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Senescent cells: A new Achilles' heel to exploit for cancer medicine?
被引:17
|作者:
Zhang, Boyi
[1
]
Lam, Eric W. -F.
[2
]
Sun, Yu
[1
,3
,4
]
机构:
[1] Univ Chinese Acad Sci, Chinese Acad Sci, Shanghai Inst Biol Sci, Key Lab Tissue Microenvironm & Tumor, Shanghai, Peoples R China
[2] Imperial Coll London, Dept Surg & Canc, London, England
[3] Univ Washington, Dept Med, Seattle, WA USA
[4] Univ Washington, VAPSHCS, Seattle, WA USA
来源:
基金:
英国医学研究理事会;
中国国家自然科学基金;
关键词:
aging-related diseases;
cancer;
cellular senescence;
clinical trial;
senescence-associated secretory phenotype;
senolytics;
ONCOGENE-INDUCED SENESCENCE;
CELLULAR SENESCENCE;
SECRETORY PHENOTYPE;
DAMAGE;
IDENTIFICATION;
CHEMOTHERAPY;
RESISTANCE;
GROWTH;
CGAS;
D O I:
10.1111/acel.12875
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Cellular senescence is a typical tumor-suppressive mechanism that restricts the proliferation of premalignant cells. However, mounting evidence suggests that senescent cells, which also persist in vivo, can promote the incidence of aging-related disorders principally via the senescence-associated secretory phenotype (SASP), among which cancer is particularly devastating. Despite the beneficial effects of the SASP on certain physiological events such as wound healing and tissue repair, more studies have demonstrated that senescent cells can substantially contribute to pathological conditions and accelerate disease exacerbation, particularly cancer resistance, relapse and metastasis. To limit the detrimental properties while retaining the beneficial aspects of senescent cells, research advancements that support screening, design and optimization of anti-aging therapeutic agents are in rapid progress in the setting of prospective development of clinical strategies, which together represent a new wave of efforts to control human malignancies or mitigate degenerative complications.
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