Mu-KRAS attenuates Hippo signaling pathway through PKCι to sustain the growth of pancreatic cancer

J Cell Physiol. 2020 Jan;235(1):408-420. doi: 10.1002/jcp.28981. Epub 2019 Jun 23.

Abstract

The atypical protein kinase C isoform ι (PKCι) is upregulated, which cooperates with mutated KRAS (mu-KRAS) to promote the development of pancreatic cancers. However, the exact role of PKCι in KRAS-mediated pancreatic tumorigenesis is not fully defined. In the present study, we demonstrate that mu-KRAS upregulates and activates PKCι, accompanied by dephosphorylation of large tumor suppressor (LATS), a key member of the growth-inhibiting Hippo signaling pathway. As a result, Yes-associated protein 1 (YAP1; a transcriptional coactivator) is dephosphorylated and translocates to the nucleus, which promotes transcription of downstream target genes to sustain the transformed growth of pancreatic cancer cells. In contrast, when PKCι is suppressed by the chemical inhibitor or small-hairpin RNA, the levels of phosphorylated LATS and YAP1 are elevated and YAP1 is excluded from the nucleus, which enhances the susceptibility of pancreatic cancer cells harboring mu-KRAS to apoptosis. These findings shed new light on the mechanisms underlying the pancreatic tumorigenesis initiated by mu-KRAS, and suggest that the PKCι-YAP1 signaling may potentially be therapeutically targeted for restricting the growth and inducing apoptosis in pancreatic tumors expressing mu-KRAS.

Keywords: KRAS; LATS; PKCι; YAP1; pancreatic cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Apoptosis / physiology
  • Cell Line, Tumor
  • Cell Transformation, Neoplastic / genetics
  • Gene Expression Regulation, Neoplastic / genetics*
  • Humans
  • Isoenzymes / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / pathology*
  • Phosphorylation
  • Protein Kinase C / metabolism*
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins p21(ras) / genetics*
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Transcription Factors / metabolism*
  • YAP-Signaling Proteins

Substances

  • Adaptor Proteins, Signal Transducing
  • Isoenzymes
  • KRAS protein, human
  • RNA, Small Interfering
  • Transcription Factors
  • YAP-Signaling Proteins
  • YAP1 protein, human
  • LATS1 protein, human
  • Protein Serine-Threonine Kinases
  • Protein Kinase C
  • protein kinase C lambda
  • Proto-Oncogene Proteins p21(ras)