Personalized Treatment Strategies via Integration of Gene Expression Biomarkers in Molecular Profiling of Laryngeal Cancer.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Antonino Maniaci, Giovanni Giurdanella, Carlos Chiesa Estomba, Simone Mauramati, Andy Bertolin, Marco Lionello, Miguel Mayo-Yanez, Paolo Boscolo Rizzo, Jerome R Lechien, Mario Lentini
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引用次数: 0

Abstract

Laryngeal cancer poses a substantial challenge in head and neck oncology, and there is a growing focus on customized medicine techniques. The present state of gene expression indicators in laryngeal cancer and their potential to inform tailored therapy choices are thoroughly examined in this review. We examine significant molecular changes, such as TP53, CDKN2A, PIK3CA, and NOTCH1 mutations, which have been identified as important participants in the development of laryngeal cancer. The study investigates the predictive and prognostic significance of these genetic markers in addition to the function of epigenetic changes such as the methylation of the MGMT promoter. We also go over the importance of cancer stem cell-related gene expression patterns, specifically CD44 and ALDH1A1 expression, in therapy resistance and disease progression. The review focuses on indicators, including PD-L1, CTLA-4, and tumor mutational burden (TMB) in predicting immunotherapy responses, highlighting recent developments in our understanding of the intricate interactions between tumor genetics and the immune milieu. We also investigate the potential for improving prognosis accuracy and treatment selection by the integration of multi-gene expression panels with clinicopathological variables. The necessity for uniform testing and interpretation techniques is one of the difficulties, in implementing these molecular insights into clinical practice, that are discussed. This review seeks to provide a comprehensive framework for promoting personalized cancer therapy by combining the most recent data on gene expression profiling in laryngeal cancer. Molecularly guided treatment options may enhance patient outcomes.

通过整合喉癌分子图谱中的基因表达生物标记物制定个性化治疗策略
喉癌给头颈部肿瘤学带来了巨大挑战,定制化医疗技术日益受到关注。本综述深入探讨了喉癌基因表达指标的现状及其为定制化治疗选择提供信息的潜力。我们研究了重要的分子变化,如 TP53、CDKN2A、PIK3CA 和 NOTCH1 突变,这些突变已被确定为喉癌发展的重要参与者。除了 MGMT 启动子甲基化等表观遗传学变化的功能外,本研究还调查了这些遗传标记的预测和预后意义。我们还探讨了癌症干细胞相关基因表达模式(特别是CD44和ALDH1A1表达)在耐药性和疾病进展中的重要性。综述重点讨论了预测免疫疗法反应的指标,包括 PD-L1、CTLA-4 和肿瘤突变负荷 (TMB),强调了我们对肿瘤遗传学和免疫环境之间错综复杂的相互作用的理解的最新进展。我们还研究了通过整合多基因表达面板和临床病理变量来提高预后准确性和治疗选择的潜力。本文讨论了将这些分子研究成果应用于临床实践的难点之一,即统一检测和解释技术的必要性。本综述旨在结合喉癌基因表达谱分析的最新数据,为促进个性化癌症治疗提供一个全面的框架。分子指导下的治疗方案可提高患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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