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The Anticancer Properties of Cordycepin and Their Underlying Mechanisms
by
Park, Yoon Jung
, Park, Soo Jung
, Yoon, So Young
in
Animals
/ Antineoplastic Agents - pharmacology
/ Apoptosis - drug effects
/ Cordyceps - chemistry
/ Deoxyadenosines - pharmacology
/ Humans
/ MAP Kinase Signaling System
/ Review
2018
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The Anticancer Properties of Cordycepin and Their Underlying Mechanisms
by
Park, Yoon Jung
, Park, Soo Jung
, Yoon, So Young
in
Animals
/ Antineoplastic Agents - pharmacology
/ Apoptosis - drug effects
/ Cordyceps - chemistry
/ Deoxyadenosines - pharmacology
/ Humans
/ MAP Kinase Signaling System
/ Review
2018
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Do you wish to request the book?
The Anticancer Properties of Cordycepin and Their Underlying Mechanisms
by
Park, Yoon Jung
, Park, Soo Jung
, Yoon, So Young
in
Animals
/ Antineoplastic Agents - pharmacology
/ Apoptosis - drug effects
/ Cordyceps - chemistry
/ Deoxyadenosines - pharmacology
/ Humans
/ MAP Kinase Signaling System
/ Review
2018
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The Anticancer Properties of Cordycepin and Their Underlying Mechanisms
Journal Article
The Anticancer Properties of Cordycepin and Their Underlying Mechanisms
2018
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Overview
Cordyceps is a genus of ascomycete fungi that has been used for traditional herbal remedies. It contains various bioactive ingredients including cordycepin. Cordycepin, also known as 3-deoxyadenosine, is a major compound and has been suggested to have anticancer potential. The treatment of various cancer cells with cordycepin in effectively induces cell death and retards their cancerous properties. However, the underlying mechanism is not fully understood. Recent evidence has shed light on the molecular pathways involving cysteine-aspartic proteases (caspases), mitogen-activated protein kinases (MAPKs), and glycogen synthase kinase 3 beta (GSK-3β). Furthermore, the pathways are mediated by putative receptors, such as adenosine receptors (ADORAs), death receptors (DRs), and the epidermal growth factor receptor (EGFR). This review provides the molecular mechanisms by which cordycepin functions as a singular or combinational anticancer therapeutic agent.
Publisher
MDPI
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