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Leukemia Research
Volume 33, Issue 2
, Pages 218-221
, February 2009
Sodium butyrate enhances the cytotoxic effect of antineoplastic drugs in human lymphoblastic T-cells
References
- . Acute lymphoblastic leukaemia. Lancet. 2008;371:1030–1043
- . Histone deacetylase inhibitors: a novel target of anticancer therapy (review). Oncol Rep. 2006;15:489–494
- . Vincristine- and cisplatin-induced apoptosis in human retinoblastoma. Potentiation by sodium butyrate. Eur J Cancer. 1998;34:1741–1748
- The histone deacetylase inhibitor sodium butyrate induces breast cancer cell apoptosis through diverse cytotoxic actions including glutathione depletion and oxidative stress. Int J Oncol. 2004;25:1701–1711
- Histone deacetylase inhibitors induce cell death and enhance the susceptibility to ionizing radiation, etoposide, and TRAIL in medulloblastoma cells. Int J Oncol. 2006;28:755–766
- The histone deacetylase inhibitor sodium butyrate induces DNA topoisomerase II alpha expression and confers hypersensitivity to etoposide in human leukemic cell lines. Mol Cancer Ther. 2001;1:121–131
- . Butyrate increases apoptosis induced by different antineoplastic drugs in monocytic leukemia cells. Chemotherapy. 2004;50:221–228
- . Increase in Ara-C cytotoxicity in the presence of valproate, a histone deacetylase inhibitor, is associated with the concurrent expression of cyclin D1 and p27(Kip 1) in acute myeloblastic leukemia cells. Leuk Res. 2005;29:1335–1342
PII: S0145-2126(08)00329-9
doi: 10.1016/j.leukres.2008.07.003
© 2008 Elsevier Ltd. All rights reserved.
« Previous
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Leukemia Research
Volume 33, Issue 2
, Pages 218-221
, February 2009
