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Review | Open Access

Tumor microenvironment-driven natural killer cell diversity: mechanisms and therapeutic opportunities

Yue Duan1,2,*Mingzhen Zhou2,*Xingxian Guo2Tianyu Cao2Yuanyuan Lu2 ( )Xiaodi Zhao2 ( )
Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, School of Medicine, Northwest University, Xi’an 710069, China
State Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, National Clinical Research Center for Digestive Diseases, Xijing Hospital of Digestive Diseases, Xijing Hospital, Fourth Military Medical University, Xi’an 710032, China

*These authors contributed equally to this work.

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Abstract

Natural killer (NK) cells are key effector cells involved in tumor immune surveillance, yet their function within the tumor microenvironment (TME) exhibits considerable complexity and plasticity that cannot be adequately explained by the classical CD56/CD16 dichotomy. This functional diversity arises from the phenotypic adaptability and dynamic differentiation of distinct NK cell subsets shaped by the TME. In this review, we systematically examine the defining characteristics and functional roles of recently identified NK cell subsets in the TME; elucidate the molecular mechanisms governing their regulation; and highlight the functional transitions and cooperative interactions among these subsets. Moreover, building on current evidence, we summarize emerging immunotherapeutic approaches targeting specific NK cell subsets. Together, these perspectives offer new insights and strategic directions for deciphering the multifaceted roles of NK cells in antitumor immunity and advancing the development of subset-targeted therapies.

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Cancer Biology & Medicine
Pages 1087-1107

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Cite this article:
Duan Y, Zhou M, Guo X, et al. Tumor microenvironment-driven natural killer cell diversity: mechanisms and therapeutic opportunities. Cancer Biology & Medicine, 2026, 23(8): 1087-1107. https://doi.org/10.20892/j.issn.2095-3941.2025.0829

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Received: 24 December 2025
Accepted: 11 March 2026
Published: 25 April 2026
©2026 The Authors.

Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0)