The role of miR-200 family in the regulation of hallmarks of cancer

被引:30
|
作者
Klicka, Klaudia [1 ,2 ]
Grzywa, Tomasz M. [1 ,3 ,4 ]
Mielniczuk, Aleksandra [1 ]
Klinke, Alicja [1 ]
Wlodarski, Pawel K. [1 ]
机构
[1] Med Univ Warsaw, Dept Methodol, Warsaw, Poland
[2] Med Univ Warsaw, Doctoral Sch, Warsaw, Poland
[3] Med Univ Warsaw, Dept Immunol, Warsaw, Poland
[4] Med Univ Warsaw, Lab Expt Med, Warsaw, Poland
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
关键词
miR-200; family; miRNA; hallmarks of cancer; tumor progression; invasiveness; metastasis; EPITHELIAL-MESENCHYMAL TRANSITION; CELL LUNG-CANCER; MICRORNA EXPRESSION PROFILE; PI3K/AKT SIGNALING PATHWAY; INHIBITS TUMOR-GROWTH; BREAST-CANCER; DOWN-REGULATION; OVARIAN-CANCER; COLORECTAL-CANCER; PROSTATE-CANCER;
D O I
10.3389/fonc.2022.965231
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MiRNAs are short non-coding RNAs that regulate gene expression post-transcriptionally contributing to the development of different diseases including cancer. The miR-200 family consists of five members, miR-200a, miR-200b, miR-200c, miR-141, and miR-429. Their expression is dysregulated in cancer tissue and their level is altered in the body fluids of cancer patients. Moreover, the levels of miR-200 family members correlate with clinical parameters such as cancer patients' survival which makes them potentially useful as diagnostic and prognostic biomarkers. MiRNAs can act as either oncomiRs or tumor suppressor miRNAs depending on the target genes and their role in the regulation of key oncogenic signaling pathways. In most types of cancer, the miR-200 family acts as tumor suppressor miRNA and regulates all features of cancer. In this review, we summarized the expression pattern of the miR-200 family in different types of cancer and their potential utility as biomarkers. Moreover, we comprehensively described the role of miR-200 family members in the regulation of all hallmarks of cancer proposed by Hanahan and Weinberg with the focus on the epithelial-mesenchymal transition, invasiveness, and metastasis of tumor cells.
引用
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页数:28
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