TY - GEN
T1 - The transforming functions of PI3-kinase-γ are linked to disruption of intercellular adhesion and promotion of cancer cell invasion
AU - Attoub, Samir
AU - De Wever, Olivier
AU - Bruyneel, Eric
AU - Mareel, Marc
AU - Gespach, Christian
PY - 2008/9
Y1 - 2008/9
N2 - The involvement of phosphoinositide 3-kinases class IA (PI3K-α and -β) in cancer cell proliferation, survival, motility, and invasiveness is now well established. However, the possible contribution of the class IB PI3Kγ in cancer cell transformation remains to be explored. In this study, we have stably transfected the PI3Kγ-deficient human colon cancer cell line HCT8/S11 with expression vectors encoding either wild-type PI3Kγ, its plasma membrane targeted form CAAX-PI3Kγ, or the PI3Kγ lipid and protein kinase-dead mutant (CAAX-K832R). We provide evidence that the constitutively active CAAX-PI3Kγ variant induced collagen type I invasion in HCT8/S11 cells through disruption of cell-cell adhesion, with no apparent impact on cell proliferation and motility. The proinvasive activity of CAAX-PI3K-γ was abolished by pharmacological inhibitors targeting PI3-K activities (wortmannin), Rho-GTPases, and the Rho-Rho kinase axis (C3T exoenzyme and Y27632, respectively). Conversely, the wild-type PI3Kγ and its double mutant CAAX-K832R were ineffective on cancer cell invasion measured under control or stimulated conditions operated with the proinvasive agents leptin and intestinal trefoil factor. Taken together, our data indicate that PI3Kγ exerts transforming functions via several mechanisms in human colon epithelial cancer cells, including alterations of homotypic cell-cell adhesion and induction of collagen type I invasion through canonical proinvasive pathways.
AB - The involvement of phosphoinositide 3-kinases class IA (PI3K-α and -β) in cancer cell proliferation, survival, motility, and invasiveness is now well established. However, the possible contribution of the class IB PI3Kγ in cancer cell transformation remains to be explored. In this study, we have stably transfected the PI3Kγ-deficient human colon cancer cell line HCT8/S11 with expression vectors encoding either wild-type PI3Kγ, its plasma membrane targeted form CAAX-PI3Kγ, or the PI3Kγ lipid and protein kinase-dead mutant (CAAX-K832R). We provide evidence that the constitutively active CAAX-PI3Kγ variant induced collagen type I invasion in HCT8/S11 cells through disruption of cell-cell adhesion, with no apparent impact on cell proliferation and motility. The proinvasive activity of CAAX-PI3K-γ was abolished by pharmacological inhibitors targeting PI3-K activities (wortmannin), Rho-GTPases, and the Rho-Rho kinase axis (C3T exoenzyme and Y27632, respectively). Conversely, the wild-type PI3Kγ and its double mutant CAAX-K832R were ineffective on cancer cell invasion measured under control or stimulated conditions operated with the proinvasive agents leptin and intestinal trefoil factor. Taken together, our data indicate that PI3Kγ exerts transforming functions via several mechanisms in human colon epithelial cancer cells, including alterations of homotypic cell-cell adhesion and induction of collagen type I invasion through canonical proinvasive pathways.
KW - Cell proliferation
KW - Leptin
KW - MAPK
KW - Motility
KW - Rho-GTPases
KW - Trefoil peptides
UR - http://www.scopus.com/inward/record.url?scp=53149114909&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=53149114909&partnerID=8YFLogxK
U2 - 10.1196/annals.1414.027
DO - 10.1196/annals.1414.027
M3 - Conference contribution
C2 - 18837901
AN - SCOPUS:53149114909
SN - 9781573317009
T3 - Annals of the New York Academy of Sciences
SP - 204
EP - 213
BT - Recent Advances in Clinical Oncology
PB - Blackwell Publishing Inc.
ER -