| Literature DB >> 28496056 |
Chaoya Ma1, Hasita Horlad1, Cheng Pan1, Hiromu Yano1, Koji Ohnishi1, Yukio Fujiwara1, Masao Matsuoka2,3, Aeju Lee4,5, Takuro Niidome6, Ryuya Yamanaka7, Motohiro Takeya1, Yoshihiro Komohara1.
Abstract
Recent studies have indicated the significance of immune checkpoint molecules including programmed death-1 (PD-1), cytotoxic T-lymphocyte associated protein 4, and T-cell immunoglobulin and mucin domain-containing molecule-3 for anti-tumor immune responses. We previously investigated PD-1 ligand 1/2 (PD-L1/2) expression in lymphoma cell lines, and found that PD-L1/2 is expressed on the adult T-cell leukemia/lymphoma (ATL-T) and B-cell lymphoma (SLVL) cell lines. In the present study, we investigated whether the Stat3 inhibitor WP1066 abrogated PD-L1/2 expression in lymphoma cell lines. Incubation with WP1066 inhibited lymphoma cell growth and induced cell apoptosis. PD-L1/2 expression in the ATL-T, SLVL, and human brain malignant lymphoma (HKBML) cell lines was significantly abrogated by WP1066 treatment. These data indicated that a Stat3 inhibitor abrogated PD-L1/2 expression in lymphoma cells. Such an inhibitor is therefore considered to be useful for additional immunotherapy in patients with advanced lymphoma.Entities:
Keywords: PD-L1; PD-L2; Stat3; lymphoma
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Year: 2017 PMID: 28496056 PMCID: PMC6144272 DOI: 10.3960/jslrt.17006
Source DB: PubMed Journal: J Clin Exp Hematop ISSN: 1346-4280