Department of Pathology, University of Utah, Salt Lake City, Utah, United States of America.
PLoS One. 2010 Apr 1;5(4):e9948. doi: 10.1371/journal.pone.0009948.
Xenotropic murine leukemia-related retrovirus (XMRV) is a recently discovered retrovirus that has been linked to human prostate cancer and chronic fatigue syndrome (CFS). Both diseases affect a large fraction of the world population, with prostate cancer affecting one in six men, and CFS affecting an estimated 0.4 to 1% of the population.
Forty-five compounds, including twenty-eight drugs approved for use in humans, were evaluated against XMRV replication in vitro. We found that the retroviral integrase inhibitor, raltegravir, was potent and selective against XMRV at submicromolar concentrations, in MCF-7 and LNCaP cells, a breast cancer and prostate cancer cell line, respectively. Another integrase inhibitor, L-000870812, and two nucleoside reverse transcriptase inhibitors, zidovudine (ZDV), and tenofovir disoproxil fumarate (TDF) also inhibited XMRV replication. When combined, these drugs displayed mostly synergistic effects against this virus, suggesting that combination therapy may delay or prevent the selection of resistant viruses.
If XMRV proves to be a causal factor in prostate cancer or CFS, these discoveries may allow for rational design of clinical trials.
嗜性鼠白血病相关病毒(XMRV)是一种最近发现的逆转录病毒,它与人类前列腺癌和慢性疲劳综合征(CFS)有关。这两种疾病都影响了世界上很大一部分人群,前列腺癌影响了六分之一的男性,而 CFS 估计影响了 0.4%到 1%的人口。
我们评估了 45 种化合物,包括 28 种已批准用于人类的药物,以对抗 XMRV 在体外的复制。我们发现,逆转录酶抑制剂拉替拉韦(raltegravir)在亚微摩尔浓度下对 MCF-7 和 LNCaP 细胞(分别为乳腺癌和前列腺癌细胞系)中的 XMRV 具有强大而选择性的抑制作用。另一种整合酶抑制剂 L-000870812 和两种核苷逆转录酶抑制剂齐多夫定(ZDV)和富马酸替诺福韦二吡呋酯(TDF)也抑制了 XMRV 的复制。当这些药物联合使用时,对这种病毒显示出大多协同作用,表明联合治疗可能延迟或防止耐药病毒的选择。
如果 XMRV 被证明是前列腺癌或 CFS 的致病因素,这些发现可能允许合理设计临床试验。