Immunohistochemically detected expression of motility-related protein-1 (MRP-1/CD9) in lung adenocarcinoma and its relation to prognosis
Open Access
- 22 April 1997
- journal article
- research article
- Published by Wiley in International Journal of Cancer
- Vol. 74 (2) , 205-211
- https://doi.org/10.1002/(sici)1097-0215(19970422)74:2<205::aid-ijc12>3.0.co;2-c
Abstract
Motility‐related protein‐1 (MRP‐1)/CD9 is a trans‐membrane glycoprotein closely associated with suppression of cell motility and reduced metastatic potential of some tumor cells. We currently report that, according to the RT‐PCR method for MRP‐1/CD9 gene expression, patients with low expression of MRP‐1/CD9 in non‐small‐cell lung cancer, especially the adenocarcinoma type, showed short overall survival. Then, to determine accurately the prognostic value of MRP‐1/CD9 product levels in lung‐adenocarcinoma cells, we immunohistochemically investigated its expression in 132 lung‐adenocarcinoma patients undergoing potentially curative surgery. Of these patients, 44 (33%) showed reduced expression of MRP‐1/CD9 in cancer cells, and an inverse association was observed between its expression and factors associated with tumor progression, such as nodal involvement (p = 0.029) or stage (p = 0.028). Patients with reduced expression of MRP‐1/CD9 showed a significantly worse prognosis in overall survival (p = 0.005) and disease‐free survival (DFS; p < 0.0001) than those with stronger expression; and even among patients with stage‐I disease, similar results were obtained (overall survival, p = 0.038; DFS, p = 0.012). In a multivariate analysis, immunohistochemical MRP‐1/CD9‐expression level was an independent prognostic factor for DFS (p = 0.021), but not for overall survival (p = 0.572). Thus, immunohistochemical MRP‐1/CD9‐expression level solely in lung‐adenocarcinoma cells within the tumor tissue appears to be a prognostic factor for DFS, and may be useful for detecting a high‐risk sub‐group of recurrence during the post‐operative clinical course of the disease. Int. J. Cancer 74:205‐211, 1997. © 1997 Wiley‐Liss, Inc.Keywords
This publication has 18 references indexed in Scilit:
- KAI1 , a Metastasis Suppressor Gene for Prostate Cancer on Human Chromosome 11p11.2Science, 1995
- The membrane protein CD9/DRAP 27 potentiates the juxtacrine growth factor activity of the membrane-anchored heparin-binding EGF-like growth factor.The Journal of cell biology, 1995
- CD9 antigen is an accessory subunit of the VLA integrin complexesEuropean Journal of Immunology, 1994
- The ins and outs of the transmembrane 4 superfamilyImmunology Today, 1994
- Anti‐CD9 monoclonal antibody elicits staurosporine inhibitable phosphatidylinositol 4,5‐bisphosphate hydrolysis, phosphatidylinositol 3,4‐bisphosphate synthesis, and protein‐tyrosine phosphorylation in human plateletsFEBS Letters, 1993
- Suppression of cell motility and metastasis by transfection with human motility-related protein (MRP-1/CD9) DNA.The Journal of Experimental Medicine, 1993
- Expression of the neuroglandular antigen and analogues in melanoma. CD9 expression appears inversely related to metastatic potential of melanomaInternational Journal of Cancer, 1993
- Identification of the motility-related protein (MRP-1), recognized by monoclonal antibody M31-15, which inhibits cell motility.The Journal of Experimental Medicine, 1991
- A new superfamily of lymphoid and melanoma cell proteins with extensive homology to Schistosoma mansoni antigen Sm23European Journal of Immunology, 1991
- The primary structure of the human leukocyte antigen CD37, a species homologue of the rat MRC OX-44 antigen.The Journal of Experimental Medicine, 1989