3 research outputs found

    Protein kinase CĪ¹ is required for Ras transformation and colon carcinogenesis in vivo

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    Protein kinase C Ī¹ (PKCĪ¹) has been implicated in Ras signaling, however, a role for PKCĪ¹ in oncogenic Ras-mediated transformation has not been established. Here, we show that PKCĪ¹ is a critical downstream effector of oncogenic Ras in the colonic epithelium. Transgenic mice expressing constitutively active PKCĪ¹ in the colon are highly susceptible to carcinogen-induced colon carcinogenesis, whereas mice expressing kinase-deficient PKCĪ¹ (kdPKCĪ¹) are resistant to both carcinogen- and oncogenic Ras-mediated carcinogenesis. Expression of kdPKCĪ¹ in Ras-transformed rat intestinal epithelial cells blocks oncogenic Ras-mediated activation of Rac1, cellular invasion, and anchorage-independent growth. Constitutively active Rac1 (RacV12) restores invasiveness and anchorage-independent growth in Ras-transformed rat intestinal epithelial cells expressing kdPKCĪ¹. Our data demonstrate that PKCĪ¹ is required for oncogenic Ras- and carcinogen-mediated colon carcinogenesis in vivo and define a procarcinogenic signaling axis consisting of Ras, PKCĪ¹, and Rac1
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