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Mutation of the nm23-H1 gene has a non-dominant role in colorectal adenocarcinoma
Author(s) -
Yueling Jin,
Zhensheng Dai
Publication year - 2016
Publication title -
molecular and clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.442
H-Index - 7
eISSN - 2049-9469
pISSN - 2049-9450
DOI - 10.3892/mco.2016.889
Subject(s) - immunostaining , colorectal cancer , oncogene , biology , point mutation , deleted in colorectal cancer , immunohistochemistry , cancer , metastasis , metastasis suppressor gene , mutation , cancer research , gene , tumor suppressor gene , gene mutation , adenocarcinoma , pathology , microbiology and biotechnology , cell cycle , genetics , carcinogenesis , medicine , immunology
Nm23-H1 is a metastasis suppressor gene, which is has a reduced expression in patients with digestive system cancer. However, the mechanistic basis for the genetic instability remains unknown. To study the expression of the nm23-H1 gene in patients with colorectal cancer, polymerase chain reaction-single strand conformation polymorphism was used to analyze any point mutation, and immunohistochemistry was used to detect the expression of nm23-H1. Results revealed that all 63 specimens of Chinese human colorectal cancer tissues exhibit no point mutation. Among those 63 specimens, 19 (30%) exhibited positive immunostaining for the nm23-H1 protein and 44 (70%) exhibited negative immunostaining. These observations suggested that the protein and gene expression levels of nm23-H1 are reduced in colorectal cancer compared with the adjacent normal tissues, and the point mutation in the nm23-H1 gene is not the dominant cause of metastatic colorectal cancer.

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