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AuthorAlmajali, Belal
AuthorNagi, Hamid Ali
AuthorTaib, Wan Rohani Wan
AuthorIsmail, Imilia Ismail
AuthorJohan, Muhammad Farid
AuthorDoolaanea, Abd Almonem
AuthorIbrahim, Wisam Nabeel
Available date2021-04-18T10:53:16Z
Publication Date2021-04-16
Publication NamePharmaceuticals
Identifierhttp://dx.doi.org/10.3390/ph14040369
CitationAlmajali, B.; Al-Jamal, H.A.N.; Taib, W.R.W.; Ismail, I.; Johan, M.F.; Doolaanea, A.A.; Ibrahim, W.N. Thymoquinone, as a Novel Therapeutic Candidate of Cancers. Pharmaceuticals 2021, 14, 369. https://doi.org/10.3390/ph14040369
URIhttp://hdl.handle.net/10576/18276
AbstractTo date, natural products are widely used as pharmaceutical agents for many human diseases and cancers. One of the most popular natural products that have been studied for anticancer properties is thymoquinone (TQ). As a bioactive compound of Nigella sativa, TQ has shown anticancer activities through the inhibition of cell proliferation, migration, and invasion. The anticancer efficacy of TQ is being investigated in several human cancers such as pancreatic cancer, breast cancer, colon cancer, hepatic cancer, cervical cancer, and leukemia. Even though TQ induces apoptosis by regulating the expression of pro- apoptotic and anti-apoptotic genes in many cancers, the TQ effect mechanism on such cancers is not yet fully understood. Therefore, the present review has highlighted the TQ effect mechanisms on several signaling pathways and expression of tumor suppressor genes (TSG). Data from relevant published experimental articles on TQ from 2015 to June 2020 were selected by using Google Scholar and PubMed search engines. The present study investigated the effectiveness of TQ alone or in combination with other anticancer therapeutic agents, such as tyrosine kinase inhibitors on cancers, as a future anticancer therapy nominee by using nanotechnology.
Languageen
PublisherMDPI
Subjectthymoquinone
cancers
proliferation
apoptosis
angiogenesis
nanoparticle
TitleThymoquinone, as a Novel Therapeutic Candidate of Cancers
TypeArticle
Issue Number4
Volume Number14
ESSN1424-8247
dc.accessType Open Access


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