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IL-1RAP:肿瘤中的关键治疗靶点

英文原题:IL-1RAP, a Key Therapeutic Target in Cancer.

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IL-1RAP, a Key Therapeutic Target in Cancer.

PubMed 2022/11/29(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

癌症是全球主要死因,尤其是在高收入和中高收入国家。尽管癌症治疗近期取得了进展,例如CAR-T(CAR-T)细胞或抗体药物偶联物(ADC),但仍需鉴定肿瘤细胞表达的新靶点,以便选择性地将这些创新疗法导向肿瘤。在此背景下,IL-1RAP 近期显示出成为这些癌症治疗新靶点之一的巨大潜力。IL-1RAP 通过白细胞介素 1、33 和 36(IL-1、IL-33、IL-36)信号通路高度参与炎症过程。炎症现已被认为是癌变的标志,提示 IL-1RAP 可能在癌症发生和进展中发挥作用。此外,IL-1RAP 被发现于多种血液系统恶性肿瘤和实体瘤的肿瘤细胞上过表达,从而证实其可能参与癌变。本综述将首先描述 IL-1RAP 的结构和遗传学及其在肿瘤发展中的作用。最后,将重点讨论基于 IL-1RAP 靶向的疗法,这些疗法目前正处于临床前或临床开发阶段。

展开英文摘要原文

Cancer is a major cause of death worldwide and especially in high- and upper-middle-income countries. Despite recent progress in cancer therapies, such as chimeric antigen receptor T (CAR-T) cells or antibody-drug conjugate (ADC), new targets expressed by the tumor cells need to be identified in order to selectively drive these innovative therapies to tumors.

In this context, IL-1RAP recently showed great potential to become one of these new targets for cancer therapy. IL-1RAP is highly involved in the inflammation process through the interleukins 1, 33, and 36 (IL-1, IL-33, IL-36) signaling pathways. Inflammation is now recognized as a hallmark of carcinogenesis, suggesting that IL-1RAP could play a role in cancer development and progression.

Furthermore, IL-1RAP was found overexpressed on tumor cells from several hematological and solid cancers, thus confirming its potential involvement in carcinogenesis. This review will first describe the structure and genetics of IL-1RAP as well as its role in tumor development.

Finally, a focus will be made on the therapies based on IL-1RAP targeting, which are now under preclinical or clinical development.

论文信息

作者
Frenay J、Bellaye PS、Oudot A、Helbling A、Petitot C、Ferrand C、Collin B、Dias AMM
单位
Plateforme d'Imagerie et Radiothérapie Précliniques, Médecine Nucléaire, Centre Georges-François Leclerc, 21000 Dijon, France.France
文献类型
综述
期刊
International journal of molecular sciences2022 Nov 29
原文标识
PubMed 36499246 · DOI 10.3390/ijms232314918