Reactivation of HIC-1 gene by saRNA inhibits clonogenicity and invasiveness in breast cancer cells

被引:11
|
作者
Zhao, Feng [1 ]
Pan, Shengli [2 ]
Gu, Yan [1 ]
Guo, Shanyu [1 ]
Dai, Qiancheng [1 ]
Yu, Yingyan [2 ]
Zhang, Wei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Dept Surg, Peoples Hosp 9, Shanghai 200011, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Dept Surg, Shanghai Ruijin Hosp, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
breast cancer; HIC-1; clonogenicity; cell invasion; saRNA; INDUCE TRANSCRIPTIONAL ACTIVATION; TUMOR-SUPPRESSOR GENE; UP-REGULATION; CARCINOMA CELL; ALLELIC LOSS; RNA; P21(WAF1/CIP1); EXPRESSION; HYPERMETHYLATION; MISREGULATION;
D O I
10.3892/ol.2014.2633
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypermethylated in cancer 1 (HIC-1) is a tumor suppressor gene, which is epigenetically silenced in breast cancer. It is known that the loss of HIC-1, caused by promoter hypermethylation, is associated with tumor aggression and poor survival in breast carcinoma. It has been shown that small activating RNA (saRNA) targeting promoter sequences may induce gene re-expression. In the current study, saRNA was used to restore HIC-1 expression, and the effects on colony formation, invasiveness and the cell cycle in breast cancer cells were explored. dsHIC1-2998, an saRNA, exhibited activating efficacy on MCF-7 and MDA-MB-231 cancer cell lines. A clonogenicity assay showed that evident colony inhibition was induced via saRNA-mediated re-expression of HIC-1 in the two cancer cell lines. Reactivation of HIC-1 significantly inhibited cell migration and invasion, resulting in G0/G1 cell cycle arrest in these cell lines. These findings suggest that HIC-1 may be a potential target in gene therapy for the treatment of breast cancer. saRNA may function as a therapeutic option for upregulating tumor suppressor genes in breast cancer.
引用
收藏
页码:159 / 164
页数:6
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