TY - JOUR
T1 - Atypical protein kinase Cτ plays a critical role in human lung cancer cell growth and tumorigenicity
AU - Regala, Roderick P.
AU - Weems, Capella
AU - Jamieson, Lee
AU - Copland, John A.
AU - Thompson, E. Aubrey
AU - Fields, Alan P.
PY - 2005/9/2
Y1 - 2005/9/2
N2 - Atypical protein kinase C (aPKC) isozyimes function in epithelial cell polarity, proliferation, and survival and have been implicated in cellular transformation. However, the role of these enzymes in human cancer is largely unexplored. Here, we report that aPKCτ is highly expressed in human non-small cell lung cancer cell lines, whereas the closely related aPKC isozyme PKCζ is undetectable in these cells. Disruption of PKCτ signaling reveals that PKCτ is dispensable for adherent growth of non-small cell lung cancer cells but is required for transformed growth in soft agar in vitro and for tumorigenicity in vivo. Molecular dissection of signaling downstream of PKCτ demonstrates that Rac1 is a critical molecular target for PKCτ-dependent transformation, whereas PKCτ is not necessary for NFκB activation in vitro or in vivo. Expression of the PB1 domain of PKCi (PKCτ-(1-113)) blocks PKCτ-dependent Rac1 activity and inhibits cellular transformation indicating a role for this domain in the transforming activity of PKCτ. Taken together, our data demonstrate that PKCτ is a critical lung cancer gene that activates a Rac1→Pak→Mek1,2→Erk1,2 signaling pathway required for transformed growth. Our data indicate that PKCτ may be an attractive molecular target for mechanism-based therapies for treatment of lung cancer.
AB - Atypical protein kinase C (aPKC) isozyimes function in epithelial cell polarity, proliferation, and survival and have been implicated in cellular transformation. However, the role of these enzymes in human cancer is largely unexplored. Here, we report that aPKCτ is highly expressed in human non-small cell lung cancer cell lines, whereas the closely related aPKC isozyme PKCζ is undetectable in these cells. Disruption of PKCτ signaling reveals that PKCτ is dispensable for adherent growth of non-small cell lung cancer cells but is required for transformed growth in soft agar in vitro and for tumorigenicity in vivo. Molecular dissection of signaling downstream of PKCτ demonstrates that Rac1 is a critical molecular target for PKCτ-dependent transformation, whereas PKCτ is not necessary for NFκB activation in vitro or in vivo. Expression of the PB1 domain of PKCi (PKCτ-(1-113)) blocks PKCτ-dependent Rac1 activity and inhibits cellular transformation indicating a role for this domain in the transforming activity of PKCτ. Taken together, our data demonstrate that PKCτ is a critical lung cancer gene that activates a Rac1→Pak→Mek1,2→Erk1,2 signaling pathway required for transformed growth. Our data indicate that PKCτ may be an attractive molecular target for mechanism-based therapies for treatment of lung cancer.
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U2 - 10.1074/jbc.M505402200
DO - 10.1074/jbc.M505402200
M3 - Article
C2 - 15994303
AN - SCOPUS:24744469442
SN - 0021-9258
VL - 280
SP - 31109
EP - 31115
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 35
ER -