Oridonin: An active diterpenoid targeting cell cycle arrest, apoptotic and autophagic pathways for cancer therapeutics

It is well-known that cell cycle arrest and/or death play a pivotal role in tumor progression, which has drawn a rising attention for cancer biologists due to their complex and intricate relationships. In this review, we demonstrate the recent research on oridonin, an active diterpenoid with remarka...

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Veröffentlicht in:The international journal of biochemistry & cell biology 2011-05, Vol.43 (5), p.701-704
Hauptverfasser: Li, Chun-yang, Wang, En-qin, Cheng, Yan, Bao, Jin-ku
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container_issue 5
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container_title The international journal of biochemistry & cell biology
container_volume 43
creator Li, Chun-yang
Wang, En-qin
Cheng, Yan
Bao, Jin-ku
description It is well-known that cell cycle arrest and/or death play a pivotal role in tumor progression, which has drawn a rising attention for cancer biologists due to their complex and intricate relationships. In this review, we demonstrate the recent research on oridonin, an active diterpenoid with remarkable anti-proliferative activities, and then further explore its molecular mechanisms of cell cycle arrest, apoptosis, autophagy and their cross-talks in various cancer cells, which may provide a new perspective of oridonin as a candidate anti-neoplastic drug for future cancer therapeutics.
doi_str_mv 10.1016/j.biocel.2011.01.020
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Anti-neoplastic drug
antineoplastic agents
Apoptosis
Apoptosis - drug effects
Autophagy
Autophagy - drug effects
Biochemistry
Biologists
Biology
Cancer
Cell Cycle - drug effects
Cell cycle arrest
cell cycle checkpoints
Cell Line, Tumor
Death
Diterpenes, Kaurane - chemistry
Diterpenes, Kaurane - pharmacology
Diterpenes, Kaurane - therapeutic use
diterpenoids
Drug Stability
Drugs
Humans
neoplasm cells
Neoplasms - drug therapy
Neoplasms - pathology
Oridonin
Pathways
Progressions
therapeutics
Tumors
title Oridonin: An active diterpenoid targeting cell cycle arrest, apoptotic and autophagic pathways for cancer therapeutics
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