Molecular mechanisms of ageing in cancer development and therapeutic response: Translational implications for precision oncology

Laiba Husain
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Abstract

Background

The intricate relationship between cellular ageing processes and cancer development represents one of the most significant challenges in contemporary oncology. As populations worldwide experience unprecedented demographic shifts towards advanced age, understanding the molecular mechanisms that link ageing to cancer initiation, progression, and therapeutic response has become essential for developing effective precision medicine approaches.

Main body

This review examines the fundamental molecular pathways through which ageing influences cancer biology, including telomere dysfunction, cellular senescence, DNA damage accumulation, and epigenetic alterations. These age-related changes create a permissive environment for oncogenesis while simultaneously affecting therapeutic efficacy and treatment tolerance. Key ageing-associated molecular signatures include p16^INK4a^ upregulation, shortened telomeres, increased DNA damage response activation, and altered chromatin structure. The accumulation of senescent cells with age contributes to chronic inflammation and tissue dysfunction that promotes tumour development. Additionally, age-related changes in drug metabolism, DNA repair capacity, and immune function significantly impact therapeutic outcomes. Recent advances in molecular ageing biomarkers, including transcriptomic ageing clocks and protein-based signatures, offer promising approaches for personalizing cancer treatment strategies. The integration of ageing biology into precision oncology frameworks presents opportunities for developing age-informed therapeutic protocols that optimize efficacy while minimizing toxicity. Emerging technologies, including artificial intelligence-driven molecular analysis and advanced imaging techniques, enable more precise characterization of ageing-cancer interactions at the cellular and tissue levels.

Conclusion

The molecular mechanisms underlying ageing-cancer relationships provide critical insights for advancing precision oncology approaches. Understanding these pathways enables the development of targeted interventions that account for age-related biological changes, ultimately improving therapeutic outcomes for older cancer patients. Future research must focus on translating molecular ageing discoveries into clinically actionable tools that enhance treatment personalization and optimize care delivery across the cancer continuum.

Abstract Image

衰老在癌症发展和治疗反应中的分子机制:对精确肿瘤学的转化意义
细胞老化过程与癌症发展之间的复杂关系是当代肿瘤学中最重大的挑战之一。随着全球人口经历前所未有的高龄人口转变,了解衰老与癌症发生、发展和治疗反应之间的分子机制对于开发有效的精准医学方法至关重要。本文综述了衰老影响癌症生物学的基本分子途径,包括端粒功能障碍、细胞衰老、DNA损伤积累和表观遗传改变。这些与年龄相关的变化为肿瘤的发生创造了一个宽松的环境,同时影响了治疗效果和治疗耐受性。衰老相关的关键分子特征包括p16^INK4a^上调、端粒缩短、DNA损伤反应激活增加和染色质结构改变。随着年龄的增长,衰老细胞的积累会导致慢性炎症和组织功能障碍,从而促进肿瘤的发展。此外,年龄相关的药物代谢、DNA修复能力和免疫功能的变化显著影响治疗结果。分子老化生物标志物的最新进展,包括转录组老化时钟和基于蛋白质的特征,为个性化癌症治疗策略提供了有希望的方法。将衰老生物学整合到精确肿瘤学框架中,为开发年龄知情的治疗方案提供了机会,这些治疗方案可以优化疗效,同时将毒性降到最低。新兴技术,包括人工智能驱动的分子分析和先进的成像技术,可以在细胞和组织水平上更精确地表征衰老与癌症的相互作用。结论衰老与癌症关系的分子机制为推进精准肿瘤学方法提供了重要见解。了解这些途径有助于开发有针对性的干预措施,以解释与年龄相关的生物学变化,最终改善老年癌症患者的治疗效果。未来的研究必须专注于将分子衰老的发现转化为临床可操作的工具,以增强治疗个性化并优化整个癌症连续体的护理交付。
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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