马拉特1
乳腺癌
癌症研究
癌变
癌症
小发夹RNA
医学
SKBR3型
内科学
肿瘤科
生物
长非编码RNA
基因敲除
细胞培养
下调和上调
人体乳房
遗传学
基因
生物化学
作者
Chuansheng Yang,Hongbo Zhu,Yeru Tan,Renjie Zhu,Xiaoping Wu,Yuehua Li,Cunchuan Wang
标识
DOI:10.2174/1568009621666210618164300
摘要
The function of MALAT1, a long non-coding RNAs (lncRNA), in HER2- positive breast cancer remains largely unexplored.This study aimed to investigate the effect of MALAT1 on tumor development in HER2-positive breast cancer.We detected MALAT1 expression in HER2-positive breast cancer cells and tissues, and analyzed the effects of MALAT1 on cell proliferation in HER2-positive breast cancer cells lines (BT-474 and SKBR3). A mouse xenograft model was established for detecting the function of MALAT1 in HER2-positive breast cancer.As a result, MALAT1 was remarkably up-regulated in HER2-positive breast cancer both in cells and tissues. In addition, the silencing of MALAT1 inhibited the proliferation of HER2-positive breast cancer cells both in vitro and in vivo. Furthermore, knockdown of MALAT1 by shRNA down-regulated DNMT1, DNMT3a, and DNMT3b, while up-regulated BRCA1 and PTEN in HER2-positive breast cancer both in cell lines and mouse xenograft models.In short, MALAT1 might be a potential biomarker and therapeutic target for HER2- positive breast cancer therapy.
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