Lnc RNA HOTAIR functions as a competing endogenous RNA to regulate HER2 expression by sponging miR-331-3p in gastric cancer

被引:849
作者
Liu, Xiang-hua [1 ]
Sun, Ming [1 ]
Nie, Feng-qi [2 ]
Ge, Ying-bin [3 ]
Zhang, Er-bao [1 ]
Yin, Dan-dan [1 ]
Kong, Rong [1 ]
Xia, Rui [1 ]
Lu, Kai-hua [2 ]
Li, Jin-hai [4 ]
De, Wei [1 ]
Wang, Ke-ming [5 ]
Wang, Zhao-xia [5 ]
机构
[1] Nanjing Med Univ, Dept Biochem & Mol Biol, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Dept Oncol, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Physiol, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Affiliated Hosp 1, Dept Gen Surg, Nanjing, Jiangsu, Peoples R China
[5] Nanjing Med Univ, Affiliated Hosp 2, Dept Oncol, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Competing endogenous RNA; HER2; HOTAIR; Gastric cancer; Proliferation and invasion; LONG NONCODING RNA; BREAST-CANCER; GENE AMPLIFICATION; POOR-PROGNOSIS; UP-REGULATION; TRASTUZUMAB; CELLS; OVEREXPRESSION; VALIDATION; CARCINOMA;
D O I
10.1186/1476-4598-13-92
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Accumulating evidence indicates that the long non-coding RNA HOTAIR plays a critical role in cancer progression and metastasis. However, the overall biological role and clinical significance of HOTAIR in gastric carcinogenesis remains largely unknown. Methods: HOTAIR expression was measured in 78 paired cancerous and noncancerous tissue samples by real-time PCR. The effects of HOTAIR on gastric cancer cells were studied by overexpression and RNA interference approaches in vitro and in vivo. Insights of the mechanism of competitive endogenous RNAs (ceRNAs) were gained from bioinformatic analysis, luciferase assays and RNA binding protein immunoprecipitation (RIP). The positive HOTAIR/HER2 interaction was identified and verified by immunohistochemistry assay and bivariate correlation analysis. Results: HOTAIR upregulation was associated with larger tumor size, advanced pathological stage and extensive metastasis, and also correlated with shorter overall survival of gastric cancer patients. Furthermore, HOTAIR overexpression promoted the proliferation, migration and invasion of gastric carcinoma cells, while HOTAIR depletion inhibited both cell invasion and cell viability, and induced growth arrest in vitro and in vivo. In particular, HOTAIR may act as a ceRNA, effectively becoming a sink for miR-331-3p, thereby modulating the derepression of HER2 and imposing an additional level of post-transcriptional regulation. Finally, the positive HOTAIR/HER2 correlation was significantly associated with advanced gastric cancers. Conclusions: HOTAIR overexpression represents a biomarker of poor prognosis in gastric cancer, and may confer malignant phenotype to tumor cells. The ceRNA regulatory network involving HOTAIR and the positive interaction between HOTAIR and HER2 may contribute to a better understanding of gastric cancer pathogenesis and facilitate the development of lncRNA-directed diagnostics and therapeutics against this disease.
引用
收藏
页数:14
相关论文
共 40 条
[1]   Complex architecture and regulated expression of the Sox2ot locus during vertebrate development [J].
Amaral, Paulo P. ;
Neyt, Christine ;
Wilkins, Simon J. ;
Askarian-Amiri, Marjan E. ;
Sunkin, Susan M. ;
Perkins, Andrew C. ;
Mattick, John S. .
RNA, 2009, 15 (11) :2013-2027
[2]   A Long Noncoding RNA Controls Muscle Differentiation by Functioning as a Competing Endogenous RNA [J].
Cesana, Marcella ;
Cacchiarelli, Davide ;
Legnini, Ivano ;
Santini, Tiziana ;
Sthandier, Olga ;
Chinappi, Mauro ;
Tramontano, Anna ;
Bozzoni, Irene .
CELL, 2011, 147 (02) :358-369
[3]   Lymph Nodes and Gastric Cancer [J].
Coburn, Natalie G. .
JOURNAL OF SURGICAL ONCOLOGY, 2009, 99 (04) :199-206
[4]   Enhanced Expression of Long Non-Coding RNA HOTAIR Is Associated with the Development of Gastric Cancer [J].
Endo, Hiroyuki ;
Shiroki, Takeharu ;
Nakagawa, Takayuki ;
Yokoyama, Misa ;
Tamai, Keiichi ;
Yamanami, Hideaki ;
Fujiya, Tsuneaki ;
Sato, Ikuro ;
Yamaguchi, Kazunori ;
Tanaka, Nobuyuki ;
Iijima, Katsunori ;
Shimosegawa, Tooru ;
Sugamura, Kazuo ;
Satoh, Kennichi .
PLOS ONE, 2013, 8 (10)
[5]   The RNA-binding Protein HuR Opposes the Repression of ERBB-2 Gene Expression by MicroRNA miR-331-3p in Prostate Cancer Cells [J].
Epis, Michael R. ;
Barker, Andrew ;
Giles, Keith M. ;
Beveridge, Dianne J. ;
Leedman, Peter J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (48) :41442-41454
[6]   Silencing of the HER2/neu gene by siRNA inhibits proliferation and induces apoptosis in HER2/neu-overexpressing breast cancer cells [J].
Faltus, T ;
Yuan, JP ;
Zimmer, B ;
Krämer, A ;
Loibl, S ;
Kaufmann, M ;
Strebhardt, K .
NEOPLASIA, 2004, 6 (06) :786-795
[7]   MiR-199b-5p targets HER2 in breast cancer cells [J].
Fang, Chen ;
Zhao, Yu ;
Guo, Baoyu .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2013, 114 (07) :1457-1463
[8]   Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? [J].
Filipowicz, Witold ;
Bhattacharyya, Suvendra N. ;
Sonenberg, Nahum .
NATURE REVIEWS GENETICS, 2008, 9 (02) :102-114
[9]   Regulation of apoptosis by a prostate-specific and prostate cancer-associated noncoding gene, PCGEM1 [J].
Fu, XQ ;
Ravindranath, L ;
Tran, N ;
Petrovics, G ;
Srivastava, S .
DNA AND CELL BIOLOGY, 2006, 25 (03) :135-141
[10]   Antitumor activity of trastuzumab in combination with chemotherapy in human gastric cancer xenograft models [J].
Fujimoto-Ouchi, Kaori ;
Sekiguchi, Fumiko ;
Yasuno, Hideyuki ;
Moriya, Yoichiro ;
Mori, Kazushige ;
Tanaka, Yutaka .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2007, 59 (06) :795-805