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射频消融不足通过自噬促进残余肝细胞癌的增殖。

Insufficient radiofrequency ablation promotes proliferation of residual hepatocellular carcinoma via autophagy.

机构信息

Department of Ultrasound, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510275, China.

Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510275, China.

出版信息

Cancer Lett. 2018 May 1;421:73-81. doi: 10.1016/j.canlet.2018.02.024. Epub 2018 Feb 16.

Abstract

Radiofrequency ablation (RFA) is considered to be a potentially curative therapy for hepatocellular carcinoma (HCC). However, insufficient RFA (IRFA) can promote rapid progression of the residual tumor. The mechanisms underlying IRFA-induced tumor promotion remain poorly understood. In the present study, we have established a subcutaneous xenograft mouse model and monitored the location and extent of IRFA by dual monitoring with ultrasonography and a thermal imager. For the first time, we provide evidence of the activation of autophagic pathways in mice exposed to IRFA. We show that autophagy plays an important role in relapse and proliferation after IRFA and that hydroxychloroquine (HCQ) can suppress these effects. Our findings indicate that autophagy is involved in experimental IRFA and that inhibition of autophagy may be a novel approach in the treatment of local recurrences of HCC after IRFA in the clinic.

摘要

射频消融 (RFA) 被认为是治疗肝细胞癌 (HCC) 的一种潜在的根治性治疗方法。然而,射频消融不足 (IRFA) 会促进残余肿瘤的快速进展。IRFA 诱导的肿瘤促进的机制仍知之甚少。在本研究中,我们建立了皮下异种移植小鼠模型,并通过超声和热像仪双重监测来监测 IRFA 的位置和范围。我们首次提供了在接受 IRFA 照射的小鼠中自噬途径被激活的证据。我们表明,自噬在 IRFA 后复发和增殖中起重要作用,而羟氯喹 (HCQ) 可以抑制这些作用。我们的研究结果表明,自噬参与了实验性 IRFA,抑制自噬可能是临床治疗 RFA 后 HCC 局部复发的一种新方法。

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