Prospective pharmacological potential of cryptotanshinone in cancer therapy

Background: Cryptotanshinone (CPT), a Traditional Chinese Medicine (TCM) has recently gained remarkable interest as a potent alternative cancer therapeutic. The sole objective of this review is to accumulate the anti-tumour activity of CPT against major cancers as well as the underlying mechanisms....

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Main Authors: Ashif Ahamed (Author), Mahmadul Hasan (Author), Arijit Samanta (Author), Syed Sahajada Mahafujul Alam (Author), Zarnain Jamil (Author), Safdar Ali (Author), Mehboob Hoque (Author)
Format: Book
Published: Elsevier, 2023-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Ashif Ahamed  |e author 
700 1 0 |a Mahmadul Hasan  |e author 
700 1 0 |a Arijit Samanta  |e author 
700 1 0 |a Syed Sahajada Mahafujul Alam  |e author 
700 1 0 |a Zarnain Jamil  |e author 
700 1 0 |a Safdar Ali  |e author 
700 1 0 |a Mehboob Hoque  |e author 
245 0 0 |a Prospective pharmacological potential of cryptotanshinone in cancer therapy 
260 |b Elsevier,   |c 2023-12-01T00:00:00Z. 
500 |a 2667-1425 
500 |a 10.1016/j.prmcm.2023.100308 
520 |a Background: Cryptotanshinone (CPT), a Traditional Chinese Medicine (TCM) has recently gained remarkable interest as a potent alternative cancer therapeutic. The sole objective of this review is to accumulate the anti-tumour activity of CPT against major cancers as well as the underlying mechanisms. Methods: This comprehensive review focuses on the experimental outcome of in vivo and in vitro investigations targeting multiple signalling pathways of various cancers and molecular mechanisms involved in hindering cancer growth. Results: CPT targets different cell signalling pathways, transcription factors (STAT1, 3, 4, 5, c-Myc), cellular markers (PD-1, CTLA-4, PDL-1), kinases (Tyrosine kinase such as IGF-1R, Bcr-Abl, Src, JAK, FAK, Serine/Threonine kinase such as Aurora A, Cyclin dependent kinase such as CDK1, 2) which are associated with stemness, growth, division, proliferation, metastasis, angiogenesis and drug resistance of a cancer cell. CPT suppresses cancer progression by inhibiting the phosphorylation of intermediate signalling molecules like STAT3, hence disrupting the STAT3 signalling pathway amongst several other signalling pathways involved in cancer progression. CPT may also induce apoptosis by modulating several pro-apoptotic (Bax, Bak, Bcl-10) and anti-apoptotic (Bcl-2, Bcl-x, Bcl-xL) proteins. Furthermore, CPT showed potential drug synergism with other chemotherapeutic drugs resulting in strategizing better cancer treatment. Conclusion: This review summarizes that CPT, being a natural product with less side-effects in long-term cancer use, may be considered as a potential alternative to the traditional cancer therapies. Although, there is substantial evidence of success in laboratory, its efficacy for clinical application may be increased with an appropriate drug delivery approach and the accurate formulation or dosage. 
546 |a EN 
690 |a Cancer therapy 
690 |a Cryptotanshinone 
690 |a Phytomedicine 
690 |a Signalling pathways 
690 |a Traditional Chinese medicine 
690 |a Other systems of medicine 
690 |a RZ201-999 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Pharmacological Research - Modern Chinese Medicine, Vol 9, Iss , Pp 100308- (2023) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2667142523000945 
787 0 |n https://doaj.org/toc/2667-1425 
856 4 1 |u https://doaj.org/article/c2e7adf59c344da384633e0af065a28a  |z Connect to this object online.