Li, WW, Johnson-Ajinwo, OR and Uche, FI (2016) Advances of Plant-Derived Natural Products in Ovarian Cancer Therapy. International Journal of Cancer Research and Prevention, 9 (1). 81 - 105.

This is the latest version of this item.

[img]
Preview
Text
1554-1134_9_1_3 _WenWu Li_review.pdf - Published Version
Available under License Creative Commons Attribution.

Download (366kB) | Preview

Abstract

Ovarian cancer is the leading cause of death in the gynaecologic cancers within the UK and US. Presently the standard treatment for ovarian cancer entails the use of chemotherapy drugs paclitaxel and carboplatin after aggressive surgical reduction in order to prolong the patient’s life for multiple years. However, prolonged use of platinum-based chemotherapy often leads to drug resistance, which causes the ovarian cancer patient to relapse and potential death. Therefore there is an urgent medical need for breakthrough drugs with an effective therapeutic impact on ovarian cancer.
Phytochemicals (plant-derived natural products) have been used for thousands of years as treatment for various diseases, because of their huge chemical diversity and wide range of biological activities.
In this review, the role of phytochemicals as chemo-preventive compounds, potential sources of new drugs for ovarian cancer and the benefits of their adoption as monotherapeutic agents or as chemosensitizers when used in-conjunction with the conventional anti-cancer drugs is highlighted. We will describe the phytochemicals: 1) clinically approved drugs such as paclitaxel and camptothecin including its semi-synthetic derivatives topotecan and irinotecan; 2) currently in clinical trials such as epipodophyllotoxin derivatives etoposide and teniposide, ventfolide, phenoxodiol, and combretastatins; 3) in preclinical trials such as quercetin, baicalein, baicalin,thymoquinone, betulinic acid and tetrandrine; and recently discovered compounds which have high potency (IC50 less than 10 µM) and have been discovered recently (last 15 years). In particular, several new compounds including bufatrienolides, ipomoeassin D,2'-(R)-O-acetylglaucarubinone, and molvizarin have IC50s lower than 100 nM in ovarian cancer cells and might have different mechanisms of action from those of platinum derivatives/paclitaxel, therefore providing potential ways to attack multidrug resistance in ovarian cancer without jeopardising the patient’s treatment.

Item Type: Article
Uncontrolled Keywords: ovarian cancer, cancer
Subjects: R Medicine > R Medicine (General)
Divisions: Faculty of Medicine and Health Sciences > Institute for Science and Technology in Medicine
Depositing User: Symplectic
Date Deposited: 15 Jun 2016 10:33
Last Modified: 11 Apr 2019 09:32
URI: http://eprints.keele.ac.uk/id/eprint/1865

Available Versions of this Item

Actions (login required)

View Item View Item