Cell death in cancer
Summary
"Evasion of cell death" is a hallmark of cancer, enabling transformed cells to withstand oncogenic and therapeutic stress. Restoring cancer cell death is an appealing strategy but requires a deep understanding of cell death programs. Over the past two decades, the cell death field has expanded from apoptosis to include necroptosis, pyroptosis, ferroptosis, and other emerging programs, reshaping cancer biology and revealing therapeutic opportunities. While apoptosis remains the primary radi
Content
# Cell death in cancer
*Published: 2026 Apr 16*
"Evasion of cell death" is a hallmark of cancer, enabling transformed cells to
withstand oncogenic and therapeutic stress. Restoring cancer cell death is an
appealing strategy but requires a deep understanding of cell death programs.
Over the past two decades, the cell death field has expanded from apoptosis to
include necroptosis, pyroptosis, ferroptosis, and other emerging programs,
reshaping cancer biology and revealing therapeutic opportunities. While
apoptosis remains the primary radiation- and chemotherapy-induced cell death
program, non-apoptotic programs can drive inflammatory responses and orchestrate
the interplay among tumor, stroma, and immune components, influencing
immunotherapy outcomes. Ferroptosis, an iron-dependent, lipid
peroxidation-driven cell death modality, lacks a canonical induction signal and
arises from perturbations in lipid, iron, and redox metabolism. This review
presents a unified framework for understanding the roles of major cell death
programs in cancer development, progression, and treatment response, as well as
addressing resistance to cancer cell death and immune suppression. "Our bodies
are made of cells that live, and just as surely, of cells that must die." -S.
Brenner.
DOI: 10.1016/j.cell.2026.03.024