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Senolytic therapy targeting CDKN2A/TP53/SASP pathway with dasatinib-quercetin

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Abstract

Selective elimination of senescent vascular smooth muscle cells expressing high CDKN2A (p16) and TP53. Reduces senescence-associated secretory phenotype (SASP) factors including IL6, TNF-α, and MMPs that contribute to aortic wall degradation in familial predisposition.