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Updated: May 19, 2026

Tractable In Vivo Reprogramming of Tumor Cells to Type 1 Conventional Dendritic Cell-like Cells
Published on: August 1, 2025
Reprogramming cancer cells: back to the future
1Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Abstract:
Reprogramming healthy somatic cells into induced pluripotent stem cells (iPSCs) with four defined factors (Oct4, Sox2, c-Myc and Klf4) has been intensively investigated. However, reprogramming diseased cells such as cancer cells has fallen much behind. In this issue of Oncogene, Zhang et al. demonstrated that reprogrammed sarcoma cells with defined factors, as well as Nanog and Lin28, lost their tumorigenicity and dedifferentiated to mesenchymal stem cells (MSC) and hematopoietic stem cell (HSC)-like cells that can be terminally differentiated into mature connective tissues and red blood cells, suggesting sarcoma cells may be reversed back to a stage of common ancestor iPSC bifurcating for HSC and MSC ontogeny. It may, therefore, provide a novel strategy for cancer treatment via ancestor pluripotency induction.
Insights
Scientists reprogrammed sarcoma cells into stem cells, reversing cancer traits. This suggests a new cancer therapy approach by inducing pluripotency in cancer cells.
Area of Science:
- Stem cell biology
- Cancer research
- Epigenetics
Background:
- Induced pluripotent stem cells (iPSCs) are generated from somatic cells using defined factors.
- Reprogramming of diseased cells, particularly cancer cells, remains challenging.
- Sarcoma is a type of cancer affecting connective tissues.
Purpose of the Study:
- To investigate the reprogramming of sarcoma cells into a pluripotent state.
- To determine if reprogramming can reverse cancer-specific characteristics.
- To explore the potential of cancer cell reprogramming for therapeutic strategies.
Main Methods:
- Sarcoma cells were reprogrammed using defined factors (Oct4, Sox2, c-Myc, Klf4) along with Nanog and Lin28.
- Characterization of reprogrammed cells for pluripotency markers and differentiation potential.
- Assessment of tumorigenicity in reprogrammed sarcoma cells.
Main Results:
- Reprogrammed sarcoma cells lost their tumorigenicity.
- Dedifferentiation occurred, yielding cells resembling mesenchymal stem cells (MSCs) and hematopoietic stem cells (HSCs).
- These cells could terminally differentiate into mature connective tissues and red blood cells.
Conclusions:
- Sarcoma cells can be reprogrammed to a pluripotent-like state, losing cancer-driving properties.
- Reprogramming may revert sarcoma cells to a common ancestral stage that can differentiate into HSCs and MSCs.
- Cancer cell reprogramming offers a potential novel therapeutic strategy through induction of ancestor pluripotency.
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