Pan-cancer analysis of ALK mutation and its association with tumor immunogenicity and the efficacy of immune checkpoint blockade

IF 14.6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Genes & Diseases Pub Date : 2026-05-01 Epub Date: 2025-05-28 DOI:10.1016/j.gendis.2025.101701
Zhiyang Huang , Jiajun Chen , Yan Huang , Hong Zhao , Bin Zhao
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引用次数: 0

Abstract

Anaplastic lymphoma kinase (ALK) plays important roles in tumorigenesis and is involved in tumor immunogenicity through various pathways. Here, we conducted a comprehensive bioinformatic and clinical analysis on the characteristics of pan-cancer ALK mutation and its association with tumor immunity and the efficacy of immune checkpoint blockade. In 2930 patients with 11 tumor types treated with immune checkpoint inhibitors, the mutation of ALK indicated favorable overall survival (hazard ratio = 0.69; 95% confidence interval, 0.57–0.83; p < 0.001). We further developed and validated a nomogram to estimate the 12-month and 24-month survival probabilities after the initiation of immunotherapy. Moreover, multi-omics analysis on both intrinsic and extrinsic immune landscapes revealed that the mutation of ALK could enrich infiltration of immune cells, enhance tumor immunogenicity, and improve immune responses. In conclusion, ALK mutation is associated with promoted cancer immunity and can be treated as a biomarker for favorable outcomes in pan-cancer immune checkpoint blockade. These results have implications for treatment decision-making and developing immunotherapy for personalized care.
泛癌分析ALK突变及其与肿瘤免疫原性和免疫检查点阻断疗效的关系
间变性淋巴瘤激酶(ALK)在肿瘤发生中起重要作用,并通过多种途径参与肿瘤的免疫原性。在此,我们对泛癌ALK突变的特征及其与肿瘤免疫的关系以及免疫检查点阻断的疗效进行了全面的生物信息学和临床分析。在接受免疫检查点抑制剂治疗的11种肿瘤类型的2930例患者中,ALK突变表明总体生存期有利(风险比= 0.69;95%可信区间为0.57-0.83;p < 0.001)。我们进一步开发并验证了一种nomogram来估计免疫治疗开始后12个月和24个月的生存概率。此外,对内、外源免疫景观的多组学分析显示,ALK突变可丰富免疫细胞浸润,增强肿瘤免疫原性,改善免疫应答。总之,ALK突变与促进癌症免疫有关,可以作为泛癌症免疫检查点阻断有利结果的生物标志物。这些结果对治疗决策和开发个性化护理的免疫疗法具有启示意义。
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来源期刊
Genes & Diseases
Genes & Diseases Multiple-
CiteScore
7.30
自引率
0.00%
发文量
347
审稿时长
49 days
期刊介绍: Genes & Diseases is an international journal for molecular and translational medicine. The journal primarily focuses on publishing investigations on the molecular bases and experimental therapeutics of human diseases. Publication formats include full length research article, review article, short communication, correspondence, perspectives, commentary, views on news, and research watch. Aims and Scopes Genes & Diseases publishes rigorously peer-reviewed and high quality original articles and authoritative reviews that focus on the molecular bases of human diseases. Emphasis will be placed on hypothesis-driven, mechanistic studies relevant to pathogenesis and/or experimental therapeutics of human diseases. The journal has worldwide authorship, and a broad scope in basic and translational biomedical research of molecular biology, molecular genetics, and cell biology, including but not limited to cell proliferation and apoptosis, signal transduction, stem cell biology, developmental biology, gene regulation and epigenetics, cancer biology, immunity and infection, neuroscience, disease-specific animal models, gene and cell-based therapies, and regenerative medicine.
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