Transformation of rat intestinal epithelial cells by overexpression of Rab25 is microtubule dependent.

Lapierre LA, Caldwell CM, Higginbotham JN, Avant KM, Hall J, Beauchamp RD, Goldenring JR
Cytoskeleton (Hoboken). 2011 68 (2): 97-111

PMID: 21246754 · PMCID: PMC3885764 · DOI:10.1002/cm.20497

Little research has addressed the role of membrane trafficking and recycling in the regulation of the transformed phenotype of neoplastic cells. The small GTPase Rab25 is an epithelial-specific modulator of membrane recycling. Recent studies have demonstrated that Rab25 expression is up-regulated in a number of epithelial cancers and overexpression may increase the aggressive phenotype of certain cancers. We have utilized the nontransformed RIE cell line to examine the influence of Rab25 on transformation. Overexpression of Rab25 in RIE cells leads to morphological transformation as well as growth in soft agar, tumor formation in nude mice, disruption of integrin-based focal adhesions, and alteration in modified microtubule subsets. Although the predominance of recent cancer research has focused on the manipulation of the actin-based cytoskeleton, recycling trafficking relies on microtubules. Transformation of RIE cells through overexpression of Rab25, but not with H-Ras(V12) , was reversed by inhibitors of microtubule polymerization. These results suggest that up-regulation of Rab25 in RIE cells leads to microtubule-dependent transformation. Thus, depolymerization of microtubules may be a potent therapeutic target for cancer therapy through the reversal of the invasive phenotype of certain cancer cells.

Copyright © 2010 Wiley-Liss, Inc.

MeSH Terms (14)

Animals Cell Transformation, Neoplastic Epithelial Cells Gene Expression Regulation, Neoplastic Intestinal Mucosa Mice Mice, Nude Microtubules Neoplasms, Experimental Neoplasm Transplantation Oncogene Protein p21(ras) rab GTP-Binding Proteins Rats Transplantation, Heterologous

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