The Cluster of miR-143 and miR-145 Affects the Risk for Esophageal Squamous Cell Carcinoma through Co-Regulating Fascin Homolog 1

被引:88
|
作者
Liu, Ran [1 ]
Liao, Juan [1 ]
Yang, Miao [1 ]
Sheng, Jingyi [1 ]
Yang, Hao [1 ]
Wang, Yi [2 ]
Pan, Enchun [2 ]
Guo, Wei [3 ]
Pu, Yuepu [1 ]
Kim, Sun Jung [4 ]
Yin, Lihong [1 ]
机构
[1] Southeast Univ, Sch Publ Hlth, Minist Educ, Key Lab Environm Med Engn, Nanjing, Jiangsu, Peoples R China
[2] Huaian Ctr Dis Control & Prevent, Huaian, Peoples R China
[3] First Peoples Hosp Huaian, Huaian, Peoples R China
[4] Dongguk Univ Seoul, Dept Life Sci, Seoul, South Korea
来源
PLOS ONE | 2012年 / 7卷 / 03期
基金
中国国家自然科学基金; 新加坡国家研究基金会; 高等学校博士学科点专项科研基金;
关键词
COMPARATIVE GENOMIC HYBRIDIZATION; PROGNOSTIC-SIGNIFICANCE; TUMOR SUPPRESSORS; PROSTATE-CANCER; FREQUENT LOSS; EXPRESSION; MICRORNA; REGIONS; PROLIFERATION; RELEVANCE;
D O I
10.1371/journal.pone.0033987
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs), 18-24 nt non-coding RNAs, are thought to play important roles in cell proliferation, differentiation, apoptosis, and development. Recent studies suggest that some of the known microRNAs map to a single genomic locale within a single polycistronic transcript. But the roles of the cluster remain to be known. In order to understand the role and mechanism of a cluster of miR-143 and miR-145 in esophageal squamous cell carcinoma (ESCC), the association of mature miR-143 and miR-145 expression with the risk for esophageal cancer was evaluated in ESCC patients with a case-control study, and target protein regulated by mature miRNA was analyzed in ESCC cell lines with 3'UTR luciferase reporter assay. The expression levels of miR-143 and miR-145 were determined in 110 pairs of esophageal cancer tissues and adjacent normal tissues using real-time reverse transcription PCR. The relative expression of miR-143 and miR-145 were statistically different between cancer tissues and matched controls. The combined expression of miR-143 and miR-145 was significantly associated with the risk for esophageal cancer. Meanwhile, the reduced expression of two miRNAs in tumor patient was supposed to have a trend of lymph node metastases. The co-expression pattern of miR-143 and miR-145 was analyzed with Pearson correlation. It showed a significant correlation between these two miRNAs expression both in tissues and tumor cell lines. 3'UTR luciferase reporter assay indicated that Fascin Homolog 1 (FSCN1) could be co-regulated by miR-143 and miR-145. The protein level of FSCN1 showed no significant linear correlation with miR-143 and miR-145 expression in ESCC cell lines with Western blotting analysis. In conclusion, since miR-143 and miR-145 could regulate oncogenic FSCN1 and take part in the modulation of metastases, the result suggested the combination variable of miR-143 and miR-145 as a potential biomarker for earlier diagnosis and prognosis of esophageal cancer.
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页数:9
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