Abilities of berberine and chemically modified berberines to inhibit proliferation of pancreatic cancer cells.
Berberine
Chemotherapeutic drugs
PDAC
Signal transduction inhibitors
Journal
Advances in biological regulation
ISSN: 2212-4934
Titre abrégé: Adv Biol Regul
Pays: England
ID NLM: 101572336
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
received:
06
10
2018
revised:
15
10
2018
accepted:
16
10
2018
pubmed:
27
10
2018
medline:
5
3
2020
entrez:
27
10
2018
Statut:
ppublish
Résumé
Berberine (BBR) is a common nutraceutical consumed by millions worldwide. BBR has many different effects on human health, e.g., diabetes, diarrhea, inflammation and now more recently it has been proposed to have potent anti-cancer effects. BBR has been shown to suppress the growth of cancer cells more than normal cells. BBR has been proposed to exert its growth-inhibitory effects by many different biochemical mechanisms including: suppression of cell cycle progression, induction of reactive oxygen species, induction of apoptosis and autophagy and interactions with DNA potentially leading to DNA damage, and altered gene expression. Pancreatic cancer is a leading cancer worldwide associated with a poor prognosis. As our population ages, pancreatic cancer has an increasing incidence and will likely become the second leading cause of death from cancer. There are few truly-effective therapeutic options for pancreatic cancer. Surgery and certain chemotherapeutic drugs are used to treat pancreatic cancer patients. Novel approaches to treat pancreatic cancer patients are direly needed as they usually survive for less than a year after being diagnosed. In the following manuscript, we discuss the abilities of BBR and certain chemically-modified BBRs (NAX compounds) to suppress growth of pancreatic cancer cells.
Identifiants
pubmed: 30361003
pii: S2212-4926(18)30149-0
doi: 10.1016/j.jbior.2018.10.003
pii:
doi:
Substances chimiques
DNA, Neoplasm
0
Berberine
0I8Y3P32UF
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
172-182Informations de copyright
Copyright © 2018 Elsevier Ltd. All rights reserved.