Emodin: A metabolite that exhibits anti-neoplastic activities by modulating multiple oncogenic targets.
Angiogenesis
Apoptosis
Cell cycle arrest
Chemoresistance
Emodin
Inflammation
Journal
Toxicology in vitro : an international journal published in association with BIBRA
ISSN: 1879-3177
Titre abrégé: Toxicol In Vitro
Pays: England
ID NLM: 8712158
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
received:
28
12
2020
revised:
11
02
2021
accepted:
09
03
2021
pubmed:
17
3
2021
medline:
9
11
2021
entrez:
16
3
2021
Statut:
ppublish
Résumé
Oncogenic transformation has been the major cause of global mortality since decades. Despite established therapeutic regimes, majority of cancer patients either present with tumor relapse, refractory disease or therapeutic resistance. Numerous drug candidates are being explored to tap the key reason being poor tumor remission rates, from novel chemotherapy agents to immunotherapy to exploring natural compound derivatives with effective anti-cancer potential. One of these natural product metabolites, emodin has present with significant potential to target tumor oncogenic processes: induction of apoptosis and cell cycle arrest, tumor angiogenesis, and metastasis to chemoresistance in malignant cells. Based on the present scientific excerpts on safety and effectiveness of emodin in targeting hallmarks of tumor progression, emodin is being promisingly explored using nanotechnology platforms for long-term sustained treatment and management of cancer patients. In this review, we summarize the up-to-date scientific literature supporting the anti-neoplastic potential of emodin. We also provide an insight into toxicity and safety profile of emodin and how emodin has emerged as an effective therapeutic alternative in synergism with established conventional chemotherapeutic regimes for management and treatment of tumor progression.
Identifiants
pubmed: 33722736
pii: S0887-2333(21)00067-9
doi: 10.1016/j.tiv.2021.105142
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Protein Kinase Inhibitors
0
Emodin
KA46RNI6HN
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
105142Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.