Cell Reprogramming Techniques: Contributions to Cancer Therapy.


Journal

Cellular reprogramming
ISSN: 2152-4998
Titre abrégé: Cell Reprogram
Pays: United States
ID NLM: 101528176

Informations de publication

Date de publication:
08 2023
Historique:
medline: 18 8 2023
pubmed: 2 8 2023
entrez: 2 8 2023
Statut: ppublish

Résumé

The reprogramming of terminally differentiated cells over the past few years has become important for induced pluripotent stem cells (iPSCs) in the field of regenerative medicine and disease drug modeling. At the same time, iPSCs have also played an important role in human cancer research. iPSCs derived from cancer patients can be used to simulate the early progression of cancer, for drug testing, and to study the molecular mechanism of cancer occurrence. In recent years, with the application of cellular immunotherapy in cancer therapy, patient-derived iPSC-induced immune cells (T, natural killer, and macrophage cells) solve the problem of immune rejection and have higher immunogenicity, which greatly improves the therapeutic efficiency of immune cell therapy. With the continuous progress of cancer differentiation therapy, iPSC technology can reprogram cancer cells to a more primitive pluripotent undifferentiated state, and successfully reverse cancer cells to a benign phenotype by changing the epigenetic inheritance of cancer cells. This article reviews the recent progress of cell reprogramming technology in human cancer research, focuses on the application of reprogramming technology in cancer immunotherapy and the problems solved, and summarizes the malignant phenotype changes of cancer cells in the process of reprogramming and subsequent differentiation.

Identifiants

pubmed: 37530737
doi: 10.1089/cell.2023.0011
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

142-153

Auteurs

Tongtong Guo (T)

College of Life Science, Northwest University, Xi'an, China.

Qi Wei (Q)

Wuhan Institute of Technology, Wuhan, China.

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Classifications MeSH