Intermittent Fasting against Cancer Development and Progression: Highlighting Potential Anticancer Molecular Mechanisms


Дәйексөз келтіру

Толық мәтін

Аннотация

Background: Intermittent fasting (IF) diets have been popular since the last few decades because of their provable clinical efficiency on weight control of the subjects. These diet types are generally safe, resulting in health promoting effects against several human diseases like cardiovascular diseases, diabetes mellitus, neurogenerative disorders and cancer.

Objective: To review whether IF can act against cancer development and progression, highlighting potential anticancer molecular mechanisms in clinical studies.

Methods: Applied summarization of the available clinical studies investigating the effectiveness of IF against cancer development and progression and cancer-induced indicators. Scientific databases, e.g., PubMed, and Scopus, were comprehensively searched using relative words to identify in vivo and in vitro data, as well as clinical studies.

Results: IF seems to exert health-promoting effects in cancer patients through induction of autophagy, which enhances the in vivo suppression of tumor development, by chemotherapy. IF provokes tumors to chemotherapy and defends the normal cells from its adverse side effects, increasing the immune response. In addition, it enhances the cytotoxic CD8(+) tumor-infiltrating lymphocytes and the bone marrow lymphoid progenitor cells, delaying the cancer progression. IF reduces oxidative stress via repression of translation and induces cellular apoptosis. Fasting exerts anti-aging properties modulating the secretion of IGF-1, IGFBP-1, glucose, and insulin while, at the same time, it integrates cell adaptive responses and activates cell signaling pathways which stimulates antioxidant defenses, DNA repairment, control of protein quality, mitochondrial synthesis while decreasing inflammation.

Conclusion: IF appears to exert health promoting effects against cancer development and progression, suppressing several kinds of cancer. There are well-recognized and not well-recognized molecular processes accentuating its anticancer outcomes; however, well-designed clinical trials and further molecular studies are strongly recommended.

Авторлар туралы

Evmorfia Psara

Department of Food Science and Nutrition, University of the Aegean

Email: info@benthamscience.net

Efthymios Poulios

Department of Food Science and Nutrition, University of the Aegean

Email: info@benthamscience.net

Sousana Papadopoulou

Department of Nutritional Science and Dietetics, International Hellenic University

Email: info@benthamscience.net

Maria Tolia

Department of Radiotherapy, School of Medicine, University of Crete

Email: info@benthamscience.net

Georgios Vasios

Department of Food Science and Nutrition, University of the Aegean

Email: info@benthamscience.net

Constantinos Giaginis

Department of Food Science and Nutrition, University of the Aegean

Хат алмасуға жауапты Автор.
Email: info@benthamscience.net

Әдебиет тізімі

  1. Mandal, S.; Simmons, N.; Awan, S.; Chamari, K.; Ahmed, I. Intermittent fasting: Eating by the clock for health and exercise performance. BMJ Open Sport Exerc. Med., 2022, 8(1), e001206. doi: 10.1136/bmjsem-2021-001206 PMID: 35070352
  2. Varady, K.A.; Roohk, D.J.; McEvoy-Hein, B.K.; Gaylinn, B.D.; Thorner, M.O.; Hellerstein, M.K. Modified alternate‐day fasting regimens reduce cell proliferation rates to a similar extent as daily calorie restriction in mice. FASEB J., 2008, 22(6), 2090-2096. doi: 10.1096/fj.07-098178 PMID: 18184721
  3. Duregon, E.; Pomatto-Watson, L.C.D.D.; Bernier, M.; Price, N.L.; de Cabo, R. Intermittent fasting: From calories to time restriction. Geroscience, 2021, 43(3), 1083-1092. doi: 10.1007/s11357-021-00335-z PMID: 33686571
  4. Moro, T.; Tinsley, G.; Bianco, A.; Marcolin, G.; Pacelli, Q.F.; Battaglia, G.; Palma, A.; Gentil, P.; Neri, M.; Paoli, A. Effects of eight weeks of time-restricted feeding (16/8) on basal metabolism, maximal strength, body composition, inflammation, and cardiovascular risk factors in resistance-trained males. J. Transl. Med., 2016, 14(1), 290. doi: 10.1186/s12967-016-1044-0 PMID: 27737674
  5. Morimoto, L.M.; White, E.; Chen, Z.; Chlebowski, R.T.; Hays, J.; Kuller, L.; Lopez, A.M.; Manson, J.; Margolis, K.L.; Muti, P.C.; Stefan-ick, M.L.; McTiernan, A. Obesity, body size, and risk of postmenopausal breast cancer: The Women's Health Initiative (United States). Cancer Causes Control, 2002, 13(8), 741-751. doi: 10.1023/A:1020239211145 PMID: 12420953
  6. International Agency for Research on Cancer; World Health Organization, 2020.
  7. Nowosad, K.; Sujka, M. Effect of various types of intermittent fasting (IF) on weight loss and improvement of diabetic parameters in hu-man. Curr. Nutr. Rep., 2021, 10(2), 146-154. doi: 10.1007/s13668-021-00353-5 PMID: 33826120
  8. Wahl, D.; LaRocca, T.J. Transcriptomic effects of healthspan-promoting dietary interventions: Current evidence and future directions. Front. Nutr., 2021, 8, 712129. doi: 10.3389/fnut.2021.712129 PMID: 34447778
  9. Brandhorst, S.; Choi, I.Y.; Wei, M.; Cheng, C.W.; Sedrakyan, S.; Navarrete, G.; Dubeau, L.; Yap, L.P.; Park, R.; Vinciguerra, M.; Di Biase, S.; Mirzaei, H.; Mirisola, M.G.; Childress, P.; Ji, L.; Groshen, S.; Penna, F.; Odetti, P.; Perin, L.; Conti, P.S.; Ikeno, Y.; Kennedy, B.K.; Co-hen, P.; Morgan, T.E.; Dorff, T.B.; Longo, V.D. A periodic diet that mimics fasting promotes multi-system regeneration, enhanced cogni-tive performance, and healthspan. Cell Metab., 2015, 22(1), 86-99. doi: 10.1016/j.cmet.2015.05.012 PMID: 26094889
  10. Abdullahi Bagudu, K.; Noreen, S.; Rizwan, B.; Bashir, S.; Khan, M.; Chishti, K.; Hussain, S.; Wahid, S. Intermittent fasting effect on weight loss. Syst. Rev., 2021.
  11. Abdellatif, M.; Sedej, S.; Carmona-Gutierrez, D.; Madeo, F.; Kroemer, G. Autophagy in cardiovascular aging. Circ. Res., 2018, 123(7), 803-824. doi: 10.1161/CIRCRESAHA.118.312208 PMID: 30355077
  12. Ahmad, A.; Khan, M.U.; Aslani, P. The role of religion, spirituality and fasting in coping with diabetes among indian migrants in Australia: A qualitative exploratory study. J. Relig. Health, 2022, 61(3), 1994-2017. doi: 10.1007/s10943-021-01438-9 PMID: 34617198
  13. AlAbdan, N.A.; Almohammed, O.A.; Altukhaim, M.S.; Farooqui, M.A.; Abdalla, M.I.; Al Otaibi, H.Q.; Alshuraym, N.R.; Alghusun, S.N.; Alotaibi, L.H.; Alsayyari, A.A. Fasting during Ramadan and acute kidney injury (AKI): A retrospective, propensity matched cohort study. BMC Nephrol., 2022, 23(1), 54. doi: 10.1186/s12882-022-02674-1 PMID: 35125093
  14. Aadil, N.; Houti, I.E.; Moussamih, S. Drug intake during Ramadan. BMJ, 2004, 329(7469), 778-782. doi: 10.1136/bmj.329.7469.778 PMID: 15459052
  15. Grindrod, K.; Alsabbagh, W. Managing medications during Ramadan fasting. Can. Pharm. J., 2017, 150(3), 146-149. doi: 10.1177/1715163517700840 PMID: 28507649
  16. Longo, V.D.; Mattson, M.P. Fasting: Molecular mechanisms and clinical applications. Cell Metab., 2014, 19(2), 181-192. doi: 10.1016/j.cmet.2013.12.008 PMID: 24440038
  17. Crudele, L.; Piccinin, E.; Moschetta, A. Visceral adiposity and cancer: Role in pathogenesis and prognosis. Nutrients, 2021, 13(6), 2101. doi: 10.3390/nu13062101 PMID: 34205356
  18. Bloom, W.L. Fasting as an introduction to the treatment of obesity. Metabolism, 1959, 8(3), 214-220. PMID: 13656492
  19. Vidoni, C.; Ferraresi, A.; Esposito, A.; Maheshwari, C.; Dhanasekaran, D.N.; Mollace, V.; Isidoro, C. Calorie restriction for cancer preven-tion and therapy: Mechanisms, expectations, and efficacy. J. Cancer Prev., 2021, 26(4), 224-236. doi: 10.15430/JCP.2021.26.4.224 PMID: 35047448
  20. Schlesinger, S.; Neuenschwander, M.; Barbaresko, J.; Lang, A.; Maalmi, H.; Rathmann, W.; Roden, M.; Herder, C. Prediabetes and risk of mortality, diabetes-related complications and comorbidities: Umbrella review of meta-analyses of prospective studies. Diabetologia, 2022, 65(2), 275-285. doi: 10.1007/s00125-021-05592-3 PMID: 34718834
  21. Galati, L.; Chiocca, S.; Duca, D.; Tagliabue, M.; Simoens, C.; Gheit, T.; Arbyn, M.; Tommasino, M. HPV and head and neck cancers: Towards early diagnosis and prevention. Tumour virus Res., 2022, 14, 200245. doi: 10.1016/j.tvr.2022.200245
  22. Gouveia, H.J.C.B.; Urquiza-Martínez, M.V.; Manhães-de-Castro, R.; Costa-de-Santana, B.J.R.; Villarreal, J.P.; Mercado-Camargo, R.; Torner, L.; de Souza Aquino, J.; Toscano, A.E.; Guzmán-Quevedo, O. Effects of the treatment with flavonoids on metabolic syndrome components in humans: A systematic review focusing on mechanisms of action. Int. J. Mol. Sci., 2022, 23(15), 8344. doi: 10.3390/ijms23158344 PMID: 35955475
  23. Majewski, M.; Mertowska, P.; Mertowski, S.; Smolak, K.; Grywalska, E.; Torres, K. Microbiota and the immune system—actors in the gastric cancer story. Cancers., 2022, 14(15), 3832. doi: 10.3390/cancers14153832 PMID: 35954495
  24. Peixoto, R.D.A.; Oliveira, L.J.C.; Passarini, T.M.; Andrade, A.C.; Diniz, P.H.; Prolla, G.; Amorim, L.C.; Gil, M.; Lino, F.; Garicochea, B.; Jácome, A.; Ng, K. Vitamin D and colorectal cancer – A practical review of the literature. In: Cancer Treat. Res. Commun; , 2022; 32, p. 100616. doi: 10.1016/j.ctarc.2022.100616 PMID: 35940119
  25. Zhao, Y.; Zhao, W.; Li, J.; Lin, S.; Li, L.; Ren, Z.; Lu, J.; Xing, X.; Liu, X. Effect of dietary consumption on the survival of esophageal squamous cell carcinoma: A prospective cohort study. Eur. J. Clin. Nutr., 2022, 77(1), 55-64. doi: 10.1038/s41430-022-01194-3 PMID: 35974139
  26. Nishioka, S.; Aragane, H.; Suzuki, N.; Yoshimura, Y.; Fujiwara, D.; Mori, T.; Kanehisa, Y.; Iida, Y.; Higashi, K.; Yoshimura-Yokoi, Y.; Sato, C.; Toyota, M.; Tanaka, M.; Ishii, Y.; Kosaka, S.; Kumagae, N.; Fujimoto, A.; Omura, K.; Yoshida, S.; Wakabayashi, H.; Momosaki, R. Clinical practice guidelines for rehabilitation nutrition in cerebrovascular disease, hip fracture, cancer, and acute illness: 2020 update. Clin. Nutr. ESPEN, 2021, 43, 90-103. doi: 10.1016/j.clnesp.2021.02.018 PMID: 34024570
  27. Laviano, A. Current guidelines for nutrition therapy in cancer: The arrival of a long journey or the starting point? JPEN. J. Parenter. Enteral Nutr., 2021, 45(S2), 12-15. doi: 10.1002/jpen.2288 PMID: 34897734
  28. Fontana, L.; Villareal, D.T.; Das, S.K.; Smith, S.R.; Meydani, S.N.; Pittas, A.G.; Klein, S.; Bhapkar, M.; Rochon, J.; Ravussin, E.; Holloszy, J.O. Effects of 2‐year calorie restriction on circulating levels of IGF‐1, IGF‐binding proteins and cortisol in nonobese men and women: a randomized clinical trial. Aging Cell, 2016, 15(1), 22-27. doi: 10.1111/acel.12400 PMID: 26443692
  29. Lee, C.; Longo, V.D. Fasting vs dietary restriction in cellular protection and cancer treatment: from model organisms to patients. Oncogene, 2011, 30(30), 3305-3316. doi: 10.1038/onc.2011.91 PMID: 21516129
  30. Cignarella, F.; Cantoni, C.; Ghezzi, L.; Salter, A.; Dorsett, Y.; Chen, L.; Phillips, D.; Weinstock, G.M.; Fontana, L.; Cross, A.H.; Zhou, Y.; Piccio, L. Intermittent fasting confers protection in CNS autoimmunity by altering the gut microbiota. Cell Metab., 2018, 27(6), 1222-1235.e6. doi: 10.1016/j.cmet.2018.05.006 PMID: 29874567
  31. Kang, D.H. Oxidative stress, DNA damage, and breast cancer. AACN Clin. Issues, 2002, 13(4), 540-549. doi: 10.1097/00044067-200211000-00007 PMID: 12473916
  32. McAllister, M.J.; Pigg, B.L.; Renteria, L.I.; Waldman, H.S. Time-restricted feeding improves markers of cardiometabolic health in physi-cally active college-age men: a 4-week randomized pre-post pilot study. Nutr. Res., 2020, 75, 32-43. doi: 10.1016/j.nutres.2019.12.001 PMID: 31955013
  33. Lo Re, O.; Panebianco, C.; Porto, S.; Cervi, C.; Rappa, F.; Di Biase, S.; Caraglia, M.; Pazienza, V.; Vinciguerra, M. Fasting inhibits hepatic stellate cells activation and potentiates anti‐cancer activity of Sorafenib in hepatocellular cancer cells. J. Cell. Physiol., 2018, 233(2), 1202-1212. doi: 10.1002/jcp.25987 PMID: 28471474
  34. Shi, Y.; Felley-Bosco, E.; Marti, T.M.; Orlowski, K.; Pruschy, M.; Stahel, R.A. Starvation-induced activation of ATM/Chk2/p53 signaling sensitizes cancer cells to cisplatin. BMC Cancer, 2012, 12(1), 571. doi: 10.1186/1471-2407-12-571 PMID: 23211021
  35. Bianchi, G.; Martella, R.; Ravera, S.; Marini, C.; Capitanio, S.; Orengo, A.; Emionite, L.; Lavarello, C.; Amaro, A.; Petretto, A.; Pfeffer, U.; Sambuceti, G.; Pistoia, V.; Raffaghello, L.; Longo, V.D. Fasting induces anti-Warburg effect that increases respiration but reduces ATP-synthesis to promote apoptosis in colon cancer models. Oncotarget, 2015, 6(14), 11806-11819. doi: 10.18632/oncotarget.3688 PMID: 25909219
  36. Leite, T.C.; Watters, R.J.; Weiss, K.R.; Intini, G. Avenues of research in dietary interventions to target tumor metabolism in osteosarcoma. J. Transl. Med., 2021, 19(1), 450. doi: 10.1186/s12967-021-03122-8 PMID: 34715874
  37. Brandhorst, S.; Longo, V.D. Fasting and caloric restriction in cancer prevention and treatment. Recent Results Cancer Res., 2016, 207, 241-266. doi: 10.1007/978-3-319-42118-6_12
  38. Greer, E.L.; Dowlatshahi, D.; Banko, M.R.; Villen, J.; Hoang, K.; Blanchard, D.; Gygi, S.P.; Brunet, A. An AMPK-FOXO pathway mediates longevity induced by a novel method of dietary restriction in C. elegans. Curr. Biol., 2007, 17(19), 1646-1656. doi: 10.1016/j.cub.2007.08.047 PMID: 17900900
  39. Lee, S.J.; Murphy, C.T.; Kenyon, C. Glucose shortens the life span of C. elegans by downregulating DAF-16/FOXO activity and aquaporin gene expression. Cell Metab., 2009, 10(5), 379-391. doi: 10.1016/j.cmet.2009.10.003 PMID: 19883616
  40. Han, Y.M.; Ramprasath, T.; Zou, M.H. β-hydroxybutyrate and its metabolic effects on age-associated pathology. Exp. Mol. Med., 2020, 52(4), 548-555. doi: 10.1038/s12276-020-0415-z PMID: 32269287
  41. Cantó, C.; Auwerx, J. Calorie restriction: Is AMPK a key sensor and effector? Physiology, 2011, 26(4), 214-224. doi: 10.1152/physiol.00010.2011 PMID: 21841070
  42. Ruderman, N.B.; Julia, Xu X.; Nelson, L.; Cacicedo, J.M.; Saha, A.K.; Lan, F.; Ido, Y. AMPK and SIRT1: A long-standing partnership? Am. J. Physiol. Endocrinol. Metab., 2010, 298(4), E751-E760. doi: 10.1152/ajpendo.00745.2009 PMID: 20103737
  43. Zhang, Y.; Wang, X.; Zhou, M.; Kang, C.; Lang, H.; Chen, M.; Hui, S.; Wang, B.; Mi, M. Crosstalk between gut microbiota and Sirtuin-3 in colonic inflammation and tumorigenesis. Exp. Mol. Med., 2018, 50(4), 1-11. doi: 10.1038/s12276-017-0002-0 PMID: 29650970
  44. Poulose, N.; Raju, R. Sirtuin regulation in aging and injury. Biochim. Biophys. Acta Mol. Basis Dis., 2015, 1852(11), 2442-2455. doi: 10.1016/j.bbadis.2015.08.017 PMID: 26303641
  45. Nagpal, R.; Mainali, R.; Ahmadi, S.; Wang, S.; Singh, R.; Kavanagh, K.; Kitzman, D.W.; Kushugulova, A.; Marotta, F.; Yadav, H. Gut mi-crobiome and aging: Physiological and mechanistic insights. Nutr. Healthy Aging, 2018, 4(4), 267-285. doi: 10.3233/NHA-170030 PMID: 29951588
  46. Lakhan, S.E.; Kirchgessner, A. Gut microbiota and sirtuins in obesity-related inflammation and bowel dysfunction. J. Transl. Med., 2011, 9(1), 202. doi: 10.1186/1479-5876-9-202 PMID: 22115311
  47. Makwana, K.; Patel, S.A.; Velingkaar, N.; Ebron, J.S.; Shukla, G.C.; Kondratov, R.V. Aging and calorie restriction regulate the expression of miR-125a-5p and its target genes Stat3, Casp2 and Stard13. Aging, 2017, 9(7), 1825-1843. doi: 10.18632/aging.101270 PMID: 28783714
  48. Pietrocola, F.; Pol, J.; Vacchelli, E.; Rao, S.; Enot, D.P.; Baracco, E.E.; Levesque, S.; Castoldi, F.; Jacquelot, N.; Yamazaki, T.; Senovilla, L.; Marino, G.; Aranda, F.; Durand, S.; Sica, V.; Chery, A.; Lachkar, S.; Sigl, V.; Bloy, N.; Buque, A.; Falzoni, S.; Ryffel, B.; Apetoh, L.; Di Virgilio, F.; Madeo, F.; Maiuri, M.C.; Zitvogel, L.; Levine, B.; Penninger, J.M.; Kroemer, G. Caloric restriction mimetics enhance anti-cancer immunosurveillance. Cancer Cell, 2016, 30(1), 147-160. doi: 10.1016/j.ccell.2016.05.016 PMID: 27411589
  49. Safdie, F.M.; Dorff, T.; Quinn, D.; Fontana, L.; Wei, M.; Lee, C.; Cohen, P.; Longo, V.D. Fasting and cancer treatment in humans: A case series report. Aging, 2009, 1(12), 988-1007. doi: 10.18632/aging.100114 PMID: 20157582
  50. Lee, C.; Safdie, F.M.; Raffaghello, L.; Wei, M.; Madia, F.; Parrella, E.; Hwang, D.; Cohen, P.; Bianchi, G.; Longo, V.D. Reduced levels of IGF-I mediate differential protection of normal and cancer cells in response to fasting and improve chemotherapeutic index. Cancer Res., 2010, 70(4), 1564-1572. doi: 10.1158/0008-5472.CAN-09-3228 PMID: 20145127
  51. Yakar, S.; Liu, J.L.; Stannard, B.; Butler, A.; Accili, D.; Sauer, B.; LeRoith, D. Normal growth and development in the absence of hepatic insulin-like growth factor I. Proc. Natl. Acad. Sci., 1999, 96(13), 7324-7329. doi: 10.1073/pnas.96.13.7324 PMID: 10377413
  52. Kari, F.W.; Dunn, S.E.; French, J.E.; Barrett, J.C. Roles for insulin-like growth factor-1 in mediating the anti-carcinogenic effects of caloric restriction. J. Nutr. Health Aging, 1999, 3(2), 92-101. PMID: 10885804
  53. Chang, S.; Hursting, S.D.; Contois, J.H.; Strom, S.S.; Yamamura, Y.; Babaian, R.J.; Troncoso, P.; Scardino, P.T.; Wheeler, T.M.; Amos, C.I.; Spitz, M.R. Leptin and prostate cancer. Prostate, 2001, 46(1), 62-67. doi: 10.1002/1097-0045(200101)46:1<62:AID-PROS1009>3.0.CO;2-V PMID: 11170133
  54. Cadoni, E.; Marongiu, F.; Fanti, M.; Serra, M.; Laconi, E. Caloric restriction delays early phases of carcinogenesis via effects on the tissue microenvironment. Oncotarget, 2017, 8(22), 36020-36032. doi: 10.18632/oncotarget.16421 PMID: 28415598
  55. Sharma, H.S.; Nyberg, F.; Gordh, T.; Alm, P.; Westman, J. Neurotrophic factors influence upregulation of constitutive isoform of heme oxygenase and cellular stress response in the spinal cord following trauma. Amino Acids, 2000, 19(1), 351-361. doi: 10.1007/s007260070066 PMID: 11026506
  56. Kozal, K.; Jóźwiak, P.; Krześlak, A. Contemporary perspectives on the warburg effect inhibition in cancer therapy. Cancer Contr., 2021, 28. doi: 10.1177/10732748211041243 PMID: 34554006
  57. Strickaert, A.; Saiselet, M.; Dom, G.; De Deken, X.; Dumont, J.E.; Feron, O.; Sonveaux, P.; Maenhaut, C. Cancer heterogeneity is not com-patible with one unique cancer cell metabolic map. Oncogene, 2017, 36(19), 2637-2642. doi: 10.1038/onc.2016.411 PMID: 27797377
  58. Sun, P.; Wang, H.; He, Z.; Chen, X.; Wu, Q.; Chen, W.; Sun, Z.; Weng, M.; Zhu, M.; Ma, D.; Miao, C. Fasting inhibits colorectal cancer growth by reducing M2 polarization of tumor-associated macrophages. Oncotarget, 2017, 8(43), 74649-74660. doi: 10.18632/oncotarget.20301 PMID: 29088814
  59. Zhou, L.; Zhang, Z.; Nice, E.; Huang, C.; Zhang, W.; Tang, Y. Circadian rhythms and cancers: The intrinsic links and therapeutic poten-tials. J. Hematol. Oncol., 2022, 15(1), 21. doi: 10.1186/s13045-022-01238-y PMID: 35246220
  60. Cathcart, P.; Craddock, C.; Stebbing, J. Fasting: Starving cancer. Lancet Oncol., 2017, 18(4), 431. doi: 10.1016/S1470-2045(17)30196-1 PMID: 28368246
  61. Salvadori, G.; Mirisola, M.G.; Longo, V.D. Intermittent and periodic fasting, hormones, and cancer prevention. Cancers, 2021, 13(18), 4587. doi: 10.3390/cancers13184587 PMID: 34572814
  62. Cheng, C.W.; Adams, G.B.; Perin, L.; Wei, M.; Zhou, X.; Lam, B.S.; Da Sacco, S.; Mirisola, M.; Quinn, D.I.; Dorff, T.B.; Kopchick, J.J.; Longo, V.D. Prolonged fasting reduces IGF-1/PKA to promote hematopoietic-stem-cell-based regeneration and reverse immunosuppres-sion. Cell Stem Cell, 2014, 14(6), 810-823. doi: 10.1016/j.stem.2014.04.014 PMID: 24905167
  63. Di Biase, S.; Lee, C.; Brandhorst, S.; Manes, B.; Buono, R.; Cheng, C.W.; Cacciottolo, M.; Martin-Montalvo, A.; de Cabo, R.; Wei, M.; Morgan, T.E.; Longo, V.D. Fasting-mimicking diet reduces HO-1 to promote T cell-mediated tumor cytotoxicity. Cancer Cell, 2016, 30(1), 136-146. doi: 10.1016/j.ccell.2016.06.005 PMID: 27411588
  64. Jardé, T.; Perrier, S.; Vasson, M.P.; Caldefie-Chézet, F. Molecular mechanisms of leptin and adiponectin in breast cancer. Eur. J. Cancer, 2011, 47(1), 33-43. doi: 10.1016/j.ejca.2010.09.005 PMID: 20889333
  65. Shim, H.S.; Wei, M.; Brandhorst, S.; Longo, V.D. Starvation promotes REV1 SUMOylation and p53-dependent sensitization of melanoma and breast cancer cells. Cancer Res., 2015, 75(6), 1056-1067. doi: 10.1158/0008-5472.CAN-14-2249 PMID: 25614517
  66. Di Biase, S.; Shim, H.S.; Kim, K.H.; Vinciguerra, M.; Rappa, F.; Wei, M.; Brandhorst, S.; Cappello, F.; Mirzaei, H.; Lee, C.; Longo, V.D. Correction: Fasting regulates EGR1 and protects from glucose- and dexamethasone-dependent sensitization to chemotherapy. PLoS Biol., 2017, 15(5), e1002603. doi: 10.1371/journal.pbio.1002603 PMID: 28459830
  67. Andrikopoulos, S.; Blair, A.R.; Deluca, N.; Fam, B.C.; Proietto, J. Evaluating the glucose tolerance test in mice. Am. J. Physiol. Endocrinol. Metab., 2008, 295(6), E1323-E1332. doi: 10.1152/ajpendo.90617.2008 PMID: 18812462
  68. Di Biase, S.; Longo, V.D. Fasting-induced differential stress sensitization in cancer treatment. Mol. Cell. Oncol., 2016, 3(3), e1117701. doi: 10.1080/23723556.2015.1117701 PMID: 27314084
  69. Faris, A.I.E.; Kacimi, S.; Al-Kurd, R.A.; Fararjeh, M.A.; Bustanji, Y.K.; Mohammad, M.K.; Salem, M.L. Intermittent fasting during Rama-dan attenuates proinflammatory cytokines and immune cells in healthy subjects. Nutr. Res., 2012, 32(12), 947-955. doi: 10.1016/j.nutres.2012.06.021 PMID: 23244540
  70. Esposito, K.; Chiodini, P.; Capuano, A.; Bellastella, G.; Maiorino, M.I.; Rafaniello, C.; Giugliano, D. Metabolic syndrome and postmeno-pausal breast cancer. Menopause, 2013, 20(12), 1301-1309. doi: 10.1097/GME.0b013e31828ce95d PMID: 23571527
  71. Hikita, H.; Nuwaysir, E.F.; Vaughan, J.; Babcock, K.; Haas, M.J.; Dragan, Y.P.; Pitot, H.C. The effect of short-term fasting, phenobarbital and refeeding on apoptotic loss, cell replication and gene expression in rat liver during the promotion stage. Carcinogenesis, 1998, 19(8), 1417-1425. doi: 10.1093/carcin/19.8.1417 PMID: 9744538
  72. Thakkar, N.; Shin, Y.B.; Sung, H.K. Nutritional regulation of mammary tumor microenvironment. Front. Cell Dev. Biol., 2022, 10, 803280. doi: 10.3389/fcell.2022.803280 PMID: 35186923
  73. Kim, K.H.; Kim, Y.H.; Son, J.E.; Lee, J.H.; Kim, S.; Choe, M.S.; Moon, J.H.; Zhong, J.; Fu, K.; Lenglin, F.; Yoo, J.A.; Bilan, P.J.; Klip, A.; Nagy, A.; Kim, J.R.; Park, J.G.; Hussein, S.M.I.; Doh, K.O.; Hui, C.; Sung, H.K. Intermittent fasting promotes adipose thermogenesis and metabolic homeostasis via VEGF-mediated alternative activation of macrophage. Cell Res., 2017, 27(11), 1309-1326. doi: 10.1038/cr.2017.126 PMID: 29039412
  74. Nencioni, A.; Caffa, I.; Cortellino, S.; Longo, V.D. Fasting and cancer: Molecular mechanisms and clinical application. Nat. Rev. Cancer, 2018, 18(11), 707-719. doi: 10.1038/s41568-018-0061-0 PMID: 30327499
  75. Lee, C.; Raffaghello, L.; Brandhorst, S.; Safdie, F.M.; Bianchi, G.; Martin-Montalvo, A.; Pistoia, V.; Wei, M.; Hwang, S.; Merlino, A.; Emi-onite, L.; de Cabo, R.; Longo, V.D. Fasting cycles retard growth of tumors and sensitize a range of cancer cell types to chemotherapy. Sci. Transl. Med., 2012, 4(124), 124ra27. doi: 10.1126/scitranslmed.3003293 PMID: 22323820
  76. Wilson, R.L.; Kang, D.W.; Christopher, C.N.; Crane, T.E.; Dieli-Conwright, C.M. Fasting and exercise in oncology: Potential synergism of combined interventions. Nutrients, 2021, 13(10), 3421. doi: 10.3390/nu13103421 PMID: 34684421
  77. Jaspers, R.T.; Zillikens, M.C.; Friesema, E.C.H.; Paoli, G.; Bloch, W.; Uitterlinden, A.G.; Goglia, F.; Lanni, A.; Lange, P. Exercise, fasting, and mimetics: Toward beneficial combinations? FASEB J., 2017, 31(1), 14-28. doi: 10.1096/fj.201600652r PMID: 27729415
  78. Newman, J.C.; Verdin, E. Ketone bodies as signaling metabolites. Trends Endocrinol. Metab., 2014, 25(1), 42-52. doi: 10.1016/j.tem.2013.09.002 PMID: 24140022
  79. Sulli, G.; Lam, M.T.Y.; Panda, S. Interplay between circadian clock and cancer: New frontiers for cancer treatment. Trends Cancer, 2019, 5(8), 475-494. doi: 10.1016/j.trecan.2019.07.002 PMID: 31421905
  80. Nicolò, E.; Trapani, D.; Berton Giachetti, P.P.M.; Zagami, P.; Curigliano, G. Fed or fasted state for oral therapies in breast cancer treat-ment? A comprehensive review of clinical practice recommendations. Cancer Treat. Rev., 2021, 100, 102281. doi: 10.1016/j.ctrv.2021.102281 PMID: 34500366
  81. Caffa, I.; D'Agostino, V.; Damonte, P.; Soncini, D.; Cea, M.; Monacelli, F.; Odetti, P.; Ballestrero, A.; Provenzani, A.; Longo, V.D.; Nencioni, A. Fasting potentiates the anticancer activity of tyrosine kinase inhibitors by strengthening MAPK signaling inhibition. Oncotarget, 2015, 6(14), 11820-11832. doi: 10.18632/oncotarget.3689 PMID: 25909220
  82. Lu, Z.; Xie, J.; Wu, G.; Shen, J.; Collins, R.; Chen, W.; Kang, X.; Luo, M.; Zou, Y.; Huang, L.J.S.; Amatruda, J.F.; Slone, T.; Winick, N.; Scherer, P.E.; Zhang, C.C. Fasting selectively blocks development of acute lymphoblastic leukemia via leptin-receptor upregulation. Nat. Med., 2017, 23(1), 79-90. doi: 10.1038/nm.4252 PMID: 27941793
  83. Phadngam, S.; Castiglioni, A.; Ferraresi, A.; Morani, F.; Follo, C.; Isidoro, C. PTEN dephosphorylates AKT to prevent the expression of GLUT1 on plasmamembrane and to limit glucose consumption in cancer cells. Oncotarget, 2016, 7(51), 84999-85020. doi: 10.18632/oncotarget.13113 PMID: 27829222
  84. Sundaram, S.; Yan, L. Time-restricted feeding mitigates high-fat diet-enhanced mammary tumorigenesis in MMTV-PyMT mice. Nutr. Res., 2018, 59, 72-79. doi: 10.1016/j.nutres.2018.07.014 PMID: 30442235
  85. Macis, D.; Guerrieri-Gonzaga, A.; Gandini, S. Circulating adiponectin and breast cancer risk: A systematic review and meta-analysis. Int. J. Epidemiol., 2014, 43(4), 1226-1236. doi: 10.1093/ije/dyu088 PMID: 24737805
  86. Palhinha, L.; Liechocki, S.; Hottz, E.D.; Pereira, J.A.S.; de Almeida, C.J.; Moraes-Vieira, P.M.M.; Bozza, P.T.; Maya-Monteiro, C.M. Lep-tin induces proadipogenic and proinflammatory signaling in adipocytes. Front. Endocrinol., 2019, 10, 841. doi: 10.3389/fendo.2019.00841 PMID: 31920961
  87. Sierra-Honigmann, M.R.; Nath, A.K.; Murakami, C.; García-Cardeña, G.; Papapetropoulos, A.; Sessa, W.C.; Madge, L.A.; Schechner, J.S.; Schwabb, M.B.; Polverini, P.J.; Flores-Riveros, J.R. Biological action of leptin as an angiogenic factor. Science, 1998, 281(5383), 1683-1686. doi: 10.1126/science.281.5383.1683 PMID: 9733517
  88. Cao, H.; Huang, Y.; Wang, L.; Wang, H.; Pang, X.; Li, K.; Dang, W.; Tang, H.; Wei, L.; Su, M.; Tang, C.; Chen, T. Leptin promotes migra-tion and invasion of breast cancer cells by stimulating IL-8 production in M2 macrophages. Oncotarget, 2016, 7(40), 65441-65453. doi: 10.18632/oncotarget.11761 PMID: 27588409
  89. Goodwin, P.J.; Ennis, M.; Fantus, I.G.; Pritchard, K.I.; Trudeau, M.E.; Koo, J.; Hood, N. Is leptin a mediator of adverse prognostic effects of obesity in breast cancer? J. Clin. Oncol., 2005, 23(25), 6037-6042. doi: 10.1200/JCO.2005.02.048 PMID: 16135472
  90. Delort, L.; Rossary, A.; Farges, M.C.; Vasson, M.P.; Caldefie-Chézet, F. Leptin, adipocytes and breast cancer: Focus on inflammation and anti-tumor immunity. Life Sci., 2015, 140, 37-48. doi: 10.1016/j.lfs.2015.04.012 PMID: 25957709
  91. Weng, M.; Chen, W.; Chen, X.; Lu, H.; Sun, Z.; Yu, Q.; Sun, P.; Xu, Y.; Zhu, M.; Jiang, N.; Zhang, J.; Zhang, J.; Song, Y.; Ma, D.; Zhang, X.; Miao, C. Fasting inhibits aerobic glycolysis and proliferation in colorectal cancer via the Fdft1-mediated AKT/mTOR/HIF1α pathway suppression. Nat. Commun., 2020, 11(1), 1869. doi: 10.1038/s41467-020-15795-8 PMID: 32313017
  92. Yun, C.; Lee, S. The roles of autophagy in cancer. Int. J. Mol. Sci., 2018, 19(11), 3466. doi: 10.3390/ijms19113466 PMID: 30400561
  93. Chung, S.J.; Nagaraju, G.P.; Nagalingam, A.; Muniraj, N.; Kuppusamy, P.; Walker, A.; Woo, J.; Győrffy, B.; Gabrielson, E.; Saxena, N.K.; Sharma, D. ADIPOQ/adiponectin induces cytotoxic autophagy in breast cancer cells through STK11/LKB1-mediated activation of the AMPK-ULK1 axis. Autophagy, 2017, 13(8), 1386-1403. doi: 10.1080/15548627.2017.1332565 PMID: 28696138
  94. Bachelot, T.; Ray-Coquard, I.; Menetrier-Caux, C.; Rastkha, M.; Duc, A.; Blay, J-Y. Prognostic value of serum levels of interleukin 6 and of serum and plasma levels of vascular endothelial growth factor in hormone-refractory metastatic breast cancer patients. Br. J. Cancer, 2003, 88(11), 1721-1726. doi: 10.1038/sj.bjc.6600956 PMID: 12771987
  95. Weisberg, S.P.; McCann, D.; Desai, M.; Rosenbaum, M.; Leibel, R.L.; Ferrante, A.W., Jr Obesity is associated with macrophage accumula-tion in adipose tissue. J. Clin. Invest., 2003, 112(12), 1796-1808. doi: 10.1172/JCI200319246 PMID: 14679176
  96. Lumeng, C.N.; Bodzin, J.L.; Saltiel, A.R. Obesity induces a phenotypic switch in adipose tissue macrophage polarization. J. Clin. Invest., 2007, 117(1), 175-184. doi: 10.1172/JCI29881 PMID: 17200717
  97. Shivappa, N.; Hébert, J.R.; Rietzschel, E.R.; De Buyzere, M.L.; Langlois, M.; Debruyne, E.; Marcos, A.; Huybrechts, I. Associations be-tween dietary inflammatory index and inflammatory markers in the Asklepios Study. Br. J. Nutr., 2015, 113(4), 665-671. doi: 10.1017/S000711451400395X PMID: 25639781
  98. Yeung, C.Y.; Tso, A.W.K.; Xu, A.; Wang, Y.; Woo, Y.C.; Lam, T.H.; Lo, S.V.; Fong, C.H.Y.; Wat, N.M.S.; Woo, J.; Cheung, B.M.Y.; Lam, K.S.L. Pro-inflammatory adipokines as predictors of incident cancers in a Chinese cohort of low obesity prevalence in Hong Kong. PLoS One, 2013, 8(10), e78594. doi: 10.1371/journal.pone.0078594 PMID: 24205276
  99. Kim, J.; Guan, K.L. Amino acid signaling in TOR activation. Annu. Rev. Biochem., 2011, 80(1), 1001-1032. doi: 10.1146/annurev-biochem-062209-094414 PMID: 21548787
  100. Christensen, R.A.G.; Kirkham, A.A. Time-restricted eating: A novel and simple dietary intervention for primary and secondary prevention of breast cancer and cardiovascular disease. Nutrients, 2021, 13(10), 3476. doi: 10.3390/nu13103476 PMID: 34684476
  101. Zeng, Q.; Dong, S.Y.; Sun, X.N.; Xie, J.; Cui, Y. Percent body fat is a better predictor of cardiovascular risk factors than body mass index. Braz. J. Med. Biol. Res., 2012, 45(7), 591-600. doi: 10.1590/S0100-879X2012007500059 PMID: 22510779
  102. Vance, V.; Mourtzakis, M.; McCargar, L.; Hanning, R. Weight gain in breast cancer survivors: prevalence, pattern and health consequenc-es. Obes. Rev., 2011, 12(4), 282-294. doi: 10.1111/j.1467-789X.2010.00805.x PMID: 20880127
  103. Gabel, K.; Varady, K.A. Current research: Effect of time restricted eating on weight and cardiometabolic health. J. Physiol., 2022, 600(6), 1313-1326. doi: 10.1113/JP280542 PMID: 33002219
  104. Wilkinson, M.J.; Manoogian, E.N.C.; Zadourian, A.; Lo, H.; Fakhouri, S.; Shoghi, A.; Wang, X.; Fleischer, J.G.; Navlakha, S.; Panda, S.; Taub, P.R. Ten-hour time-restricted eating reduces weight, blood pressure, and atherogenic lipids in patients with metabolic syndrome. Cell Metab., 2020, 31(1), 92-104.e5. doi: 10.1016/j.cmet.2019.11.004 PMID: 31813824
  105. Caffa, I.; Spagnolo, V.; Vernieri, C.; Valdemarin, F.; Becherini, P.; Wei, M.; Brandhorst, S.; Zucal, C.; Driehuis, E.; Ferrando, L.; Piacente, F.; Tagliafico, A.; Cilli, M.; Mastracci, L.; Vellone, V.G.; Piazza, S.; Cremonini, A.L.; Gradaschi, R.; Mantero, C.; Passalacqua, M.; Ballestrero, A.; Zoppoli, G.; Cea, M.; Arrighi, A.; Odetti, P.; Monacelli, F.; Salvadori, G.; Cortellino, S.; Clevers, H.; De Braud, F.; Sukkar, S.G.; Provenzani, A.; Longo, V.D.; Nencioni, A. Fasting-mimicking diet and hormone therapy induce breast cancer regression. Nature, 2020, 583(7817), 620-624. doi: 10.1038/s41586-020-2502-7 PMID: 32669709
  106. DeVita, V.T.; Steven, A.R. MD DeVita, Hellman, and Rosenberg's Cancer: Principles & Practice of Oncology (Cancer Principles and Practice of Oncology), 11th Edition; , 2019.
  107. Pinho, C.P.S.; Diniz, A.S.; Arruda, I.K.G.; Leite, A.P.D.L.; Rodrigues, I.G. Effects of weight loss on adipose visceral and subcutaneous tissue in overweight adults. Clin. Nutr., 2018, 37(4), 1252-1258. doi: 10.1016/j.clnu.2017.05.011 PMID: 28571712
  108. Bauersfeld, S.P.; Kessler, C.S.; Wischnewsky, M.; Jaensch, A.; Steckhan, N.; Stange, R.; Kunz, B.; Brückner, B.; Sehouli, J.; Michalsen, A. The effects of short-term fasting on quality of life and tolerance to chemotherapy in patients with breast and ovarian cancer: A randomized cross-over pilot study. BMC Cancer, 2018, 18(1), 476. doi: 10.1186/s12885-018-4353-2 PMID: 29699509
  109. Dorff, T.B.; Groshen, S.; Garcia, A.; Shah, M.; Tsao-Wei, D.; Pham, H.; Cheng, C.W.; Brandhorst, S.; Cohen, P.; Wei, M.; Longo, V.; Quinn, D.I. Safety and feasibility of fasting in combination with platinum-based chemotherapy. BMC Cancer, 2016, 16(1), 360. doi: 10.1186/s12885-016-2370-6 PMID: 27282289
  110. Smith, W.J.; Underwood, L.E.; Clemmons, D.R. Effects of caloric or protein restriction on insulin-like growth factor-I (IGF-I) and IGF-binding proteins in children and adults. J. Clin. Endocrinol. Metab., 1995, 80(2), 443-449. doi: 10.1210/jcem.80.2.7531712 PMID: 7531712
  111. de Groot, S.; Vreeswijk, M.P.G.; Welters, M.J.P.; Gravesteijn, G.; Boei, J.J.W.A.; Jochems, A.; Houtsma, D.; Putter, H.; van der Hoeven, J.J.M.; Nortier, J.W.R.; Pijl, H.; Kroep, J.R. The effects of short-term fasting on tolerance to (neo) adjuvant chemotherapy in HER2-negative breast cancer patients: A randomized pilot study. BMC Cancer, 2015, 15(1), 652. doi: 10.1186/s12885-015-1663-5 PMID: 26438237
  112. Chan, L.N.; Chen, Z.; Braas, D.; Lee, J.W.; Xiao, G.; Geng, H.; Cosgun, K.N.; Hurtz, C.; Shojaee, S.; Cazzaniga, V.; Schjerven, H.; Ernst, T.; Hochhaus, A.; Kornblau, S.M.; Konopleva, M.; Pufall, M.A.; Cazzaniga, G.; Liu, G.J.; Milne, T.A.; Koeffler, H.P.; Ross, T.S.; Sánchez-García, I.; Borkhardt, A.; Yamamoto, K.R.; Dickins, R.A.; Graeber, T.G.; Müschen, M. Metabolic gatekeeper function of B-lymphoid tran-scription factors. Nature, 2017, 542(7642), 479-483. doi: 10.1038/nature21076 PMID: 28192788
  113. Dupertuis, Y.M.; Meguid, M.M.; Pichard, C. Colon cancer therapy: New perspectives of nutritional manipulations using polyunsaturated fatty acids. Curr. Opin. Clin. Nutr. Metab. Care, 2007, 10(4), 427-432. doi: 10.1097/MCO.0b013e3281e2c9d4 PMID: 17563460
  114. Scheim, D.E. Cytotoxicity of unsaturated fatty acids in fresh human tumor explants: concentration thresholds and implications for clinical efficacy. Lipids Health Dis., 2009, 8(1), 54. doi: 10.1186/1476-511X-8-54 PMID: 20003514
  115. Comba, A.; Lin, Y.H.; Eynard, A.R.; Valentich, M.A.; Fernandez-Zapico, M.E.; Pasqualini, M.E. Basic aspects of tumor cell fatty acid-regulated signaling and transcription factors. Cancer Metastasis Rev., 2011, 30(3-4), 325-342. doi: 10.1007/s10555-011-9308-x PMID: 22048864
  116. Dashti, S.G.; Simpson, J.A.; Viallon, V.; Karahalios, A.; Moreno-Betancur, M.; Brasky, T.; Pan, K.; Rohan, T.E.; Shadyab, A.H.; Thom-son, C.A.; Wild, R.A.; Wassertheil-Smoller, S.; Ho, G.Y.F.; Strickler, H.D.; English, D.R.; Gunter, M.J. Adiposity and breast, endometrial, and colorectal cancer risk in postmenopausal women: Quantification of the mediating effects of leptin, C‐reactive protein, fasting insulin, and estradiol. Cancer Med., 2022, 11(4), 1145-1159. doi: 10.1002/cam4.4434 PMID: 35048536
  117. Safdie, F.; Brandhorst, S.; Wei, M.; Wang, W.; Lee, C.; Hwang, S.; Conti, P.S.; Chen, T.C.; Longo, V.D. Fasting enhances the response of glioma to chemo- and radiotherapy. PLoS One, 2012, 7(9), e44603. doi: 10.1371/journal.pone.0044603 PMID: 22984531
  118. Raffaghello, L.; Lee, C.; Safdie, F.M.; Wei, M.; Madia, F.; Bianchi, G.; Longo, V.D. Starvation-dependent differential stress resistance protects normal but not cancer cells against high-dose chemotherapy. Proc. Natl. Acad. Sci., 2008, 105(24), 8215-8220. doi: 10.1073/pnas.0708100105 PMID: 18378900
  119. Marsh, J.; Mukherjee, P.; Seyfried, T.N. Akt-dependent proapoptotic effects of dietary restriction on late-stage management of a phospha-tase and tensin homologue/tuberous sclerosis complex 2-deficient mouse astrocytoma. Clin. Cancer Res., 2008, 14(23), 7751-7762. doi: 10.1158/1078-0432.CCR-08-0213 PMID: 19047102
  120. Ajona, D.; Ortiz-Espinosa, S.; Lozano, T.; Exposito, F.; Calvo, A.; Valencia, K.; Redrado, M.; Remírez, A.; Lecanda, F.; Alignani, D.; Lasarte, J.J.; Macaya, I.; Senent, Y.; Bértolo, C.; Sainz, C.; Gil-Bazo, I.; Eguren-Santamaría, I.; Lopez-Picazo, J.M.; Gonzalez, A.; Perez-Gracia, J.L.; de Andrea, C.E.; Vicent, S.; Sanmamed, M.F.; Montuenga, L.M.; Pio, R. Short-term starvation reduces IGF-1 levels to sensi-tize lung tumors to PD-1 immune checkpoint blockade. Nat. Can., 2020, 1(1), 75-85. doi: 10.1038/s43018-019-0007-9 PMID: 35121837
  121. Chen, H.; Zhang, H.; Cao, L.; Cui, J.; Ma, X.; Zhao, C.; Yin, S.; Hu, H. Glucose limitation sensitizes cancer cells to selenite-induced cyto-toxicity via slc7a11-mediated redox collapse. Cancers, 2022, 14(2), 345. doi: 10.3390/cancers14020345 PMID: 35053507
  122. Wang, X.; Xu, W.; Hu, X.; Yang, X.; Zhang, M. The prognostic role of glycemia in patients with pancreatic carcinoma: A systematic review and meta-analysis. Front. Oncol., 2022, 12, 780909. doi: 10.3389/fonc.2022.780909 PMID: 35223469
  123. Cheon, Y.K.; Koo, J.K.; Lee, Y.S.; Lee, T.Y.; Shim, C.S. Elevated hemoglobin A1c levels are associated with worse survival in advanced pancreatic cancer patients with diabetes. Gut Liver, 2014, 8(2), 205-214. doi: 10.5009/gnl.2014.8.2.205 PMID: 24672663
  124. Gapstur, S.M.; Gann, P.H.; Lowe, W.; Liu, K.; Colangelo, L.; Dyer, A. Abnormal glucose metabolism and pancreatic cancer mortality. JAMA, 2000, 283(19), 2552-2558. doi: 10.1001/jama.283.19.2552 PMID: 10815119
  125. D'Aronzo, M.; Vinciguerra, M.; Mazza, T.; Panebianco, C.; Saracino, C.; Pereira, S.P.; Graziano, P.; Pazienza, V. Fasting cycles potentiate the efficacy of gemcitabine treatment in in vitro and in vivo pancreatic cancer models. Oncotarget, 2015, 6(21), 18545-18557. doi: 10.18632/oncotarget.4186 PMID: 26176887
  126. Tinkum, K.L.; Stemler, K.M.; White, L.S.; Loza, A.J.; Jeter-Jones, S.; Michalski, B.M.; Kuzmicki, C.; Pless, R.; Stappenbeck, T.S.; Piwni-ca-Worms, D.; Piwnica-Worms, H. Fasting protects mice from lethal DNA damage by promoting small intestinal epithelial stem cell sur-vival. Proc. Natl. Acad. Sci., 2015, 112(51), E7148-E7154. doi: 10.1073/pnas.1509249112 PMID: 26644583
  127. Murphy, N.; Song, M.; Papadimitriou, N.; Carreras-Torres, R.; Langenberg, C.; Martin, R.M.; Tsilidis, K.K.; Barroso, I.; Chen, J.; Frayling, T.M.; Bull, C.J.; Vincent, E.E.; Cotterchio, M.; Gruber, S.B.; Pai, R.K.; Newcomb, P.A.; Perez-Cornago, A.; van Duijnhoven, F.J.B.; Van Guelpen, B.; Vodicka, P.; Wolk, A.; Wu, A.H.; Peters, U.; Chan, A.T.; Gunter, M.J. Associations between glycemic traits and colorectal cancer: A mendelian randomization analysis. J. Natl. Cancer Inst., 2022, 114(5), 740-752. doi: 10.1093/jnci/djac011 PMID: 35048991
  128. Joshi, R.K.; Kim, W.J.; Lee, S-A. Association between obesity-related adipokines and colorectal cancer: A case-control study and meta-analysis. World J. Gastroenterol., 2014, 20(24), 7941-7949. doi: 10.3748/wjg.v20.i24.7941 PMID: 24976730
  129. Su, J.; Wang, Y.; Zhang, X.; Ma, M.; Xie, Z.; Pan, Q.; Ma, Z.; Peppelenbosch, M.P. Remodeling of the gut microbiome during Ramadan-associated intermittent fasting. Am. J. Clin. Nutr., 2021, 113(5), 1332-1342. doi: 10.1093/ajcn/nqaa388 PMID: 33842951
  130. Su, J.; Braat, H.; Peppelenbosch, M.P. Gut microbiota-derived propionate production may explain beneficial effects of intermittent fasting in experimental colitis. J. Crohn's Colitis, 2021, 15(6), 1081-1082. doi: 10.1093/ecco-jcc/jjaa248 PMID: 33277656
  131. Bian, X.; Wu, W.; Yang, L.; Lv, L.; Wang, Q.; Li, Y.; Ye, J.; Fang, D.; Wu, J.; Jiang, X.; Shi, D.; Li, L. Administration of Akkermansia mu-ciniphila ameliorates dextran sulfate sodium-induced ulcerative colitis in mice. Front. Microbiol., 2019, 10, 2259. doi: 10.3389/fmicb.2019.02259 PMID: 31632373
  132. Wang, L.; Tang, L.; Feng, Y.; Zhao, S.; Han, M.; Zhang, C.; Yuan, G.; Zhu, J.; Cao, S.; Wu, Q.; Li, L.; Zhang, Z. A purified membrane protein from Akkermansia muciniphila or the pasteurised bacterium blunts colitis associated tumourigenesis by modulation of CD8+ T cells in mice. Gut, 2020, 69(11), 1988-1997. doi: 10.1136/gutjnl-2019-320105 PMID: 32169907
  133. Hou, X.; Zhang, P.; Du, H.; Chu, W.; Sun, R.; Qin, S.; Tian, Y.; Zhang, Z.; Xu, F. Akkermansia Muciniphila potentiates the antitumor effi-cacy of FOLFOX in colon cancer. Front. Pharmacol., 2021, 12, 725583. doi: 10.3389/fphar.2021.725583 PMID: 34603035
  134. Su, J.; Braat, H.; Verhaar, A.; Peppelenbosch, M. Commentary: Intermittent fasting and akkermansia muciniphila potentiate the antitumor efficacy of FOLFOX in colon cancer. Front. Pharmacol., 2022, 13, 843133. doi: 10.3389/fphar.2022.843133 PMID: 35222050
  135. Eriau, E.; Paillet, J.; Kroemer, G.; Pol, J.G. Metabolic reprogramming by reduced calorie intake or pharmacological caloric restriction mi-metics for improved cancer immunotherapy. Cancers, 2021, 13(6), 1260. doi: 10.3390/cancers13061260 PMID: 33809187
  136. Qian, H.; Chao, X.; Williams, J.; Fulte, S.; Li, T.; Yang, L.; Ding, W.X. Autophagy in liver diseases: A review. Mol. Aspects Med., 2021, 82, 100973. doi: 10.1016/j.mam.2021.100973 PMID: 34120768
  137. Schwarz, J.M.; Linfoot, P.; Dare, D.; Aghajanian, K. Hepatic de novo lipogenesis in normoinsulinemic and hyperinsulinemic subjects consuming high-fat, low-carbohydrate and low-fat, high-carbohydrate isoenergetic diets. Am. J. Clin. Nutr., 2003, 77(1), 43-50. doi: 10.1093/ajcn/77.1.43 PMID: 12499321
  138. Minehira, K.; Bettschart, V.; Vidal, H.; Vega, N.; Di Vetta, V.; Rey, V.; Schneiter, P.; Tappy, L. Effect of carbohydrate overfeeding on whole body and adipose tissue metabolism in humans. Obes. Res., 2003, 11(9), 1096-1103. doi: 10.1038/oby.2003.150 PMID: 12972680
  139. Ameer, F.; Scandiuzzi, L.; Hasnain, S.; Kalbacher, H.; Zaidi, N. De novo lipogenesis in health and disease. Metabolism, 2014, 63(7), 895-902. doi: 10.1016/j.metabol.2014.04.003 PMID: 24814684
  140. Menendez, J.A.; Lupu, R. Fatty acid synthase and the lipogenic phenotype in cancer pathogenesis. Nat. Rev. Cancer, 2007, 7(10), 763-777. doi: 10.1038/nrc2222 PMID: 17882277
  141. Alkhouri, N.; Gornicka, A.; Berk, M.P.; Thapaliya, S.; Dixon, L.J.; Kashyap, S.; Schauer, P.R.; Feldstein, A.E. Adipocyte apoptosis, a link between obesity, insulin resistance, and hepatic steatosis. J. Biol. Chem., 2010, 285(5), 3428-3438. doi: 10.1074/jbc.M109.074252 PMID: 19940134
  142. Gucalp, A.; Iyengar, N.M.; Hudis, C.A.; Dannenberg, A.J. Targeting obesity-related adipose tissue dysfunction to prevent cancer develop-ment and progression. Semin. Oncol., 2016, 43(1), 154-160. doi: 10.1053/j.seminoncol.2015.09.012 PMID: 26970134
  143. Kubota, N.; Terauchi, Y.; Yamauchi, T.; Kubota, T.; Moroi, M.; Matsui, J.; Eto, K.; Yamashita, T.; Kamon, J.; Satoh, H.; Yano, W.; Froguel, P.; Nagai, R.; Kimura, S.; Kadowaki, T.; Noda, T. Disruption of adiponectin causes insulin resistance and neointimal formation. J. Biol. Chem., 2002, 277(29), 25863-25866. doi: 10.1074/jbc.C200251200 PMID: 12032136
  144. Cai, L.; Xu, S.; Piao, C.; Qiu, S.; Li, H.; Du, J. Adiponectin induces CXCL1 secretion from cancer cells and promotes tumor angiogenesis by inducing stromal fibroblast senescence. Mol. Carcinog., 2016, 55(11), 1796-1806. doi: 10.1002/mc.22428 PMID: 27092462
  145. Zhong, Z.; Mao, S.; Lin, H.; Li, H.; Lin, J.; Lin, J.M. Alteration of intracellular metabolome in osteosarcoma stem cells revealed by liquid chromatography-tandem mass spectrometry. Talanta, 2019, 204, 6-12. doi: 10.1016/j.talanta.2019.05.088 PMID: 31357340
  146. Sadeghian, M.; Rahmani, S.; Khalesi, S.; Hejazi, E. A review of fasting effects on the response of cancer to chemotherapy. Clin. Nutr., 2021, 40(4), 1669-1681. doi: 10.1016/j.clnu.2020.10.037 PMID: 33153820
  147. Oyabu, M.; Takigawa, K.; Mizutani, S.; Hatazawa, Y.; Fujita, M.; Ohira, Y.; Sugimoto, T.; Suzuki, O.; Tsuchiya, K.; Suganami, T.; Ogawa, Y.; Ishihara, K.; Miura, S.; Kamei, Y. FOXO1 cooperates with C/EBPδ and ATF4 to regulate skeletal muscle atrophy transcriptional pro-gram during fasting. FASEB J., 2022, 36(2), e22152. doi: 10.1096/fj.202101385RR PMID: 35061305
  148. Ibrahim, E.M.; Al-Foheidi, M.H.; Al-Mansour, M.M. Energy and caloric restriction, and fasting and cancer: a narrative review. Support. Care Cancer, 2021, 29(5), 2299-2304. doi: 10.1007/s00520-020-05879-y PMID: 33190181
  149. de Groot, S.; Pijl, H.; van der Hoeven, J.J.M.; Kroep, J.R. Effects of short-term fasting on cancer treatment. J. Exp. Clin. Cancer Res., 2019, 38(1), 209. doi: 10.1186/s13046-019-1189-9 PMID: 31113478
  150. Ariaans, G.; Jalving, M.; Vries, E.G.E.; Jong, S. Anti-tumor effects of everolimus and metformin are complementary and glucose-dependent in breast cancer cells. BMC Cancer, 2017, 17(1), 232. doi: 10.1186/s12885-017-3230-8 PMID: 28356082
  151. O'Flanagan, C.H.; Smith, L.A.; McDonell, S.B.; Hursting, S.D. When less may be more: Calorie restriction and response to cancer therapy. BMC Med., 2017, 15(1), 106. doi: 10.1186/s12916-017-0873-x PMID: 28539118

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML

© Bentham Science Publishers, 2023