HPV18 E7 inhibits LATS1 kinase and activates YAP1 by degrading PTPN14

William J Blakely1, Joshua Hatterschide1, Elizabeth A White1

  • 1Department of Otorhinolaryngology: Head and Neck Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.

Mbio
|September 9, 2024
PubMed

Insights

High-risk human papillomavirus (HPV) oncoprotein E7 degrades tumor suppressor PTPN14, inhibiting the Hippo pathway. This promotes YAP1 activity, driving keratinocyte stemness and blocking differentiation, thus contributing to HPV-driven carcinogenesis.

Area of Science:

  • Cell Biology
  • Molecular Oncology
  • Virology

Background:

  • High-risk human papillomavirus (HPV) oncoproteins disrupt cellular tumor suppressors, reprogramming host signaling.
  • YAP1, a transcriptional coactivator driving epithelial stemness, is negatively regulated by the Hippo kinase pathway.
  • The Hippo pathway is frequently inactivated in cancers, and HPV E7 oncoprotein activity requires YAP1.

Purpose of the Study:

  • To investigate the effect of high-risk HPV18 E7 oncoprotein on Hippo pathway activity.
  • To elucidate the mechanism by which HPV E7 activates YAP1 and promotes keratinocyte dedifferentiation.

Main Methods:

  • Investigated HPV18 E7 effects on Hippo pathway components in human keratinocytes.
  • Utilized PTPN14 knockout and assessed phosphorylation of LATS1 and YAP1.
  • Examined the role of LATS kinases and PTPN14 motifs in keratinocyte differentiation.

Main Results:

  • PTPN14 knockout or HPV18 E7-mediated degradation of PTPN14 reduced LATS1 T1079 and YAP1 S127 phosphorylation.
  • This reduction in phosphorylation inhibited keratinocyte differentiation.
  • PTPN14-dependent differentiation necessitated LATS kinases and specific PTPN14 motifs, but not MST1/2 kinases or PTPN14 phosphatase activity.

Conclusions:

  • HPV18 E7 degrades PTPN14, leading to reduced LATS1 kinase activity.
  • Inhibition of LATS1 kinase promotes YAP1 activation, driving keratinocyte stemness and inhibiting differentiation.
  • These findings strengthen the link between PTPN14, Hippo signaling, and HPV-mediated carcinogenesis.

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