Can 3D bioprinting solve the mystery of senescence in cancer therapy?

衰老 肿瘤微环境 休眠 癌症 生物 癌细胞 机制(生物学) 神经科学 癌症研究 肿瘤进展 生物信息学 细胞生物学 遗传学 哲学 认识论 发芽 植物
作者
Sofian Al Shboul,Valerie DeLuca,Yazan Al Dweiri,Tareq Saleh
出处
期刊:Ageing Research Reviews [Elsevier BV]
卷期号:81: 101732-101732 被引量:8
标识
DOI:10.1016/j.arr.2022.101732
摘要

Tumor dormancy leading to cancer relapse is still a poorly understood mechanism. Several cell states such as quiescence and diapause can explain the persistence of tumor cells in a dormant state, but the potential role of tumor cell senescence has been met with hesitance given the historical understanding of the senescent growth arrest as irreversible. However, recent evidence has suggested that senescence might contribute to dormancy and relapse, although its exact role is not fully developed. This limited understanding is largely due to the paucity of reliable study models. The current 2D cell modeling is overly simplistic and lacks the appropriate representation of the interactions between tumor cells (senescent or non-senescent) and the other cell types within the tumor microenvironment (TME), as well as with the extracellular matrix (ECM). 3D cell culture models, including 3D bioprinting techniques, offer a promising approach to better recapitulate the native cancer microenvironment and would significantly improve our understanding of cancer biology and cellular response to treatment, particularly Therapy-Induced Senescence (TIS), and its contribution to cancer recurrence. Fabricating a novel 3D bioprinted model offers excellent opportunities to investigate both the role of TIS in tumor dormancy and the utility of senolytics (drugs that selectively eliminate senescent cells) in targeting dormant cancer cells and mitigating the risk for resurgence. In this review, we discuss literature on the possible contribution of TIS in tumor dormancy, provide examples on the current 3D models of senescence, and propose a novel 3D model to investigate the ultimate role of TIS in mediating overall response to therapy. • Therapy-Induced Senescence (TIS) is a major component of tumor cell response to therapy. • TIS might be a potential mechanism for tumor dormancy • 3D bioprinting is an advantageous approach to investigate the role of TIS in tumor dormancy • 3D bioprinting provides an avenue to screen for more effective senolytics for cancer therapy
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