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Therapy-induced senescence is finally escapable, what is next?

Tareq Saleh

2024Cell Cycle15 citationsDOIOpen Access PDF

Abstract

Several breakthrough articles have recently confirmed the ability of tumor cells to escape the stable cell cycle arrest imposed by Therapy-Induced Senescence (TIS). Subsequently, accepting the hypothesis that TIS is escapable should encourage serious reassessments of the fundamental roles of senescence in cancer treatment. The potential for escape from TIS undermines the well-established tumor suppressor function of senescence, proposes it as a mechanism of tumor dormancy leading to disease recurrence and invites for further investigation of its unfavorable contribution to cancer therapy outcomes. Moreover, escaping TIS strongly indicates that the elimination of senescent tumor cells, primarily through pharmacological means, is a suitable approach for increasing the efficacy of cancer treatment, one that still requires further exploration. This commentary provides an overview of the recent evidence that unequivocally demonstrated the ability of therapy-induced senescent tumor cells in overcoming the terminal growth arrest fate and provides future perspectives on the roles of TIS in tumor biology.

Topics & Concepts

SenescenceSuppressorCancer therapyCancerMechanism (biology)DormancyCellular senescenceCell cycle checkpointFunction (biology)Cancer researchDiseaseBiologyTumor cellsCell cycleCell biologyMedicineGeneticsInternal medicineEpistemologyPhilosophyPhenotypeBotanyGerminationGeneTelomeres, Telomerase, and SenescenceSingle-cell and spatial transcriptomicsAdvanced biosensing and bioanalysis techniques
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