Literature DB >> 10092128

Comparative genomic hybridization analysis of primary colorectal carcinomas and their synchronous metastases.

F Al-Mulla1, W N Keith, I R Pickford, J J Going, G D Birnie.   

Abstract

We have analyzed 26 tumors from 12 patients with metastatic colorectal adenocarcinoma by comparative genomic hybridization (CGH). Primary tumors and their lymph node metastases from five Dukes' C patients as well as primary tumors and their liver metastases from seven Dukes' D patients were used to assess the extent of genetic differences between primary and secondary colorectal carcinomas from the same patients, to calculate the degree of clonal divergence and genetic heterogeneity in metastatic colorectal cancer, and to determine the differences in genetic imbalances between Dukes' C and D stage tumors. We show that the same genetic aberrations were frequently found in the primary tumors and their metastases. However, metastases often contained genetic aberrations not found in the corresponding primary tumors. The comparison of Dukes' stages C and D revealed genetic aberrations common to both. However, reduced copy number of chromosome arm 17p (5/5 vs. 0/7; P = 0.001) was significantly associated with Dukes' stage C and lymph node metastases, while increased copy number of chromosome arms 6p (6/7 vs. 0/5; P = 0.007) and 17q (5/7 vs. 0/5; P = 0.027) was associated more with Dukes' stage D and liver metastases. Our results established a repertoire of chromosomal alterations associated with metastatic colorectal cancer and suggest that Dukes' C (lymph node metastasis) tumors are not always simply an earlier stage of Dukes' D (liver metastasis) tumors and, thus, in some instances at least, they are distinct forms of the disease.

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Year:  1999        PMID: 10092128     DOI: 10.1002/(sici)1098-2264(199904)24:4<306::aid-gcc3>3.0.co;2-5

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


  35 in total

1.  Expressive genomic hybridisation: gene expression profiling at the cytogenetic level.

Authors:  F Al-Mulla; M Al-Maghrebi; G Varadharaj
Journal:  Mol Pathol       Date:  2003-08

2.  Metastatic recurrence of early-stage colorectal cancer is linked to loss of heterozygosity on chromosomes 4 and 14q.

Authors:  F Al-Mulla; S AlFadhli; A H Al-Hakim; J J Going; M S Bitar
Journal:  J Clin Pathol       Date:  2006-06       Impact factor: 3.411

Review 3.  Chromosome 6p amplification and cancer progression.

Authors:  Gda C Santos; M Zielenska; M Prasad; J A Squire
Journal:  J Clin Pathol       Date:  2006-06-21       Impact factor: 3.411

4.  Telomere loss provokes multiple pathways to apoptosis and produces genomic instability in Drosophila melanogaster.

Authors:  Simon W A Titen; Kent G Golic
Journal:  Genetics       Date:  2008-10-09       Impact factor: 4.562

5.  Hypermethylation of the TPEF/HPP1 gene in primary and metastatic colorectal cancers.

Authors:  Matthias P A Ebert; Suzanne H Mooney; Lori Tonnes-Priddy; Joe Lograsso; Juliane Hoffmann; Jie Chen; Christoph Röcken; Hans-Ulrich Schulz; Peter Malfertheiner; Catherine Lofton-Day
Journal:  Neoplasia       Date:  2005-08       Impact factor: 5.715

Review 6.  Implementing prognostic and predictive biomarkers in CRC clinical trials.

Authors:  Sandra Van Schaeybroeck; Wendy L Allen; Richard C Turkington; Patrick G Johnston
Journal:  Nat Rev Clin Oncol       Date:  2011-02-15       Impact factor: 66.675

Review 7.  Is there a genetic signature for liver metastasis in colorectal cancer?

Authors:  Cristina Nadal; Joan Maurel; Pere Gascon
Journal:  World J Gastroenterol       Date:  2007-11-28       Impact factor: 5.742

8.  Biological resonance for cancer metastasis, a new hypothesis based on comparisons between primary cancers and metastases.

Authors:  Dongwei Gao; Sha Li
Journal:  Cancer Microenviron       Date:  2013-11-10

9.  Reduced level of the spindle checkpoint protein BUB1B is associated with aneuploidy in colorectal cancers.

Authors:  E Burum-Auensen; P M DeAngelis; A R Schjølberg; J Røislien; O Mjåland; O P F Clausen
Journal:  Cell Prolif       Date:  2008-08       Impact factor: 6.831

10.  Predominant modifier of extreme liver cancer susceptibility in C57BR/cdJ female mice localized to 6 Mb on chromosome 17.

Authors:  Stephanie E-M Peychal; Andrea Bilger; Henry C Pitot; Norman R Drinkwater
Journal:  Carcinogenesis       Date:  2009-03-02       Impact factor: 4.944

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