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Increased Expression of the Laminin Receptor in Human Colon Cancer

Authors :
Vittoria Cioce
Lance A. Liotta
Spiridione Garbisa
Barry M. Shmookler
Walter F. Grigioni
Mark E. Sobel
Vincent Castronovo
Source :
JNCI Journal of the National Cancer Institute. 83:29-36
Publication Year :
1991
Publisher :
Oxford University Press (OUP), 1991.

Abstract

It has been proposed that among the various cell-surface proteins capable of interacting with laminin, the 67-kd high-affinity laminin receptor plays a crucial role during tumor invasion and metastasis. In this study, the expression of laminin-receptor-precursor messenger RNA (mRNA) and 67-kd protein was analyzed in human colon adenocarcinoma. In 22 of 23 patients with colon cancer, we found a 2- to 23-fold increase in levels of laminin-receptor-precursor mRNA in the cancer tissues compared with those in matched normal adjacent colonic mucosa. In 10 of 11 cases studied, the level of 67-kd laminin receptor, detected by affinity-purified anti-laminin-receptor synthetic peptide antibodies on immunoblots of matched tumor and normal tissue extracts, was higher in the colon carcinoma tissue. Immunodetection of laminin receptor in tissue sections using anti-laminin-receptor-peptide antibodies confirmed that the increased expression of laminin receptor was specifically associated with the cancer cells. In a series of 72 paraffin sections of colon lesions, we observed a correlation between the expression of the laminin receptor and the Dukes' classification. Our observations indicate that increased expression of laminin-receptor-precursor mRNA is associated with enhanced levels of the 67-kd laminin receptor as well as with the invasive phenotype of colon carcinoma. Detection of this metastasis-associated gene product may be a valuable adjunct in the evaluation of human colon cancer.

Details

ISSN :
14602105 and 00278874
Volume :
83
Database :
OpenAIRE
Journal :
JNCI Journal of the National Cancer Institute
Accession number :
edsair.doi.dedup.....21ebd7286ceb6dbd6a5aea18dda755ef
Full Text :
https://doi.org/10.1093/jnci/83.1.29