Calpain activity is generally elevated during transformation but has oncogene-specific biological functions

Carragher, N.O., Fonseca, B.D. and Frame, M.C. (2004) Calpain activity is generally elevated during transformation but has oncogene-specific biological functions. Neoplasia, 6, pp. 53-73.

Full text not currently available from Enlighten.

Abstract

Several oncogene and tumor-suppressor gene products are known substrates for the calpain family of cysteine proteases, and calpain is required for transformation by v-src and tumor invasion. Thus, we have now addressed whether calpain is generally associated with transformation and how calpain contributes to oncogene function. Our results demonstrate that calpain activity is enhanced upon transformation induced by the v-Src, v-Jun, v-Myc, k-Ras, and v-Fos oncoproteins. Furthermore, elevated calpain activity commonly promotes focal adhesion remodelling, disruption of actin cytoskeleton, morphological transformation, and cell migration, although proteolysis of target substrates (such as focal adhesion kinase, talin, and spectrin) is differently specified by individual oncoproteins. Interestingly, v-Fos differs from other common oncoproteins in not requiring calpain activity for actin/adhesion remodelling or migration of v-Fos transformed cells. However, anchorage-independent growth of all transformed cells is sensitive to calpain inhibition. In addition, elevated calpain activity contributes to oncogene-induced apoptosis associated with transformation by v-Myc. Taken together, these studies demonstrate that calpain activity is necessary for full cellular transformation induced by common oncoproteins, but has distinct roles in oncogenic events induced by individual transforming proteins. Thus, targeting calpain activity may represent a useful general strategy for interfering with activated proto-oncogenes in cancer cells.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Frame, Prof Margaret
Authors: Carragher, N.O., Fonseca, B.D., and Frame, M.C.
College/School:College of Medical Veterinary and Life Sciences > School of Cancer Sciences
Journal Name:Neoplasia
ISSN:1522-8002

University Staff: Request a correction | Enlighten Editors: Update this record