Singh, VishakhaKhurana, AmitNavik, UmashankerAllawadhi, PrinceBharani, Kala KumarWeiskirchen, Ralf2024-01-212024-08-142024-01-212024-08-142022-04-082413415510.3390/sci4020015http://10.2.3.109/handle/32116/4317Apoptosis is an evolutionarily conserved sequential process of cell death to maintain a homeostatic balance between cell formation and cell death. It is a vital process for normal eukaryotic development as it contributes to the renewal of cells and tissues. Further, it plays a crucial role in the elimination of unnecessary cells through phagocytosis and prevents undesirable immune responses. Apoptosis is regulated by a complex signaling mechanism, which is driven by interactions among several protein families such as caspases, inhibitors of apoptosis proteins, B-cell lymphoma 2 (BCL-2) family proteins, and several other proteases such as perforins and granzyme. The signaling pathway consists of both pro-apoptotic and pro-survival members, which stabilize the selection of cellular survival or death. However, any aberration in this pathway can lead to abnormal cell proliferation, ultimately leading to the development of cancer, autoimmune disorders, etc. This review aims to elaborate on apoptotic signaling pathways and mechanisms, interacting members involved in signaling, and how apoptosis is associated with carcinogenesis, along with insights into targeting apoptosis for disease resolution. � 2022 by the authors.en-USapoptosisBCL-2carcinogenesiscaspaseextrinsic pathwayinhibitorsintrinsic pathwaysignalingtherapytumor suppressorReviewhttps://www.mdpi.com/2413-4155/4/2/15