Abstract
Introduction
MicroRNAs, also known as miRNAs, are small regulatory RNAs, and they also include many different types in terms of size and commission that do not code the proteins but are crucial for many biological activities, such as formation, regulation, and inhibition in biological pathways.
miRNA-202
Our aim in this study was to analyze miRNA-202 in reproductive system settings, including the formation and function of reproductive systems. MiRNA-202 has been identified as a tumor suppressor in ovarian, endometrial, and cervical malignancies; in addition, it is essential for follicular growth and oogenesis.
Conclusion
This study reviews the most recent evidence supporting the concept that dysregulation of miRNA-202 may contribute to gynecological malignancies.
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Data availability
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References
O’Brien J, Hayder H, Zayed Y, Peng C. Overview of microRNA biogenesis, mechanisms of actions, and circulation. Front Endocrinol. 2018;9:402.
Khan HL, Bhatti S, Abbas S, Kaloglu C, Isa AM, Younas H, et al. Extracellular microRNAs: key players to explore the outcomes of in vitro fertilization. Reprod Biol Endocrinol. 2021;19(1):1–17.
Santamaria X, Taylor H. MicroRNA and gynecological reproductive diseases. Fertil Steril. 2014;101(6):1545–51.
Brunetti M, Panagopoulos I, Vitelli V, Andersen K, Hveem TS, Davidson B, et al. Endometrial carcinoma: molecular cytogenetics and transcriptomic profile. Cancers. 2022;14(14):3536.
Monk BJ, Tan DS, Chagüi JDH, Takyar J, Paskow MJ, Nunes AT, et al. Proportions and incidence of locally advanced cervical cancer: a global systematic literature review. Int J Gynecol Cancer. 2022. https://doi.org/10.1136/ijgc-2022-003801.
Zhu JW, Charkhchi P, Akbari MR. Potential clinical utility of liquid biopsies in ovarian cancer. Mol Cancer. 2022;21(1):1–24.
Zhang D, Wang L, Guo HL, Zhang ZW, Wang C, Chian RC, et al. MicroRNA-202 inhibits endometrial stromal cell migration and invasion by suppressing the K-Ras/Raf1/MEK/ERK signaling pathway. Int J Mol Med. 2020;46(6):2078–88.
Zheng Y, Xie L, Xu S, Yan W, Zhang H, Meng Y, et al. Effects of miR-202-5p silencing PIK3CA gene expression on proliferation, invasion, and epithelial–mesenchymal transition of cervical cancer SiHa cells through inhibiting PI3K/Akt/mTOR signaling pathway activation. Mol Cell Biochem. 2021;476(11):4031–44.
Yi Y, Li H, Lv Q, Wu K, Zhang W, Zhang J, et al. miR-202 inhibits the progression of human cervical cancer through inhibition of cyclin D1. Oncotarget. 2016;7(44):72067.
Deng X, Hou C, Liang Z, Wang H, Zhu L, Xu H. miR-202 suppresses cell proliferation by targeting FOXR2 in endometrial adenocarcinoma. Dis mark. 2017. https://doi.org/10.1155/2017/2827435.
Zhang M, Zhang Y, Li L, Ma L, Zhou C. Dysregulation of miR-202-3p affects migration and invasion of endometrial stromal cells in endometriosis via targeting ROCK1. Reprod Sci. 2020;27(2):731–42.
Fassina A, Cappellesso R, Fassan M. Classification of non-small cell lung carcinoma in transthoracic needle specimens using microRNA expression profiling. Chest. 2011;140(5):1305–11.
Yu H, Pan S. MiR-202-5p suppressed cell proliferation, migration and invasion in ovarian cancer via regulating HOXB2. Eur Rev Med Pharmacol Sci. 2020;24:2256–63.
Mallender WD, Yager D, Onstead L, Nichols MR, Eckman C, Sambamurti K, et al. Characterization of recombinant, soluble β-secretase from an insect cell expression system. Mol Pharmacol. 2001;59(3):619–26.
Wahid F, Shehzad A, Khan T. Kim YY 2010 MicroRNAs: synthesis, mechanism, function, and recent clinical trials. Biochimica et Biophysica Acta (BBA)-Molecular Cell Res. 1803;11:1231–43.
Melamed ZE, Levy A, Ashwal-Fluss R, Lev-Maor G, Mekahel K, Atias N, et al. Alternative splicing regulates biogenesis of miRNAs located across exon-intron junctions. Mol cell. 2013;50(6):869–81.
Hoffman AE, Liu R, Fu A, Zheng T, Slack F, Zhu Y. Targetome profiling, pathway analysis and genetic association study implicate miR-202 in lymphomagenesismiR-202 and lymphomagenesis. Cancer Epidemiol Biomark Prev. 2013;22(3):327–36.
Bizuayehu TT, Babiak I. MicroRNA in teleost fish. Genome Biol Evol. 2014;6(8):1911–37.
Di Fiore R, Suleiman S, Pentimalli F, O’toole SA, O’leary JJ, Ward MP, et al. Could MicroRNAs be useful tools to improve the diagnosis and treatment of rare gynecological cancers? A brief overview. Int j mol sci. 2021;22(8):3822.
Wongwarangkana C, Fujimori KE, Akiba M, Kinoshita S, Teruya M, Nezuo M, et al. Deep sequencing, profiling and detailed annotation of microRNAs in Takifugu rubripes. BMC Genomics. 2015;16(1):1–14.
Rosa A, Brivanlou AH. Regulatory non-coding RNAs in pluripotent stem cells. Int J Mol Sci. 2013;14(7):14346–73.
Ahmed EA, Rajendran P, Scherthan H. The microRNA-202 as a diagnostic biomarker and a potential tumor suppressor. Int J Mol Sci. 2022;23(11):5870.
Hashemipour M, Boroumand H, Mollazadeh S, Tajiknia V, Nourollahzadeh Z, Borj MR, et al. Exosomal microRNAs and exosomal long non-coding RNAs in gynecologic cancers. Gynecol Oncol. 2021;161(1):314–27.
Ledford LR, Lockwood S, editors. Scope and epidemiology of gynecologic cancers: an overview. Seminars in oncology nursing; 2019: Elsevier.
Mills AM, Bullock TN, Ring KL. Targeting immune checkpoints in gynecologic cancer: updates & perspectives for pathologists. Mod Pathol. 2022;35(2):142–51.
Razavi ZS, Tajiknia V, Majidi S, Ghandali M, Mirzaei HR, Rahimian N, et al. Gynecologic cancers and non-coding RNAs: epigenetic regulators with emerging roles. Crit Rev Oncol Hematol. 2021;157: 103192.
Wang Q, Peng H, Qi X, Wu M, Zhao X. Targeted therapies in gynecological cancers: a comprehensive review of clinical evidence. Signal Transduct Target Ther. 2020;5(1):137.
Gonçalves V. Long-term quality of life in gynecological cancer survivors. Curr Opin Obstet Gynecol. 2010;22(1):30–5.
Crusz SM, Miller RE. Targeted therapies in gynaecological cancers. Histopathology. 2020;76(1):157–70.
De Almeida BC, Garcia N, Maffazioli G, Gonzalez dos Anjos L, ChadaBaracat E, CandidoCarvalho K. Oncomirs expression profiling in uterine leiomyosarcoma cells. Int j mol sci. 2017;19(1):52.
Kim J, Park S, Hwang D, Kim SI, Lee H. Diagnostic value of circulating miR-202 in early-stage breast cancer in South Korea. Medicina. 2020;56(7):340.
Zheng Y, Xie L, Xu S, Yan W, Zhang H, Meng Y, et al. Effects of miR-202-5p silencing PIK3CA gene expression on proliferation, invasion, and epithelial–mesenchymal transition of cervical cancer SiHa cells through inhibiting PI3K/Akt/mTOR signaling pathway activation. Mol Cell Biochem. 2021;476:4031–44.
Chang RK, Li X, Mu N, Hrydziuszko O, Garcia-Majano B, Larsson C, et al. MicroRNA expression profiles in non-epithelial ovarian tumors. Int J Oncol. 2018;52(1):55–66.
Yu H, Pan S. MiR-202–5p suppressed cell proliferation, migration and invasion in ovarian cancer via regulating HOXB2. Eur Rev Med Pharmacol Sci. 2020;24:2256–63.
Xu C, Zhai J, Fu Y. Overexpression of Nuclear Enriched Autosomal Transcript 1 Facilitates Cell Proliferation, Migration Invasion, and Suppresses Apoptosis in Endometrial Cancer by Targeting MicroRNA-202-3p/T Cell Immunoglobulin and Mucin Domain 4 Axis. Cancer Biother Radiopharm. 2022;37(9):815–23.
Chen P, Xing T, Wang Q, Liu A, Liu H, Hu Y, et al. MicroRNA-202 inhibits cell migration and invasion through targeting FGF2 and inactivating Wnt/β-catenin signaling in endometrial carcinoma. 2019. Biosci Rep. https://doi.org/10.1042/BSR20190680.
Han X, Wang Q, Wang Y, Hu B, Dong X, Zhang H, et al. Long non-coding RNA metastasis-associated lung adenocarcinoma transcript 1/microRNA-202-3p/periostin axis modulates invasion and epithelial–mesenchymal transition in human cervical cancer. J Cell Physiol. 2019;234(8):14170–80.
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This work was financially supported by Behbahan Faculty of Medical Sciences, Behbahan, Iran (Grant number: 401109).
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Vahedi, F., Hasani, F., Rezaee, M. et al. MiRNA-202 Role in Reproductive System and Gynecological Cancers. Indian J Gynecol Oncolog 22, 75 (2024). https://doi.org/10.1007/s40944-024-00833-w
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DOI: https://doi.org/10.1007/s40944-024-00833-w