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Expression of laminin γ2 chain monomer enhances invasive growth of human carcinoma cells in vivo
Author(s) -
Tsubota Yoshiaki,
Ogawa Takashi,
Oyanagi Jun,
Nagashima Yoji,
Miyazaki Kaoru
Publication year - 2010
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.25231
Subject(s) - matrigel , laminin , cell culture , biology , cancer research , stromal cell , cell growth , growth factor , in vivo , epidermal growth factor , pathology , microbiology and biotechnology , angiogenesis , extracellular matrix , medicine , biochemistry , genetics , receptor
Laminin γ2 chain is a subunit of the heterotrimeric basement membrane protein laminin‐332 (α3β3γ2). The γ2 chain is highly expressed by human cancers at the invasion fronts and this expression correlates with poor prognosis of the cancers. Our previous study showed that the γ2 chain is expressed as a monomer form in invading carcinoma cells. However, the role of the γ2 protein in tumor invasion remains unknown. Here, we demonstrate that the monomeric γ2 chain promotes invasive growth of human cancer cells in vivo . First, we analyzed regulatory factors for the γ2 chain expression using 2 gastric carcinoma cell lines. It was found that tumor necrosis factor‐α, by itself or in a combination with transforming growth factor‐β1, strongly induced the secretion of the monomeric γ2 chain. In addition, epidermal growth factor families appeared to function as the γ2 chain inducers in human cancers. Next, we established T‐24 bladder carcinoma cell lines expressing the full‐length or the short arm of the laminin γ2 chain. When these cell lines were i.p . injected into nude mice, they produced larger tumors in the abdominal cavity and showed much stronger invasive growth onto the diaphragms than the control cell line. The γ2‐expressing T‐24 cells often produced ascites fluid, but scarcely the control cells. In culture, the γ2‐expressing cells migrated through Matrigel more efficiently than the control cells. These findings imply that the γ2 monomer is induced in human cancers by inflammatory and stromal cytokines and promotes their invasive growth in vivo .