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Oct4

ZEB2 Facilitates Peritoneal Metastasis by Regulating the Invasiveness and Tumorigenesis of Cancer Stem-Like Cells in High-Grade Serous Ovarian Cancers

[Oncogene] Investigators demonstrated that ZEB2, the transcription factor of epithelial–mesenchymal transition, was upregulated in ascites cells from high-grade serous ovarian cancer patients and in CD133+ cancer stem-like cells from epithelial ovarian cancer cell lines.

Auxin-Degron System Identifies Immediate Mechanisms of OCT4

[Stem Cell Reports] Researchers developed a rapid protein-level OCT4 depletion system that demonstrated that the immediate downstream response to loss of OCT4 was reduced expression of key pluripotency factors.

Subtype-Specific Collaborative Transcription Factor Networks Are Promoted by OCT4 in the Progression of Prostate Cancer

[Nature Communications] Researchers showed the essential role of disease phase-specific transcription factor collaboration changes in advanced prostate cancer.

Biological Importance of OCT Transcription Factors in Reprogramming and Development

[Experimental & Molecular Medicine] Investigators discuss the roles of the structural components of Oct proteins in reprogramming and how donor cell epigenomes endow Oct proteins with different reprogramming competences.

Biological Characteristics of a Sub-Population of Cancer Stem Cells from Two Triple-Negative Breast Tumor Cell Lines

[Heliyon] The authors determined differences in ultrastructural morphology, proliferative capacity, and mouse-xenotransplantation characteristics of the MDA-MB-231 and MDA-MB-436 triple-negative breast tumor cell lines with the CD44high/CD24low phenotype in order to study their exosomes.

AP-1 Is a Temporally Regulated Dual Gatekeeper of Reprogramming to Pluripotency

[Proceedings of the National Academy of Sciences of the United States of America] Scientists examined epigenome remodeling at the onset of human nuclear reprogramming by profiling human fibroblasts after fusion with murine ESCs. Efficient reprogramming of human fibroblasts to iPSCs was achieved by transduction with vectors expressing SOX2, KLF4, and inducible dnAP-1, demonstrating that dnAP-1 can substitute for exogenous human OCT4.

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