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The Ability of Versican to Simultaneously Cause Apoptotic Resistance and Sensitivity

¹ Sunnybrook Health Sciences Centre and ² Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada; ³ Guangdong Institute of Microbiology, Guangdong Academy of Sciences; and ⁴ School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China

Requests for reprints: Burton B. Yang, Sunnybrook Health Sciences Centre, Research Building, 2075 Bayview Avenue, Toronto, Canada M4N 3M5. Phone: 416-480-5874; Fax: 416-480-5737; E-mail: burton.yang{at}sri.utoronto.ca.

Expression of the extracellular matrix proteoglycan versican is associated with more than 10 types of cancers, often being secreted by stromal cells in response to tumor signals. Previous work in our lab has shown that overexpression of the V1 versican isoform in cultured fibroblasts (V1 cells) increases both proliferation and apoptotic resistance. We show here that V1 cells induced tumor formation in nude mice and that, in keeping with previously shown apoptotic resistance, V1 cells have down-regulated Fas mRNA and protein levels. Unexpectedly, however, V1 cells were found to be sensitized to a wide range of cytotoxic agents. This combination of selective apoptotic resistance and sensitivity is often seen in cancer cells. V1 cells were also shown to have high resting levels of p53 and murine double minute-2 proteins, correlating with apoptotic sensitivity. Treatment with UV radiation induced p21 expression in vector-transfected cells but not in V1 cells. As p21 induces cell cycle arrest and inhibits apoptosis, its loss in V1 cells, coupled with high resting levels of proapoptotic p53, may be at least partially involved in their premature death following cytotoxic treatment. This study further supports the importance of versican in cancer cell biology and the complexity of apoptosis regulation. [Cancer Res 2007;67(10):4742–50]

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