The Met receptor and alpha 6 beta 4 integrin can function independently to promote carcinoma invasion

UMMS Affiliation

Department of Cancer Biology

Publication Date


Document Type



3T3 Cells; Animals; Carcinoma; Cell Line, Tumor; Culture Media, Conditioned; Hepatocyte Growth Factor; Humans; Immunoblotting; Integrin alpha6beta4; Integrin beta4; Lysophospholipids; Mice; Neoplasm Invasiveness; Precipitin Tests; Proteins; *Proto-Oncogene Proteins; RNA Interference; RNA, Small Interfering; *Receptors, Growth Factor; Retroviridae; Time Factors


Cancer Biology | Neoplasms


It has been proposed that a constitutive, physical association of the Met receptor and the alpha(6)beta(4) integrin exists on the surface of invasive carcinoma cells and that hepatocyte growth factor (HGF)-mediated invasion is dependent on alpha(6)beta(4) (Trusolino, L., Bertotti, A., and Comoglio, P. M. (2001) Cell 107, 643-654). The potential significance of these results prompted us to re-examine this hypothesis. Using three different carcinoma cell lines that express both Met and alpha(6)beta(4), we were unable to detect the constitutive association of these receptors by co-immunoprecipitation. Moreover, carcinoma cells that lacked expression of alpha(6)beta(4) exhibited Met-dependent invasion toward HGF, and increasing Met expression by viral infection of these cells enhanced invasion without inducing alpha(6)beta(4) expression. Although expression of alpha(6)beta(4) in such cells enhanced their invasion to HGF, it also enhanced their ability to invade toward other chemoattractants such as lysophosphatidic acid, and this latter invasion was not inhibited by a function-blocking Met antibody. Finally, depletion of beta(4) by RNA interference in invasive carcinoma cells that express both receptors reduced the ability of these cells to invade toward HGF by approximately 25%, but it did not abrogate their invasion. These data argue that the invasive function of Met can be independent of alpha(6)beta(4) and that alpha(6)beta(4) has a generic influence on the invasion of carcinoma cells that is not specific to Met.

DOI of Published Version



J Biol Chem. 2004 Jul 30;279(31):32287-93. Epub 2004 May 25. Link to article on publisher's site

Journal/Book/Conference Title

The Journal of biological chemistry

Related Resources

Link to Article in PubMed

PubMed ID