癌症免疫疗法中免疫检查点调节的新兴药物靶点:冰山就在表面之下。

IF 6.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Apoptosis Pub Date : 2024-10-01 DOI:10.1007/s10495-024-02022-8
Sakuntala Gayen, Swarupananda Mukherjee, Sandipan Dasgupta, Souvik Roy
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引用次数: 0

摘要

免疫系统是防止癌症发生和发展的基本屏障。免疫系统失效会增强免疫抑制作用,从而导致癌症的发生。这种免疫抑制作用源于与肿瘤进展相关的免疫检查点表达的显著改变。肿瘤微环境会促进免疫逃逸机制,进一步扩大免疫抑制作用。值得注意的是,大量针对免疫检查点的研究已成为癌症研究进展中的务实之举。本研究重点综述了旨在调节免疫检查点协同抑制和协同刺激分子以应对免疫系统激活的新兴药物靶点。这种调节促使人们开发出更新的治疗方法,最终通过免疫调节作用诱导免疫原性细胞死亡。这项研究强调了免疫检查点在癌症发病的免疫调节中的作用,并探索了癌症免疫疗法的潜在治疗途径。
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Emerging druggable targets for immune checkpoint modulation in cancer immunotherapy: the iceberg lies beneath the surface

The immune system serves as a fundamental defender against the initiation and progression of cancer. Failure of the immune system augments immunosuppressive action that leading to cancer manifestation. This immunosuppressive effect causes from significant alterations in immune checkpoint expression associated with tumoral progression. The tumor microenvironment promotes immune escape mechanisms that further amplifying immunosuppressive actions. Notably, substantial targeting of immune checkpoints has been pragmatic in the advancement of cancer research. This study highlights a comprehensive review of emerging druggable targets aimed at modulating immune checkpoint co-inhibitory as well as co-stimulatory molecules in response to immune system activation. This modulation has prompted to the development of newer therapeutic insights, eventually inducing immunogenic cell death through immunomodulatory actions. The study emphasizes the role of immune checkpoints in immunogenic regulation of cancer pathogenesis and explores potential therapeutic avenues in cancer immunotherapy.

Graphical Abstract

Modulation of Immunosuppressive and Immunostimulatory pathways of immune checkpoints in cancer immunotherapy

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来源期刊
Apoptosis
Apoptosis 生物-生化与分子生物学
CiteScore
9.10
自引率
4.20%
发文量
85
审稿时长
1 months
期刊介绍: Apoptosis, a monthly international peer-reviewed journal, focuses on the rapid publication of innovative investigations into programmed cell death. The journal aims to stimulate research on the mechanisms and role of apoptosis in various human diseases, such as cancer, autoimmune disease, viral infection, AIDS, cardiovascular disease, neurodegenerative disorders, osteoporosis, and aging. The Editor-In-Chief acknowledges the importance of advancing clinical therapies for apoptosis-related diseases. Apoptosis considers Original Articles, Reviews, Short Communications, Letters to the Editor, and Book Reviews for publication.
期刊最新文献
Advancements in programmed cell death research in antitumor therapy: a comprehensive overview. Dysregulation of R-loop homeostasis shapes the immunosuppressive microenvironment and induces malignant progression in melanoma. FBXO2 as a switch guides a special fate of tumor clones evolving into a highly malignant transcriptional subtype in oral squamous cell carcinoma. MRG15 promotes cell apoptosis through inhibition of mitophagy in hyperlipidemic acute pancreatitis. Correction: The extracellular lactate-to-pyruvate ratio modulates the sensitivity to oxidative stress-induced apoptosis via the cytosolic NADH/NAD + redox state
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