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细胞衰老与重编程之间的相互作用塑造了衰老和癌症的生物学格局,揭示了新的治疗途径。

The interplay of cellular senescence and reprogramming shapes the biological landscape of aging and cancer revealing novel therapeutic avenues.

作者信息

Ding Fuan, Yu Ying, Zhao Jiangqi, Wei Shibo, Zhang Yan, Han Jung Ho, Li Zhuo, Jiang Hong-Bo, Ryu Dongryeol, Cho Minkyoung, Bae Sung-Jin, Park Wonyoung, Ha Ki-Tae, Gao Bo

机构信息

Department of Vascular Surgery, The Second Hospital of Jilin University, Changchun, China.

Department of Surgery, Changchun University of Chinese Medicine, Changchun, China.

出版信息

Front Cell Dev Biol. 2025 Apr 28;13:1593096. doi: 10.3389/fcell.2025.1593096. eCollection 2025.

Abstract

Cellular senescence and cellular reprogramming represent two fundamentally intertwined processes that profoundly influence aging and cancer. This paper explores how the permanent cell-cycle arrest of senescent cells and the identity-resetting capacity of reprogramming jointly shape biological outcomes in later life and tumor development. We synthesize recent findings to show that senescent cells, while halting the proliferation of damaged cells, can paradoxically promote tissue dysfunction and malignancy via their secretory phenotype. Conversely, induced reprogramming of somatic cells-exemplified by Yamanaka factors-resets cellular age and epigenetic marks, offering a potential to rejuvenate aged cells. Key findings highlight shared mechanisms (e.g., DNA damage responses and epigenetic remodeling) and bidirectional crosstalk between these processes: senescence signals can facilitate neighboring cell plasticity, whereas reprogramming attempts can trigger intrinsic senescence programs as a barrier. In aging tissues, transient (partial) reprogramming has been shown to erase senescence markers and restore cell function without inducing tumorigenesis, underlining a novel strategy to combat age-related degeneration. In cancer, we discuss how therapy-induced senescence of tumor cells may induce stem-cell-like traits in some cells and drive relapse, revealing a delicate balance between tumor suppression and tumor promotion. Understanding the interplay between senescence and reprogramming is crucial for developing innovative therapies. By targeting the senescence-reprogramming axis-for instance, via senolytic drugs, SASP inhibitors, or safe reprogramming techniques-there is significant therapeutic potential to ameliorate aging-related diseases and improve cancer treatment. Our findings underscore that carefully modulating cellular senescence and rejuvenation processes could pave the way for novel regenerative and anti-cancer strategies.

摘要

细胞衰老和细胞重编程是两个基本相互交织的过程,对衰老和癌症产生深远影响。本文探讨了衰老细胞的永久性细胞周期停滞和重编程的身份重置能力如何共同塑造晚年生活和肿瘤发展中的生物学结果。我们综合了最近的研究结果,表明衰老细胞虽然阻止了受损细胞的增殖,但却能通过其分泌表型反常地促进组织功能障碍和恶性肿瘤。相反,以山中因子为代表的体细胞诱导重编程可重置细胞年龄和表观遗传标记,为使衰老细胞恢复活力提供了潜力。关键发现突出了这些过程之间的共同机制(如DNA损伤反应和表观遗传重塑)以及双向串扰:衰老信号可促进邻近细胞的可塑性,而重编程尝试可触发内在衰老程序作为障碍。在衰老组织中,已证明短暂(部分)重编程可消除衰老标记并恢复细胞功能而不诱导肿瘤发生,这凸显了一种对抗与年龄相关的退化的新策略。在癌症方面,我们讨论了治疗诱导的肿瘤细胞衰老如何在某些细胞中诱导干细胞样特征并导致复发,揭示了肿瘤抑制和肿瘤促进之间的微妙平衡。了解衰老和重编程之间的相互作用对于开发创新疗法至关重要。通过靶向衰老 - 重编程轴——例如,通过衰老细胞溶解药物、衰老相关分泌表型抑制剂或安全的重编程技术——有显著的治疗潜力来改善与衰老相关的疾病并改善癌症治疗。我们的研究结果强调,仔细调节细胞衰老和年轻化过程可为新的再生和抗癌策略铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acdc/12066513/77e190aa3890/fcell-13-1593096-g001.jpg

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