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Herbal therapeutics that block the oncogenic kinase PAK1: a practical approach towards PAK1-dependent diseases and longevity.

Abstract
Over 35 years research on PAKs, RAC/CDC42(p21)-activated kinases, comes of age, and in particular PAK1 has been well known to be responsible for a variety of diseases such as cancer (mainly solid tumors), Alzheimer's disease, acquired immune deficiency syndrome and other viral/bacterial infections, inflammatory diseases (asthma and arthritis), diabetes (type 2), neurofibromatosis, tuberous sclerosis, epilepsy, depression, schizophrenia, learning disability, autism, etc. Although several distinct synthetic PAK1-blockers have been recently developed, no FDA-approved PAK1 blockers are available on the market as yet. Thus, patients suffering from these PAK1-dependent diseases have to rely on solely a variety of herbal therapeutics such as propolis and curcumin that block PAK1 without affecting normal cell growth. Furthermore, several recent studies revealed that some of these herbal therapeutics significantly extend the lifespan of nematodes (C. elegans) and fruit flies (Drosophila), and PAK1-deficient worm lives longer than the wild type. Here, I outline mainly pathological phenotypes of hyper-activated PAK1 and a list of herbal therapeutics that block PAK1, but cause no side (harmful) effect on healthy people or animals.
AuthorsHiroshi Maruta
JournalPhytotherapy research : PTR (Phytother Res) Vol. 28 Issue 5 Pg. 656-72 (May 2014) ISSN: 1099-1573 [Electronic] England
PMID23943274 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2013 John Wiley & Sons, Ltd.
Chemical References
  • Antineoplastic Agents, Phytogenic
  • Propolis
  • p21-Activated Kinases
  • Curcumin
Topics
  • Animals
  • Antineoplastic Agents, Phytogenic (pharmacology)
  • Communicable Diseases (drug therapy)
  • Curcumin (pharmacology)
  • Humans
  • Inflammation (drug therapy)
  • Longevity (drug effects)
  • Neoplasms (drug therapy)
  • Phytotherapy
  • Plants, Medicinal (chemistry)
  • Propolis (pharmacology)
  • p21-Activated Kinases (antagonists & inhibitors)

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