Marine macroalga Caulerpa: role of its metabolites in modulating cancer signaling. View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-04-12

AUTHORS

Richa Mehra, Satej Bhushan, Felix Bast, Sandeep Singh

ABSTRACT

Cancer, the leading causes of death worldwide, causes multiple metabolic and physiological alterations, leading to an unregulated proliferation of cells. The existing anticancer therapies are usually nonspecific with side effects and or are extremely expensive, thus hunt for better therapeutics is still on, specially efforts are made to look for naturally occurring molecules. Sea harbors several organisms which are unexplored for their biological potentials. Green macroalga genus, Caulerpa, is one such invaluable repository of bioactive metabolites like alkaloids, terpenoids, flavonoids, steroids and tannins with reported bioactivities against many diseases including cancer. Anti-cancerous metabolites of Caulerpa like caulerpenyne (Cyn), caulerpin, caulersin, and racemosin C, possess unique structural moieties and are known to exhibit distinct effects on cancer cells. Theses metabolites are reported to affect microtubule dynamics, unfolded protein response, mitochondrial health, cell cycle progression, metabolic and stress pathways by their cross-talk with signalling proteins like AMPK, GRP78, GADD153, Bid, Bax, AIF, Bcl2, P21, cyclin D, cyclin E, caspase 9, and PTP1B. Targeting of multiple cancer hallmarks by Caulerpa metabolites, with concomitant modulations of multiple signalling cascades, displays its multifactorial approach against cancer. Evaluation of anti-cancer properties of this genus is particularly important as Caulerpa species are widely edible and utilized in several delicacies in the coastal countries. This is the first review article providing a consolidated information about the role of Caulerpa in cancer with major contributing metabolites and plausible modulations in cancer signaling and prospects. More... »

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11033-019-04743-5

DOI

http://dx.doi.org/10.1007/s11033-019-04743-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1113380591

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30980271


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