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
相关论文
共 50 条
  • [1] HIC-1: A gene silenced in cancer stem cells of glioma
    Bhagat, Mohita
    Sinha, Subrata
    Chattopadhyay, Parthaprasad
    CANCER RESEARCH, 2014, 74 (19)
  • [2] Expression of the hypermethylated in cancer gene (HIC-1) is associated with good outcome in human breast cancer
    G Nicoll
    D N Crichton
    H E McDowell
    N Kernohan
    T R Hupp
    A M Thompson
    British Journal of Cancer, 2001, 85 : 1878 - 1882
  • [3] Methylation of the HIC-1 candidate tumor suppressor gene in human breast cancer
    Hiroaki Fujii
    Margaret A Biel
    Weibo Zhou
    Sigmund A Weitzman
    Stephen B Baylin
    Edward Gabrielson
    Oncogene, 1998, 16 : 2159 - 2164
  • [4] Methylation of the HIC-1 candidate tumor suppressor gene in human breast cancer
    Fujii, H
    Biel, MA
    Zhou, WB
    Weitzman, SA
    Baylin, SB
    Gabrielson, E
    ONCOGENE, 1998, 16 (16) : 2159 - 2164
  • [5] Expression of the hypermethylated in cancer gene (HIC-1) is associated with good outcome in human breast cancer
    Nicoll, G
    Crichton, DN
    McDowell, HE
    Kernohan, N
    Hupp, TR
    Thompson, AM
    BRITISH JOURNAL OF CANCER, 2001, 85 (12) : 1878 - 1882
  • [6] Loss of expression of the HIC-1 gene (hypermethylated in cancer) from 17P13.3 in breast cancer
    Nicoll, G
    Crichton, DN
    Thompson, AM
    BRITISH JOURNAL OF CANCER, 2000, 83 : 38 - 38
  • [7] Epigenetic silencing of the HIC-1 gene in human medulloblastomas
    Waha, A
    Waha, A
    Koch, A
    Meyer-Puttlitz, B
    Weggen, S
    Sörensen, N
    Tonn, JC
    Albrecht, S
    Goodyer, CG
    Berthold, F
    Wiestler, OD
    Pietsch, T
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2003, 62 (11): : 1192 - 1201
  • [8] Small Activating RNA Restores the Activity of the Tumor Suppressor HIC-1 on Breast Cancer
    Zhao, Feng
    Pan, Shengli
    Gu, Yan
    Guo, Shanyu
    Dai, Qiancheng
    Yu, Yingyan
    Zhang, Wei
    PLOS ONE, 2014, 9 (01):
  • [9] Silencing of the IKKε gene by siRNA inhibits invasiveness and growth of breast cancer cells
    Bin Qin
    Kun Cheng
    Breast Cancer Research, 12
  • [10] Silencing of the IKKε gene by siRNA inhibits invasiveness and growth of breast cancer cells
    Qin, Bin
    Cheng, Kun
    BREAST CANCER RESEARCH, 2010, 12 (05)