Oncogene GAEC1 regulates CAPN10 expression which predicts survival in esophageal squamous cell carcinoma

被引:21
作者
Chan, Dessy [1 ]
Tsoi, Miriam Yuen-Tung [1 ]
Di Liu, Christina [1 ]
Chan, Sau-Hing [1 ]
Law, Simon Ying-Kit [2 ]
Chan, Kwok-Wah [3 ]
Chan, Yuen-Piu [3 ]
Gopalan, Vinod [4 ,5 ]
Lam, Alfred King-Yin [4 ,5 ]
Tang, Johnny Cheuk-On [1 ]
机构
[1] Hong Kong Polytech Univ, State Key Lab Chirosci, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
[2] Univ Hong Kong, Li Ka Shing Fac Med, Dept Surg, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Li Ka Shing Fac Med, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
[4] Griffith Univ, Griffith Med Sch, Dept Pathol, Gold Coast, Qld 4222, Australia
[5] Griffith Univ, Griffith Hlth Inst, Gold Coast, Qld 4222, Australia
关键词
Esophageal squamous cell carcinoma; Oncogene; RNA interference; Calpain; 10; Tissue microarray; GENETIC ALTERATIONS; GENOMIC IMBALANCES; ABERRATIONS; SEQUENCE; CANCER; RNAI; INVASION; PROTEIN; 7Q22; CGH;
D O I
10.3748/wjg.v19.i18.2772
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To identify the downstream regulated genes of GAEC1 oncogene in esophageal squamous cell carcinoma and their clinicopathological significance. METHODS: The anti-proliferative effect of knocking down the expression of GAEC1 oncogene was studied by using the RNA interference (RNAi) approach through transfecting the GAEC1-overexpressed esophageal carcinoma cell line KYSE150 with the pSilencer vector cloned with a GAEC1-targeted sequence, followed by MTS cell proliferation assay and cell cycle analysis using flow cytometry. RNA was then extracted from the parental, pSilencer-GAEC1-targeted sequence transfected and pSilencer negative control vector transfected KYSE150 cells for further analysis of different patterns in gene expression. Genes differentially expressed with suppressed GAEC1 expression were then determined using Human Genome U133 Plus 2.0 cDNA microarray analysis by comparing with the parental cells and normalized with the pSilencer negative control vector transfected cells. The most prominently regulated genes were then studied by immunohistochemical staining using tissue microarrays to determine their clinicopathological correlations in esophageal squamous cell carcinoma by statistical analyses. RESULTS: The RNAi approach of knocking down gene expression showed the effective suppression of GAEC1 expression in esophageal squamous cell carcinoma cell line KYSE150 that resulted in the inhibition of cell proliferation and increase of apoptotic population. cDNA microarray analysis for identifying differentially expressed genes detected the greatest levels of downregulation of calpain 10 (CAPN10) and upregulation of trinucleotide repeat containing 6C (TNRC6C) transcripts when GAEC1 expression was suppressed. At the tissue level, the high level expression of calpain 10 protein was significantly associated with longer patient survival (month) of esophageal squamous cell carcinoma compared to the patients with low level of calpain 10 expression (37.73 +/- 16.33 vs 12.62 +/- 12.44, P = 0.032). No significant correction was observed among the TNRC6C protein expression level and the clinocopathologcial features of esophageal squamous cell carcinoma. CONCLUSION: GAEC1 regulates the expression of CAPN10 and TNRC6C downstream. Calpain 10 expression is a potential prognostic marker in patients with esophageal squamous cell carcinoma. (C) 2013 Baishideng. All rights reserved. et
引用
收藏
页码:2772 / 2780
页数:9
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