Quiescence-Origin Senescence: A New Paradigm in Cellular Aging

被引:2
作者
Yao, Guang [1 ,2 ]
机构
[1] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[2] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85719 USA
关键词
quiescence; senescence; quiescence deepening; dormancy state continuum; Rb-E2F switch threshold; geroconversion; STEM-CELLS; FIBROBLASTS; E2F; PROLIFERATION; STIMULATION; COMMITMENT; TRANSITION; UNDERLIES; AUTOPHAGY; REVERSAL;
D O I
10.3390/biomedicines12081837
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular senescence, traditionally viewed as a consequence of proliferating and growing cells overwhelmed by extensive stresses and damage, has long been recognized as a critical cellular aging mechanism. Recent research, however, has revealed a novel pathway termed "quiescence-origin senescence", where cells directly transition into senescence from the quiescent state, bypassing cell proliferation and growth. This opinion paper presents a framework conceptualizing a continuum between quiescence and senescence with quiescence deepening as a precursor to senescence entry. We explore the triggers and controllers of this process and discuss its biological implications. Given that the majority of cells in the human body are dormant rather than proliferative, understanding quiescence-origin senescence has significant implications for tissue homeostasis, aging, cancer, and various disease processes. The new paradigm in exploring this previously overlooked senescent cell population may reshape our intervention strategies for age-related diseases and tissue regeneration.
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页数:8
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