Oncovirology Laboratory, Bone Marrow Transplantation Center (CEMO), Instituto Nacional de Câncer (INCA), Rio de Janeiro 20230-130, Brazil.
Laboratório Célula-Tronco, CEMO, Instituto Nacional de Câncer (INCA), Rio de Janeiro 20230-130, Brazil.
Int J Mol Sci. 2018 Mar 13;19(3):836. doi: 10.3390/ijms19030836.
Classical Hodgkin lymphoma (cHL) cells overexpress heat-shock protein 90 (HSP90), an important intracellular signaling hub regulating cell survival, which is emerging as a promising therapeutic target. Here, we report the antitumor effect of celastrol, an anti-inflammatory compound and a recognized HSP90 inhibitor, in Hodgkin and Reed-Sternberg cell lines. Two disparate responses were recorded. In KM-H2 cells, celastrol inhibited cell proliferation, induced G0/G1 arrest, and triggered apoptosis through the activation of caspase-3/7. Conversely, L428 cells exhibited resistance to the compound. A proteomic screening identified a total of 262 differentially expressed proteins in sensitive KM-H2 cells and revealed that celastrol's toxicity involved the suppression of the MAPK/ERK (extracellular signal regulated kinase/mitogen activated protein kinase) pathway. The apoptotic effects were preceded by a decrease in RAS (proto-oncogene protein Ras), p-ERK1/2 (phospho-extracellular signal-regulated Kinase-1/2), and c-Fos (proto-oncogene protein c-Fos) protein levels, as validated by immunoblot analysis. The L428 resistant cells exhibited a marked induction of HSP27 mRNA and protein after celastrol treatment. Our results provide the first evidence that celastrol has antitumor effects in cHL cells through the suppression of the MAPK/ERK pathway. Resistance to celastrol has rarely been described, and our results suggest that in cHL it may be mediated by the upregulation of HSP27. The antitumor properties of celastrol against cHL and whether the disparate responses observed in vitro have clinical correlates deserve further research.
经典型霍奇金淋巴瘤 (cHL) 细胞过表达热休克蛋白 90 (HSP90),这是一种重要的细胞内信号枢纽,调节细胞存活,正成为有前途的治疗靶点。在这里,我们报告了 celastrol(一种抗炎化合物和公认的 HSP90 抑制剂)在霍奇金和 Reed-Sternberg 细胞系中的抗肿瘤作用。记录了两种不同的反应。在 KM-H2 细胞中,celastrol 通过激活 caspase-3/7 抑制细胞增殖、诱导 G0/G1 期阻滞并触发细胞凋亡。相反,L428 细胞对该化合物表现出抗性。蛋白质组学筛选鉴定了敏感的 KM-H2 细胞中总共 262 种差异表达的蛋白质,并表明 celastrol 的毒性涉及 MAPK/ERK(细胞外信号调节激酶/有丝分裂原激活蛋白激酶)途径的抑制。凋亡作用之前,RAS(原癌基因蛋白 Ras)、p-ERK1/2(磷酸化细胞外信号调节激酶-1/2)和 c-Fos(原癌基因蛋白 c-Fos)蛋白水平下降,免疫印迹分析验证了这一点。在 celastrol 处理后,L428 耐药细胞中 HSP27 mRNA 和蛋白明显诱导。我们的结果首次证明,celastrol 通过抑制 MAPK/ERK 通路对 cHL 细胞具有抗肿瘤作用。celastrol 耐药性很少被描述,我们的结果表明,在 cHL 中,它可能是通过 HSP27 的上调介导的。celastrol 对 cHL 的抗肿瘤特性以及体外观察到的不同反应是否具有临床相关性值得进一步研究。