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  2. Anti-tumor effects of pigment epithelium-derived factor (PEDF): implication for cancer therapy. A mini-review

Anti-tumor effects of pigment epithelium-derived factor (PEDF): implication for cancer therapy. A mini-review

  • J Exp Clin Cancer Res. 2016 Jan 8;35:4. doi: 10.1186/s13046-015-0278-7.
Louiza Belkacemi 1 Shaun Xiaoliu Zhang 2 3
Affiliations

Affiliations

  • 1 Center for Nuclear Receptors and Cell Signaling, University of Houston, Houston, TX, 77204, USA. lbelkace@central.uh.edu.
  • 2 Department of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA. xzhang5@central.uh.edu.
  • 3 Center for Nuclear Receptors and Cell Signaling, University of Houston, Houston, TX, 77204, USA. xzhang5@central.uh.edu.
Abstract

Pigment epithelium-derived factor (PEDF) is a secreted glycoprotein and a non-inhibitory member of the Serine Protease Inhibitor (serpin) family. It is widely expressed in human fetal and adult tissues but its expression decreases with age and in malignant tissues. The main anti-cancer activities of PEDF derive from its dual effects, either indirectly on the tumor microenvironment (indirect antitumor action) or directly on the tumor itself (direct antitumor influence). The indirect antitumor activities of PEDF were uncovered from the early findings that it stimulates retinoblastoma cell differentiation and that additionally it possesses anti-angiogenic, anti-tumorigenic and anti-metastatic properties. The mechanisms of its direct antitumor effect, however, have not been fully elucidated. This review highlights recent progress in our understanding of the multifunctional activities of PEDF and, in particular, its anti-cancer signaling mechanisms. Additionally, we discuss the possibility of using novel phosphaplatin compounds that can upregulate PEDF expression as a chemotherapy for Cancer treatment.

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