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Data from Analysis of MiR-195 and MiR-497 Expression, Regulation and Role in Breast Cancer

Authors :
Lihui Lai
Bing-Hua Jiang
Feng Mao
Ling-Zhi Liu
Hallgeir Rui
Hsiang-Fu Kung
Marie C. Lin
Andreas Dress
Zhenbing Zeng
Qiang Sun
Dan Zhao
Xuejing Wang
Shunying Liu
Xiaolong Zhang
Chao Zou
Yue Jiang
Yanting Qi
Xiaona Chen
Changxing Liu
Yulan Zhao
Dan Li
Publication Year :
2023
Publisher :
American Association for Cancer Research (AACR), 2023.

Abstract

Purpose: To investigate expression, regulation, potential role and targets of miR-195 and miR-497 in breast cancer.Experimental Design: The expression patterns of miR-195 and miR-497 were initially examined in breast cancer tissues and cell lines by Northern blotting and quantitative real-time PCR. Combined bisulfite restriction analysis and bisulfite sequencing were carried out to study the DNA methylation status of miR-195 and miR-497 genes. Breast cancer cells stably expressing miR-195 and miR-497 were established to study their role and targets. Finally, normal, fibroadenoma and breast cancer tissues were employed to analyze the correlation between miR-195/497 levels and malignant stages of breast tumor tissues.Results: MiR-195 and miR-497 were significantly downregulated in breast cancer. The methylation state of CpG islands upstream of the miR-195/497 gene was found to be responsible for the downregulation of both miRNAs. Forced expression of miR-195 or miR-497 suppressed breast cancer cell proliferation and invasion. Raf-1 and Ccnd1 were identified as novel direct targets of miR-195 and miR-497. miR-195/497 expression levels in clinical specimens were found to be correlated inversely with malignancy of breast cancer.Conclusions: Our data imply that both miR-195 and miR-497 play important inhibitory roles in breast cancer malignancy and may be the potential therapeutic and diagnostic targets. Clin Cancer Res; 17(7); 1722–30. ©2011 AACR.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....3459aa02b57ed82c8ad0f87915915ba1
Full Text :
https://doi.org/10.1158/1078-0432.c.6519554.v1