Division of Morphological Pathology, Department of Basic Laboratory Sciences, School of Health Sciences, University of the Ryukyus, 207 Uehara, Nishihara, Okinawa, 903-0215, Japan.
Department of Oral and Maxillofacial Functional Rehabilitation, Graduate School of Medicine, University of the Ryukyus, 207 Uehara, Nishihara, Okinawa, 903-0215, Japan.
Sci Rep. 2019 Apr 23;9(1):6416. doi: 10.1038/s41598-019-42763-0.
Kaposi's sarcoma-associated herpesvirus (KSHV) causes both AIDS-related Kaposi's sarcoma (KS) and classic KS, but their clinical presentations are different, and respective mechanisms remain to be elucidated. The KSHV K1 gene is reportedly involved in tumorigenesis through the immunoreceptor tyrosine-based activation motif (ITAM). Since we found the sequence variations in the K1 gene of KSHV isolated from AIDS-related KS and classic KS, we hypothesized that the transformation activity of the K1 gene contributes to the different clinical presentations. To evaluate our hypothesis, we compared the transformation activities of the K1 gene between AIDS-related KS and classic KS. We also analyzed ITAM activities and the downstream AKT and NF-κB. We found that the transformation activity of AIDS-related K1 was greater than that of classic K1, and that AIDS-related K1 induced higher ITAM activity than classic K1, causing more potent Akt and NF-κB activities. K1 downregulation by siRNA in AIDS-related K1 expressing cells induced a loss of transformation properties and decreased both Akt and NF-κB activities, suggesting a correlation between the transformation activity of K1 and ITAM signaling. Our study indicates that the increased transformation activity of AIDS-related K1 is associated with its clinical aggressiveness, whereas the weak transformation activity of classic type K1 is associated with a mild clinical presentation and spontaneous regression. The mechanism of spontaneous regression of classic KS may provide new therapeutic strategy to cancer.
卡波氏肉瘤相关疱疹病毒(KSHV)可引起艾滋病相关卡波氏肉瘤(KS)和经典 KS,但它们的临床表现不同,各自的机制仍需阐明。据报道,KSHV 的 K1 基因通过免疫受体酪氨酸激活基序(ITAM)参与肿瘤发生。由于我们发现了从艾滋病相关 KS 和经典 KS 分离的 KSHV K1 基因中的序列变异,我们假设 K1 基因的转化活性导致了不同的临床表现。为了验证我们的假设,我们比较了艾滋病相关 KS 和经典 KS 中 K1 基因的转化活性。我们还分析了 ITAM 活性及其下游的 AKT 和 NF-κB。我们发现,艾滋病相关 K1 的转化活性大于经典 K1,艾滋病相关 K1 诱导的 ITAM 活性高于经典 K1,导致 Akt 和 NF-κB 活性更强。在表达 AIDS 相关 K1 的细胞中用 siRNA 下调 K1 会导致转化特性丧失,并降低 Akt 和 NF-κB 活性,表明 K1 的转化活性与 ITAM 信号之间存在相关性。我们的研究表明,艾滋病相关 K1 的转化活性增加与其临床侵袭性相关,而经典型 K1 的弱转化活性与其轻度临床表现和自发消退相关。经典 KS 自发消退的机制可能为癌症提供新的治疗策略。