Affiliations 

  • 1 Faculty of Applied Sciences, UCSI University, 56000 Cheras, Kuala Lumpur, Malaysia. Electronic address: chanwc@ucsiuniversity.edu.my
  • 2 Faculty of Applied Sciences, UCSI University, 56000 Cheras, Kuala Lumpur, Malaysia
  • 3 School of Science, Monash University Sunway, 46150 Petaling Jaya, Selangor, Malaysia
  • 4 Xiamen University Malaysia, Bandar Sunsuria, 43900 Sepang, Selangor, Malaysia
J Integr Med, 2019 May;17(3):155-160.
PMID: 30928277 DOI: 10.1016/j.joim.2019.03.003

Abstract

Ursolic acid (UA) is a pentacyclic triterpene of the ursane type. As a common chemical constituent among species of the family Lamiaceae, UA possesses a broad spectrum of pharmacological properties. This overview focuses on the anticancer properties of UA against breast cancer (BC) and colorectal cancer (CRC) that are most common among women and men, respectively. In vitro studies have shown that UA inhibited the growth of BC and CRC cell lines through various molecular targets and signaling pathways. There are several in vivo studies on the cytotoxic activity of UA against BC and CRC. UA also inhibits the growth of other types of cancer. Studies on structural modifications of UA have shown that the -OH groups at C3 and at C28 are critical factors influencing the cytotoxic activity of UA and its derivatives. Some needs for future research are suggested. Sources of information were from ScienceDirect, Google Scholar and PubMed.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.