Natazuka T, Umemiya-Okada T, Matsui T, Saida T, Nakao Y
Department of Medicine, Kobe University School of Medicine, Japan.
Int J Cancer. 1993 May 8;54(2):348-54. doi: 10.1002/ijc.2910540230.
Human T-cell-leukemia-virus-type-1 (HTLV-1) infection is associated with adult T-cell leukemia/lymphoma (ATL) and HTLV-1-associated myelopathy (HAM)/tropical spastic paraparesis (TSP). The T-cell-targeting immunosuppressants, FK506 and cyclosporin A (CsA), suppressed proliferation of the HAM/TSP-derived T-cell lines, H89-59, H89-79 and H109. FK506 and CsA also reduced expression of the proto-oncogenes, c-myc and c-fos, but not c-jun and interleukin-2-receptor-alpha (IL-2R alpha) gene in H109 cells. The growth-inhibitory effects of FK506 and CsA were not abrogated by interleukin 2 (IL-2). These results suggest that the inhibitory effects of FK506 and CsA are independent of IL-2, and are associated with the reduction of c-myc and c-fos gene expression.
人类T细胞白血病病毒1型(HTLV-1)感染与成人T细胞白血病/淋巴瘤(ATL)以及HTLV-1相关脊髓病(HAM)/热带痉挛性截瘫(TSP)有关。靶向T细胞的免疫抑制剂FK506和环孢素A(CsA)可抑制源自HAM/TSP的T细胞系H89-59、H89-79和H109的增殖。FK506和CsA还可降低原癌基因c-myc和c-fos的表达,但对H109细胞中的c-jun和白细胞介素2受体α(IL-2Rα)基因无影响。FK506和CsA的生长抑制作用不会被白细胞介素2(IL-2)消除。这些结果表明,FK506和CsA的抑制作用独立于IL-2,且与c-myc和c-fos基因表达的降低有关。