TY - JOUR
T1 - Molecular targets and anticancer potential of sanguinarine—a benzophenanthridine alkaloid
AU - Galadari, Sehamuddin
AU - Rahman, Anees
AU - Pallichankandy, Siraj
AU - Thayyullathil, Faisal
N1 - Funding Information:
This work was financially supported by grants from the Al Jalila Foundation Research Centre ( AJF201413 ), UAEU Program for Advanced Research ( 31M192 ), the Terry Fox Foundation for Cancer Research ( 21M093 ), the Abu Dhabi Educational Council (ADEC) ( 21M110 ), and in part from the College of Medicine and Health Sciences. The funding sources had no role in the design, collection, analysis, data interpretation or writing of the manuscript.
Publisher Copyright:
© 2017 Elsevier GmbH
PY - 2017/10/15
Y1 - 2017/10/15
N2 - Background Cancer is an enormous global health burden, and should be effectively addressed with better therapeutic strategies. Currently, over 60% of the clinically approved anticancer agents are either directly isolated from natural sources or are modified from natural lead molecules. Sanguinarine (SNG), a quaternary benzophenanthridine alkaloid has gained increasing attention in recent years as a potential anticancer agent. Purpose There is a large untapped source of phytochemical-based anticancer agents remaining to be explored. This review article aims to recapitulate different anticancer properties of SNG, and describes some of the molecular targets involved in exerting its effect. It also depicts the pharmacokinetic and toxicological properties of SNG, two parameters important in determining the druggability of a molecule. Methods Numerous in vivo and in vitro published studies have signified the anticancer properties of SNG. In order to collate and decipher these properties, an extensive literature search was conducted in PubMed, ScienceDirect, and Scopus using keywords followed by the evaluation of the relevant articles where the relevant reports are integrated and analyzed. Results Apart from inducing cell death, SNG inhibits pro-tumorigenic processes such as invasion, angiogenesis, and metastasis in different cancers. Moreover, SNG has been shown to synergistically enhance the sensitivity of several chemotherapeutic agents and is effective against a variety of multi-drug resistant cancers.
AB - Background Cancer is an enormous global health burden, and should be effectively addressed with better therapeutic strategies. Currently, over 60% of the clinically approved anticancer agents are either directly isolated from natural sources or are modified from natural lead molecules. Sanguinarine (SNG), a quaternary benzophenanthridine alkaloid has gained increasing attention in recent years as a potential anticancer agent. Purpose There is a large untapped source of phytochemical-based anticancer agents remaining to be explored. This review article aims to recapitulate different anticancer properties of SNG, and describes some of the molecular targets involved in exerting its effect. It also depicts the pharmacokinetic and toxicological properties of SNG, two parameters important in determining the druggability of a molecule. Methods Numerous in vivo and in vitro published studies have signified the anticancer properties of SNG. In order to collate and decipher these properties, an extensive literature search was conducted in PubMed, ScienceDirect, and Scopus using keywords followed by the evaluation of the relevant articles where the relevant reports are integrated and analyzed. Results Apart from inducing cell death, SNG inhibits pro-tumorigenic processes such as invasion, angiogenesis, and metastasis in different cancers. Moreover, SNG has been shown to synergistically enhance the sensitivity of several chemotherapeutic agents and is effective against a variety of multi-drug resistant cancers.
KW - Anticancer
KW - Apoptosis
KW - Cell death
KW - Phytochemicals
KW - ROS
KW - Sanguinarine
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U2 - 10.1016/j.phymed.2017.08.006
DO - 10.1016/j.phymed.2017.08.006
M3 - Review article
C2 - 28899497
AN - SCOPUS:85028539259
SN - 0944-7113
VL - 34
SP - 143
EP - 153
JO - Phytomedicine
JF - Phytomedicine
ER -