Literature DB >> 17268177

Inverted duplication pattern in anaphase bridges confirms the breakage-fusion-bridge (BFB) cycle model for 11q13 amplification.

S C Reshmi1, S Roychoudhury, Z Yu, E Feingold, D Potter, W S Saunders, S M Gollin.   

Abstract

The homogeneously staining region (hsr) involving chromosome band 11q13 includes amplified genes from this chromosome segment and carries a relatively poor prognosis in oral squamous cell carcinomas (OSCC), with shorter time to recurrence and reduced overall survival. We previously identified an inverted duplication pattern of genes within the 11q13 hsr in OSCC cells, supporting a breakage-fusion-bridge (BFB) cycle model for gene amplification. To validate our hypothesis that 11q13 gene amplification in OSCC occurs via BFB cycles, we carried out fluorescence in situ hybridization (FISH) using probes for band 11q13 on 29 OSCC cell lines. We demonstrate that all OSCC cell lines with 11q13 amplification express a significantly higher frequency of anaphase bridges containing 11q13 sequences compared to cell lines without amplification, providing further experimental evidence that 11q13 gene amplification in OSCC cells occurs via BFB cycles. Elucidation of mechanisms responsible for initiating and promoting gene amplification provides opportunities to identify new biomarkers to aid in the diagnosis and prognosis of oral cancer, and may be useful for developing novel therapeutic strategies for patients with OSCC. Copyright 2007 S. Karger AG, Basel.

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Year:  2007        PMID: 17268177     DOI: 10.1159/000097425

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  11 in total

1.  Reconstructing breakage fusion bridge architectures using noisy copy numbers.

Authors:  Shay Zakov; Vineet Bafna
Journal:  J Comput Biol       Date:  2015-06       Impact factor: 1.479

2.  Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure.

Authors:  Clelia Tiziana Storlazzi; Angelo Lonoce; Maria C Guastadisegni; Domenico Trombetta; Pietro D'Addabbo; Giulia Daniele; Alberto L'Abbate; Gemma Macchia; Cecilia Surace; Klaas Kok; Reinhard Ullmann; Stefania Purgato; Orazio Palumbo; Massimo Carella; Peter F Ambros; Mariano Rocchi
Journal:  Genome Res       Date:  2010-07-14       Impact factor: 9.043

3.  Targeted inhibition of ATR or CHEK1 reverses radioresistance in oral squamous cell carcinoma cells with distal chromosome arm 11q loss.

Authors:  Madhav Sankunny; Rahul A Parikh; Dale W Lewis; William E Gooding; William S Saunders; Susanne M Gollin
Journal:  Genes Chromosomes Cancer       Date:  2013-11-25       Impact factor: 5.006

Review 4.  Chromosomal imbalances in oral squamous cell carcinoma: examination of 31 cell lines and review of the literature.

Authors:  Christa Lese Martin; Shalini C Reshmi; Thomas Ried; William Gottberg; John W Wilson; Jaya K Reddy; Poornima Khanna; Jonas T Johnson; Eugene N Myers; Susanne M Gollin
Journal:  Oral Oncol       Date:  2007-08-02       Impact factor: 5.337

Review 5.  Genome rearrangements associated with aberrant telomere maintenance.

Authors:  Ragini Bhargava; Matthias Fischer; Roderick J O'Sullivan
Journal:  Curr Opin Genet Dev       Date:  2020-03-04       Impact factor: 5.578

6.  Genomic profiling of advanced-stage oral cancers reveals chromosome 11q alterations as markers of poor clinical outcome.

Authors:  Srikant Ambatipudi; Moritz Gerstung; Ravindra Gowda; Prathamesh Pai; Anita M Borges; Alejandro A Schäffer; Niko Beerenwinkel; Manoj B Mahimkar
Journal:  PLoS One       Date:  2011-02-28       Impact factor: 3.240

7.  Characterization at nucleotide resolution of the homogeneously staining region sites of insertion in two cancer cell lines.

Authors:  Anne Gibaud; Nicolas Vogt; Olivier Brison; Michelle Debatisse; Bernard Malfoy
Journal:  Nucleic Acids Res       Date:  2013-07-02       Impact factor: 16.971

8.  Characterization of genetic rearrangements in esophageal squamous carcinoma cell lines by a combination of M-FISH and array-CGH: further confirmation of some split genomic regions in primary tumors.

Authors:  Jia-Jie Hao; Zhi-Zhou Shi; Zhi-Xin Zhao; Yu Zhang; Ting Gong; Chun-Xiang Li; Ting Zhan; Yan Cai; Jin-Tang Dong; Song-Bin Fu; Qi-Min Zhan; Ming-Rong Wang
Journal:  BMC Cancer       Date:  2012-08-24       Impact factor: 4.430

9.  Copy number alterations identify a smoking-associated expression signature predictive of poor outcome in head and neck squamous cell carcinoma.

Authors:  Brenen W Papenberg; James Ingles; Si Gao; Jun Feng; Jessica L Allen; Steven M Markwell; Erik T Interval; Phillip A Montague; Sijin Wen; Scott A Weed
Journal:  Cancer Genet       Date:  2021-05-28

10.  A common copy-number breakpoint of ERBB2 amplification in breast cancer colocalizes with a complex block of segmental duplications.

Authors:  Michael Marotta; Xiongfong Chen; Ayako Inoshita; Robert Stephens; G Thomas Budd; Joseph P Crowe; Joanne Lyons; Anna Kondratova; Raymond Tubbs; Hisashi Tanaka
Journal:  Breast Cancer Res       Date:  2012-11-26       Impact factor: 6.466

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