TRIM21 is a novel regulator of Par-4 in colon and pancreatic cancer cells.

Cancer Biol Ther

a Department of Medicine and Penn State Hershey Cancer Institute , Penn State College of Medicine, Hershey , PA , USA.

Published: January 2017

AI Article Synopsis

  • Par-4 is a tumor-suppressor protein that selectively induces apoptosis in cancer cells, and understanding its regulation is crucial for developing new cancer treatments.
  • Research identified TRIM21 as a novel interacting partner of Par-4, which downregulates Par-4 levels in response to the chemotherapy drug cisplatin.
  • High TRIM21 levels correlate with increased resistance to cisplatin in colon cancer cells and predict poorer survival outcomes in pancreatic cancer patients, suggesting it as a potential therapeutic target and prognostic marker.

Article Abstract

The prostate apoptosis response protein 4 (Par-4) is a tumor-suppressor that has been shown to induce cancer-cell selective apoptosis in a variety of cancers. The regulation of Par-4 expression and activity is a relatively understudied area, and identifying novel regulators of Par-4 may serve as novel therapeutic targets. To identify novel regulators of Par-4, a co-immunoprecipitation was performed in colon cancer cells, and co-precipitated proteins were identified by mass-spectometry. TRIM21 was identified as a novel interacting partner of Par-4, and further shown to interact with Par-4 endogenously and through its PRY-SPRY domain. Additional studies show that TRIM21 downregulates Par-4 levels in response to cisplatin, and that TRIM21 can increase the resistance of colon cancer cells to cisplatin. Furthermore, forced Par-4 expression can sensitize pancreatic cancer cells to cisplatin. Finally, we demonstrate that TRIM21 expression predicts survival in pancreatic cancer patients. Our work highlights a novel mechanism of Par-4 regulation, and identifies a novel prognostic marker and potential therapeutic target for pancreatic cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323013PMC
http://dx.doi.org/10.1080/15384047.2016.1252880DOI Listing

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