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The term 'Dysfunctional cells' refers to a broad cellular state or phenotype rather than a specific molecular target such as a receptor, enzyme, or transporter. In modern pharmacology and regenerative medicine, this term most frequently identifies senescent cells—cells that have permanently ceased division in response to stress or damage but remain metabolically active (PMID: 31034451). These cells often contribute to chronic disease by secreting pro-inflammatory cytokines, proteases, and growth factors, collectively known as the Senescence-Associated Secretory Phenotype (SASP) (PMID: 24703831). While 'senolytic' drugs like Navitoclax and the Dasatinib/Quercetin combination are designed to eliminate these populations, they do so by targeting specific proteins like BCL-2 or BCL-XL rather than the 'cell' as a whole (PMID: 25754861, 26738515). Consequently, 'Dysfunctional cells' is an imprecise classification for a drug target; effective therapeutic development requires identifying the specific molecular drivers or markers unique to these cells (National Institute on Aging).
Selective induction of apoptosis in cells exhibiting pathological phenotypes or senescence-associated anti-apoptotic pathways.
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