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Therapy-induced selective loss of leukemia-initiating activity in murine adult T cell leukemia

Chronic HTLV-I (human T cell lymphotropic virus type I) infection may cause adult T cell leukemia/lymphoma (ATL), a disease with dismal long-term prognosis. The HTLV-I transactivator, Tax, initiates ATL in transgenic mice. In this study, we demonstrate that an As(2)O(3) and IFN-α combination, known...

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Detalles Bibliográficos
Autores principales: El Hajj, Hiba, El-Sabban, Marwan, Hasegawa, Hideki, Zaatari, Ghazi, Ablain, Julien, Saab, Shahrazad T., Janin, Anne, Mahfouz, Rami, Nasr, Rihab, Kfoury, Youmna, Nicot, Christophe, Hermine, Olivier, Hall, William, de Thé, Hugues, Bazarbachi, Ali
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005222/
https://www.ncbi.nlm.nih.gov/pubmed/21135137
http://dx.doi.org/10.1084/jem.20101095
Descripción
Sumario:Chronic HTLV-I (human T cell lymphotropic virus type I) infection may cause adult T cell leukemia/lymphoma (ATL), a disease with dismal long-term prognosis. The HTLV-I transactivator, Tax, initiates ATL in transgenic mice. In this study, we demonstrate that an As(2)O(3) and IFN-α combination, known to trigger Tax proteolysis, cures Tax-driven ATL in mice. Unexpectedly, this combination therapy abrogated initial leukemia engraftment into secondary recipients, whereas the primary tumor bulk still grew in the primary hosts, only to ultimately abate later on. This loss of initial transplantability required proteasome function. A similar regimen recently yielded unprecedented disease control in human ATL. Our demonstration that this drug combination targeting Tax stability abrogates tumor cell immortality but not short-term growth may foretell a favorable long-term efficiency of this regimen in patients.