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Colorectal cancer desmoplastic reaction affects tumor cell invasion
Author(s) -
CoulsonThomas Vivien Jane,
CoulsonThomas Yvette May,
Gesteira Tarsis Ferreira,
Pinhal Maria AS,
Friedl Andreas,
Toma Leny,
Nader Helena Bonciani
Publication year - 2011
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.25.1_supplement.915.6
Subject(s) - desmoplasia , extracellular matrix , myofibroblast , microbiology and biotechnology , cancer cell , colorectal cancer , cell , pathology , chemistry , cell migration , cancer research , cancer , biology , pancreatic cancer , medicine , fibrosis , biochemistry
During cancer cell growth many tumors exhibit various grades of desmoplasia, unorganized production of fibrous or connective tissue, composed mainly of collagen fibers and myofibroblasts. The accumulation of extracellular matrix (ECM) surrounding tumors directly affects cancer cell proliferation, migration and spread, therefore the study of desmoplasia is of vital importance. Myofibroblasts synthesize an amalgam of products including collagens and other ECM proteins, such as proteoglycans and are activated during a desmoplastic reaction. Small leucine rich proteoglycans have been characterized surrounding breast and pancreatic tumors and have the ability to suppress cell proliferation. In this study we have analyzed desmoplasia co‐cultivating colorectal cancer cells (Caco‐2 and HCT116) and myofibroblasts using various co‐culture systems. Our findings demonstrate that direct cell‐cell contact between myofibroblasts and colorectal cancer cells evokes an up‐regulation of the expression of ECM by myofibroblasts. The ECM accumulation produced when myofibroblasts are co‐cultivated with colorectal cancer cells appears unorganized and in bundles. This ECM accumulation slowed the migration and invasion of the colorectal tumor cells in both 2‐D and 3‐D co‐culture systems.