Literature DB >> 21802380

Altered JS-2 expression in colorectal cancers and its clinical pathological relevance.

Alfred King-Yin Lam1, Vinod Gopalan, Mohammad Reza Nassiri, Kais Kasim, Jayampathy Dissanayake, Johnny Chuek-On Tang, Robert Anthony Smith.   

Abstract

JS-2 is a novel gene located at 5p15.2 and originally detected in primary oesophageal cancer. There is no study on the role of JS-2 in colorectal cancer. The aim of this study is to determine the gene copy number and expression of JS-2 in a large cohort of patients with colorectal tumours and correlate these to the clinicopathological features of the cancer patients. We evaluated the DNA copy number and mRNA expression of JS-2 in 176 colorectal tissues (116 adenocarcinomas, 30 adenomas and 30 non-neoplastic tissues) using real-time polymerase chain reaction. JS-2 expression was also evaluated in two colorectal cancer cell lines and a benign colorectal cell line. JS-2 amplification was noted in 35% of the colorectal adenocarcinomas. Significant differences in relative expression levels for JS-2 mRNA between different colorectal tissues were noted (p = 0.05). Distal colorectal adenocarcinoma had significantly higher copy number than proximal adenocarcinoma (p = 0.005). The relative expression level of JS-2 was different between colonic and rectal adenocarcinoma (p = 0.007). Mucinous adenocarcinoma showed higher JS-2 expression than non-mucinous adenocarcinoma (p = 0.02). Early T-stage cancers appear to have higher JS-2 copy number and lower expression of JS-2 mRNA than later stage cancers (p = 0.001 and 0.03 respectively). Colorectal cancer cell lines showed lower expression of JS-2 than the benign colorectal cell line. JS-2 copy number change and expression were shown for the first time to be altered in the carcinogenesis of colorectal cancer. In addition, genetic alteration of JS-2 was found to be related to location, pathological subtypes and staging of colorectal cancer.
Copyright © 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21802380      PMCID: PMC5528300          DOI: 10.1016/j.molonc.2011.06.003

Source DB:  PubMed          Journal:  Mol Oncol        ISSN: 1574-7891            Impact factor:   6.603


  23 in total

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Authors:  Sarwat Fatima; Chung H Chui; Wing K Tang; Kin S Hui; Ho W Au; Wing Y Li; Mei M Wong; Filly Cheung; S W Tsao; King Y Lam; Philip S L Beh; John Wong; Simon Law; Gopesh Srivastava; Kwok P Ho; Albert S C Chan; Johnny C O Tang
Journal:  Int J Mol Med       Date:  2006-01       Impact factor: 4.101

2.  Altered JS-2 expression in colorectal cancers and its clinical pathological relevance.

Authors:  Alfred King-Yin Lam; Vinod Gopalan; Mohammad Reza Nassiri; Kais Kasim; Jayampathy Dissanayake; Johnny Chuek-On Tang; Robert Anthony Smith
Journal:  Mol Oncol       Date:  2011-07-12       Impact factor: 6.603

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Journal:  Cancer Genet Cytogenet       Date:  2008-04-01

10.  hTERT expression in colorectal adenocarcinoma: correlations with p21, p53 expressions and clinicopathological features.

Authors:  Alfred King-Yin Lam; Kate Ong; Yik-Hong Ho
Journal:  Int J Colorectal Dis       Date:  2008-03-06       Impact factor: 2.571

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2.  Altered JS-2 expression in colorectal cancers and its clinical pathological relevance.

Authors:  Alfred King-Yin Lam; Vinod Gopalan; Mohammad Reza Nassiri; Kais Kasim; Jayampathy Dissanayake; Johnny Chuek-On Tang; Robert Anthony Smith
Journal:  Mol Oncol       Date:  2011-07-12       Impact factor: 6.603

Review 3.  Somatic gene copy number alterations in colorectal cancer: new quest for cancer drivers and biomarkers.

Authors:  H Wang; L Liang; J-Y Fang; J Xu
Journal:  Oncogene       Date:  2015-08-10       Impact factor: 9.867

4.  VEGF-A/VEGF-B/VEGF-C expressions in non-hereditary, non-metastatic phaeochromocytoma.

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