Selective Inhibition of HTLV-1-infected Cell Proliferation by a Novel Tetramethylnaphthalene Derivative

被引:0
作者
Hamasaki, Takayuki [1 ]
Toyama, Masaaki [1 ]
Aoyama, Hiroshi [3 ]
White, Yohann [2 ]
Okamoto, Mika [1 ]
Arima, Naomichi [2 ]
Hashimoto, Yuichi [3 ]
Baba, Masanori [1 ]
机构
[1] Kagoshima Univ, Grad Sch Med & Dent Sci, Ctr Chron Viral Dis, Div Antiviral Chemotherapy, Kagoshima 8908544, Japan
[2] Kagoshima Univ, Grad Sch Med & Dent Sci, Ctr Chron Viral Dis, Div Hematol & Immunol, Kagoshima 8908544, Japan
[3] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
关键词
HTLV-1; ATL; tetramethylnaphthalene; inhibitor; cell cycle; NF-KAPPA-B; VIRUS TYPE-I; RETRACTED ARTICLE. SEE; LEUKEMIA-CELLS; RETINOBLASTOMA PROTEIN; DEPSIPEPTIDE FR901228; T-CELLS; LINES; APOPTOSIS; LYMPHOMA;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adult T-cell leukemia (ATL) is caused by infection with human T-lymphotropic virus type 1 (HTLV-1). A novel tetramethylnaphthalene derivative, TMNAA, selectively inhibited the proliferation of various HTLV-1-infected cells, including ATL cell lines and peripheral blood mononuclear cells (PBMCs) from ATL patients. In contrast, the proliferation of uninfected cell lines and PBMCs from healthy donors was hardly affected by the compound. Cell-cycle analysis revealed that TMNAA increased the population of the G(0)/G(1) phase and reduced that of the S phase in HTLV-1-infected cells. TMNAA was found to suppress the phosphorylation of retinoblastoma protein and the expression of cyclin-dependent kinase 4 in HTLV-1-infected cells. Furthermore, the inhibition of cell proliferation was partially annihilated by removing the compound. These results indicate that TMNAA exerts selective inhibition of HTLV-1-infected cells through a novel mechanism, presumably modulating cell cycle regulatory proteins associated with the G(0)/G(1) phase.
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页码:2241 / 2247
页数:7
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