Broad spectrum targeting of tumor vasculature by medicinal plants: An updated review

dc.contributor.authorYehya, Ashwaq H. S.
dc.contributor.authorAsif, Muhammad
dc.contributor.authorTan, Yi J.
dc.contributor.authorSasidharan, Sreenivasan
dc.contributor.authorAbdul Majid, Amin Malik Shah Bin
dc.contributor.authorOon, Chern Ein
dc.date.accessioned2019-12-16T01:04:16Z
dc.date.issued2017-03-08
dc.date.updated2019-07-28T08:19:37Z
dc.description.abstractDeregulated angiogenesis plays a central role in the development and metastasis of solid cancers. Tumor vasculature expressing a variety of biomarkers offers some novel therapeutic options which can be selectively targeted with anti-angiogenic agents without significantly affecting the normal vasculature. However, anti-angiogenic agents currently available commercially (synthetic compounds and humanized monoclonal antibodies) have been designed to target specific molecular markers within the cell signalling networks in addition to being expensive as well as toxic. Therefore, it is highly desirable to search for new therapeutic moieties which can simultaneously treat multiple aberrant pathways yet being less toxic and inexpensive. Several studies have highlighted that medicinal plants either as crude extracts or as pure isolated compounds can meet these criteria. The unique combination of different classes of phytochemicals present in plant extracts have been shown simultaneously to target multiple abnormal pathways in the tumor angiogenic cascade thus arresting growth of tumor cells at various stages. In addition, these phytochemicals have health promoting benefits making them ideal candidates to be pursued for drug development. The current review provides an update on the broad spectrum anti-angiogenic activities of different classes of phytochemicals present in the medicinal plants. Although preclinical studies have shown promising results, further studies are required to explore the in-depth molecular mechanisms responsible for the observed pharmacological activities and to test the efficacy of isolated compounds or standardised extracts in properly designed experiments. In addition, long term toxicity studies and data on interaction with other drugs are also required to establish the safety profile of extracts before the commencement of clinical trials.en_AU
dc.description.sponsorshipAshwaq, H. S. Yehya and Muhammad Asif were supported by TWAS (The Academy of Sciences for the Developing World, Italy) and IPS USM (USM fellowship) respectively and NKEA Grant by Ministry of Agriculture Malaysia (304/CIPPM/650736/k123). Chern. E. Oon was supported by the RUI Universiti Sains Malaysia Grant (1001/CIPPM/812156).en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn2210-8041en_AU
dc.identifier.urihttp://hdl.handle.net/1885/195316
dc.language.isoen_AUen_AU
dc.publisherElsevier GmbHen_AU
dc.rights© 2017 Elsevier GmbHen_AU
dc.sourceJournal of Herbal Medicineen_AU
dc.subjectMedicinal plantsen_AU
dc.subjectPhytochemicalsen_AU
dc.subjectAnti-angiogenesisen_AU
dc.subjectCrude extractsen_AU
dc.titleBroad spectrum targeting of tumor vasculature by medicinal plants: An updated reviewen_AU
dc.typeJournal articleen_AU
dcterms.dateAccepted2017-03-06
local.bibliographicCitation.lastpage13en_AU
local.bibliographicCitation.startpage1en_AU
local.contributor.affiliationYehya, Ashwaq H. S., University of Science Malaysiaen_AU
local.contributor.affiliationAsif, Muhammad, Universti Sains Malaysiaen_AU
local.contributor.affiliationTan, Yi J., Universti Sains Malaysiaen_AU
local.contributor.affiliationSasidharan, Sreenivasan, Universti Sains Malaysiaen_AU
local.contributor.affiliationAbdul Majid, Amin Malik Shah Bin, College of Health and Medicine, ANUen_AU
local.contributor.affiliationOon, Chern Ein, Universti Sains Malaysiaen_AU
local.contributor.authoremailu1026638@anu.edu.auen_AU
local.contributor.authoruidAbdul Majid, Amin Malik Shah Bin, u1026638en_AU
local.description.embargo2037-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor111200 - ONCOLOGY AND CARCINOGENESISen_AU
local.identifier.absseo860803 - Human Pharmaceutical Treatments (e.g. Antibiotics)en_AU
local.identifier.ariespublicationu4485658xPUB1091en_AU
local.identifier.citationvolume9en_AU
local.identifier.doi10.1016/j.hermed.2017.03.003en_AU
local.identifier.scopusID2-s2.0-85016034069
local.identifier.thomsonID000418086300001
local.identifier.uidSubmittedByu4485658en_AU
local.publisher.urlhttps://www.sciencedirect.comen_AU
local.type.statusPublished Versionen_AU

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