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Natarajan, Jawahar
- Discovery of Immunomodulators from Plant Kingdom Targeting IL-6 for the Effective Management Therapy of SARS-CoV-2
Abstract Views :164 |
PDF Views:93
Authors
Akey Krishna Swaroop
1,
Palathoti Nagarjuna
1,
P. Naresh
1,
P. Shyam Sundar
1,
S. Jubie
1,
Jawahar Natarajan
2,
P. Vasanth
3
Affiliations
1 Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, The Nilgiris – 643001, Tamil Nadu, IN
2 Department of Pharmaceutics, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, The Nilgiris – 643001, Tamil Nadu, IN
3 Department of Biotechnology, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, The Nilgiris – 643001, Tamil Nadu, IN
1 Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, The Nilgiris – 643001, Tamil Nadu, IN
2 Department of Pharmaceutics, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, The Nilgiris – 643001, Tamil Nadu, IN
3 Department of Biotechnology, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, The Nilgiris – 643001, Tamil Nadu, IN
Source
Journal of Natural Remedies, Vol 22, No 2 (2022), Pagination: 249 - 260Abstract
The present study was conducted because of the recent scenario of this pandemic coronavirus outbreak worldwide. Currently, this disease cannot be treated through specific vaccines and therapeutic medicines. While many vaccines are being investigated, it would take some time for these to be accessible to the masses. Eventual evidence indicates that many COVID-19 patients may die from an irregular release of cytokines called as Cytokine Release Syndrome (CRS) due to the excessive reaction of their immune systems. In worsening patients with COVID-19, CRS played a significant role, from pneumonia via ARDS to cumulative systemic inflammation and eventually to a failing of the multi-system organ. In COVID-19 individuals, a large number of cytokines, including IL-6, IL-1, IL-2, IL-10, TNF- α, and IFN- α, participate in the ‘cytokine storm,’ but IL-6, whose higher serum levels are associated with respiratory failure, ARDS, and adverse clinical outcomes, tends to be a critical factor. In China, the COVID-19 mortality indicator has been tested by a multi-centre retrospective analysis in 150 COVID-19 patients. The study analysed that 82 cases are resolved from COVID-19 and 68 cases are dead due to enhancement of IL-6 levels in the serum. In this research, the secondary plant metabolites from Indian traditional medicine are identified through a computational technique and the selected seedling metabolite is sealed to block the IL-6 receptor.Keywords
Covid-19, IL-6, Cytokine Release Syndrome, Secondary MetabolitesReferences
- Abbasifard M, Khorramdelazad H. The bio-mission of interleukin-6 in the pathogenesis of COVID-19: A brief look at potential therapeutic tactics. Life Sci. 2020; 257. https://doi.org/10.1016/j.lfs.2020.118097. PMid:32679148. PMCid:PMC7361088
- Tang Y, Liu J, Zhang D, Xu Z, Ji J, Wen C. Cytokine Storm in COVID-19: The Current evidence and treatment strategies. Front Immunol. 2020; 11(July):1–13. https:// doi.org/10.3389/fimmu.2020.01708. PMid:32754163. PMCid:PMC7365923
- Rana MM. Cytokine storm in COVID-19: Potential therapeutics for immunomodulation. J Res Clin Med. 2020; 8(1):38. https://doi.org/10.34172/jrcm.2020.038
- Zhang C, Wu Z, Li J-W, Zhao H, Wang G-Q. Cytokine release syndrome in severe COVID-19: Interleukin-6 receptor antagonist tocilizumab may be the key to reduce mortality. Int J Antimicrob Agents. 2020; 55(5):105954. https://doi. org/10.1016/j.ijantimicag.2020.105954. PMid:32234467. PMCid:PMC7118634
- Sinha P, Matthay MA, Calfee CS. Is a “Cytokine Storm” relevant to COVID-19? JAMA Intern Med. 2020; 180(9):1152. https://doi.org/10.1001/jamainternmed.2020.3313. PMid:32602883.
- Liu B, Li M, Zhou Z, Guan X, Xiang Y. Can we use interleukin-6 (IL-6) blockade for coronavirus disease 2019 (COVID-19)-induced cytokine release syndrome (CRS)? J Autoimmun. 2020; 111:102452. https://doi.org/10.1016/j. jaut.2020.102452. PMid:32291137. PMCid:PMC7151347
- Han H, Ma Q, Li C, Liu R, Zhao L, Wang W, et al. Profiling serum cytokines in COVID-19 patients reveals IL-6 and IL-10 are disease severity predictors. Emerg Microbes Infect. 2020; 9(1):1123–30. https://doi.org/10.1080/222217 51.2020.1770129. PMid:32475230. PMCid:PMC7473317
- Copaescu A, Smibert O, Gibson A, Phillips EJ, Trubiano JA. The role of IL-6 and other mediators in the cytokine storm associated with SARS-CoV-2 infection. J Allergy Clin Immunol. 2020; 146(3):518–34. https://doi.org/10.1016/j. jaci.2020.07.001. PMid:32896310. PMCid:PMC7471766
- Chen X, Zhao B, Qu Y, Chen Y, Xiong J, Feng Y, et al. Detectable serum SARS-CoV-2 viral load (RNAaemia) is closely correlated with drastically elevated interleukin 6 (IL6) level in critically ill COVID-19 patients. Clin Infect Dis. 2020. https://doi.org/10.1101/2020.02.29.20029520
- Chen LYC, Hoiland RL, Stukas S, Wellington CL, Sekhon MS. Confronting the controversy: Interleukin-6 and the COVID-19 cytokine storm syndrome. Eur Respir J. 2020; 56(4). https://doi.org/10.1183/13993003.03006-2020. PMid:32883678. PMCid:PMC7474149
- Gubernatorova EO, Gorshkova EA, Polinova AI, Drutskaya MS. IL-6: relevance for immunopathology of SARS-CoV-2. Cytokine Growth Factor Rev. 2020; 53:13–24. https:// doi.org/10.1016/j.cytogfr.2020.05.009. PMid:32475759. PMCid:PMC7237916
- Rees C, Costin J, Fink R, Mcmichael M, Fontaine K, Isern S, et al. In vitro inhibition of dengue virus entry by p-sulfoxy-cinnamic acid and structurally related combinatorial chemistries. Antivir. Res. 2008; 80(2):135–42. https://doi. org/10.1016/j.antiviral.2008.05.007. PMid:18606464
- Berman HM, Kleywegt GJ, Nakamura H, Markley JL. The protein data bank archive as an open data resource. J Comput Aided Mol Des. 2014; 28(10):1009–14. https:// doi.org/10.1007/s10822-014-9770-y. PMid:25062767. PMCid:PMC4196035
- Alhazmi HA, Najmi A, Javed SA, Sultana S, Al Bratty M, Makeen HA, et al. Medicinal plants and isolated molecules demonstrating immunomodulation activity as potential alternative therapies for viral diseases including COVID19. Front Immunol. 2021; 12:1721. https://doi.org/10.3389/ fimmu.2021.637553. PMid:34054806. PMCid:PMC8155592
- Wagner H. Immunomodulatory agents from plants. Part of the Progress in Inflammation Research book series (PIR). Springer Science & Business Media; 1999. https://doi. org/10.1007/978-3-0348-8763-2
- Dahanukar SA, Thatte UM. Current status of Ayurveda in phytomedicine. Phytomedicine. 1997; 4(4):359–68. https:// doi.org/10.1016/S0944-7113(97)80048-7
- Dorsch W, Stuppner H, Wagner H, Gropp M, Demoulin S, Ring J. Antiasthmatic effects of Picrorhiza kurroa: Androsin prevents allergen-and PAF-induced bronchial obstruction in guinea pigs. Int Arch Allergy Immunol. 1991; 95(2–3):128–33. https://doi.org/10.1159/000235416. PMid:1718906
- Jantan I, Ahmad W, Bukhari SNA. Plant-derived immunomodulators: An insight on their preclinical evaluation and clinical trials. Front Plant Sci. 2015; 6:655. https:// doi.org/10.3389/fpls.2015.00655. PMid:26379683 PMCid:PMC4548092
- Nair A, Chattopadhyay D, Saha B. Plant-derived immunomodulators. In: New look to phytomedicine. Elsevier; 2019. p. 435–99. https://doi.org/10.1016/B978-0-12-814619- 4.00018-5. PMid:30794457
- Swaroop AK, Mvnl C, S M, Subramanian G, Natarajan J, Selvaraj J. Plant derived immunomodulators: A Critical Review [Internet]. 2021. [cited 2021 Nov 9]. Available from: https://apb.tbzmed.ac.ir/Article/apb-32199. https://doi. org/10.34172/apb.2022.074
- Akey KS, Jubie S, Vasanth P, Jeyaprakash M, Jawahar N. Dual modulation of IL-6 pathway by flavonoid-metal complexes as immune boosters for SARS-CoV-2 therapy. SPAST Abstracts. 2021; 1(01).
- Cousins KR. Computer review of Chem Draw Ultra 12.0. J Am Chem Soc. 2011; 133(21):8388. https://doi.org/10.1021/ ja204075s. PMid:21561109
- Usha T, Goyal AK, Lubna S, Prashanth HP, Mohan TM, Pande V, et al. Identification of anti-cancer targets of eco-friendly waste punica granatum peel by dual reverse virtual screening and binding analysis. Asian Pac J Cancer Prev. 2015; 15(23):10345–50. https://doi.org/10.7314/ APJCP.2014.15.23.10345. PMid:25556473
- Sarvagalla S, Singh VK, Ke Y-Y, Shiao H-Y, Lin W-H, Hsieh H-P, et al. Identification of ligand efficient, fragment-like hits from an HTS library: Structure-based virtual screening and docking investigations of 2H- and 3H-pyrazolo tautomers for Aurora kinase A selectivity. J Comput Aided Mol Des. 2015; 29(1):89–100. https://doi.org/10.1007/s10822- 014-9807-2. PMid:25344840
- Geerts T, Vander Heyden Y. In Silico predictions of ADME-Tox properties: Drug absorption. Comb Chem High Throughput Screen. 2011; 14(5):339–61. https://doi. org/10.2174/138620711795508359. PMid:21470183
- Naresh P, Selvaraj A, Sundar PS, Murugesan S, Sathianarayanan S, Namboori PKK, et al. Targeting a conserved pocket (n-octyl-β-D-glucoside) on the dengue virus envelope protein by small bioactive molecule inhibitors. J Biomol Struct Dyn. 2020; 1–13. https://doi.org/10.1080/073 91102.2020.1862707. PMid:33345726
- Prabha T, Kapoor VK, Selvamani P, Latha S, Sivakumar T, Jubie S. Dual modulators of selected plant secondary metabolites targeting COVID-19 main protease and Interleukin-2: An in-silico approach based novel hypothesis. COVID. 2021; 2(2):223–34. https://doi.org/10.2174/2 666796701999200929124556
- Chemopreventive Potential of Phytoestrogens on Hormone-Sensitive Cancer - An Updated Review
Abstract Views :101 |
PDF Views:78
Authors
Affiliations
1 Department of Pharmacognosy, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, Nilgiris - 643001, Tamil Nadu, IN
2 Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, Nilgiris - 643001, Tamil Nadu, IN
3 Department of Pharmaceutics, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, Nilgiris - 643001, Tamil Nadu, IN
1 Department of Pharmacognosy, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, Nilgiris - 643001, Tamil Nadu, IN
2 Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, Nilgiris - 643001, Tamil Nadu, IN
3 Department of Pharmaceutics, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, Nilgiris - 643001, Tamil Nadu, IN
Source
Journal of Natural Remedies, Vol 23, No 1 (2023), Pagination: 23-33Abstract
Hormone-dependent cancers contribute to the majority of cancer deaths in women. Treatment options for hormonal cancer such as breast, endometrial, prostate, and ovarian cancer aim at inhibiting key signalling pathways and hormones responsible for cell proliferation. Hormonal therapies in the long run cause musculoskeletal disorders, Disease reoccurrence, and drug resistance. There is a need for new alternative therapies to prevent and treat hormonal carcinomas. Phytoestrogens, a naturally occurring polyphenol have potent effects on hormonal cancers due to their estrogenic effects. Evidence suggests that phytoestrogens exert their apoptotic potential by interfering with steroidogenesis, gene expressions, and down-regulation of Protein Tyrosine Kinases, Matrix Metalloproteinases. They also act as topo-poisons. This review explains the key mechanisms of phytoestrogens in inhibiting cell proliferation in hormonal cancers by evidence from recent clinical studies, meta-analyses, and cohort study reports. Phytoestrogens have multi-target potential with both preventive and treatment properties on cancer cell lines. Combination therapies with phytoestrogens are more beneficial in controlling cell progression. Hence further research is required to explore their epigenetic properties on tumour suppressor genes which stay an important target in cancer research.Keywords
Breast Cancer, Chemoprevention, Endometrial Cancer, Ovarian Cancer, Phytoestrogens.References
- Korde LA, Wu AH, Fears T, Nomura AMY, West DW, Kolonel LN, Pike MC, Hoover RN, Ziegler RG. Childhood Soy Intake and Breast Cancer Risk in Asian American Women. Cancer Epidemiol. Biomark. Prev. Publ. Am. Assoc. Cancer Res. Cosponsored Am. Soc. Prev. Oncol. 2009; 18(4):1050-1059. https://doi. org/10.1158/1055-9965.EPI-08-0405
- Ronghe A, Chatterjee A, Singh B, Dandawate P, Murphy L, Bhat NK, Padhye S, Bhat HK. Differential Regulation of Estrogen Receptors α and β by 4-(E)-{(4- Hydroxyphenylimino)-Methylbenzene,1,2-Diol}, a Novel Resveratrol Analog. J. Steroid Biochem. Mol. Biol. 2014; 144:500-512. https://doi.org/10.1016/j. jsbmb.2014.09.015
- He J, Wang S, Zhou M, Yu W, Zhang Y, He X. Phytoestrogens and Risk of Prostate Cancer: A MetaAnalysis of Observational Studies. World J. Surg. Oncol. 2015; 13(1):231. https://doi.org/10.1186/ s12957-015-0648-9
- Horn-Ross P L, John EM, Canchola AJ, Stewart SL, Lee MM. Phytoestrogen Intake and Endometrial Cancer Risk. JNCI J. Natl. Cancer Inst. 2003; 95(15):1158- 1164. https://doi.org/10.1093/jnci/djg015
- Rice S, Whitehead S.A. Phytoestrogens and Breast Cancer–Promoters or Protectors? Endocr. Relat. Cancer. 2006; 13(4):995-1015. https://doi. org/10.1677/erc.1.01159
- Sudhesh Dev S, Zainal Abidin SA, Farghadani R, Othman I, Naidu R. Receptor Tyrosine Kinases and Their Signaling Pathways as Therapeutic Targets of Curcumin in Cancer. Front. Pharmacol. 2021; 12:772510. https://doi.org/10.3389/ fphar.2021.772510
- Pottier C, Fresnais M, Gilon M, Jerusalem G, Longuespee R, Sounni NE. Tyrosine Kinase Inhibitors in Cancer: Breakthrough and Challenges of Targeted Therapy. Cancers. 2020; 12(3):731. https://doi. org/10.3390/cancers12030731
- Butti R, Das S, Gunasekaran VP, Yadav AS, Kumar D, Kundu GC. Receptor Tyrosine Kinases (RTKs) in Breast Cancer: Signaling, Therapeutic Implications and Challenges. Mol. Cancer. 2018; 17(1):34. https:// doi.org/10.1186/s12943-018-0797-x
- Nynca A, Nynca J, Wąsowska B, Kolesarova A, Kołomycka A, Ciereszko RE. Effects of the Phytoestrogen, Genistein, and Protein Tyrosine Kinase Inhibitor–Dependent Mechanisms on Steroidogenesis and Estrogen Receptor Expression in Porcine Granulosa Cells of Medium Follicles. Domest. Anim. Endocrinol. 2013; 44(1):10-18. https:// doi.org/10.1016/j.domaniend.2012.07.002
- Pratheeshkumar P, Sreekala C, Zhang Z, Budhraja A, Ding S, Son Y-O, Wang X, Hitron A, HyunJung K, Wang L, Lee J-C, Shi X. Cancer Prevention with Promising Natural Products: Mechanisms of Action and Molecular Targets. Anticancer Agents Med. Chem. 2012; 12(10):1159-1184. https://doi. org/10.2174/187152012803833035
- Kang NJ, Lee KW, Rogozin EA, Cho Y-Y, Heo Y-S, Bode AM, Lee HJ, Dong Z. Equol, a Metabolite of the Soybean Isoflavone Daidzein, Inhibits Neoplastic Cell Transformation by Targeting the MEK/ERK/ P90RSK/Activator Protein-1 Pathway. J. Biol. Chem. 2007; 282(45):32856-32866. https://doi.org/10.1074/ jbc.M701459200
- Polier G, Ding J, Konkimalla BV, Eick D, Ribeiro N, Kohler R, Giaisi M, Efferth T, Desaubry L, Krammer PH, Li-Weber M. Wogonin and Related Natural Flavones Are Inhibitors of CDK9 That Induce Apoptosis in Cancer Cells by Transcriptional Suppression of Mcl1. Cell Death Dis. 2011; 2(7):e182-e182. https://doi. org/10.1038/cddis.2011.66
- Holder S, Zemskova M, Zhang C, Tabrizizad M, Bremer R, Neidigh JW, Lilly MB. Characterization of a Potent and Selective Small-Molecule Inhibitor of the PIM1 Kinase. Mol. Cancer Ther. 2007; 6(1):163-172. https://doi.org/10.1158/1535-7163.MCT-06-0397
- Balakrishnan L, Bambara RA. Flap Endonuclease 1. Annu. Rev. Biochem. 2013; 82(1):119-138. https://doi. org/10.1146/annurev-biochem-072511-122603
- Balian A, Hernandez FJ. Nucleases as Molecular Targets for Cancer Diagnosis. Biomark. Res. 2021; 9(1):86. https://doi.org/10.1186/s40364-021-00342-4
- Thakur S, Sarkar B, Cholia RP, Gautam N, Dhiman M, Mantha AK. APE1/Ref-1 as an Emerging Therapeutic Target for Various Human Diseases: Phytochemical Modulation of Its Functions. Exp. Mol. Med. 2014; 46(7):e106-e106. https://doi.org/10.1038/ emm.2014.42
- Chen B, Zhang Y, Wang Y, Rao J, Jiang X, Xu Z. Curcumin Inhibits Proliferation of Breast Cancer Cells through Nrf2-Mediated down-Regulation of Fen1 Expression. J. Steroid Biochem. Mol. Biol. 2014; 143:11-18. https://doi.org/10.1016/j. jsbmb.2014.01.009
- Rice S, Whitehead SA. Phytoestrogens and Breast Cancer–Promoters or Protectors? Endocr. Relat. Cancer. 2006; 13(4):995-1015. https://doi. org/10.1677/erc.1.01159
- Vann KR, Oviatt AA, Osheroff N. Topoisomerase II Poisons: Converting Essential Enzymes into Molecular Scissors. Biochemistry. 2021; 60(21):1630- 1641. https://doi.org/10.1021/acs.biochem.1c00240
- Bandele OJ, Osheroff N. Bioflavonoids as Poisons of Human Topoisomerase IIα and IIβ. Biochemistry. 2007; 46(20):6097-6108. https://doi.org/10.1021/ bi7000664
- Basso E, Fiore M, Leone S, Degrassi F, Cozzi R. Effects of Resveratrol on Topoisomerase IIActivity: Induction of Micronuclei and Inhibition of Chromosome Segregation in CHO-K1 Cells. Mutagenesis. 2013; 28(3):243-248. https://doi. org/10.1093/mutage/ges067
- Karsli-Ceppioglu S, Ngollo M, Judes G, PenaultLLorca F, Bignon Y-J, Guy L, Bernard-Gallon D. The Role of Soy Phytoestrogens on Genetic and Epigenetic Mechanisms of Prostate Cancer. In The Enzymes. Elsevier. 2015; 37:193-221. https://doi.org/10.1016/ bs.enz.2015.05.004
- Adjakly M, Bosviel R, Rabiau N, Boiteux J-P, Bignon Y-J, Guy L, Bernard-Gallon D. DNA Methylation and Soy Phytoestrogens: Quantitative Study in DU-145 and PC-3 Human Prostate Cancer Cell Lines. Epigenomics. 2011; 3(6):795-803. https://doi. org/10.2217/epi.11.103
- Mayo B, Vazquez L, Florez AB. Equol: A Bacterial Metabolite from the Daidzein Isoflavone and Its Presumed Beneficial Health Effects. Nutrients. 2019; 11(9):2231. https://doi.org/10.3390/nu11092231
- Phillip CJ, Giardina CK, Bilir B, Cutler DJ, Lai Y-H, Kucuk O, Moreno CS. Genistein Cooperates with the Histone Deacetylase Inhibitor Vorinostat to Induce Cell Death in Prostate Cancer Cells. BMC Cancer. 2012; 12(1):145. https://doi.org/10.1186/1471-2407- 12-145
- Hsieh C-J, Hsu Y-L, Huang Y-F, Tsai E-M. Molecular Mechanisms of Anticancer Effects of Phytoestrogens in Breast Cancer. Curr. Protein Pept. Sci. 2018; 19(3). https://doi.org/10.2174/138920371 8666170111121255
- Waite KA, Sinden MR, Eng C. Phytoestrogen Exposure Elevates PTEN Levels. 7. 28. Phytoestrogens Regulate MRNA and Protein Levels of Guanine Nucleotide-Binding Protein, Beta-1 Subunit (GNB1) in MCF-7 Cells. J. Cell. Physiol. 11.
- Yasin HK, Taylor AH, Ayakannu T. A Narrative Review of the Role of Diet and Lifestyle Factors in the Development and Prevention of Endometrial Cancer. Cancers. 2021; 13(9):2149. https://doi.org/10.3390/ cancers13092149
- Zhong X, Ge J, Chen S, Xiong Y, Ma S, Chen Q. Association between Dietary Isoflavones in Soy and Legumes and Endometrial Cancer: A Systematic Review and Meta-Analysis. J. Acad. Nutr. Diet. 2018; 118(4):637-651. https://doi.org/10.1016/j. jand.2016.09.036
- Rudzitis-Auth J, Menger MD, Laschke MW. Resveratrol Is a Potent Inhibitor of Vascularization and Cell Proliferation in Experimental Endometriosis. Hum. Reprod. 2013; 28(5):1339-1347. https://doi. org/10.1093/humrep/det031
- Kim J, Woo J, Kim H, Oh M, Jang D, Choi J. Anti‐ Endometriotic Effects of Pueraria Flower Extract in Human Endometriotic Cells and Mice. Nutrients. 2017; 9(3):212. https://doi.org/10.3390/nu9030212
- Park S, Lim W, Bazer FW, Song G. Naringenin Induces Mitochondria-Mediated Apoptosis and Endoplasmic Reticulum Stress by Regulating MAPK and AKT Signal Transduction Pathways in Endometriosis Cells. MHR Basic Sci. Reprod. Med. 2017; 23(12):842- 854. https://doi.org/10.1093/molehr/gax057
- Arablou T. Delbandi A, Khodaverdi S, Arefi S, Kolahdouz‐Mohammadi R, Heidari S, Mohammadi T, Aryaeian N. Resveratrol Reduces the Expression of Insulin‐like Growth Factor‐1 and Hepatocyte Growth Factor in Stromal Cells of Women with Endometriosis Compared with Nonendometriotic Women. Phytother. Res. 2019; 33(4):1044-1054. https://doi.org/10.1002/ptr.6298
- Bartiromo L, Schimberni M, Villanacci R, Ottolina J, Dolci C, Salmeri N, Vigano P, Candiani M. Endometriosis and Phytoestrogens: Friends or Foes? A Systematic Review. Nutrients. 2021; 13(8):2532. https://doi.org/10.3390/nu13082532
- Zhou Y, Liu X. The Role of Estrogen Receptor Beta in Breast Cancer. Biomark. Res. 2020; 8(1):39. https:// doi.org/10.1186/s40364-020-00223-2
- Paterni I, Granchi C, Katzenellenbogen JA, Minutolo F. Estrogen Receptors Alpha (ERα) and Beta (ERβ): Subtype-Selective Ligands and Clinical Potential. Steroids. 2014; 9:13-29. https://doi.org/10.1016/j.steroids.2014.06.012
- Jordan VC, O’Malley BW. Selective EstrogenReceptor Modulators and Antihormonal Resistance in Breast Cancer. J. Clin. Oncol. 2007; 25(36):5815- 5824. https://doi.org/10.1200/JCO.2007.11.3886
- Kala R, Shah HN, Martin SL, Tollefsbol TO. EpigeneticBased Combinatorial Resveratrol and Pterostilbene Alters DNA Damage Response by Affecting SIRT1 and DNMT Enzyme Expression, Including SIRT1- Dependent γ-H2AX and Telomerase Regulation in Triple-Negative Breast Cancer. BMC Cancer. 2015; 15:672. https://doi.org/10.1186/s12885-015-1693-z
- Zhao T-T, Jin F, Li J-G, Xu Y-Y, Dong H-T, Liu Q, Xing P, Zhu G-L, Xu H, Miao Z-F. Dietary Isoflavones or Isoflavone-Rich Food Intake and Breast Cancer Risk: A Meta-Analysis of Prospective Cohort Studies. Clin. Nutr. 2019; 38(1):136-145. https://doi.org/10.1016/j. clnu.2017.12.006
- Yang Y-CSH, Li Z-L, Huang T-Y, Su K-W, Lin C-Y, Huang C-H, Chen H-Y, Lu M-C, Huang H-M, Lee S-Y, Whang-Peng J, Lin H-Y, Davis PJ, Wang K. Effect of Estrogen on Heteronemin-Induced Anti-Proliferative Effect in Breast Cancer Cells With Different Estrogen Receptor Status. Front. Cell Dev. Biol. 2021; 9:688607. https://doi.org/10.3389/fcell.2021.688607
- Shirabe R, Saito E, Sawada N, Ishihara J, Takachi R, Abe SK, Shimazu T, Yamaji T, Goto A, Iwasaki M,Inoue M, Tsugane S. JPHC Study Group. Fermented and Nonfermented Soy Foods and the Risk of Breast Cancer in a Japanese Population‐based Cohort Study. Cancer Med. 2021; 10(2):757-771. https://doi.org/10.1002/cam4.3677
- Zhang H-W, Hu J-J, Fu R-Q, Liu X, Zhang Y-H, Li J, Liu L, Li Y-N, Deng Q, Luo Q-S, Ouyang Q, Gao N. Flavonoids Inhibit Cell Proliferation and Induce Apoptosis and Autophagy through Downregulation of PI3Kγ Mediated PI3K/AKT/MTOR/P70S6K/ULK Signaling Pathway in Human Breast Cancer Cells. Sci. Rep. 2018; 8(1):11255. https://doi.org/10.1038/ s41598-018-29308-7
- Nag S, Aggarwal S, Rauthan A, Warrier N. Maintenance Therapy for Newly Diagnosed Epithelial Ovarian Cancer – A Review. J. Ovarian Res. 2022; 15(1):88. https://doi.org/10.1186/s13048-022-01020-1
- Chien J, Poole EM. Ovarian Cancer Prevention, Screening, and Early Detection: Report From the 11th Biennial Ovarian Cancer Research Symposium. Int. J. Gynecol. Cancer. 2017; 27:S20-S22. https://doi. org/10.1097/IGC.0000000000001118
- Bell SG, Dalton L, McNeish BL; Fang F, Henry NL, Kidwell KM, McLean K. Aromatase Inhibitor Use, Side Effects and Discontinuation Rates in Gynecologic Oncology Patients. Gynecol. Oncol. 2020; 159(2):509- 514. https://doi.org/10.1016/j.ygyno.2020.08.015
- Shen F, Weber G. Synergistic Action of Quercetin and Genistein in Human Ovarian Carcinoma Cells. Oncol. Res. 1997; 9(11–12):597-602.
- Zhao E. Phytoestrogen Biological Actions on Mammalian Reproductive System and Cancer Growth. Sci. Pharm. 2011; 79(1):1-20. https://doi. org/10.3797/scipharm.1007-15
- Tanaka T, Kohno H, Tanino M, Yanaida Y. Inhibitory Effects of Estrogenic Compounds, 4-Nonylphenol and Genistein, on 7,12-Dimethylbenz[a]AnthraceneInduced Ovarian Carcinogenesis in Rats. Ecotoxicol. Environ. Saf. 2002; 52(1):38-45. https://doi. org/10.1006/eesa.2002.2159
- Lim W, Jeong W, Song G. Coumestrol Suppresses Proliferation of ES2 Human Epithelial Ovarian Cancer Cells. J. Endocrinol. 2016; 228(3):149-160. https://doi.org/10.1530/JOE-15-0418
- Eilati E, Hales K, Zhuge Y, Ansenberger Fricano K, Yu R, van Breemen RB, Hales DB. Flaxseed Enriched Diet-Mediated Reduction in Ovarian Cancer Severity Is Correlated to the Reduction of Prostaglandin E2 in Laying Hen Ovaries. Prostaglandins Leukot. Essent. Fatty Acids. 2013; 89(4):179-187. https://doi. org/10.1016/j.plefa.2013.08.001
- Chhabra G, Singh CK, Ndiaye MA, Fedorowicz S, Molot A, Ahmad N. Prostate Cancer Chemoprevention by Natural Agents: Clinical Evidence and Potential Implications. Cancer Lett. 2018; 422:9-18. https://doi. org/10.1016/j.canlet.2018.02.025
- Umlauff L, Weber M, Freitag N, Fairman CM, Heidenreich A, Bloch W, Schumann M. Dietary Interventions to Improve Body Composition in Men Treated with Androgen Deprivation Therapy for Prostate Cancer: A Solution for the Growing Problem? Prostate Cancer Prostatic Dis. 2022; 25(2):149-158. https://doi.org/10.1038/s41391-021-00411-7
- Zhang Q,Feng H, Qluwakemi B, Wang J, Yao S, Cheng G, Xu H, Qiu H, Zhu L, Yuan M. Phytoestrogens and Risk of Prostate Cancer: An Updated Meta-Analysis of Epidemiologic Studies. Int. J. Food Sci. Nutr. 2017; 68(1):28-42. https://doi.org/10.1080/09637486.2016. 1216525
- Hnit SST, Yao M, Xie C, Bi L, Wong M, Liu T, De Souza P, Li Z, Dong Q. Apigenin Impedes Cell Cycle Progression at G2 Phase in Prostate Cancer Cells Discov. Oncol. 2022; 13(1):44. https://doi.org/10.1007/ s12672-022-00505-1
- Bilir B, Sharma NV, Lee J, Hammarstrom B, Svindland A, Kucuk O, Moreno CS. Effects of Genistein Supplementation on Genome-wide DNA Methylation and Gene Expression in Patients with Localized Prostate Cancer. Int. J. Oncol. 2017; 51(1):223-234. https://doi.org/10.3892/ijo.2017.4017
- Azrad M, Vollmer RT, Madden J, Dewhirst M, Polascik TJ, Snyder DC, Ruffin MT, Moul JW, Brenner DE, Demark-Wahnefried W. Flaxseed-Derived Enterolactone Is Inversely Associated with Tumor Cell Proliferation in Men with Localized Prostate Cancer. J. Med. Food. 2013; 16(4):357-360. https:// doi.org/10.1089/jmf.2012.0159
- Seo Y, Ryu K, Park J, Jeon D, Jo S, Lee HK, Namkung W. Inhibition of ANO1 by Luteolin and Its Cytotoxicity in Human Prostate Cancer PC-3 Cells. PLOS ONE. 2017; 12(3):e0174935. https://doi.org/10.1371/journal.pone.0174935
- Fontana F, Raimondi M, Marzagalli M, Di Domizio A, Limonta P. Natural Compounds in Prostate Cancer Prevention and Treatment: Mechanisms of Action and Molecular Targets. Cells. 2020; 9(2):E460. https:// doi.org/10.3390/cells9020460