RETRACTED: Mir-655 up-regulation suppresses cell invasion by targeting pituitary tumor-transforming gene-1 in esophageal squamous cell carcinoma (Retracted Article)

被引:37
作者
Wang, Yuanyuan [1 ]
Zang, Wenqiao [1 ]
Du, Yuwen [1 ]
Ma, Yunyun [1 ]
Li, Min [1 ]
Li, Ping [2 ]
Chen, Xudong [3 ]
Wang, Tao [4 ]
Dong, Ziming [1 ]
Zhao, Guoqiang [1 ]
机构
[1] Zhengzhou Univ, Coll Basic Med Sci, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Resp Med, Zhengzhou 450052, Henan, Peoples R China
[3] Luohe Med Coll, Dept Histol & Embryol, Luohe 462002, Henan, Peoples R China
[4] Henan Univ TCM, Affiliated Hosp 1, Dept Hematotumor, Zhengzhou 450000, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Esophageal squamous cell carcinoma; miR-655; Invasion; PTTG1; MATRIX METALLOPROTEINASES; MICRORNA SIGNATURES; EXPRESSION; CANCER; PTTG; PROFILES; GENOMICS;
D O I
10.1186/1479-5876-11-301
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: MicroRNAs (miRNAs) can act as either oncogenes or tumor suppressor genes under different conditions and thus can play a significant role in cancer development. We investigated miR-655 expression in a cohort of esophageal squamous cell carcinoma (ESCC) to assess the impact of this miRNA on ESCC cell invasion and metastasis. Methods: A qRT-PCR assay was used to quantify miR-655 expression levels in 34 paired ESCC samples and adjacent non-tumor tissues. Wound healing and transwell assays were used to evaluate the effects of miR-655 expression on the invasiveness of ESCC cells. Luciferase reporter and western blot assays were used to determine whether the mRNA encoding pituitary tumor-transforming gene-1 (PTTG1) is a major target of miR-655. Results: The expression level of miR-655 in ESCC tissues was found to be lower than in adjacent non-tumor tissues (P < 0.05). This relatively low expression level was significantly associated with the occurrence of lymph node metastases (P < 0.05). Migration rates were significantly lower for two ESCC-derived cell lines (EC9706 and KYSE150) transfected with miR-429 mimics (P < 0.05). Subsequent western blot and luciferase reporter assays demonstrated that miR-655 could bind to putative binding sites within the PTTG1 mRNA 3'-untranslated region (3'-UTR) and thus reduce the expression. Conclusions: miR-655 is expressed at low levels in primary ESCC tissues, and up-regulation of miR-655 inhibits ESCC cell invasiveness by targeting PTTG1. Our findings suggest that PTTG1 may act as a major target of miR-655. This study improves our understanding of the mechanisms underlying ESCC pathogenesis and may promote the development of novel targeted therapies.
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页数:8
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