| Literature DB >> 30061950 |
Miho Hachiman1, Makoto Yoshimitsu1, Chibueze Ezinne1, Ayako Kuroki1, Tomohiro Kozako2, Naomichi Arima1.
Abstract
Despite the efficacy of combination chemotherapy with arsenic trioxide (ATO), interferon α (IFN) and zidovudine (AZT) for adult T cell leukemia/lymphoma (ATL), the precise mechanism underlying this combination treatment effect is unknown. In the present study, ATO/IFN/AZT was examined in an ATL leukemic cell line (S1T, non-Tax expressing), a human T-lymphotropic virus 1 (HTLV-1)-infected cell line (MT2, Tax-expressing) and primary ATL cells from patients with acute and chronic ATL. IFN/AZT marginally inhibited MT2 cell proliferation, but substantially inhibited S1T cell proliferation. IFN/AZT increased the cleavage of numerous caspases and PARP in S1T cells, and regulated the signal transducer and activator of transcription 1 and nuclear factor-κB signaling pathway. These effects represent the potential anti-ATL mechanisms of INF/AZT in vitro. In addition, the combination of ATO and IFN/AZT demonstrated synergistic effects on S1T cells. Therefore, the Tax-independent mechanism underlying the anti-ATL effect of ATO must be further elucidated.Entities:
Keywords: Tax; adult T cell leukemia lymphoma; arsenic trioxide; human T-lymphotropic virus 1; interferon α; zidovudine
Year: 2018 PMID: 30061950 PMCID: PMC6063039 DOI: 10.3892/ol.2018.8771
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967