Immune evasion in cancer: mechanisms and cutting-edge therapeutic approaches

Abstract Immune evasion represents a significant challenge in oncology. It allows tumors to evade immune surveillance and destruction, thereby complicating therapeutic interventions and contributing to suboptimal patient outcomes. This review addresses the critical need to understand how cancers eva...

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Main Authors: Muhammad Tufail, Can-Hua Jiang, Ning Li
Format: Article
Language:English
Published: Nature Publishing Group 2025-07-01
Series:Signal Transduction and Targeted Therapy
Online Access:https://doi.org/10.1038/s41392-025-02280-1
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author Muhammad Tufail
Can-Hua Jiang
Ning Li
author_facet Muhammad Tufail
Can-Hua Jiang
Ning Li
author_sort Muhammad Tufail
collection DOAJ
description Abstract Immune evasion represents a significant challenge in oncology. It allows tumors to evade immune surveillance and destruction, thereby complicating therapeutic interventions and contributing to suboptimal patient outcomes. This review addresses the critical need to understand how cancers evade immune surveillance. It aims to provide a comprehensive overview of strategies of tumors to escape immune detection by examining tumor-induced immune suppression, immune checkpoint regulation, and genetic and epigenetic influences. Moreover, it explores the dynamic role of the tumor microenvironment (TME) in fostering immune resistance and highlights the impact of metabolic reprogramming on immune suppression. Additionally, this review focuses on how tumor heterogeneity influences immune evasion and discusses the limitations of current immunotherapies. The role of key signaling pathways, including programmed cell death protein 1/programmed cell death ligand 1 (PD-1/PD-L1), cytotoxic T-lymphocyte–associated antigen 4 (CTLA-4), transforming growth factor-β (TGF-β), nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), and cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS–STING) is analyzed to elucidate their contributions to immune escape. Emphasizing the complexities of immune evasion, this review underscores the importance of personalized approaches and the integration of multi-omics data to combat therapeutic resistance. Furthermore, it discusses novel and emerging therapeutic strategies, such as bispecific antibodies, oncolytic viruses, and nanotechnology-driven immunotherapies, showcasing innovative avenues in cancer treatment. The significance of this review lies in its potential to guide future research and innovations in immunotherapy, ultimately improving patient outcomes and advancing our understanding of cancer immunology.
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spelling doaj-art-9dc63cbbcf024af1a02bdb0d5c8c6ab92025-08-20T03:46:29ZengNature Publishing GroupSignal Transduction and Targeted Therapy2059-36352025-07-0110114910.1038/s41392-025-02280-1Immune evasion in cancer: mechanisms and cutting-edge therapeutic approachesMuhammad Tufail0Can-Hua Jiang1Ning Li2Department of Oral and Maxillofacial Surgery, Center of Stomatology, Xiangya Hospital, Central South UniversityDepartment of Oral and Maxillofacial Surgery, Center of Stomatology, Xiangya Hospital, Central South UniversityDepartment of Oral and Maxillofacial Surgery, Center of Stomatology, Xiangya Hospital, Central South UniversityAbstract Immune evasion represents a significant challenge in oncology. It allows tumors to evade immune surveillance and destruction, thereby complicating therapeutic interventions and contributing to suboptimal patient outcomes. This review addresses the critical need to understand how cancers evade immune surveillance. It aims to provide a comprehensive overview of strategies of tumors to escape immune detection by examining tumor-induced immune suppression, immune checkpoint regulation, and genetic and epigenetic influences. Moreover, it explores the dynamic role of the tumor microenvironment (TME) in fostering immune resistance and highlights the impact of metabolic reprogramming on immune suppression. Additionally, this review focuses on how tumor heterogeneity influences immune evasion and discusses the limitations of current immunotherapies. The role of key signaling pathways, including programmed cell death protein 1/programmed cell death ligand 1 (PD-1/PD-L1), cytotoxic T-lymphocyte–associated antigen 4 (CTLA-4), transforming growth factor-β (TGF-β), nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), and cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS–STING) is analyzed to elucidate their contributions to immune escape. Emphasizing the complexities of immune evasion, this review underscores the importance of personalized approaches and the integration of multi-omics data to combat therapeutic resistance. Furthermore, it discusses novel and emerging therapeutic strategies, such as bispecific antibodies, oncolytic viruses, and nanotechnology-driven immunotherapies, showcasing innovative avenues in cancer treatment. The significance of this review lies in its potential to guide future research and innovations in immunotherapy, ultimately improving patient outcomes and advancing our understanding of cancer immunology.https://doi.org/10.1038/s41392-025-02280-1
spellingShingle Muhammad Tufail
Can-Hua Jiang
Ning Li
Immune evasion in cancer: mechanisms and cutting-edge therapeutic approaches
Signal Transduction and Targeted Therapy
title Immune evasion in cancer: mechanisms and cutting-edge therapeutic approaches
title_full Immune evasion in cancer: mechanisms and cutting-edge therapeutic approaches
title_fullStr Immune evasion in cancer: mechanisms and cutting-edge therapeutic approaches
title_full_unstemmed Immune evasion in cancer: mechanisms and cutting-edge therapeutic approaches
title_short Immune evasion in cancer: mechanisms and cutting-edge therapeutic approaches
title_sort immune evasion in cancer mechanisms and cutting edge therapeutic approaches
url https://doi.org/10.1038/s41392-025-02280-1
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