The retinoid X receptor-selective retinoid, LGD1069, prevents the development of estrogen receptor-negative mammary tumors in transgenic mice

Despite the effectiveness of the selective estrogen receptor (ER) modulators in preventing ER-positive breast cancer, chemopreventive agents still need to be developed for the prevention of ER-negative breast cancers. The naturally occurring retinoids are promising agents for the prevention of human...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2002-11, Vol.62 (22), p.6376-6380
Hauptverfasser: WU, Kendall, YUN ZHANG, BROWN, Powel H, XU, Xiao-Chun, HILL, Jamal, CELESTINO, Joseph, KIM, Hee-Tae, MOHSIN, Syed K, HILSENBECK, Susan G, LAMPH, William W, BISSONETTE, Reid
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Sprache:eng
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Zusammenfassung:Despite the effectiveness of the selective estrogen receptor (ER) modulators in preventing ER-positive breast cancer, chemopreventive agents still need to be developed for the prevention of ER-negative breast cancers. The naturally occurring retinoids are promising agents for the prevention of human cancers but are too toxic for long-term chronic use. We previously demonstrated that the chemopreventive effects of the retinoids could be separated from the toxicity by using an RXR-selective retinoid, LGD1069. The studies described here demonstrate that LGD1069 effectively suppresses ER-negative tumor development in mouse mammary tumor virus-erbB2 transgenic mice with minimal toxicity. These studies suggest that receptor-selective retinoids are promising agents for the prevention of breast cancer and that they may be particularly useful in preventing ER-negative breast cancer.
ISSN:0008-5472
1538-7445