Expression and function of the 67 kDa high-affinity laminin receptor in nonsmall cell lung carcinoma
A. A. Mancini, G. G. Marsico, A. A. Russo, P. P. Ragno, N. N. Montuori, G. G. Rossi, M. M. Caputi (Naples, Italy)
Source: Annual Congress 2002 - Lung cancer biology
Session: Lung cancer biology
Session type: Oral Presentation
Number: 219
Disease area: Thoracic oncology
Abstract Cell surface receptors for laminin mediate cell adhesion to basal membranes, a critical step in the metastasis cascade. The 67 kDa high affinity laminin receptor (67LR), a non-integrin laminin receptor, is overexpressed in a large variety of human cancers and is associated with the invasive and metastatic phenotype. We studied the expression and the function of 67LR in cell lines, tissues and primary cell cultures derived from non-small cell lung carcinoma (NSCLC). The 67LR was highly expressed in lung mucoepidermoid- (NCI-H292), epidermoid- (Calu-1) and adeno- (GLC-82) carcinoma cell lines, while it was absent in the immortalized normal lung cell line MRC-5. The expression of 67LR was also increased in 21 out of 34 tumor tissues derived from patients affected by NSCLC (62%), as compared to adjacent normal tissues. In addition, primary cell cultures were prepared from normal and tumor tissues of 7 NSCLC patients: tumor cells showed increased expression of 67LR in 6 patients, as compared to the respective normal cells. Tumor cells overexpressing the 67LR showed an increased cell adhesion to laminin (LM), that could be dramatically inhibited by a recombinant polypeptide (r37LRP) containing laminin-binding domains of the 67LR. Therefore, the adhesion of NSCLC cells to LM was mostly mediated by the 67LR. Interestingly, the ability of NSCLC-derived cells to invade matrigel-coated membranes was also related to the level of 67LR expression and was specifically inhibited by r37LRP. These findings suggest that NSCLC overexpress a functional 67LR that conferes to the cells the ability to bind LM with high affinity and to migrate through basal membranes.
Rating:
You must login to grade this presentation.
Share or cite this content
Citations should be made in the following way:
A. A. Mancini, G. G. Marsico, A. A. Russo, P. P. Ragno, N. N. Montuori, G. G. Rossi, M. M. Caputi (Naples, Italy). Expression and function of the 67 kDa high-affinity laminin receptor in nonsmall cell lung carcinoma. Eur Respir J 2002; 20: Suppl. 38, 219
You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.
Member's Comments
Related content which might interest you:
Related content which might interest you:
The effect of adhesion molecule CEACAM1 and chemokine receptor CXCR4 expression on prognosis of non-small cell lung cancer Source: Eur Respir J 2005; 26: Suppl. 49, 324s Year: 2005
Toll-like receptor 3 is up-regulated and enhances anti-proliferative function in human non-small cell lung cancer Source: Annual Congress 2008 - Lung cancer and other malignant diseases involving the lungs Year: 2008
Expression and significance of VE-cadherin and E-cadherin in non-small cell lung cancer Source: Annual Congress 2011 - Progress in pathology of lung cancer Year: 2011
Loss of polymeric immunoglobulin receptor expression is associated with lung tumourigenesis Source: Eur Respir J 2012; 39: 1171-1180 Year: 2012
Expression of sex hormone receptors in non-small cell lung cancer patients Source: Eur Respir J 2004; 24: Suppl. 48, 79s Year: 2004
The value of CD44 and MMP-2 expression in non-small cell lung cancer Source: Eur Respir J 2004; 24: Suppl. 48, 77s Year: 2004
Management of EGFR mutated nonsmall cell lung carcinoma patients Source: Eur Respir J 2015; 45: 1132-1141 Year: 2015
Differential cytokine expression in non-small cell lung carcinomas Source: Eur Respir J 2007; 30: Suppl. 51, 512s Year: 2007
Bile acid receptor mediates cancer-associated fibroblasts-induced migration and invasion of non-small cell lung cancer cells Source: International Congress 2017 – Basic research in lung cancer: a scientific potpourri from genetic alterations to immune cells Year: 2017
FGFR1 gene aberrations and FGFR1 protein expression in squamous non-small cell lung cancer (Sq-NSCLC). Source: Virtual Congress 2021 – Biology of lung cancer: preclinical and translational research Year: 2021
Expression of Fhit protein in non-small cell lung cancer (NSCLC) and its correlation with Ki-67, a proliferative marker Source: Eur Respir J 2002; 20: Suppl. 38, 230s Year: 2002
Alpha and beta estrogen and progesterone receptors expression in non-small cell lung cancer patients Source: Annual Congress 2008 - Biology and prognosis in thoracic oncology Year: 2008
Choice of endogenous control for gene expression in nonsmall cell lung cancer Source: Eur Respir J 2005; 26: 1002-1008 Year: 2005
An analysis of EGFR expression and tumour imaging in non-small cell carcinomas of lung Source: Annual Congress 2011 - Imaging, functional evaluation and staging for lung cancer patients Year: 2011
Expression of βig-h3 as a marker of local tumor invasion in non-small cell lung cancer Source: Eur Respir J 2006; 28: Suppl. 50, 770s Year: 2006
MRP1 and -3 protein expression in non-small cells carcinomas and survey Source: Eur Respir J 2006; 28: Suppl. 50, 811s Year: 2006
Expression of Her-2/neu and Bcl-2 in patients with non-small cell lung cancer Source: International Congress 2017 – Gene signatures in bronchial diseases Year: 2017
Association of KIR genes and their ligands with non-small cell lung cancer Source: Annual Congress 2010 - Prognostic factors for lung cancer Year: 2010
Transcriptional regulation of the human osteopontin promoter in non-small cell lung cancer Source: Annual Congress 2011 - Progress in pathology of lung cancer Year: 2011
Prognostic significance of epidermal growth factor receptor expression in nonsmall cell lung cancer Source: Eur Respir J 2002; 20: Suppl. 38, 72s Year: 2002