Influence of laminin substratum on cell proliferation and CALC I gene expression in medullary thyroid carcinoma C cell lines

被引:9
作者
Lekmine, F
Lausson, S
Pidoux, E
Segond, N
Roos, B
Treilhou-Lahille, F
Jeanne, N
机构
[1] Univ Paris Sud, Lab Endocrinol Cellulaire & Evolut, F-91405 Orsay, France
[2] Hop Lariboisiere, Ctr Viggo Petersen, Inst Natl Sante & Rech Med, U349, F-75475 Paris 10, France
[3] Univ Miami, Sch Med, Dept Med, Div Endocrinol, Miami, FL 33101 USA
基金
澳大利亚研究理事会;
关键词
extracellular matrix; medullary thyroid carcinoma; laminin; calcitonin; calcitonin gene-related peptide;
D O I
10.1016/S0303-7207(99)00138-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Medullary thyroid carcinoma (MTC) originates from C cells, which secrete calcitonin (CT) and CT gene-related peptide (CGRP), the two splice peptide products of the CALC I gene. Normal and hyperplastic C cells are intrafollicular, in contact with the basement membrane (BM) that is maintained around the differentiated tumors. To investigate the relationships between MTC evolution and BM constituents, we examined the modifications induced by laminin-l and -2 (merosin), two isoforms colocalized in the follicular BM, on three MTC cell lines: murine rMTC 6-23 and CA-77 cells, and human TT cells. Laminin exerted a mitogenic activity on rMTC 6-23 and on TT cells, causing a concurrent decrease in both CT and CGRP mRNA levels and production of the peptides. Conversely, laminin reduced the proliferation rate and enhanced CGRP synthesis and secretion in CA-77 cells. This antiproliferative response, which coincides with an increase in differentiation markers, is comparable to that reported in normal cells and also in the neoplastic Caco-2 cell line. This suggests that laminin could exert opposite effects depending on the stage of tumor evolution. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:181 / 189
页数:9
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