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Effect of melanoma stem cells on melanoma metastasis.
Yin, Qiliang; Shi, Xiumin; Lan, Shijie; Jin, Haofan; Wu, Di.
Afiliación
  • Yin Q; Department of Tumor Center, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
  • Shi X; Department of Tumor Center, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
  • Lan S; Department of Tumor Center, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
  • Jin H; Department of Tumor Center, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
  • Wu D; Department of Tumor Center, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Oncol Lett ; 22(1): 566, 2021 Jul.
Article en En | MEDLINE | ID: mdl-34113394
ABSTRACT
Cancer stem cells (CSCs) are involved in the metastatic process, the resistance of many types of cancer to therapeutic treatments and consequently the onset of recurrences. The CSC concept therefore significantly extends our understanding of melanoma biology. More recently, melanoma stem cells (MSCs) have been described in melanoma as expressing specific biomarkers. These primitive melanoma cells are not only capable of self-renewal and differentiation plasticity, but may also confer virulence via immune evasion and multidrug resistance, and potentially, via vasculogenic mimicry and transition to migratory and metastasizing derivatives. This review will present the specific biomarkers of MSCs, including CD133, ATP binding cassette subfamily B member 5, CD271, CD20 and aldehyde dehydrogenase, which can regulate the transduction of tumor-related signals. These signal molecules can reversely act on tumor cells and regulate tumor angiogenesis, leading to the occurrence of melanoma metastasis. Targeting these specific biomarkers could inhibit the progression of melanoma and may help the development of novel therapeutic strategies for melanoma.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Oncol Lett Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Oncol Lett Año: 2021 Tipo del documento: Article
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