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PMID: 7746054 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Genetic diagnosis of lymph-node metastasis in colorectal cancer.

Lancet (London, England) ·Vol. 345 ·No. 8960 ·1995-05-20 ·Pages 1257-9

Hayashi N, Ito I, Yanagisawa A, Kato Y, Nakamori S, Imaoka S, Watanabe H, Ogawa M, Nakamura Y

Abstract

If a regional lymph node taken during surgery for colorectal cancer is found to be free of tumour on histological examination this is taken to be a good sign. However, conventional staining may not be sensitive enough. Mutant-allele-specific amplification (MASA) is a technique that can detect, at the level of an individual cell, micrometastases to lymph nodes that are histologically diagnosed as negative. To examine the prognostic significance of such genetically detectable tumour cells we screened 120 colorectal cancers from patients who had no histologically detectable lymph-node metastasis at the time of surgery for mutations in K-ras (codons 12, 13, and 61) or p53 (exons 5-8). Somatic mutations were identified by MASA in 71 tumours. We next examined preserved tissues from corresponding regional lymph nodes, using MASA to look for the specific mutation found in the primary. Of 37 patients with genetically positive lymph nodes 27 had had a tumour recurrence within 5 years of surgery; none of the 34 patients who were MASA negative for lymph node metastasis had had a recurrence. Genetic diagnosis of lymph node metastasis may be a useful prognostic factor in colorectal cancer, and it could also serve as a selective marker for intensive postoperative adjuvant chemotherapy.

Related Genes
MeSH Terms
Colorectal Neoplasms/genetics,pathology,surgery DNA, Neoplasm/genetics Genes, p53 Genes, ras Humans Immunohistochemistry Lymphatic Metastasis/diagnosis,genetics Mutation Neoplasm Metastasis Neoplasm Recurrence, Local Polymerase Chain Reaction/methods Predictive Value of Tests Prognosis
Chemicals
DNA, Neoplasm
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Hayashi N
Department of Biochemistry, Cancer Institute, Tokyo, Japan.
Ito I
Yanagisawa A
Kato Y
Nakamori S
Imaoka S
Watanabe H
Ogawa M
Nakamura Y
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
0140-6736
Published
1995-05-20
Pages
1257-9
Language
English
Region
England
NLM ID
2985213R
Subset
IM
Corrections
CommentIn
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