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Induced pluripotent stem cell reprogramming via Yamanaka factors (iPSC reprogramming (Yamanaka factors))

Target
iPSC reprogramming (Yamanaka factors)
Molecular classification
Transcription factor (for the individual Yamanaka factors), Epigenetic modification (process level), Other (cellular process, not a single molecule or receptor)
01

Overview

Cellular differentiation potential restoration via Yamanaka factor-mediated nuclear reprogramming" refers not to a single molecule or receptor but rather a process in which differentiated somatic cells are reverted back into an embryonic-like pluripotent state. This is achieved by introducing four key transcription factors—OCT4, SOX2, KLF4, and c-MYC—collectively known as the "Yamanaka factors." These proteins act on the genome to erase cell-type-specific epigenetic marks and reactivate genes associated with stemness. The resulting induced pluripotent stem cells (iPSCs) can then be directed toward various cell fates for research or therapeutic purposes. While this technology has revolutionized regenerative medicine research by providing an alternative source for patient-specific stem cells without using embryos[1], it is not itself a druggable target but rather describes a method/process involving multiple molecular targets. The process shares molecular pathways with cancer biology due to its reliance on proliferation and dedifferentiation mechanisms.[1][2]

Other names
Yamanaka factor-mediated nuclear reprogrammingOSKM-mediated cellular reprogrammingInduced pluripotency via Yamanaka factorsCellular dedifferentiation by OSKM
02

Mechanism of action

Induction of epigenetic changes and activation of signaling pathways that revert differentiated cells to a pluripotent state; inhibition of HDACs and TGFβ signaling; activation/inhibition of Wnt/β-catenin and MAPK pathways[1][2]

03

Biological functions

Restoration of cellular differentiation potentialInduction of pluripotencyCell fate conversionEpigenetic remodeling
04

Disease associations

Cancer (shared pathways with carcinogenesis)[2]Aging and longevity[2]Regenerative medicine applications[1][2]
05

Safety considerations

Potential for tumorigenicity/cancer due to overlap with oncogenic pathways[2]risk from genomic integration when using viral vectors for gene delivery[1]incomplete or aberrant reprogramming leading to dysfunctional cells
06

Interacting drugs

Valproic acid

4 more in the full profile.

07

Biomarkers

Expression of pluripotency genes such as OCT4, SOX2, NANOGloss of lineage-specific markers[1]

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