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热消融后肝细胞癌复发与进展的机制及治疗策略

Mechanisms and therapeutic strategies to combat the recurrence and progression of hepatocellular carcinoma after thermal ablation.

作者信息

Ye Feilong, Xie Lulu, Liang Licong, Zhou Zhimei, He Siqin, Li Rui, Lin Liteng, Zhu Kangshun

机构信息

Laboratory of Interventional Radiology, Department of Minimally Invasive Interventional Radiology and Department of Radiology, The Second Affiliated Hospital of Guangzhou Medical University, 250 East Changgang Road, Guangzhou, Guangdong Province, 510260, China.

出版信息

J Interv Med. 2023 Oct 18;6(4):160-169. doi: 10.1016/j.jimed.2023.10.004. eCollection 2023 Nov.

Abstract

Thermal ablation (TA), including radiofrequency ablation (RFA) and microwave ablation (MWA), has become the main treatment for early-stage hepatocellular carcinoma (HCC) due to advantages such as safety and minimal invasiveness. However, HCC is prone to local recurrence, with more aggressive malignancies after TA closely related to TA-induced changes in epithelial-mesenchymal transition (EMT) and remodeling of the tumor microenvironment (TME). According to many studies, various components of the TME undergo complex changes after TA, such as the recruitment of innate and adaptive immune cells, the release of tumor-associated antigens (TAAs) and various cytokines, the formation of a hypoxic microenvironment, and tumor angiogenesis. Changes in the TME after TA can partly enhance the anti-tumor immune response; however, this response is weak to kill the tumor completely. Certain components of the TME can induce an immunosuppressive microenvironment through complex interactions, leading to tumor recurrence and progression. How the TME is remodeled after TA and the mechanism by which the TME promotes HCC recurrence and progression are unclear. Thus, in this review, we focused on these issues to highlight potentially effective strategies for reducing and preventing the recurrence and progression of HCC after TA.

摘要

热消融(TA),包括射频消融(RFA)和微波消融(MWA),由于具有安全性和微创性等优点,已成为早期肝细胞癌(HCC)的主要治疗方法。然而,HCC易于局部复发,TA后更具侵袭性的恶性肿瘤与TA诱导的上皮-间质转化(EMT)和肿瘤微环境(TME)重塑密切相关。根据许多研究,TA后TME的各种成分会发生复杂变化,如先天性和适应性免疫细胞的募集、肿瘤相关抗原(TAA)和各种细胞因子的释放、缺氧微环境的形成以及肿瘤血管生成。TA后TME的变化可部分增强抗肿瘤免疫反应;然而,这种反应不足以完全杀死肿瘤。TME的某些成分可通过复杂的相互作用诱导免疫抑制微环境,导致肿瘤复发和进展。TA后TME如何重塑以及TME促进HCC复发和进展的机制尚不清楚。因此,在本综述中,我们聚焦于这些问题,以突出减少和预防TA后HCC复发和进展的潜在有效策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8451/10831380/95083ad0a2a8/gr1.jpg

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