Therapeutic Potential of Pigment Epithelium-derived Factor in Cancer.


Journal

Current pharmaceutical design
ISSN: 1873-4286
Titre abrégé: Curr Pharm Des
Pays: United Arab Emirates
ID NLM: 9602487

Informations de publication

Date de publication:
2019
Historique:
received: 13 02 2019
accepted: 13 03 2019
pubmed: 21 3 2019
medline: 23 2 2020
entrez: 21 3 2019
Statut: ppublish

Résumé

Pigment epithelium-derived factor (PEDF) is one of the serine protease inhibitors with multifunctional properties, which is produced by various types of organs and tissues. There is an accumulating body of evidence that PEDF plays an important role in the maintenance of tissue homeostasis. Indeed, PEDF not only works as an endogenous inhibitor of angiogenesis, but also suppresses oxidative stress, inflammatory and thrombotic reactions in cell culture systems, animal models, and humans. Furthermore, we, along with others, have found that PEDF inhibits proliferation of, and induces apoptotic cell death in, numerous kinds of tumors. In addition, circulating as well as tumor expression levels of PEDF have been inversely associated with tumor growth and metastasis. These observations suggest that supplementation of PEDF proteins and/or enhancement of endogenous PEDF expression could be a novel therapeutic strategy for the treatment of cancer. Therefore, in this paper, we review the effects of PEDF on diverse types of cancer, and discuss its therapeutic perspectives.

Identifiants

pubmed: 30892156
pii: CPD-EPUB-97413
doi: 10.2174/1381612825666190319112106
doi:

Substances chimiques

Eye Proteins 0
Nerve Growth Factors 0
Serpins 0
pigment epithelium-derived factor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

313-324

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Sho-Ichi Yamagishi (SI)

Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume 830-0011, Japan.

Yoshinori Koga (Y)

Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume 830-0011, Japan.
Department of Pediatric Surgery, Kurume University School of Medicine, Kurume 830-0011, Japan.

Ami Sotokawauchi (A)

Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume 830-0011, Japan.

Naoki Hashizume (N)

Department of Pediatric Surgery, Kurume University School of Medicine, Kurume 830-0011, Japan.

Suguru Fukahori (S)

Department of Pediatric Surgery, Kurume University School of Medicine, Kurume 830-0011, Japan.

Takanori Matsui (T)

Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume 830-0011, Japan.

Minoru Yagi (M)

Department of Pediatric Surgery, Kurume University School of Medicine, Kurume 830-0011, Japan.

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Classifications MeSH