References
- 1E. A. Stewart, C. Cookson, R. A. Gandolfo, and R. Schulze-Rath, “Epidemiology of Uterine Fibroids: A Systematic Review,” BJOG 124 (2017): 1501–1512.
- 2S. E. Bulun, “Uterine Fibroids,” New England Journal of Medicine 369 (2013): 1344–1355.
- 3B. J. Borah, W. K. Nicholson, L. Bradley, and E. A. Stewart, “The Impact of Uterine Leiomyomas: A National Survey of Affected Women,” American Journal of Obstetrics and Gynecology 209 (2013): 319.e1–319.e20.
- 4E. A. Stewart, S. K. Laughlin-Tommaso, W. H. Catherino, et al., “Uterine Fibroids,” Nature Reviews Disease Primers 2 (2016): 1–18.
- 5D. Day Baird, D. B. Dunson, M. C. Hill, D. Cousins, and J. M. Schectman, “High Cumulative Incidence of Uterine Leiomyoma in Black and White Women: Ultrasound Evidence,” American Journal of Obstetrics and Gynecology 188 (2003): 100–107.
- 6E. R. Cardozo, A. D. Clark, N. K. Banks, et al., “The Estimated Annual Cost of Uterine Leiomyomata in the United States,” American Journal of Obstetrics and Gynecology 206 (2012): 211.e1–211.e9.
- 7A. E. Commandeur, A. K. Styer, and J. M. Teixeira, “Epidemiological and Genetic Clues for Molecular Mechanisms Involved in Uterine Leiomyoma Development and Growth,” Human Reproduction Update 21 (2015): 593–615.
- 8M. S. Islam, O. Protic, P. Stortoni, et al., “Complex Networks of Multiple Factors in the Pathogenesis of Uterine Leiomyoma,” Fertility and Sterility 100 (2013): 178–193.
- 9D. D. Baird, M. C. Hill, J. M. Schectman, and B. W. Hollis, “Vitamin D and the Risk of Uterine Fibroids,” Epidemiology (Cambridge, Mass.) 24 (2013): 447–453.
- 10M. S. Islam, M. M. Akhtar, and J. H. Segars, “Vitamin D Deficiency and Uterine Fibroids: An Opportunity for Treatment or Prevention?,” Fertility and Sterility 115 (2021): 1175–1176.
- 11M. Sabry, S. K. Halder, A. S. A. Allah, et al., “Serum Vitamin D3 Level Inversely Correlates With Uterine Fibroid Volume in Different Ethnic Groups: A Cross-Sectional Observational Study,” International Journal of Women's Health 5 (2013): 93–100.
- 12F. Xu, F. Li, L. Li, et al., “Vitamin D as a Risk Factor for the Presence of Asymptomatic Uterine Fibroids in Premenopausal Han Chinese Women,” Fertility and Sterility 115 (2021): 1288–1293.
- 13M. Ciebiera, M. Włodarczyk, A. Słabuszewska-Jóźwiak, G. Nowicka, and G. Jakiel, “Influence of Vitamin D and Transforming Growth Factor β3 Serum Concentrations, Obesity, and Family History on the Risk for Uterine Fibroids,” Fertility and Sterility 106 (2016): 1787–1792.
- 14S. Christakos, P. Dhawan, A. Verstuyf, L. Verlinden, and G. Carmeliet, “Vitamin D: Metabolism, Molecular Mechanism of Action, and Pleiotropic Effects,” Physiological Reviews 96 (2016): 365–408.
- 15S. K. Halder, J. S. Goodwin, and A. Al-Hendy, “1,25-Dihydroxyvitamin D Reduces TGF-β3-Induced Fibrosis-Related Gene Expression in Human Uterine Leiomyoma Cells,” Journal of Clinical Endocrinology and Metabolism 96 (2011): E754–E762.
- 16S. K. Halder, C. Sharan, and A. Al-Hendy, “1,25-Dihydroxyvitamin D3 Treatment Shrinks Uterine Leiomyoma Tumors in the Eker Rat Model,” Biology of Reproduction 86 (2012): 116.
- 17C. Sharan, S. K. Halder, C. Thota, et al., “Vitamin D Inhibits Proliferation of Human Uterine Leiomyoma Cells via Catechol-O-Methyltransferase,” Fertility and Sterility 95 (2011): 247–253.
- 18A. Paffoni, E. Somigliana, P. Vigano', et al., “Vitamin D Status in Women With Uterine Leiomyomas,” Journal of Clinical Endocrinology and Metabolism 98 (2013): E1374–E1378.
- 19A. Ciavattini, G. D. Carpini, M. Serri, et al., “Hypovitaminosis D and “Small Burden” Uterine Fibroids: Opportunity for a Vitamin D Supplementation,” Medicine 95 (2016): 5698.
- 20D. Hazimeh, G. Massoud, M. Parish, et al., “Green Tea and Benign Gynecologic Disorders: A New Trick for an Old Beverage?,” Nutrients 15 (2023): 1439.
- 21M. S. Islam, M. Parish, J. T. Brennan, B. L. Winer, and J. H. Segars, “Targeting Fibrotic Signaling Pathways by EGCG as a Therapeutic Strategy for Uterine Fibroids,” Scientific Reports 13 (2023): 8492.
- 22D. Zhang, M. Al-Hendy, G. Richard-Davis, et al., “Antiproliferative and Proapoptotic Effects of Epigallocatechin Gallate on Human Leiomyoma Cells,” Fertility and Sterility 94 (2010): 1887–1893.
- 23D. Zhang, M. Al-Hendy, G. Richard-Davis, et al., “Green Tea Extract Inhibits Proliferation of Uterine Leiomyoma Cells In Vitro and in Nude Mice,” American Journal of Obstetrics and Gynecology 202 (2010): 289.e1–289.e9.
- 24J. V. Higdon and B. Frei, “Tea Catechins and Polyphenols: Health Effects, Metabolism, and Antioxidant Functions,” Critical Reviews in Food Science and Nutrition 43 (2003): 89–143.
- 25E. Roshdy, V. Rajaratnam, S. Maitra, et al., “Treatment of Symptomatic Uterine Fibroids With Green Tea Extract: A Pilot Randomized Controlled Clinical Study,” International Journal of Women's Health 5 (2013): 477–486.
- 26G. Grandi, M. C. Del Savio, C. Melotti, L. Feliciello, and F. Facchinetti, “Vitamin D and Green Tea Extracts for the Treatment of Uterine Fibroids in Late Reproductive Life: A Pilot, Prospective, Daily-Diary Based Study,” Gynecological Endocrinology 38 (2022): 63–67.
- 27G. Porcaro and P. Angelozzi, “Uterine Fibroid Treatment With Vitamin D Combined With Epigallocatechin Gallate and Vitamin B6: A Controlled Pilot Study,” IJMDAT 4 (2021): 300.
- 28Q. Yang, M. Ciebiera, M. V. Bariani, et al., “Comprehensive Review of Uterine Fibroids: Developmental Origin, Pathogenesis, and Treatment,” Endocrine Reviews 43 (2022): 678–719.
- 29L. A. Wise, J. R. Palmer, E. A. Stewart, and L. Rosenberg, “Age-Specific Incidence Rates for Self-Reported Uterine Leiomyomata in the Black Women's Health Study,” Obstetrics and Gynecology 105 (2005): 563–568.
- 30E. Faerstein, M. Szklo, and N. Rosenshein, “Risk Factors for Uterine Leiomyoma: A Practice-Based Case-Control Study. I. African-American Heritage, Reproductive History, Body Size, and Smoking,” American Journal of Epidemiology 153 (2001): 1–10.
- 31R. Boynton-Jarrett, J. Rich-Edwards, S. Malspeis, S. A. Missmer, and R. Wright, “A Prospective Study of Hypertension and Risk of Uterine Leiomyomata,” American Journal of Epidemiology 161 (2005): 628–638.
- 32J. Goad, J. Rudolph, M. Zandigohar, et al., “Single-Cell Sequencing Reveals Novel Cellular Heterogeneity in Uterine Leiomyomas,” Human Reproduction 37 (2022): 2334–2349.
- 33M. S. Islam, A. Ciavattini, F. Petraglia, M. Castellucci, and P. Ciarmela, “Extracellular Matrix in Uterine Leiomyoma Pathogenesis: A Potential Target for Future Therapeutics,” Human Reproduction Update 24 (2018): 59–85.
- 34M. S. Islam, S. Afrin, B. Singh, et al., “Extracellular Matrix and Hippo Signaling as Therapeutic Targets of Antifibrotic Compounds for Uterine Fibroids,” Clinical and Translational Medicine 11 (2021): 475.
- 35C. N. C. Mitchell, M. S. Islam, S. Afrin, et al., “Mechanical Stiffness Augments Ligand-Dependent Progesterone Receptor B Activation via MEK 1/2 and Rho/ROCK–Dependent Signaling Pathways in Uterine Fibroid Cells,” Fertility and Sterility 116 (2021): 255–265.
- 36H. Matsuo, O. Kurachi, Y. Shimomura, T. Samoto, and T. Maruo, “Molecular Bases for the Actions of Ovarian Sex Steroids in the Regulation of Proliferation and Apoptosis of Human Uterine Leiomyoma,” Oncology 57 (1999): 49–58.
- 37M. Ono, P. Yin, A. Navarro, et al., “Paracrine Activation of WNT/β-Catenin Pathway in Uterine Leiomyoma Stem Cells Promotes Tumor Growth,” PNAS 110 (2013): 17053–17058.
- 38M. Ciebiera, M. Włodarczyk, M. Wrzosek, et al., “Role of Transforming Growth Factor β in Uterine Fibroid Biology,” International Journal of Molecular Sciences 18 (2017): 2435.
- 39M. F. Holick, “Vitamin D Deficiency,” New England Journal of Medicine 357 (2007): 266–281.
- 40A. W. Norman, “From Vitamin D to Hormone D: Fundamentals of the Vitamin D Endocrine System Essential for Good Health,” American Journal of Clinical Nutrition 88 (2008): 491S–499S.
- 41M. F. Holick, “Sunlight and Vitamin D for Bone Health and Prevention of Autoimmune Diseases, Cancers, and Cardiovascular Disease,” American Journal of Clinical Nutrition 80 (2004): 1678S–1688S.
- 42J. B. Cheng, D. L. Motola, D. J. Mangelsdorf, and D. W. Russell, “De-Orphanization of Cytochrome P450 2R1: A Microsomal Vitamin D 25-Hydroxylase,” Journal of Biological Chemistry 278 (2003): 38084–38093.
- 43G. Jones, “Metabolism and Biomarkers of Vitamin D,” Scandinavian Journal of Clinical and Laboratory Investigation 72 (2012): 7–13.
- 44Y. Tanaka and H. F. DeLuca, “Rat Renal 25-Hydroxyvitamin D3 1-and 24-Hydroxylases: Their In Vivo Regulation,” American Journal of Physiology. Endocrinology and Metabolism 246 (1984): E168–E173.
- 45H. L. Brenza and H. F. DeLuca, “Regulation of 25-Hydroxyvitamin D3 1α-Hydroxylase Gene Expression by Parathyroid Hormone and 1, 25-Dihydroxyvitamin D3,” Archives of Biochemistry and Biophysics 381 (2000): 143–152.
- 46H. L. Henry, “Regulation of Vitamin D Metabolism,” Best Practice & Research Clinical Endocrinology & Metabolism 25 (2011): 531–541.
- 47R. Bouillon, G. Carmeliet, L. Verlinden, et al., “Vitamin D and Human Health: Lessons From Vitamin D Receptor Null Mice,” Endocrine Reviews 29 (2008): 726–776.
- 48G. Jones, D. E. Prosser, and M. Kaufmann, “Cytochrome P450-Mediated Metabolism of Vitamin D,” Journal of Lipid Research 55 (2014): 13–31.
- 49D. E. Prosser and G. Jones, “Enzymes Involved in the Activation and Inactivation of Vitamin D,” Trends in Biochemical Sciences 29 (2004): 664–673.
- 50C. Aranow, “Vitamin D and the Immune System,” Journal of Investigative Medicine 59 (2011): 881–886.
- 51G. Jones, S. A. Strugnell, and H. F. DeLuca, “Current Understanding of the Molecular Actions of Vitamin D,” Physiological Reviews 78 (1998): 1193–1231.
- 52H. F. DeLuca, “Overview of General Physiologic Features and Functions of Vitamin D,” American Journal of Clinical Nutrition 80 (2004): 1689S–1696S.
- 53L. Issa, G. Leong, and J. Eisman, “Molecular Mechanism of Vitamin D Receptor Action,” Inflammation Research 47 (1998): 451–475.
- 54F. Barletta, L. P. Freedman, and S. Christakos, “Enhancement of VDR-Mediated Transcription by Phosphorylation: Correlation With Increased Interaction Between the VDR and DRIP205, a Subunit of the VDR-Interacting Protein Coactivator Complex,” Molecular Endocrinology 16 (2002): 301–314.
- 55G. Jones, D. E. Prosser, and M. Kaufmann, “25-Hydroxyvitamin D-24-Hydroxylase (CYP24A1): Its Important Role in the Degradation of Vitamin D,” Archives of Biochemistry and Biophysics 523 (2012): 9–18.
- 56C. Carlberg, “Current Understanding of the Function of the Nuclear Vitamin D Receptor in Response to Its Natural and Synthetic Ligands,” Vitamin D Analogs in Cancer Prevention and Therapy 164 (2003): 29–42.
- 57M. R. Haussler, P. W. Jurutka, M. Mizwicki, and A. W. Norman, “Vitamin D Receptor (VDR)-Mediated Actions of 1α,25(OH)2vitamin D3: Genomic and Non-Genomic Mechanisms,” Best Practice & Research Clinical Endocrinology & Metabolism 25 (2011): 543–559.
- 58A. Olszewska and M. Zmijewski, “Genomic and Non-Genomic Action of Vitamin D on Ion Channels–Targeting Mitochondria,” Mitochondrion 77 (2024): 101891.
- 59Y. Zhang, J. Zhang, and G. P. Studzinski, “AKT Pathway Is Activated by 1, 25-Dihydroxyvitamin D3 and Participates in Its Anti-Apoptotic Effect and Cell Cycle Control in Differentiating HL60 Cells,” Cell Cycle 5 (2006): 447–451.
- 60Z. Zhang, P. Kovalenko, M. Cui, et al., “Constitutive Activation of the Mitogen-Activated Protein Kinase Pathway Impairs Vitamin D Signaling in Human Prostate Epithelial Cells,” Journal of Cellular Physiology 224 (2010): 433–442.
- 61L. Nonn, L. Peng, D. Feldman, and D. M. Peehl, “Inhibition of p38 by Vitamin D Reduces Interleukin-6 Production in Normal Prostate Cells via Mitogen-Activated Protein Kinase Phosphatase 5: Implications for Prostate Cancer Prevention by Vitamin D,” Cancer Research 66 (2006): 4516–4524.
- 62M. A. Rivera-Bermúdez, P. J. Bertics, R. M. Albrecht, R. Mosavin, and W. S. Mellon, “1, 25-Dihydroxyvitamin D3 Selectively Translocates PKCα to Nuclei in ROS 17/2.8 Cells,” Molecular and Cellular Endocrinology 188 (2002): 227–239.
- 63N. Pendas-Franco, O. Aguilera, F. Pereira, J. M. González-Sancho, and A. Munoz, “Vitamin D and Wnt/β-Catenin Pathway in Colon Cancer: Role and Regulation of DICKKOPF Genes,” Anticancer Research 28 (2008): 2613–2623.
- 64R. Bouillon, F. Schuit, L. Antonio, and F. Rastinejad, “Vitamin D Binding Protein: A Historic Overview,” Frontiers in Endocrinology 10 (2020): 484325.
- 65B. Cao, T. Wen, M. Wei, et al., “Transcriptomic Analysis Reveal the Responses of Dendritic Cells to VDBP,” Genes & Genomics 44 (2022): 1271–1282.
- 66M. F. Holick, N. C. Binkley, H. A. Bischoff-Ferrari, et al., “Evaluation, Treatment, and Prevention of Vitamin D Deficiency: An Endocrine Society Clinical Practice Guideline,” Journal of Clinical Endocrinology and Metabolism 96 (2011): 1911–1930.
- 67C. R. McCartney, M. E. McDonnell, M. D. Corrigan, and R. W. Lash, “Vitamin D Insufficiency and Epistemic Humility: An Endocrine Society Guideline Communication,” Journal of Clinical Endocrinology and Metabolism 109 (2024): 1948–1954.
- 68Z. A. Oskovi Kaplan, Y. Taşçi, H. O. Topçu, and S. Erkaya, “25-Hydroxy Vitamin D Levels in Premenopausal Turkish Women With Uterine Leiomyoma,” Gynecological Endocrinology 34 (2018): 261–264.
- 69V. Singh, A. Barik, and N. Imam, “Vitamin D 3 Level in Women With Uterine Fibroid: An Observational Study in Eastern Indian Population,” Journal of Obstetrics and Gynecology of India 69 (2019): 161–165.
- 70P. Srivastava, H. P. Gupta, S. Singhi, S. Khanduri, and B. Rathore, “Evaluation of 25-Hydroxy Vitamin D3 Levels in Patients With a Fibroid Uterus,” Journal of Obstetrics and Gynaecology 40 (2020): 710–714.
- 71S. Li, B. Chen, B. Sheng, J. Wang, and X. Zhu, “The Associations Between Serum Vitamin D, Calcium and Uterine Fibroids in Chinese Women: A Case-Controlled Study,” Journal of International Medical Research 48 (2020): 0300060520923492.
- 72K. A. Tunau, J. A. Garba, A. A. Panti, et al., “Low Plasma Vitamin D as a Predictor of Uterine Fibroids in a Nigerian Population,” Nigerian Postgraduate Medical Journal 28 (2021): 181–186.
- 73L. A. Huseman-Plascencia, F. Villa-Villagrana, A. Ballesteros-Manzo, et al., “Body Mass Index and Vitamin D as Risk Factors for the Development of Uterine Leiomyomas in Mexican Women,” Journal of Endometriosis and Pelvic Pain Disorders 14 (2022): 14–18.
- 74Q. E. Harmon, S. A. Patchel, S. Denslow, et al., “Vitamin D and Uterine Fibroid Growth, Incidence, and Loss: A Prospective Ultrasound Study,” Fertility and Sterility 118 (2022): 1127–1136.
- 75R. Kumari, B. Nath, H. S. Gaikwad, and M. Sharma, “Association Between Serum Vitamin D Level and Uterine Fibroid in Premenopausal Women in Indian Population,” Drug Discoveries & Therapeutics 16 (2022): 8–13.
- 76Z. Latifi, F. Oghbaei, Z. Salemi, S. Kamalipoya, and A. Fattahi, “Vitamin D and Its Binding Protein in Patients With Leiomyomas,” Journal of Obstetrics and Gynaecology Research 50 (2024): 691–698.
- 77C. C. Okoro, O. C. Ikpeze, G. U. Eleje, et al., “Association Between Serum Vitamin D Status and Uterine Leiomyomas: A Case-Control Study,” Obstetrics & Gynecology Science 67 (2024): 101.
- 78L. Feng, F. Jayes, S.-H. Jung, and P. Leppert, “Vitamin D Receptor (VDR) Is Over-Expressed in the Center of Uterine Fibroids,” Fertility and Sterility 94 (2010): S75.
- 79M. S. O. Lima, B. B. da Silva, M. L. de Medeiros, et al., “Evaluation of Vitamin D Receptor Expression in Uterine Leiomyoma and Nonneoplastic Myometrial Tissue: A Cross-Sectional Controlled Study,” Reproductive Biology and Endocrinology [Electronic Resource]: RB&E 19 (2021): 67.
- 80A. Markowska, P. Kurzawa, W. Bednarek, et al., “Immunohistochemical Expression of Vitamin D Receptor in Uterine Fibroids,” Nutrients 14 (2022): 3371.
- 81M. Bläuer, P. H. Rovio, T. Ylikomi, and P. K. Heinonen, “Vitamin D Inhibits Myometrial and Leiomyoma Cell Proliferation In Vitro,” Fertility and Sterility 91 (2009): 1919–1925.
- 82S. Mangioni, P. Viganò, D. Lattuada, et al., “Overexpression of the Wnt5b Gene in Leiomyoma Cells: Implications for a Role of the Wnt Signaling Pathway in the Uterine Benign Tumor,” Journal of Clinical Endocrinology and Metabolism 90 (2005): 5349–5355.
- 83P. S. Tanwar, H.-J. Lee, L. Zhang, et al., “Constitutive Activation of Beta-Catenin in Uterine Stroma and Smooth Muscle Leads to the Development of Mesenchymal Tumors in Mice,” Biology of Reproduction 81 (2009): 545–552.
- 84M. Ono, P. Yin, A. Navarro, et al., “Inhibition of Canonical WNT Signaling Attenuates Human Leiomyoma Cell Growth,” Fertility and Sterility 101 (2014): 1441–1449.
- 85A. Corachán, H. Ferrero, A. Aguilar, et al., “Inhibition of Tumor Cell Proliferation in Human Uterine Leiomyomas by Vitamin D via Wnt/β-Catenin Pathway,” Fertility and Sterility 111 (2019): 397–407.
- 86A. Al-Hendy, M. P. Diamond, T. G. Boyer, and S. K. Halder, “Vitamin D3 Inhibits Wnt/β-Catenin and mTOR Signaling Pathways in Human Uterine Fibroid Cells,” Journal of Clinical Endocrinology and Metabolism 101 (2016): 1542–1551.
- 87M. Ali, S. M. Shahin, N. A. Sabri, A. Al-Hendy, and Q. Yang, “Hypovitaminosis D Exacerbates the DNA Damage Load in Human Uterine Fibroids, Which Is Ameliorated by Vitamin D3 Treatment,” Acta Pharmacologica Sinica 40 (2019): 957–970.
- 88F. M. Reis, E. Bloise, and T. M. Ortiga-Carvalho, “Hormones and Pathogenesis of Uterine Fibroids,” Best Practice & Research. Clinical Obstetrics & Gynaecology 34 (2016): 13–24.
- 89A. Al-Hendy, M. P. Diamond, A. El-Sohemy, and S. K. Halder, “25-Dihydroxyvitamin D3 Regulates Expression of Sex Steroid Receptors in human Uterine Fibroid Cells,” Journal of Clinical Endocrinology and Metabolism 1 (2015): E572–E582.
10.1210/jc.2014-4011Google Scholar
- 90D. D. Bikle, “Vitamin D Metabolism, Mechanism of Action, and Clinical Applications,” Chemistry & Biology 21 (2014): 319–329.
- 91E. R. Othman, E. Ahmed, A. A. Sayed, et al., “Human Uterine Leiomyoma Contains Low Levels of 1, 25 Dihdroxyvitamin D3, and Shows Dysregulated Expression of Vitamin D Metabolizing Enzymes,” European Journal of Obstetrics & Gynecology and Reproductive Biology 229 (2018): 117–122.
- 92S. K. Halder, K. G. Osteen, and A. Al-Hendy, “Vitamin D3 Inhibits Expression and Activities of Matrix Metalloproteinase-2 and-9 in Human Uterine Fibroid Cells,” Human Reproduction 28 (2013): 2407–2416.
- 93A. Corachán, M. G. Trejo, M. C. Carbajo-García, et al., “Vitamin D as an Effective Treatment in Human Uterine Leiomyomas Independent of Mediator Complex Subunit 12 Mutation,” Fertility and Sterility 115 (2021): 512–521.
- 94C. I. Cross, P. H. Driggers, B. E. McCarthy, et al., “A-Kinase Anchoring Protein 13 Interacts With the Vitamin D Receptor to Alter Vitamin D-Dependent Gene Activation in Uterine Leiomyoma Cells,” F&S Science 2 (2021): 303–314.
- 95S. S. M. Ng, S. Jorge, M. Malik, et al., “A-Kinase Anchoring Protein 13 (AKAP13) Augments Progesterone Signaling in Uterine Fibroid Cells,” Journal of Clinical Endocrinology and Metabolism 104 (2018): 970–980.
10.1210/jc.2018-01216Google Scholar
- 96R. Rogers, J. Norian, M. Malik, et al., “Mechanical Homeostasis Is Altered in Uterine Leiomyoma,” American Journal of Obstetrics and Gynecology 198 (2008): 474.e1–474.11.
- 97A. Corachán, H. Ferrero, J. Escrig, et al., “Long-Term Vitamin D Treatment Decreases Human Uterine Leiomyoma Size in a Xenograft Animal Model,” Fertility and Sterility 113 (2020): 205–216.e4.
- 98M. Ivanova, A. Soule, J. Pudwell, and O. Bougie, “The Association of Vitamin D With Uterine Fibroids in Premenopausal Patients: A Systematic Review and Meta-Analysis,” Journal of Obstetrics and Gynaecology Canada 46 (2024): 102632.
- 99A. Combs, B. Singh, E. Nylander, et al., “A Systematic Review of Vitamin D and Fibroids: Pathophysiology, Prevention, and Treatment,” Reproductive Sciences 30 (2023): 1049–1064.
- 100S. A. Alsharif, S. Baradwan, M. S. Alshahrani, et al., “Effect of Oral Consumption of Vitamin D on Uterine Fibroids: A Systematic Review and Meta-Analysis of Randomized Clinical Trials,” Nutrition and Cancer 76 (2024): 226–235.
- 101M. Hajhashemi, M. Ansari, F. Haghollahi, and B. Eslami, “The Effect of Vitamin D Supplementation on the Size of Uterine Leiomyoma in Women With Vitamin D Deficiency,” Caspian Journal of Internal Medicine 10 (2019): 125.
- 102S. Arjeh, F. Darsareh, Z. A. Asl, and M. A. Kutenaei, “Effect of Oral Consumption of Vitamin D on Uterine Fibroids: A Randomized Clinical Trial,” Complementary Therapies in Clinical Practice 39 (2020): 101159.
- 103F. D. Tanha, E. Feizabad, M. V. Farahani, et al., “The Effect of Vitamin D Deficiency on Overgrowth of Uterine Fibroids: A Blinded Randomized Clinical Trial,” International Journal of Fertility & Sterility 15 (2021): 95.
- 104A. Suneja, F. Faridi, S. Bhatt, et al., “Effect of Vitamin D3 Supplementation on Symptomatic Uterine Leiomyoma in Women With Hypovitaminosis D,” Journal of Mid-Life Health 12 (2021): 53–60.
- 105K. Tabrizian, R. Shokouhinia, F. D. Tanha, et al., “Effect of Two Different Doses of Vitamin D Supplementation on Uterine Myoma on South East Iranian Population: A Clinical Trial,” Journal of Family & Reproductive Health 15 (2021): 248.
- 106Q. Wang, P. Tian, W. Sun, et al., “A Multimodal Ultrasound Observation Study on the Effect of Vitamin D on Uterine Fibroids in Non-Menopausal Women,” Current Medical Imaging 20 (2024): e15734056281479.
- 107H. N. Graham, “Green Tea Composition, Consumption, and Polyphenol Chemistry,” Preventive Medicine 21 (1992): 334–350.
- 108C. Cabrera, R. Artacho, and R. Giménez, “Beneficial Effects of Green Tea—A Review,” Journal of the American College of Nutrition 25 (2006): 79–99.
- 109D. Del Rio, A. J. Stewart, W. Mullen, et al., “HPLC-MSn Analysis of Phenolic Compounds and Purine Alkaloids in Green and Black Tea,” Journal of Agricultural and Food Chemistry 52 (2004): 2807–2815.
- 110J. D. Lambert and R. J. Elias, “The Antioxidant and Pro-Oxidant Activities of Green Tea Polyphenols: A Role in Cancer Prevention,” Archives of Biochemistry and Biophysics 501 (2010): 65–72.
- 111S. A. Mandel, T. Amit, L. Kalfon, et al., “Cell Signaling Pathways and Iron Chelation in the Neurorestorative Activity of Green Tea Polyphenols: Special Reference to Epigallocatechin Gallate (EGCG),” Journal of Alzheimer's Disease 15 (2008): 211–222.
- 112K. F. Pirker, M. C. Baratto, R. Basosi, and B. A. Goodman, “Influence of pH on the Speciation of Copper (II) in Reactions With the Green Tea Polyphenols, Epigallocatechin Gallate and Gallic Acid,” Journal of Inorganic Biochemistry 112 (2012): 10–16.
- 113S. Azam, N. Hadi, N. U. Khan, and S. M. Hadi, “Prooxidant Property of Green Tea Polyphenols Epicatechin and Epigallocatechin-3-Gallate: Implications for Anticancer Properties,” Toxicology In Vitro 18 (2004): 555–561.
- 114A. Negri, V. Naponelli, F. Rizzi, and S. Bettuzzi, “Molecular Targets of Epigallocatechin—Gallate (EGCG): A Special Focus on Signal Transduction and Cancer,” Nutrients 10 (2018): 1936.
- 115M. Moradzadeh, A. Hosseini, S. Erfanian, and H. Rezaei, “Epigallocatechin-3-Gallate Promotes Apoptosis in Human Breast Cancer T47D Cells Through Down-Regulation of PI3K/AKT and Telomerase,” Pharmacological Reports 69 (2017): 924–928.
- 116G. Jin, Y. Yang, K. Liu, et al., “Combination Curcumin and (−)-Epigallocatechin-3-Gallate Inhibits Colorectal Carcinoma Microenvironment-Induced Angiogenesis by JAK/STAT3/IL-8 Pathway,” Oncogenesis 6 (2017): e384–e384.
- 117M. Shimizu, Y. Shirakami, and H. Moriwaki, “Targeting Receptor Tyrosine Kinases for Chemoprevention by Green Tea Catechin, EGCG,” International Journal of Molecular Sciences 9 (2008): 1034–1049.
- 118Y. Chen, X.-Q. Wang, Q. Zhang, et al., “(−)-Epigallocatechin-3-Gallate Inhibits Colorectal Cancer Stem Cells by Suppressing Wnt/β-Catenin Pathway,” Nutrients 9 (2017): 572.
- 119S. Shankar, G. Suthakar, and R. K. Srivastava, “Epigallocatechin-3-Gallate Inhibits Cell Cycle and Induces Apoptosis in Pancreatic Cancer,” Frontiers in Bioscience 12 (2007): 5039–5051.
- 120F. A. Olotu, C. Agoni, E. Adeniji, M. Abdullahi, and M. E. Soliman, “Probing Gallate-Mediated Selectivity and High-Affinity Binding of Epigallocatechin Gallate: A Way-Forward in the Design of Selective Inhibitors for Anti-Apoptotic Bcl-2 Proteins,” Applied Biochemistry and Biotechnology 187 (2019): 1061–1080.
- 121Q. Hu, X. Chang, R. Yan, et al., “(−)-Epigallocatechin-3-Gallate Induces Cancer Cell Apoptosis via Acetylation of Amyloid Precursor Protein,” Medical Oncology 32 (2015): 1–11.
- 122S.-R. Kim, K.-J. Seong, W.-J. Kim, and J.-Y. Jung, “Epigallocatechin Gallate Protects Against Hypoxia-Induced Inflammation in Microglia via NF-κB Suppression and Nrf-2/HO-1 Activation,” International Journal of Molecular Sciences 23 (2022): 4004.
- 123M. Sazuka, H. Imazawa, Y. Shoji, et al., “Inhibition of Collagenases From Mouse Lung Carcinoma Cells by Green Tea Catechins and Black Tea Theaflavins,” Bioscience, Biotechnology, and Biochemistry 61 (1997): 1504–1506.
- 124G. Deb, V. S. Thakur, A. M. Limaye, and S. Gupta, “Epigenetic Induction of Tissue Inhibitor of Matrix Metalloproteinase-3 by Green Tea Polyphenols in Breast Cancer Cells,” Molecular Carcinogenesis 54 (2015): 485–499.
- 125J. Shi, F. Liu, W. Zhang, et al., “Epigallocatechin-3-Gallate Inhibits Nicotine‑Induced Migration and Invasion by the Suppression of Angiogenesis and Epithelial‑Mesenchymal Transition in Non-Small Cell Lung Cancer Cells Corrigendum in/10.3892/or. 2023.8614,” Oncology Reports 33 (2015): 2972–2980.
- 126M. Pandey, S. Shukla, and S. Gupta, “Promoter Demethylation and Chromatin Remodeling by Green Tea Polyphenols Leads to Re-Expression of GSTP1 in Human Prostate Cancer Cells,” International Journal of Cancer 126 (2010): 2520–2533.
- 127M. A. Khan, A. Hussain, M. K. Sundaram, et al., “(-)-Epigallocatechin-3-Gallate Reverses the Expression of Various Tumor-Suppressor Genes by Inhibiting DNA Methyltransferases and Histone Deacetylases in Human Cervical Cancer Cells,” Oncology Reports 33 (2015): 1976–1984.
- 128H. Wang, S. Bian, and C. S. Yang, “Green Tea Polyphenol EGCG Suppresses Lung Cancer Cell Growth Through Upregulating miR-210 Expression Caused by Stabilizing HIF-1α,” Carcinogenesis 32 (2011): 1881–1889.
- 129J.-Y. Jang, J.-K. Lee, Y.-K. Jeon, and C.-W. Kim, “Exosome Derived From Epigallocatechin Gallate Treated Breast Cancer Cells Suppresses Tumor Growth by Inhibiting Tumor-associated Macrophage Infiltration and M2 Polarization,” BMC Cancer 13 (2013): 1–12.
- 130J. C.-C. Wei, H.-C. Huang, W.-J. Chen, et al., “Epigallocatechin Gallate Attenuates Amyloid β-Induced Inflammation and Neurotoxicity in EOC 13.31 Microglia,” European Journal of Pharmacology 770 (2016): 16–24.
- 131D. Zhang, V. Rajaratnam, O. Al-Hendy, S. Halder, and A. Al-Hendy, “Green Tea Extract Inhibition of Human Leiomyoma Cell Proliferation Is Mediated via Catechol-o-Methyltransferase,” Gynecologic and Obstetric Investigation 78 (2014): 109–118.
- 132I. H. Ozercan, N. Sahin, F. Akdemir, et al., “Chemoprevention of Fibroid Tumors by [-]-Epigallocatechin-3-Gallate in Quail,” Nutrition Research 28 (2008): 92–97.
- 133R. Biro, R. Richter, M. Ortiz, J. Sehouli, and M. David, “Effects of Epigallocatechin Gallate-Enriched Green Tea Extract Capsules in Uterine Myomas: Results of an Observational Study,” Archives of Gynecology and Obstetrics 303 (2021): 1235–1243.
- 134G. Porcaro, A. Santamaria, D. Giordano, and P. Angelozzi, “Vitamin D Plus Epigallocatechin Gallate: A Novel Promising Approach for Uterine Myomas,” European Review for Medical and Pharmacological Sciences 24 (2020): 3344–3351.
- 135D. Miriello, F. Galanti, P. Cignini, et al., “Uterine Fibroids Treatment: Do We Have New Valid Alternative? Experiencing the Combination of Vitamin D Plus Epigallocatechin Gallate in Childbearing Age Affected Women,” European Review for Medical and Pharmacological Sciences 25 (2021): 2843–2851.
- 136A. Tinelli, G. Panese, M. Licchelli, et al., “The Impact of Epigallocatechin Gallate, Vitamin D, and D-Chiro-Inositol on Early Surgical Outcomes of Laparoscopic Myomectomy: A Pilot Study,” Archives of Gynecology and Obstetrics 309 (2024): 1021–1026.
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Elkins, L. J., & Spiegelman, M. (2021). pyUserCalc: A revised Jupyter notebook calculator for uranium-series disequilibria in basalts. Earth and Space Science, 8, e2020EA001619. https://doi.org/10.1029/2020EA001619
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