Tutusaus Anna, Sanduzzi-Zamparelli Marco, Boix Loreto, Rider Patricia, Subías Silvia, García de Frutos Pablo, Colell Anna, Marí Montserrat, Reig María, Morales Albert
Department of Cell Death and Proliferation, IIBB-CSIC, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 08036 Barcelona, Spain.
Barcelona Clinic Liver Cancer (BCLC) Group, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 08036 Barcelona, Spain.
Cancers (Basel). 2024 Apr 13;16(8):1491. doi: 10.3390/cancers16081491.
During the last decade, tyrosine kinase inhibitors (TKIs) sorafenib and regorafenib have been standard systemic treatments for advanced hepatocellular carcinoma (HCC). Previous data associated sorafenib with inflammasome activation. However, the role of the inflammasome in sorafenib and regorafenib signaling has not been described in liver cancer patients. For this purpose, we analyzed inflammasome-related transcriptomic changes in a murine HCC model. Our data confirmed inflammasome activation after both TKI treatments, sharing a similar pattern of increased gene expression. According to human database results, transcriptional increase of inflammasome genes is associated with poorer prognosis for male liver cancer patients, suggesting a sex-dependent role for inflammasome activation in HCC therapy. In biopsies of HCC and its surrounding tissue, we detected durable increases in the inflammasome activation pattern after sorafenib or regorafenib treatment in male patients. Further supporting its involvement in sorafenib action, inflammasome inhibition (MCC950) enhanced sorafenib anticancer activity in experimental HCC models, while no direct in vitro effect was observed in HCC cell lines. Moreover, activated human THP-1 macrophages released IL-1β after sorafenib administration, while 3D Hep3B spheres displayed increased tumor growth after IL-1β addition, pointing to the liver microenvironment as a key player in inflammasome action. In summary, our results unveil the inflammasome pathway as an actionable target in sorafenib or regorafenib therapy and associate an inflammasome signature in HCC and surrounding tissue with TKI administration. Therefore, targeting inflammasome activation, principally in male patients, could help to overcome sorafenib or regorafenib resistance and enhance the efficacy of TKI treatments in HCC.
在过去十年中,酪氨酸激酶抑制剂(TKIs)索拉非尼和瑞戈非尼一直是晚期肝细胞癌(HCC)的标准全身治疗药物。先前的数据表明索拉非尼与炎性小体激活有关。然而,炎性小体在索拉非尼和瑞戈非尼信号传导中的作用在肝癌患者中尚未得到描述。为此,我们在小鼠肝癌模型中分析了炎性小体相关的转录组变化。我们的数据证实了两种TKI治疗后炎性小体的激活,呈现出相似的基因表达增加模式。根据人类数据库结果,炎性小体基因的转录增加与男性肝癌患者较差的预后相关,这表明炎性小体激活在肝癌治疗中存在性别依赖性作用。在肝癌及其周围组织的活检中,我们在男性患者中检测到索拉非尼或瑞戈非尼治疗后炎性小体激活模式的持续增加。进一步支持其参与索拉非尼作用的是,炎性小体抑制(MCC950)在实验性肝癌模型中增强了索拉非尼的抗癌活性,而在肝癌细胞系中未观察到直接的体外效应。此外,索拉非尼给药后活化的人THP-1巨噬细胞释放白细胞介素-1β(IL-1β),而添加IL-1β后3D Hep3B球体显示肿瘤生长增加,这表明肝脏微环境是炎性小体作用的关键参与者。总之,我们的结果揭示炎性小体途径是索拉非尼或瑞戈非尼治疗中的一个可操作靶点,并将肝癌及其周围组织中的炎性小体特征与TKI给药相关联。因此,主要针对男性患者靶向炎性小体激活可能有助于克服索拉非尼或瑞戈非尼耐药性,并提高TKI治疗肝癌的疗效。