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肿瘤微环境中的免疫调节:联合抑制肿瘤缺氧与PD-1/PD-L1的治疗潜力

[Immunomodulation in the tumor microenvironment: Therapeutic potential of combined inhibition of tumor hypoxia and PD-1/ PD-L1].

作者信息

Svajda Laura, Cserepes Mihály, Hegyi Barbara, Niczky Theodora, Tóvári József

机构信息

Kísérletes Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary.

Nemzeti Tumorbiológiai Laboratórium, Országos Onkológiai Intézet, Budapest, Hungary.

出版信息

Magy Onkol. 2024 Jul 16;68(2):126-135. Epub 2024 Jun 3.

PMID:39013086
Abstract

Tumor hypoxia plays an important role in controlling tumor progression through signaling pathways related to the transcription factor HIF-1. In addition to enhancing migration, promoting angiogenesis and regulating metabolism, the hypoxic environment also affects immune function. In this hypoxic microenvironment an immunosuppressive milieu is established, where HIF-1 upregulates the expression of PD-L1, a key regulator of the immune response. We have found that elevated expression of PD-L1 correlates with increased HIF-1 levels in cancer cell lines and clinical samples. Thus, the co-inhibition of HIF-1 and PD-1/PD-L1 offers promising therapeutic possibilities. In this review we have examined the limitations of HIF-1 and PD-1/PD-L1 inhibition as monotherapy, explored their combined benefits and evaluated the feasibility of targeting PD-L1 with HIF-1 inhibitors.

摘要

肿瘤缺氧通过与转录因子HIF-1相关的信号通路在控制肿瘤进展中发挥重要作用。除了增强迁移、促进血管生成和调节代谢外,缺氧环境还影响免疫功能。在这种缺氧微环境中建立了一种免疫抑制环境,其中HIF-1上调免疫反应的关键调节因子PD-L1的表达。我们发现在癌细胞系和临床样本中,PD-L1表达升高与HIF-1水平增加相关。因此,联合抑制HIF-1和PD-1/PD-L1提供了有前景的治疗可能性。在本综述中,我们研究了HIF-1和PD-1/PD-L1单一疗法的局限性,探讨了它们联合使用的益处,并评估了用HIF-1抑制剂靶向PD-L1的可行性。

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