Stemness as a Systems-Level State: From Ancestral Plasticity to Systemic Control in Regeneration, Aging, and Cancer

Multicellularity necessitated the evolution of cellular diversity and specialization, yet across organisms, the retention of cellular plasticity within defined physiological contexts is a recurring principle. Here, we examine early-diverging metazoans to reevaluate the evolutionary logic of stemness. Rather than viewing stem cells as exceptional, we argue that cellular plasticity represents a deeply conserved attribute of early life. The ability of cells to remain responsive, multipotent, and regenerative under ecological or physiological contexts challenges the notion of cellular identity. We integrate evidence across three layers: evolutionary origins of cellular plasticity, systemic physiological axes that govern stem cell behavior, and metabolic and epigenetic mechanisms that execute fate decisions. This synthesis reveals that stemness is not a default cellular state but a licensed state, permitted when organism-level physiological signals align with local tissue demands. Within this framework, regeneration, age-associated decline, and cancer emerge as evidence of how effectively systemic governance regulates cellular plasticity across multicellular life.

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Publication Details

Journal
Annual Review of Genetics
Published
2026-09-01
DOI
https://doi.org/10.1146/annurev-genet-013026-083508
Primary Topic
Planarian Biology and Electrostimulation
Type
article
Field-Weighted Citation Impact
0.00
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article

Stemness as a Systems-Level State: From Ancestral Plasticity to Systemic Control in Regeneration, Aging, and Cancer

Sakshi Tiwari, Dasaradhi Palakodeti, Tina Mukherjee, Jagriti Arora
Annual Review of Genetics
Planarian Biology and Electrostimulation
article

Stemness as a Systems-Level State: From Ancestral Plasticity to Systemic Control in Regeneration, Aging, and Cancer

Sakshi Tiwari, Dasaradhi Palakodeti, Tina Mukherjee, Jagriti Arora
article en

Abstract

Multicellularity necessitated the evolution of cellular diversity and specialization, yet across organisms, the retention of cellular plasticity within defined physiological contexts is a recurring principle. Here, we examine early-diverging metazoans to reevaluate the evolutionary logic of stemness. Rather than viewing stem cells as exceptional, we argue that cellular plasticity represents a deeply conserved attribute of early life. The ability of cells to remain responsive, multipotent, and regenerative under ecological or physiological contexts challenges the notion of cellular identity. We integrate evidence across three layers: evolutionary origins of cellular plasticity, systemic physiological axes that govern stem cell behavior, and metabolic and epigenetic mechanisms that execute fate decisions. This synthesis reveals that stemness is not a default cellular state but a licensed state, permitted when organism-level physiological signals align with local tissue demands. Within this framework, regeneration, age-associated decline, and cancer emerge as evidence of how effectively systemic governance regulates cellular plasticity across multicellular life.

Annual Review of Genetics
Manipal Academy of Higher Education (IN), Institute for Stem Cell Biology and Regenerative Medicine (IN), Regional Centre for Biotechnology (IN)
Openalex Percentile: Top 18%
Planarian Biology and Electrostimulation
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