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钙信号调节蛋白 II 抑制剂:肝癌治疗中免疫检查点抑制剂的潜在增敏剂。

CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment.

机构信息

Department of Chinese Medicine Oncology, The First Affiliated Hospital of Naval Medical University, Shanghai, China.

Department of Chinese Medicine, Naval Medical University, Shanghai, China.

出版信息

Front Immunol. 2023 Mar 16;14:1052657. doi: 10.3389/fimmu.2023.1052657. eCollection 2023.

Abstract

Hepatocellular carcinoma (HCC) is a lethal malignancy with a lack of effective treatments particularly for the disease at an advanced stage. Even though immune checkpoint inhibitors (ICIs) have made great progress in the treatment of HCC, durable and ideal clinical benefits still cannot be achieved in plenty of patients with HCC. Therefore, novel and refined ICI-based combination therapies are still needed to enhance the therapeutic effect. The latest study has reported that the carbonic anhydrase XII inhibitor (CAXIIi), a novel type of anticancer drug, can modify the tumor immunosuppression microenvironment by affecting hypoxic/acidic metabolism and alter the functions of monocytes and macrophages by regulating the expression of C-C motif chemokine ligand 8 (CCL8). These observations shine a light on improving programmed cell death protein 1 (PD-1)/programmed cell death ligand-1 (PD-L1) immunotherapy in combination with CAXIIis. This mini-review aims to ignite enthusiasm to explore the potential application of CAXIIis in combination with immunotherapy for HCC.

摘要

肝细胞癌(HCC)是一种致命的恶性肿瘤,缺乏有效的治疗方法,特别是对于晚期疾病。尽管免疫检查点抑制剂(ICI)在 HCC 的治疗方面取得了重大进展,但仍有大量 HCC 患者无法获得持久和理想的临床获益。因此,仍需要新型、精细化的基于 ICI 的联合治疗来增强治疗效果。最近的一项研究报告称,碳酸酐酶 XII 抑制剂(CAXIIi)是一种新型抗癌药物,通过影响缺氧/酸性代谢来改变肿瘤免疫抑制微环境,并通过调节 C-C 基序趋化因子配体 8(CCL8)的表达来改变单核细胞和巨噬细胞的功能。这些观察结果为改善程序性细胞死亡蛋白 1(PD-1)/程序性细胞死亡配体 1(PD-L1)免疫疗法与 CAXIIis 的联合应用提供了思路。本综述旨在激发探索 CAXIIis 与免疫疗法联合应用于 HCC 的潜力的热情。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a137/10061011/204608c534e3/fimmu-14-1052657-g001.jpg

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