Mechanisms of apoptosis by the tumor suppressor Par-4

J Cell Physiol. 2012 Dec;227(12):3715-21. doi: 10.1002/jcp.24098.

Abstract

Par-4 is a pro-apoptotic, tumor suppressor protein that induces apoptosis selectively in cancer cells. Endoplasmic reticulum-stress and higher levels of protein kinase A in tumor cells confer the coveted feature of cancer selective response to extracellular and intracellular Par-4, respectively. Recent studies have shown that systemic Par-4 confers resistance to tumor growth in mice, and that tumor-resistance is transferable by bone-marrow transplantation. Moreover, recombinant Par-4 inhibits the growth of tumors in mice. As systemic Par-4 induces apoptosis via cell surface GRP78, strategies that promote GRP78 trafficking to the cell surface are expected sensitize cancer cells to circulating levels of Par-4. This review illustrates the domains and mechanisms by which Par-4 orchestrates the apoptotic process in both cell culture models and in physiological settings.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Endoplasmic Reticulum Chaperone BiP
  • Gene Expression Regulation, Neoplastic / physiology*
  • Genetic Predisposition to Disease
  • Humans
  • Neoplasms / metabolism
  • Receptors, Thrombin / genetics
  • Receptors, Thrombin / metabolism*

Substances

  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Hspa5 protein, mouse
  • Receptors, Thrombin
  • protease-activated receptor 4