Abstract
Alopecia (hair loss) is experienced by thousands of cancer patients every year. Substantial-to-severe alopecia is induced by anthracyclines (e.g., adriamycin), taxanes (e.g., taxol), alkylating compounds (e.g., cyclophosphamide), and the topisomerase inhibitor etoposide, agents that are widely used in the treatment of leukemias and breast, lung, ovarian, and bladder cancers. Currently, no treatment appears to be generally effective in reliably preventing this secondary effect of chemotherapy. We observed in experiments using different rodent models that localized administration of heat or subcutaneous/intradermal injection of geldanamycin or 17-(allylamino)-17-demethoxygeldanamycin induced a stress protein response in hair follicles and effectively prevented alopecia from adriamycin, cyclophosphamide, taxol, and etoposide. Model tumor therapy experiments support the presumption that such localized hair-saving treatment does not negatively affect chemotherapy efficacy.
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Acknowledgments
We thank M. Fenna, J. He, J. Xie, and S.L. Hsia for their help with certain experiments, and Walter Scott and David Barber for the critical review of the manuscript. This study was supported in part by the Rockefeller Brothers Fund (02-237), NCI grant R01 CA093489, and HSF Pharmaceuticals S.A.
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Jimenez, J.J., Roberts, S.M., Mejia, J. et al. Prevention of chemotherapy-induced alopecia in rodent models. Cell Stress and Chaperones 13, 31–38 (2008). https://doi.org/10.1007/s12192-007-0005-1
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DOI: https://doi.org/10.1007/s12192-007-0005-1