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.
Original language | English |
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Pages (from-to) | 3715-3721 |
Number of pages | 7 |
Journal | Journal of Cellular Physiology |
Volume | 227 |
Issue number | 12 |
DOIs | |
State | Published - Dec 2012 |
ASJC Scopus subject areas
- Physiology
- Clinical Biochemistry
- Cell Biology