Increased antitumor potential of the raloxifene prodrug, raloxifene diphosphate

✍ Scribed by Yoshinori Okamoto; Xiaoping Liu; Naomi Suzuki; Kanako Okamoto; Masashi Sekimoto; Y.R. Santosh Laxmi; Shinya Shibutani

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: French
• Weight: 164 KB
• Volume: 122
• Category: Article
• ISSN: 0020-7136
• DOI: 10.1002/ijc.23362

✦ Synopsis

Abstract

Raloxifene (RAL) significantly reduced the incidence of breast cancer in women at high risk of developing the disease. Unlike tamoxifen (TAM), an increased incidence of endometrial cancer was not observed in women treated with RAL. However, RAL, having two hydroxyl moieties, can be conjugated rapidly through phase II metabolism and excreted, making it difficult to achieve adequate bioavailability by oral administration in humans. As a result, higher doses must be administered to obtain an efficacy equivalent to that achieved with TAM. To improve oral bioavailability and antitumor potential, RAL diphosphate was prepared as a prodrug. RAL diphosphate showed several orders of magnitude lower binding potential to both ERα and ERβ and weak antiproliferative potency on cultured human MCF‐7 and ZR‐75‐1 breast cancer cells, as compared to RAL. However, RAL diphosphate has a much higher bioavailability than RAL, endowing it with higher antitumor potential than RAL against both 7,12‐dimethylbenz(a)anthracene‐induced mammary carcinoma in rats and human MCF‐7 breast cancer implanted in athymic nude mice. The RAL prodrug may provide greater clinical benefit for breast cancer therapy and prevention. © 2008 Wiley‐Liss, Inc.