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Cancer cell reprogramming to identify the genes competent for generating liver cancer stem cells

期刊

INFLAMMATION AND REGENERATION
卷 37, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s41232-017-0041-x

关键词

c-JUN oncogene; Induced pluripotent stem cells; Liver cancer; OCT4; Reprogramming

资金

  1. Ministry of Science and Technology [MOST 104-2320-B-037-033-My2, MOST 104-2314-B-033-002]
  2. National Health Research Institutes in Taiwan [NHRI-Ex102-10109B1, NHRI-Ex104-10416S1]
  3. Kaohsiung Medical University in Taiwan [KMU-TP103G00, KMU-TP103G01, KMU-TP103G03, KMU-TP103G04, KMU-TP103G05, KMU-TP103A104, KMU-TP104A04, KMU-TP104E24, KMU-TP104PR22, KMU-DT104001]

向作者/读者索取更多资源

The cancer stem cell (CSC) hypothesis postulates that cancer originates from the malignant transformation of stem/progenitor cells and is considered to apply to many cancers, including liver cancer. Identification that CSCs are responsible for drug resistance, metastasis, and secondary tumor appearance suggests that these populations are novel obligatory targets for the treatment of cancer. Here, we describe our new method for identifying potential CSC candidates. The reprogramming of cancer cells via induced pluripotent stem cell (iPSC) technology is a novel therapy for the treatment and for the study of CSC-related genes. This technology has advantages for studying the interactions between CSC-related genes and the cancer niche microenvironment. This technology may also provide a useful platform for studying the genes involved in the generation of CSCs before and after reprogramming, and for elucidating the mechanisms underlying cancer initiation and progression. The present review summarizes the current understanding of transcription factors involved in the generation of liver CSCs from liver cancer cell-derived iPSCs and how these contribute to oncogenesis, and discusses the modeling of liver cancer development.

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