Chromosomal Alterations during Lymphatic and Liver Metastasis Formation of Colorectal Cancer
Comparative genomic hybridization (CGH) was used to screen colorectal carcinomas for chromosomal aberrations that are associated with metastatic phenotype. In total, 63 tumor specimens from 40 patients were investigated, comprising 30 primary tumors, 22 systemic metastases (12 liver, 6 brain, and 4...
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doaj-ed79af34b7a74cb18a3bca947f6b1c092020-11-24T22:51:07ZengElsevierNeoplasia: An International Journal for Oncology Research1476-55861522-80022004-01-0161232810.1016/S1476-5586(04)80050-2Chromosomal Alterations during Lymphatic and Liver Metastasis Formation of Colorectal CancerThomas Knösel0Karsten Schlüns1Ulrike Stein2Holger Schwabe3Peter Michael Schlag4Manfred Dietel5Iver Petersen6Institute of Pathology, Charité-Campus Mitte, Berlin, GermanyInstitute of Pathology, Charité-Campus Mitte, Berlin, GermanyDepartment of Surgery and Oncology, RRC, Charité Campus Buch, Berlin, GermanyDepartment of Surgery and Oncology, RRC, Charité Campus Buch, Berlin, GermanyDepartment of Surgery and Oncology, RRC, Charité Campus Buch, Berlin, GermanyInstitute of Pathology, Charité-Campus Mitte, Berlin, GermanyInstitute of Pathology, Charité-Campus Mitte, Berlin, Germany Comparative genomic hybridization (CGH) was used to screen colorectal carcinomas for chromosomal aberrations that are associated with metastatic phenotype. In total, 63 tumor specimens from 40 patients were investigated, comprising 30 primary tumors, 22 systemic metastases (12 liver, 6 brain, and 4 abdominal wall metastases) and 11 lymph node tumors. Using statistical analysis and histograms to evaluate the chromosomal imbalances, overrepresentations were detected most frequently at 20q11.2-20q13.2, 7q11.17q12, 13q11.2-13q14, 16p12, 19p13, 9q34, and 19q13.1-19q13.2. Deletions were prominent at 18q12-18q23, 4q27-4q28, 4p14, 5q21, 1p21-1p22, 21q21, 6q16-6q21, 3p12, 8p22-8p23, 9p21, 11g22, and 14q13-14q21. Hematogenous metastases showed more alterations than lymph node tumors, particularly more deletions at 1p, 3, 4, 5q, 10q, 14, and 21q21 and gains at 1q, 7p, 12gter, 13, 16, and 22q. Comparing liver metastases with their corresponding primary tumors, particularly deletions at 2q, 5q, 8p, 9p, 10q, and 21q21 and gains at 1q, 11, 12gter, 17g12-q21, 19, and 22q were more often observed. The analysis suggested that the different pathways of tumor dissemination are reflected by a nonrandom accumulation of chromosomal alterations with specific changes being responsible for the different characteristics of the metastatic phenotype. http://www.sciencedirect.com/science/article/pii/S1476558604800502CGHcolorectal cancermetastasislymph node metastasesliver metastases |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Thomas Knösel Karsten Schlüns Ulrike Stein Holger Schwabe Peter Michael Schlag Manfred Dietel Iver Petersen |
spellingShingle |
Thomas Knösel Karsten Schlüns Ulrike Stein Holger Schwabe Peter Michael Schlag Manfred Dietel Iver Petersen Chromosomal Alterations during Lymphatic and Liver Metastasis Formation of Colorectal Cancer Neoplasia: An International Journal for Oncology Research CGH colorectal cancer metastasis lymph node metastases liver metastases |
author_facet |
Thomas Knösel Karsten Schlüns Ulrike Stein Holger Schwabe Peter Michael Schlag Manfred Dietel Iver Petersen |
author_sort |
Thomas Knösel |
title |
Chromosomal Alterations during Lymphatic and Liver Metastasis Formation of Colorectal Cancer |
title_short |
Chromosomal Alterations during Lymphatic and Liver Metastasis Formation of Colorectal Cancer |
title_full |
Chromosomal Alterations during Lymphatic and Liver Metastasis Formation of Colorectal Cancer |
title_fullStr |
Chromosomal Alterations during Lymphatic and Liver Metastasis Formation of Colorectal Cancer |
title_full_unstemmed |
Chromosomal Alterations during Lymphatic and Liver Metastasis Formation of Colorectal Cancer |
title_sort |
chromosomal alterations during lymphatic and liver metastasis formation of colorectal cancer |
publisher |
Elsevier |
series |
Neoplasia: An International Journal for Oncology Research |
issn |
1476-5586 1522-8002 |
publishDate |
2004-01-01 |
description |
Comparative genomic hybridization (CGH) was used to screen colorectal carcinomas for chromosomal aberrations that are associated with metastatic phenotype. In total, 63 tumor specimens from 40 patients were investigated, comprising 30 primary tumors, 22 systemic metastases (12 liver, 6 brain, and 4 abdominal wall metastases) and 11 lymph node tumors. Using statistical analysis and histograms to evaluate the chromosomal imbalances, overrepresentations were detected most frequently at 20q11.2-20q13.2, 7q11.17q12, 13q11.2-13q14, 16p12, 19p13, 9q34, and 19q13.1-19q13.2. Deletions were prominent at 18q12-18q23, 4q27-4q28, 4p14, 5q21, 1p21-1p22, 21q21, 6q16-6q21, 3p12, 8p22-8p23, 9p21, 11g22, and 14q13-14q21. Hematogenous metastases showed more alterations than lymph node tumors, particularly more deletions at 1p, 3, 4, 5q, 10q, 14, and 21q21 and gains at 1q, 7p, 12gter, 13, 16, and 22q. Comparing liver metastases with their corresponding primary tumors, particularly deletions at 2q, 5q, 8p, 9p, 10q, and 21q21 and gains at 1q, 11, 12gter, 17g12-q21, 19, and 22q were more often observed. The analysis suggested that the different pathways of tumor dissemination are reflected by a nonrandom accumulation of chromosomal alterations with specific changes being responsible for the different characteristics of the metastatic phenotype.
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topic |
CGH colorectal cancer metastasis lymph node metastases liver metastases |
url |
http://www.sciencedirect.com/science/article/pii/S1476558604800502 |
work_keys_str_mv |
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