Literature DB >> 8993977

Genomic instability in sporadic colorectal cancer quantitated by inter-simple sequence repeat PCR analysis.

M Basik1, D L Stoler, K C Kontzoglou, M A Rodriguez-Bigas, N J Petrelli, G R Anderson.   

Abstract

Genomic instability plays a major role in cancer by facilitating tumor progression and tumor heterogeneity. Inter-simple sequence repeat (inter-SSR) PCR has been developed to provide a rapid and reproducible technique for quantitation of the major type of genomic instability observed in sporadic tumors, namely, that manifesting itself as amplifications, deletions, translocations, and insertions. Evaluation of 59 sporadic colorectal cancers by inter-SSR PCR has demonstrated a wide range of instability, independent of tumor stage at diagnosis. Comparison of these data and the results of microsatellite PCR analysis reveals an association of high genomic instability with loss of heterozygosity but no association with the replication error phenomenon arising from defects in mismatch repair.

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Year:  1997        PMID: 8993977

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


  17 in total

1.  How many mutations does it take to make a tumor?

Authors:  C R Boland; L Ricciardiello
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

2.  Uniparentalism in sporadic colorectal cancer is independent of imprint status, and coordinate for chromosomes 14 and 18.

Authors:  Huferesh K Darbary; Smitha S Dutt; Sheila J Sait; Norma J Nowak; Roy E Heinaman; Daniel L Stoler; Garth R Anderson
Journal:  Cancer Genet Cytogenet       Date:  2009-03

3.  Genomic instability measured by inter-(simple sequence repeat) PCR and high-resolution microsatellite instability are prognostic of colorectal carcinoma survival after surgical resection.

Authors:  Bruce M Brenner; Helen Swede; Beth A Jones; Garth R Anderson; Daniel L Stoler
Journal:  Ann Surg Oncol       Date:  2011-04-13       Impact factor: 5.344

4.  The onset and extent of genomic instability in sporadic colorectal tumor progression.

Authors:  D L Stoler; N Chen; M Basik; M S Kahlenberg; M A Rodriguez-Bigas; N J Petrelli; G R Anderson
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

5.  Allelic losses at genomic instability-associated loci in villous adenomas and adjacent colorectal cancers.

Authors:  Bruce M Brenner; Daniel L Stoler; Luz Rodriguez; Matthew J Karpenko; Helen Swede; Nicholas J Petrelli; Garth R Anderson
Journal:  Cancer Genet Cytogenet       Date:  2007-04-01

Review 6.  Aberrant crypt foci as precursors in colorectal cancer progression.

Authors:  Frank A Orlando; Dongfeng Tan; Juan D Baltodano; Thaer Khoury; John F Gibbs; Victor J Hassid; Bestoun H Ahmed; Sadir J Alrawi
Journal:  J Surg Oncol       Date:  2008-09-01       Impact factor: 3.454

7.  DNA fingerprinting abnormalities can distinguish ulcerative colitis patients with dysplasia and cancer from those who are dysplasia/cancer-free.

Authors:  Ru Chen; Peter S Rabinovitch; David A Crispin; Mary J Emond; Kent M Koprowicz; Mary P Bronner; Teresa A Brentnall
Journal:  Am J Pathol       Date:  2003-02       Impact factor: 4.307

8.  Colorectal cancers in patients with the (9A/6A) polymorphism of TGFBR1 exhibit lesser inter-(simple sequence repeat) PCR genomic instability and present clinically at greater age.

Authors:  Smitha S Dutt; Neng Chen; Huferesh K Darbary; Helen Swede; Nicholas J Petrelli; Daniel L Stoler; Garth R Anderson
Journal:  Mutat Res       Date:  2008-08-20       Impact factor: 2.433

9.  Amplification of repeat-containing transcribed sequences (ARTS): a transcriptome fingerprinting strategy to detect functionally relevant microsatellite mutations in cancer.

Authors:  Martina Olivero; Tina Ruggiero; Nadia Coltella; Antonella Maffe'; Raffaele Calogero; Enzo Medico; Maria Flavia Di Renzo
Journal:  Nucleic Acids Res       Date:  2003-04-01       Impact factor: 16.971

10.  A truncated isoform of the protein phosphatase 2A B56gamma regulatory subunit may promote genetic instability and cause tumor progression.

Authors:  Akihiko Ito; Yu-Ichiro Koma; Kenji Watabe; Teruaki Nagano; Yuichi Endo; Hiroshi Nojima; Yukihiko Kitamura
Journal:  Am J Pathol       Date:  2003-01       Impact factor: 4.307

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