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微小 RNA-22 在女性恶性肿瘤中的作用:聚焦于乳腺癌、宫颈癌和卵巢癌。

MicroRNA-22 in female malignancies: Focusing on breast, cervical, and ovarian cancers.

机构信息

Pharmaceutical Sciences Research Center, Ardabil University of Medical Sciences, Ardabil, Iran.

Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Pathol Res Pract. 2021 Jul;223:153452. doi: 10.1016/j.prp.2021.153452. Epub 2021 May 2.


DOI:10.1016/j.prp.2021.153452
PMID:33993061
Abstract

MicroRNAs (miRNAs), a novelty-defined class of regulatory genes, have revolutionized principles of classical bimolecular. These RNAs regulate the expression of a gene through inhibition of translational initiation or targeting mRNAs for degradation. MiRNAs act in several biological operations, including proliferation, differentiation, and cell death, and their expression is often abnormal in human diseases such as cancer. In recent years, miR-22 has attracted much attention from researchers. Its expression is downregulated in female malignancies such as breast, cervical, and ovarian cancers, exhibiting that miR-22 plays a tumor-suppressive function in these cancers. Also, different reports exist about the involvement of miR-22 in non-tumor diseases. In the present review, we report the results of performed studies on the potential roles of miR-22 in female malignancies with a focus on breast, cervical, and ovarian cancers. Also, we summary its predicted target genes in various cancers. In conclusion, it is effective for researchers to understand the role of miR-22 in different cellular operations.

摘要

微小 RNA(miRNAs),一类新定义的调控基因家族,彻底改变了经典双分子的原理。这些 RNA 通过抑制翻译起始或靶向 mRNA 降解来调节基因的表达。miRNAs 参与多种生物学过程,包括增殖、分化和细胞死亡,并且它们的表达在癌症等人类疾病中经常异常。近年来,miR-22 引起了研究人员的极大关注。它在女性恶性肿瘤如乳腺癌、宫颈癌和卵巢癌中的表达下调,表明 miR-22 在这些癌症中发挥肿瘤抑制功能。此外,也有不同的报告表明 miR-22 参与非肿瘤疾病。在本综述中,我们报告了关于 miR-22 在女性恶性肿瘤中(重点是乳腺癌、宫颈癌和卵巢癌)的潜在作用的研究结果。此外,我们总结了其在各种癌症中的预测靶基因。总之,研究人员了解 miR-22 在不同细胞操作中的作用是有效的。

相似文献

[1]
MicroRNA-22 in female malignancies: Focusing on breast, cervical, and ovarian cancers.

Pathol Res Pract. 2021-7

[2]
microRNA-802 inhibits cell proliferation and induces apoptosis in human cervical cancer by targeting serine/arginine-rich splicing factor 9.

J Cell Biochem. 2018-12-19

[3]
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Expert Rev Mol Diagn. 2018-10-29

[4]
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[5]
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Oncol Res. 2018-1-10

[6]
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[7]
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[8]
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[9]
microRNA-145 modulates epithelial-mesenchymal transition and suppresses proliferation, migration and invasion by targeting SIP1 in human cervical cancer cells.

Cell Oncol (Dordr). 2017-4

[10]
Down-regulation of microRNA-135b inhibited growth of cervical cancer cells by targeting FOXO1.

Int J Clin Exp Pathol. 2015-9-1

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J Appl Genet. 2025-6-18

[2]
Exosomal miRNA-based theranostics in cervical cancer: bridging diagnostics and therapy.

Med Oncol. 2025-5-4

[3]
Metformin reverses 5-FU chemoresistance by downregulating DKK1, WNT5A, and ABCB1 expressions in gastric cancer: An experimental and bioinformatic study.

Naunyn Schmiedebergs Arch Pharmacol. 2025-2-15

[4]
Review of the Different Outcomes Produced by Genetic Knock Out of the Long Non-coding microRNA-host-gene MIR22HG Pharmacologic Antagonism of its Intragenic microRNA product miR-22-3p.

Microrna. 2025

[5]
Role of microRNAs in host defense against porcine reproductive and respiratory syndrome virus infection: a hidden front line.

Front Immunol. 2024

[6]
Cytotoxicity of curcumin against CD44 prostate cancer cells: Roles of miR-383 and miR-708.

Avicenna J Phytomed. 2023

[7]
Fabrication of Antibody Conjugated Super Magnetic Oxide Nanoparticles for Early Detection of Prostate Cancer.

Asian Pac J Cancer Prev. 2023-6-1

[8]
G Protein-Coupled Receptor 75 (GPR75) As a Novel Molecule for Targeted Therapy of Cancer and Metabolic Syndrome.

Asian Pac J Cancer Prev. 2023-5-1

[9]
miR-22-enriched breast cancer cells display repressed glycolytic metabolism, increased glycogen synthesis, and reduced survival in low glucose conditions.

Mol Biol Rep. 2023-6

[10]
An Immunocompetent Environment Unravels the Proto-Oncogenic Role of miR-22.

Cancers (Basel). 2022-12-19

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