Literature DB >> 24481768

A selected group of large common fragile site genes have decreased expression in oropharyngeal squamous cell carcinomas.

Ge Gao1, Jan L Kasperbauer, Nicole M Tombers, Vivian Wang, Kevin Mayer, David I Smith.   

Abstract

The common fragile sites (CFSs) are large regions of profound genomic instability found in all individuals. The frequent deletions and other alterations in these regions in multiple cancers has led to the discovery of a number of extremely large genes contained within these regions and several of the large CFS genes have already been demonstrated to function as tumor suppressors involved in the formation of many different cancers. To study the large CFS genes in oropharyngeal squamous cell carcinoma (OPSCC), we did RNA seq analysis from 11 head and neck cancer patients. This revealed that there are six large CFS genes which consistently had decreased expression in the tumor samples compared to their matched normal tissues. These six genes are PARK2, DLG2, NBEA, CTNNA3, DMD, and FHIT. PARK2 and FHIT are located within the two most frequently expressed CFSs and both have been demonstrated to function as tumor suppressors, while the other large genes are found to have frequent alterations in multiple cancers. Validation experiments using real time PCR indicated that over 60% of OPSCC tumors showed decreased expression for all six genes. Both HPV-positive and HPV-negative OPSCCs had similar proportions with loss of expression of these genes. Our results suggest that this selected group of large genes might serve as potential tumor suppressors involved in the development of OPSCCs. Further studies are needed to investigate whether the decreased expression observed is due to genomic instability within the CFS regions or the selection for alterations of specific large CFS genes.
Copyright © 2014 Wiley Periodicals, Inc.

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Year:  2014        PMID: 24481768     DOI: 10.1002/gcc.22150

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  15 in total

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Review 2.  Fragility Extraordinaire: Unsolved Mysteries of Chromosome Fragile Sites.

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Review 3.  WWOX, large common fragile site genes, and cancer.

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4.  MicroRNA-23a depletion promotes apoptosis of ovarian cancer stem cell and inhibits cell migration by targeting DLG2.

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5.  A knockdown with smoke model reveals FHIT as a repressor of Heme oxygenase 1.

Authors:  Jennifer A Boylston; Charles Brenner
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Review 6.  The common fragile site FRA16D gene product WWOX: roles in tumor suppression and genomic stability.

Authors:  Rami I Aqeilan; Muhannad Abu-Remaileh; Mohammad Abu-Odeh
Journal:  Cell Mol Life Sci       Date:  2014-09-23       Impact factor: 9.261

Review 7.  Very large common fragile site genes and their potential role in cancer development.

Authors:  Ge Gao; David I Smith
Journal:  Cell Mol Life Sci       Date:  2014-10-10       Impact factor: 9.261

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Authors:  Leanne Jones; Michael Naidoo; Lee R Machado; Karen Anthony
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9.  DNA secondary structure at chromosomal fragile sites in human disease.

Authors:  Ryan G Thys; Christine E Lehman; Levi C T Pierce; Yuh-Hwa Wang
Journal:  Curr Genomics       Date:  2015-02       Impact factor: 2.236

Review 10.  Updating the mechanisms of common fragile site instability: how to reconcile the different views?

Authors:  Benoît Le Tallec; Stéphane Koundrioukoff; Therese Wilhelm; Anne Letessier; Olivier Brison; Michelle Debatisse
Journal:  Cell Mol Life Sci       Date:  2014-09-24       Impact factor: 9.261

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