Chloroform Fraction of Drymaria cordata Linn (CFDC) Suppresses Estradiol Benzoate- Induced Endometrial Hyperplasia
- Авторы: Olowofolahan A.1, Akinjiola O.1, Olanlokun J.2, Oyebode O.2, Aina O.3, Olorunsogo O.1
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Учреждения:
- Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine, University of Ibadan
- Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine,, University of Ibadan
- Department of Veterinary Anatomy,, University of Ibadan
- Выпуск: Том 23, № 11 (2023)
- Страницы: 1298-1308
- Раздел: Oncology
- URL: https://kld-journal.fedlab.ru/1871-5206/article/view/694299
- DOI: https://doi.org/10.2174/1871520623666230209144428
- ID: 694299
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Аннотация
Background: The diagnosis of uterine dysfunction (endometrial hyperplasia) is on the rise. The available treatment is quite expensive and associated with some side effects. The therapeutic potential of natural products is now being explored, as they are easily available with little or no side effects. Drymaraia cordata is folklorically utilized in the treatment of diverse ailments including uterine fibroids
Objectives: This study aims to investigate the potential therapeutic effect of chloroform fraction of methanol extract of Drymaria cordata (CFDC) in estradiol benzoate (EB)-induced endometrial hyperplasia.
Methods: Thirty-six rats were randomly divided equally into six groups. These included control group, CFDC: (100 mg/kg), CFDC: (200 mg/kg), EB: (2 mg/kg), EB + CFDC (100 mg/kg), and EB + CFDC (200 mg/kg). Endometrial hyperplasia (EH) was induced by intraperitoneal injection of EB. The levels of estrogen (E2), progesterone (PG), Follicle stimulating hormone (FSH), Luteinizing hormone (LH), Malondialdehyde (MDA), Superoxide dismutase (SOD), and Glutathione peroxidase (GSH-Px) activities were determined using ELISA technique. The uterine histological assessment and immunohistochemical expression levels of estrogen receptor, Ki-67, cytochrome c, and caspase 3 were carried out.
Results: EH was severely expressed in the uterine section of EB-treated rats. However, CFDC administration improved the pathological features of the animal model. The sex hormones levels were increased in the EB-treated group, which were significantly reduced by CFDC. The antioxidant indices were also restored by CFDC. Immunoexpression levels of ERα and Ki-67 were downregulated while cytochrome c and caspase 3 were upregulated by CFDC.
Conclusion: This study suggests that CFDC contains phytochemicals that can protect against EB-induced EH via modulation of hormonal signaling, apoptotic machinery, and oxidative indices.
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Об авторах
Adeola Olowofolahan
Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine, University of Ibadan
Автор, ответственный за переписку.
Email: info@benthamscience.net
Oluwatofunmi Akinjiola
Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine, University of Ibadan
Email: info@benthamscience.net
John Olanlokun
Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine,, University of Ibadan
Email: info@benthamscience.net
Olubukola Oyebode
Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine,, University of Ibadan
Email: info@benthamscience.net
Oluwasanmi Aina
Department of Veterinary Anatomy,, University of Ibadan
Email: info@benthamscience.net
Olufunso Olorunsogo
Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine, University of Ibadan
Email: info@benthamscience.net
Список литературы
- Nair, A.; Taylor, H. The mechanism of menstruation.In: Amenorrhea. Contemporary Endocrinology; Santoro, N.F.; Neal-Perry, G., Eds.; Humana Press: Totowa, 2010, pp. 21-34.
- Palmer, J.E.; Perunovic, B.; Tidy, J.A. Endometrial hyperplasia. Obstet. Gynaecol., 2008, 10(4), 211-216. doi: 10.1576/toag.10.4.211.27436
- Lacey, J.V., Jr; Chia, V.M. Endometrial hyperplasia and the risk of progression to carcinoma. Maturitas, 2009, 63(1), 39-44. doi: 10.1016/j.maturitas.2009.02.005 PMID: 19285814
- Parkash, V.; Fadare, O.; Tornos, C.; McCluggage, W.G. Committee Opinion No. 631: Endometrial intraepithelial neoplasia. Obstet. Gynecol., 2015, 126(4), 897. doi: 10.1097/AOG.0000000000001071 PMID: 26393443
- Chandra, V.; Kim, J.J.; Benbrook, D.M.; Dwivedi, A.; Rai, R. Therapeutic options for management of endometrial hyperplasia. J. Gynecol. Oncol., 2016, 27(1), e8. doi: 10.3802/jgo.2016.27.e8 PMID: 26463434
- Medh, R.D.; Thompson, E.B. Hormonal regulation of physiological cell turnover and apoptosis. Cell Tissue Res., 2000, 301(1), 101-124. doi: 10.1007/s004419900159 PMID: 10928284
- Horne, F.M.; Blithe, D.L. Progesterone receptor modulators and the endometrium: Changes and consequences. Hum. Reprod. Update, 2007, 13(6), 567-580. doi: 10.1093/humupd/dmm023 PMID: 17630398
- Deroo, B.J.; Korach, K.S. Estrogen receptors and human disease. J. Clin. Invest., 2006, 116(3), 561-570. doi: 10.1172/JCI27987 PMID: 16511588
- Acconcia, F.; Marino, M. The effects of 17β-estradiol in cancer are mediated by estrogen receptor signaling at the plasma membrane. Front. Physiol., 2011, 2, 30. doi: 10.3389/fphys.2011.00030 PMID: 21747767
- Skrzypczak, M.; Merx, I.; Schüler-Toprak, S.; Weber, F.; Inwald, E.C.; Ortmann, O.; Treeck, O. Molecular profiling of estrogen receptor α and progesterone receptor transcript variants in endometrial cancer. Steroids, 2015, 104, 122-128. doi: 10.1016/j.steroids.2015.09.004 PMID: 26428028
- Dimitrakopoulos, F.I.; Kottorou, A.; Tzezou, A. Endocrine resistance and epigenetic reprogramming in estrogen receptor positive breast cancer. Cancer Lett., 2021, 517, 55-65. doi: 10.1016/j.canlet.2021.05.030 PMID: 34077785
- Ozdegirmenci, O.; Kayikcioglu, F.; Bozkurt, U.; Akgul, M.A.; Haberal, A. Comparison of the efficacy of three progestins in the treatment of simple endometrial hyperplasia without atypia. Gynecol. Obstet. Invest., 2011, 72(1), 10-14. doi: 10.1159/000321390 PMID: 21266792
- Daud, S.; Jalil, S.S.A.; Griffin, M.; Ewies, A.A.A. Endometrial hyperplasia - the dilemma of management remains: A retrospective obser-vational study of 280 women. Eur. J. Obstet. Gynecol. Reprod. Biol., 2011, 159(1), 172-175. doi: 10.1016/j.ejogrb.2011.06.023 PMID: 21764501
- Nieman, K.M.; Romero, I.L.; Van Houten, B.; Lengyel, E. Adipose tissue and adipocytes support tumorigenesis and metastasis. Biochim. Biophys. Acta Mol. Cell Biol. Lipids, 2013, 1831(10), 1533-1541. doi: 10.1016/j.bbalip.2013.02.010 PMID: 23500888
- Zhang, Q.; Shen, Q.; Celestino, J.; Milam, M.R.; Westin, S.N.; Lacour, R.A.; Meyer, L.A.; Shipley, G.L.; Davies, P.J.A.; Deng, L.; McCampbell, A.S.; Broaddus, R.R.; Lu, K.H. Enhanced estrogen-induced proliferation in obese rat endometrium. Am. J. Obstet. Gynecol., 2009, 200(2), 186.e1-186.e8. doi: 10.1016/j.ajog.2008.08.064 PMID: 19185100
- Deligdisch, L. Hormonal pathology of the endometrium. Mod. Pathol., 2000, 13(3), 285-294. doi: 10.1038/modpathol.3880050 PMID: 10757339
- Silverberg, S.G. Problems in the differential diagnosis of endometrial hyperplasia and carcinoma. Mod. Pathol., 2000, 13(3), 309-327. doi: 10.1038/modpathol.3880053 PMID: 10757341
- Gunin, A.G.; Mashin, I.N.; Zakharov, D.A. Proliferation, mitosis orientation and morphogenetic changes in the uterus of mice following chronic treatment with both estrogen and glucocorticoid hormones. J. Endocrinol., 2001, 169(1), 23-31. doi: 10.1677/joe.0.1690023 PMID: 11250643
- Burns, K.A.; Korach, K.S. Estrogen receptors and human disease: An update. Arch. Toxicol., 2012, 86(10), 1491-1504. doi: 10.1007/s00204-012-0868-5 PMID: 22648069
- Caldon, C.E. Estrogen signaling and the DNA damage response in hormone dependent breast cancers. Front. Oncol., 2014, 4, 106. doi: 10.3389/fonc.2014.00106 PMID: 24860786
- Williamson, L.M.; Lees-Miller, S.P. Estrogen receptor α-mediated transcription induces cell cycle-dependent DNA double-strand breaks. Carcinogenesis, 2011, 32(3), 279-285. doi: 10.1093/carcin/bgq255 PMID: 21112959
- Ashby, J.; Tinwell, H.; Soames, A.; Foster, J. Induction of hyperplasia and increased DNA content in the uterus of immature rats exposed to coumestrol. Environ. Health Perspect., 1999, 107(10), 819-822. doi: 10.1289/ehp.99107819 PMID: 10504149
- Yager, J.D.; Davidson, N.E. Estrogen carcinogenesis in breast cancer. N. Engl. J. Med., 2006, 354(3), 270-282. doi: 10.1056/NEJMra050776 PMID: 16421368
- El-Sharkawy, S.L.; Abbas, N.F.; El-Henawy, A.M.Y.; Badawi, M.A.E.M.; Yasseen, N.N. Morphometric and DNA image analysis of en-dometrial hyperplasia and carcinoma. Appl. Immunohistochem. Mol. Morphol., 2017, 25(1), 32-38. doi: 10.1097/PAI.0000000000000259 PMID: 26469331
- Lumachi, F.; Luisetto, G.; Basso, S.M.; Basso, U.; Brunello, A.; Camozzi, V. Endocrine therapy of breast cancer. Curr. Med. Chem., 2011, 18(4), 513-522. doi: 10.2174/092986711794480177 PMID: 21143113
- Omar, M.; Laknaur, A.; Al-Hendy, A.; Yang, Q. Myometrial progesterone hyper-responsiveness associated with increased risk of human uterine fibroids. BMC Womens Health, 2019, 19(1), 92. doi: 10.1186/s12905-019-0795-1 PMID: 31288815
- Magon, N.; Kumar, P. Hormones in pregnancy. Niger. Med. J., 2012, 53(4), 179-183. doi: 10.4103/0300-1652.107549 PMID: 23661874
- Arab, H.; Alharbi, A.; Oraif, A.; Sagr, E.; Al Madani, H.; Abduljabbar, H.; Bajouh, O.S.; Faden, Y.; Sabr, Y. The role of progestogens in threatened and idiopathic recurrent miscarriage. Int. J. Womens Health, 2019, 11, 589-596. doi: 10.2147/IJWH.S224159 PMID: 31807086
- Rein, M.S.; Barbieri, R.L.; Friedman, A.J. Progesterone: A critical role in the pathogenesis of uterine myomas. Am. J. Obstet. Gynecol., 1995, 172(1), 14-18. doi: 10.1016/0002-9378(95)90077-2 PMID: 7847524
- William, J. Endometrial hyperplasia and apoptosis following neonatal diethylstilbestrol exposure and subsequent estrogen stimulation in both host and transplanted hamster. Cancer Res., 1997, 57, 1903-1908. PMID: 9157983
- Chuang, T.D.; Khorram, O. Regulation of cell cycle regulatory proteins by micro RNAs in uterine leiomyoma. Reprod. Sci., 2019, 26(2), 250-258. doi: 10.1177/1933719118768692 PMID: 29642801
- Rubio, N.; España, L.; Fernández, Y.; Blanco, J.; Sierra, A. Metastatic behavior of human breast carcinomas overexpressing the Bcl-x(L) gene: A role in dormancy and organospecificity. Lab. Invest., 2001, 81(5), 725-734. doi: 10.1038/labinvest.3780281 PMID: 11351044
- Kastratović, T.; Arsenijević, S.; Matović, Z.; Mitrović, M.; Nikolić, I.; Milosavljević, Z.; Protrka, Z.; orak, M.; Đurić, J. Methotrexate and myotrexate induce apoptosis in human myoma fibroblasts (T hES cell line) via mitochondrial pathway. Acta Pol. Pharm., 2015, 72(3), 455-464. PMID: 26642654
- Sreevalsan, S.; Safe, S. Reactive oxygen species and colorectal cancer. Curr. Colorectal Cancer Rep., 2013, 9(4), 350-357. doi: 10.1007/s11888-013-0190-5 PMID: 25584043
- Marinescu, S.; Anghel, R.; Gruia, M.I.; Beuran, M. Involvement of reactive oxygen species in the mechanisms associated with cervical cancer specific treatment. Chirurgia, 2014, 109(6), 806-811. PMID: 25560505
- Chiou, J.F.; Hu, M.L. Elevated lipid peroxidation and disturbed antioxidant enzyme activities in plasma and erythrocytes of patients with uterine cervicitis and myoma. Clin. Biochem., 1999, 32(3), 189-192. doi: 10.1016/S0009-9120(98)00110-6 PMID: 10383079
- Thyagarajan, A.; Sahu, R.P. Potential contributions of antioxidants to cancer therapy: Immunomodulation and radiosensitization. Integr. Cancer Ther., 2018, 17(2), 210-216. doi: 10.1177/1534735416681639 PMID: 28627256
- Raffoul, J.J.; Banerjee, S.; Che, M.; Knoll, Z.E.; Doerge, D.R.; Abrams, J.; Kucuk, O.; Sarkar, F.H.; Hillman, G.G. Soy isoflavones enhance radiotherapy in a metastatic prostate cancer model. Int. J. Cancer, 2007, 120(11), 2491-2498. doi: 10.1002/ijc.22548 PMID: 17304503
- Yasueda, A.; Urushima, H.; Ito, T. Efficacy and interaction of antioxidant supplements as adjuvant therapy in cancer treatment: A system-atic review. Integr. Cancer Ther., 2016, 15(1), 17-39. doi: 10.1177/1534735415610427 PMID: 26503419
- Singh-Gupta, V.; Joiner, M.C.; Runyan, L.; Yunker, C.K.; Sarkar, F.H.; Miller, S.; Gadgeel, S.M.; Konski, A.A.; Hillman, G.G. Soy isofla-vones augment radiation effect by inhibiting APE1/Ref-1 DNA repair activity in non-small cell lung cancer. J. Thorac. Oncol., 2011, 6(4), 688-698. doi: 10.1097/JTO.0b013e31821034ae PMID: 21325978
- Tak, J.K.; Lee, J.H.; Park, J.W. Resveratrol and piperine enhance radiosensitivity of tumor cells. BMB Rep., 2012, 45(4), 242-246. doi: 10.5483/BMBRep.2012.45.4.242 PMID: 22531135
- Mut-Salud, N.; Álvarez, P.J.; Garrido, J.M.; Carrasco, E.; Aránega, A.; Rodríguez-Serrano, F. Antioxidant intake and antitumor therapy: Toward nutritional recommendations for optimal results. Oxid. Med. Cell. Longev., 2016, 2016, 1-19. doi: 10.1155/2016/6719534 PMID: 26682013
- de Martel, C.; Ferlay, J.; Franceschi, S.; Vignat, J.; Bray, F.; Forman, D.; Plummer, M. Global burden of cancers attributable to infections in 2008: A review and synthetic analysis. Lancet Oncol., 2012, 13(6), 607-615. doi: 10.1016/S1470-2045(12)70137-7 PMID: 22575588
- Yajid, A.I.; Ab Rahman, H.S.; Pak Kai, M.W.; Wan Zain, W.Z. Potential benefits of Annona muricata in combating cancer: A review. Malays. J. Med. Sci., 2018, 25(1), 5-15. doi: 10.21315/mjms2018.25.1.2 PMID: 29599630
- Bulun, S.E. Uterine Fibroids. N. Engl. J. Med., 2013, 369(14), 1344-1355. doi: 10.1056/NEJMra1209993 PMID: 24088094
- Yong, Y.K.; Tan, J.J.; The, S.S.; Mah, S.H.; Ee, G.C.L.; Chiong, H.S.; Ahmad, Z. Clinacanthus nutans extracts are antioxidant with antipro-liferative efect on cultured human cancer cell lines. Evid-Based Compl Alt., 2013, (462751), 1-8.
- Deng, S.; Shanmugam, M.K.; Kumar, A.P.; Yap, C.T.; Sethi, G.; Bishayee, A. Targeting autophagy using natural compounds for cancer prevention and therapy. Cancer, 2019, 125(8), 1228-1246. doi: 10.1002/cncr.31978 PMID: 30748003
- Olowofolahan, A.O.; Olorunsogo, O.O. Effect of Gloriosa superba linn (EEGS) on mPT and monosodium glutamate-induced proliferative disorder using rat model. J. Ethnopharmacol., 2021, 267, 113498. doi: 10.1016/j.jep.2020.113498 PMID: 33091496
- Olowofolahan, A.O.; Olorunsogo, O.O. Fractions of Ageratum conyzoides L. (Compositae) induce mitochondrial-mediated apoptosis in rats: Possible option in monosodium glutamate-induced hepatic and uterine pathological disorder. J. Ethnopharmacol., 2021, 277, 114192. b doi: 10.1016/j.jep.2021.114192 PMID: 33974943
- Mishra, S.; Ahmad, S.; Kumar, N.; Sharma, B.K. Annona muricata (the cancer killer): A review. Glob J Pharma Res, 2013, 2, 1613-1618.
- Burkill, H.M. The Useful Plants of West Tropical Africa 2nd Edition; Royal Botanic Gardens, Kew, 1985, 1, p. 343.
- Mukherjee, P.K.; Saha, K.; Bhattacharya, S.; Giri, S.N.; Pal, M.; Saha, B.P. Studies on antitussive activity of Drymaria cordata Willd. (Car-yophyllaceae). J. Ethnopharmacol., 1997, 56(1), 77-80. doi: 10.1016/S0378-8741(97)01512-2 PMID: 9147257
- Mukherjee, P.K.; Bhattacharya, S.; Saha, K.; Giri, S.N.; Pal, M.; Saha, B.P. Antibacterial evaluation of Drymaria cordata willd.(Fam. Cary-ophyllaceae) extract. Phytother. Res., 1998, 11, 249-250.
- Adeyemi, O.O.; Akindele, A.J.; Ndubuisi, N. Anti-inflammatory activity of Drymaria cordata extract. J. Nat. Rem., 2008, 8(1), 93-100.
- Barua, C.C.; Roy, J.D.; Buragohain, B.; Barua, A.G.; Borah, P.; Lahkar, M. Anxiolytic effect of hydroethanolic extract of Drymaria cordata L Willd. Indian J. Exp. Biol., 2009, 47(12), 969-973. PMID: 20329700
- Sowemimo, A.; van de Venter, M.; Baatjies, L.; Koekemoer, T. Cytotoxic activity of selected Nigerian plants. Afr. J. Tradit. Complement. Altern. Med., 2009, 6(4), 526-528. PMID: 20606772
- Akindele, A.J.; Ibe, I.F.; Adeyemi, O.O. Analgesic and Antipyretic activities of Drymaria cordata (Linn.) Willd. Afr. J. Tradit. Complement. Altern. Med., 2012, 9(1), 25-35. PMID: 23983316
- Olowofolahan, A.O.; Adeoye, O.A.; Offor, G.N.; Adebisi, L.A.; Olorunsogo, O.O. Induction of mitochondrial membrane permeability transition pore opening and cytochrome C release by fractions of Drymaria cordata. Arch. Basic Appl. Med., 2015, 3, 135-144.
- Olowofolahan, A.O.; Olorunsogo, O.O. Induction of apoptosis in rat liver cells via caspase activation by chloroform fraction of methanol extract of Drymaria cordata. European J. Biomed. Pharm. Sci., 2018, 5(4), 73-83.
- Olowofolahan, A.; Aina, O.; Hassan, E.; Olorunsogo, O. Ameliorative potentials of methanol extract and chloroform fraction of Drymaria cordata on MSG-induced uterine hyperplasia in female wistar rats. European J. Med. Plants, 2017, 20(4), 1-9. doi: 10.9734/EJMP/2017/36335
- Huang, H.C.; Tsai, W.J.; Liaw, C.C.; Wu, S.H.; Wu, Y.C.; Kuo, Y.H. Anti-platelet aggregation triterpene saponins from the galls of Sapin-dus mukorossi. Chem. Pharm. Bull., 2007, 55(9), 1412-1415. doi: 10.1248/cpb.55.1412 PMID: 17827775
- Solomon, T.; Largesse, Z.; Mekbeb, A.; Eyasu, M.; Asfaw, D. Effect of Rumex steudelii methanolic root extract on ovarian folliculogene-sis and uterine histology in female albino rats. Afr. Health Sci., 2010, 10(4), 353-361. PMID: 21416037
- Reitman, S.; Frankel, S. A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am. J. Clin. Pathol., 1957, 28(1), 56-63. doi: 10.1093/ajcp/28.1.56 PMID: 13458125
- Sbrana, E.; Newman, P.C.; Popov, V.L.; Xiao, S-Y.; Tesh, R.B.; Mateo, R. Clinical laboratory, virologic, and pathologic changes in ham-sters experimentally infected with Pirital virus (Arenaviridae): A rodent model of Lassa fever. Am. J. Trop. Med. Hyg., 2006, 74(6), 1096-1102. doi: 10.4269/ajtmh.2006.74.1096 PMID: 16760527
- Olowofolahan, A.O.; Oyebode, O.T.; Olorunsogo, O.O. Methyl palmitate reversed estradiol benzoate-induced endometrial hyperplasia in female rats. Toxicol. Mech. Methods, 2021, 31(1), 43-52. a doi: 10.1080/15376516.2020.1827329 PMID: 32967526
- Olowofolahan, A.O.; Olanlokun, J.O.; Olorunsogo, O.O. GCMS analysis and phytoprotective effect of chloroform fraction of methanol leaf extract of Drymaria cordata against MSG-induced lesions in specific tissues. Afr. J. Med. Med. Sci., 2020, 49, 409-419. b
- You, Z.; Sun, J.; Xie, F.; Chen, Z.; Zhang, S.; Chen, H.; Liu, F.; Li, L.; Chen, G.; Song, Y.; Xuan, Y.; Zheng, G.; Xin, Y. Modulatory effect of fermented papaya extracts on mammary gland hyperplasia induced by estrogen and progestin in female rats. Oxid. Med. Cell. Longev., 2017, 2017, 1-11. doi: 10.1155/2017/8235069 PMID: 29359010
- Ngokere, A.A.; Ezeofor, C.P.; Okoye, J.O.; Ibekailo, S.N.; Ude, T.; Awalu, C.J.; Amadi, M.S. Antiprogesteronic and estrogenic effect of Mangifera Indica. J. Pharmacol. Toxicol, 2014, 9(2), 82-89. doi: 10.3923/jpt.2014.82.89
- Das Gupta, S.; So, J.Y.; Wall, B.; Wahler, J.; Smolarek, A.K.; Sae-tan, S.; Soewono, K.Y.; Yu, H.; Lee, M.J.; Thomas, P.E.; Yang, C.S.; Suh, N. Tocopherols inhibit oxidative and nitrosative stress in estrogen-induced early mammary hyperplasia in ACI rats. Mol. Carcinog., 2015, 54(9), 916-925. doi: 10.1002/mc.22164 PMID: 24782330
- Chen, T.; Li, J.; Chen, J.; Yang, C. Anti-hyperplasia effects of Rosa rugosa polyphenols in rats with hyperplasia of mammary gland. Environ. Toxicol. Pharmacol., 2015, 39(2), 990-996. doi: 10.1016/j.etap.2015.02.014
- Weroha, S.J.; Li, S.A.; Tawfik, O.; Li, J.J. Overexpression of cyclins D1 and D3 during estrogen-induced breast oncogenesis in female ACI rats. Carcinogenesis, 2006, 27(3), 491-498. doi: 10.1093/carcin/bgi278 PMID: 16311245
- Singh, K.P.; Treas, J.; Tyagi, T.; Gao, W. DNA demethylation by 5-aza-2-deoxycytidine treatment abrogates 17 beta-estradiol-induced cell growth and restores expression of DNA repair genes in human breast cancer cells. Cancer Lett., 2012, 316(1), 62-69. doi: 10.1016/j.canlet.2011.10.022 PMID: 22082530
- Islam, M.S.; Protic, O.; Stortoni, P.; Grechi, G.; Lamanna, P.; Petraglia, F.; Castellucci, M.; Ciarmela, P. Complex networks of multiple factors in the pathogenesis of uterine leiomyoma. Fertil. Steril., 2013, 100(1), 178-193. doi: 10.1016/j.fertnstert.2013.03.007 PMID: 23557758
- Rizzello, A.; Franck, J.; Pellegrino, M.; Nuccio, F.; Simeone, P.; Fiore, G.; Tommaso, S.; Malvasi, A.; Tinelli, A.; Fournier, I.; Salzet, M.; Maffia, M.; Vergara, D. A proteomic analysis of human uterine myoma. Curr. Protein Pept. Sci., 2016, 18(2), 167-174. doi: 10.2174/1389203717666160322150603 PMID: 27001059
- Xu, Q.; Chen, C.; Liu, B.; Lin, Y.; Zheng, P.; Zhou, D.; Xie, Y.; Lin, Y.; Guo, C.; Liu, J.; Li, L. Association of iRhom1 and iRhom2 ex-pression with prognosis in patients with cervical cancer and possible signaling pathways. Oncol. Rep., 2020, 43(1), 41-54. PMID: 31661139
- Li, X.; Pishdari, B.; Cui, P.; Hu, M.; Yang, H.P.; Guo, Y.R.; Jiang, H.Y.; Feng, Y.; Billig, H.; Shao, R. Regulation of androgen receptor ex-pression alters AMPK phosphorylation in the endometrium: In vivo and in vitro studies in women with polycystic ovary syndrome. Int. J. Biol. Sci., 2015, 11(12), 1376-1389. doi: 10.7150/ijbs.13109 PMID: 26681917
- Hu, M.; Zhang, Y.; Feng, J.; Xu, X.; Zhang, J.; Zhao, W.; Guo, X.; Li, J.; Vestin, E.; Cui, P.; Li, X.; Wu, X.; Brännström, M.; Shao, L.R.; Billig, H. Uterine progesterone signaling is a target for metformin therapy in PCOS-like rats. J. Endocrinol., 2018, 237(2), 123-137. doi: 10.1530/JOE-18-0086 PMID: 29535146
- Olowofolahan, A.O.; Tobih, S.E.; Olorunsogo, O.O. Amelioration of oestradiol valerate-induced endometrial hyperplasia in female rats by methanol fraction of Mangifera indica Linn via modulation of estrogen receptor signaling pathway. Indian J. Physiol. Pharmacol., 2021, 2021(65), 2.
- Strubbe-Rivera, J.O.; Schrad, J.R.; Pavlov, E.V.; Conway, J.F.; Parent, K.N.; Bazil, J.N. The mitochondrial permeability transition phenom-enon elucidated by cryo-EM reveals the genuine impact of calcium overload on mitochondrial structure and function. Sci. Rep., 2021, 11(1), 1037. doi: 10.1038/s41598-020-80398-8 PMID: 33441863
- Green, D.R.; Walczak, H. Apoptosis therapy: Driving cancers down the road to ruin. Nat. Med., 2013, 19(2), 131-133. doi: 10.1038/nm.3076 PMID: 23389605
- Wu, H.; Medeiros, L.J.; Young, K.H. Apoptosis signaling and BCL-2 pathways provide opportunities for novel targeted therapeutic strate-gies in hematologic malignances. Blood Rev., 2018, 32(1), 8-28. doi: 10.1016/j.blre.2017.08.004 PMID: 28802908
- Sermakkani, M.; Thangapandian, V. GC-MS analysis of Cassia italic leaf methanol extract. Asian J. Pharm. Clin. Res., 2012, 5, 90-94.
- Gomathi, D.; Kalaiselvi, M.; Ravikumar, G.; Devaki, K.; Uma, C. GC-MS analysis of bioactive compounds from the whole plant ethanolic extract of Evolvulus alsinoides (L.). J. Food Sci. Technol., 2015, 52(2), 1212-1217. doi: 10.1007/s13197-013-1105-9 PMID: 25694742
- Vijisaral, E.D.; Subramanian, A. GC-MS analysis of ethanol extract of Cyperus rotundus leaves. Int. J. Curr. Biotechnol., 2014, 2, 19-23.
- Dandekar, R.; Fegade, B.; Bhaskar, V.H. GC-MS analysis of phytoconstituents in alcohol extract of Epiphyllum oxipetalum leaves. J. Pharmacogn. Phytochem., 2015, 4, 149-154.
- Rajab, M.; Cantrell, C.; Franzblau, S.; Fischer, N. Antimycobacterial activity of (E)-phytol and derivatives: A preliminary structure-activity study. Planta Med., 1998, 64(1), 2-4. doi: 10.1055/s-2006-957354 PMID: 9491760
- Rajeswari, G.; Murugan, M.; Mohan, V.R. GC-MS analysis of bioactive components of Hugonia mystax L (Linaceae). Res. J. Pharm. Biol. Chem. Sci., 2012, 3, 301-308.
- Saikia, D.; Parihar, S.; Chanda, D.; Ojha, S.; Kumar, J.K.; Chanotiya, C.S.; Shanker, K.; Negi, A.S. Antitubercular potential of some sem-isynthetic analogues of phytol. Bioorg. Med. Chem. Lett., 2010, 20(2), 508-512. doi: 10.1016/j.bmcl.2009.11.107 PMID: 20004575
- Ryu, K.R.; Choi, J.Y.; Chung, S.; Kim, D.H. Anti-scratching behavioral effect of the essential oil and phytol isolated from Artemisia prin-ceps Pamp. in mice. Planta Med., 2011, 77(1), 22-26. doi: 10.1055/s-0030-1250119 PMID: 20645242
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