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Therapy resistance mediated by exosomes

期刊

MOLECULAR CANCER
卷 18, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12943-019-0970-x

关键词

MDR genes; Apoptosis; Cancer stem cells; Immune surveillance; Dormancy; EMT

资金

  1. Austrian Science Fund (FWF) [P29457]
  2. Anniversary Fund of Austrian National Bank [ONB 17620]
  3. Ingrid Shaker-Nessmann Cancer Research Foundation
  4. Austrian Science Fund (FWF) [P29457] Funding Source: Austrian Science Fund (FWF)

向作者/读者索取更多资源

Therapy resistance can arise within tumor cells because of genetic or phenotypic changes (intrinsic resistance), or it can be the result of an interaction with the tumor microenvironment (extrinsic resistance). Exosomes are membranous vesicles 40 to 100nm in diameter constitutively released by almost all cell types, and mediate cell-to-cell communication by transferring mRNAs, miRNAs, DNAs and proteins causing extrinsic therapy resistance. They transfer therapy resistance by anti-apoptotic signalling, increased DNA-repair or delivering ABC transporters to drug sensitive cells. As functional mediators of tumor-stroma interaction and of epithelial to mesenchymal transition, exosomes also promote environment-mediated therapy resistance.Exosomes may be used in anticancer therapy exploiting their delivery function. They may effectively transfer anticancer drugs or RNAs in the context of gene therapy reducing immune stimulatory effects of these drugs and hydrophilic qualities facilitating crossing of cell membranes.

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