A New Micronized Formulation of 2-Methoxyestradiol-bis-sulfamate (STX140) is Therapeutically Potent against Breast Cancer

There is a continued need for orally bioavailable anticancer compounds that exhibit good efficacy against breast cancer. STX140, a derivative of 2-methoxyestradiol (2-MeOE2), has been shown to have excellent oral bioavailability and significantly reduces tumor growth. A new micronized formulation of...

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Veröffentlicht in:Anticancer research 2008-03, Vol.28 (2A), p.577-581
Hauptverfasser: FOSTER, Paul A, NEWMAN, Simon P, REED, Michael J, PUROHIT, Atul, LEESE, Mathew P, BERNETIERE, Sonia, DIOLEZ, Christian, CAMARA, Jose, HACHER, Beatrice, BARONNET, Marie-Madeleine, ALI, Tauhid, POTTER, Barry V. L
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container_end_page 581
container_issue 2A
container_start_page 577
container_title Anticancer research
container_volume 28
creator FOSTER, Paul A
NEWMAN, Simon P
REED, Michael J
PUROHIT, Atul
LEESE, Mathew P
BERNETIERE, Sonia
DIOLEZ, Christian
CAMARA, Jose
HACHER, Beatrice
BARONNET, Marie-Madeleine
ALI, Tauhid
POTTER, Barry V. L
description There is a continued need for orally bioavailable anticancer compounds that exhibit good efficacy against breast cancer. STX140, a derivative of 2-methoxyestradiol (2-MeOE2), has been shown to have excellent oral bioavailability and significantly reduces tumor growth. A new micronized formulation of STX140 has now been developed and its pharmacokinetics (PK) in rats and effect on MDA-MB-231 breast cancer growth in nude mice was investigated. Materials and Methods: For the PK studies, female Wistar rats were treated orally with STX140 in two separate vehicles (10% tetrahydrofuran (THF) in propylene glycol (PG) or 0.5% methyl cellulose (MC) in saline) and plasma samples taken for high performance liquid chromatography analysis over 48 h. For the tumor efficacy studies, female nude mice were inoculated with MDA-MB-231 breast cancer cells and then treated orally with a range of doses of STX140. Results: The PK studies demonstrated that the THF/PG vehicle resulted in a greater oral bioavailability of STX140 compared to the 0.5% MC vehicle. However, this was not translated to the tumor efficacy studies where STX140 at 20 mg/kg in either vehicle caused a significant reduction in tumor volume. Conclusion: The new micronized formulation of STX140 is orally bioavailable and efficacious at inhibiting MDA-MB-231 breast tumor growth.
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Materials and Methods: For the PK studies, female Wistar rats were treated orally with STX140 in two separate vehicles (10% tetrahydrofuran (THF) in propylene glycol (PG) or 0.5% methyl cellulose (MC) in saline) and plasma samples taken for high performance liquid chromatography analysis over 48 h. For the tumor efficacy studies, female nude mice were inoculated with MDA-MB-231 breast cancer cells and then treated orally with a range of doses of STX140. Results: The PK studies demonstrated that the THF/PG vehicle resulted in a greater oral bioavailability of STX140 compared to the 0.5% MC vehicle. However, this was not translated to the tumor efficacy studies where STX140 at 20 mg/kg in either vehicle caused a significant reduction in tumor volume. 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L</creatorcontrib><title>A New Micronized Formulation of 2-Methoxyestradiol-bis-sulfamate (STX140) is Therapeutically Potent against Breast Cancer</title><title>Anticancer research</title><addtitle>Anticancer Res</addtitle><description>There is a continued need for orally bioavailable anticancer compounds that exhibit good efficacy against breast cancer. STX140, a derivative of 2-methoxyestradiol (2-MeOE2), has been shown to have excellent oral bioavailability and significantly reduces tumor growth. A new micronized formulation of STX140 has now been developed and its pharmacokinetics (PK) in rats and effect on MDA-MB-231 breast cancer growth in nude mice was investigated. Materials and Methods: For the PK studies, female Wistar rats were treated orally with STX140 in two separate vehicles (10% tetrahydrofuran (THF) in propylene glycol (PG) or 0.5% methyl cellulose (MC) in saline) and plasma samples taken for high performance liquid chromatography analysis over 48 h. 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L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A New Micronized Formulation of 2-Methoxyestradiol-bis-sulfamate (STX140) is Therapeutically Potent against Breast Cancer</atitle><jtitle>Anticancer research</jtitle><addtitle>Anticancer Res</addtitle><date>2008-03</date><risdate>2008</risdate><volume>28</volume><issue>2A</issue><spage>577</spage><epage>581</epage><pages>577-581</pages><issn>0250-7005</issn><eissn>1791-7530</eissn><abstract>There is a continued need for orally bioavailable anticancer compounds that exhibit good efficacy against breast cancer. STX140, a derivative of 2-methoxyestradiol (2-MeOE2), has been shown to have excellent oral bioavailability and significantly reduces tumor growth. A new micronized formulation of STX140 has now been developed and its pharmacokinetics (PK) in rats and effect on MDA-MB-231 breast cancer growth in nude mice was investigated. 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Conclusion: The new micronized formulation of STX140 is orally bioavailable and efficacious at inhibiting MDA-MB-231 breast tumor growth.</abstract><cop>Attiki</cop><pub>International Institute of Anticancer Research</pub><pmid>18506995</pmid><tpages>5</tpages></addata></record>
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subjects Administration, Oral
Animals
Biological and medical sciences
Cell Line, Tumor
Dosage Forms
Estrenes - administration & dosage
Estrenes - pharmacokinetics
Estrenes - therapeutic use
Female
Gynecology. Andrology. Obstetrics
Male
Mammary gland diseases
Mammary Neoplasms, Experimental - drug therapy
Mammary Neoplasms, Experimental - metabolism
Medical sciences
Mice
Mice, Nude
Rats
Rats, Sprague-Dawley
Tumors
Viscosity
Xenograft Model Antitumor Assays
title A New Micronized Formulation of 2-Methoxyestradiol-bis-sulfamate (STX140) is Therapeutically Potent against Breast Cancer
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