Literature DB >> 29555101

GAEC1 mutations and copy number aberration is associated with biological aggressiveness of colorectal cancer.

Katherine Ting-Wei Lee1, Vinod Gopalan1, Farhadul Islam2, Riajul Wahab1, Afraa Mamoori1, Cu-Tai Lu3, Robert Anthony Smith4, Alfred King-Yin Lam5.   

Abstract

GAEC1 (gene amplified in oesophageal cancer 1) is a transforming oncogene with tumorigenic potential observed in both oesophageal squamous cell carcinoma and colorectal cancer. Nonetheless, there has been a lack of study done on this gene to understand how this gene exert its oncogenic properties in cancer. This study aims to identify novel mutation sites in GAEC1. To do so, seventy-nine matched colorectal cancers were tested for GAEC1 mutation via Sanger sequencing. The mutations noted were investigated for the correlations with the clinicopathological parameters of the patients with the cancer. Additionally, GAEC1 copy number aberration (CNA), mRNA and protein expression were determined with the use of droplet digital (dd) polymerase chain reaction (PCR), real-time PCR and Western blot (confirmed with immunofluorescence analysis). GAEC1 mutation was noted in 8.8% (n = 7/79) of the cancer tissues including one missense mutation, four loss of heterozygosity (LOH) and two substitutions. These mutations were significantly associated with cancer perforation (p = 0.021). GAEC1 mutation is frequently associated with increased GAEC1 protein expression. Nevertheless, GAEC1 mRNA and protein are only weakly associated. Taken together, GAEC1 mutation affects GAEC1 expression and is associated with poorer clinical outcomes. This further strengthens the role of GAEC1 as an oncogene.
Copyright © 2018 Elsevier GmbH. All rights reserved.

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Keywords:  Colorectal cancer; Copy number aberration; Mutation; Polymorphism; Sequencing; ddPCR

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Year:  2018        PMID: 29555101     DOI: 10.1016/j.ejcb.2018.03.002

Source DB:  PubMed          Journal:  Eur J Cell Biol        ISSN: 0171-9335            Impact factor:   4.492


  2 in total

1.  Overexpression of family with sequence similarity 134, member B (FAM134B) in colon cancers and its tumor suppressive properties in vitro.

Authors:  Katherine Ting-Wei Lee; Farhadul Islam; Jelena Vider; Jeremy Martin; Anna Chruścik; Cu-Tai Lu; Vinod Gopalan; Alfred Kin-Yan Lam
Journal:  Cancer Biol Ther       Date:  2020-08-28       Impact factor: 4.742

Review 2.  Copy Number Variation and Rearrangements Assessment in Cancer: Comparison of Droplet Digital PCR with the Current Approaches.

Authors:  Vincenza Ylenia Cusenza; Alessandra Bisagni; Monia Rinaldini; Chiara Cattani; Raffaele Frazzi
Journal:  Int J Mol Sci       Date:  2021-04-29       Impact factor: 5.923

  2 in total

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