AI Article Synopsis

  • Extracellular vesicles (EVs), including tumor-derived exosomes, play significant roles in cancer development by transporting mediators from cancer cells and reflecting the tumor environment.
  • Current research focuses on identifying molecules in these exosomes that contribute to tumor growth and metastasis, as well as the mechanisms that allow their inclusion.
  • Bacterial outer membrane vesicles (OMVs) are also linked to gastrointestinal tumors and inflammation, suggesting that both eukaryotic and microbial EVs are crucial for cell communication, tumor survival, and drug resistance, thus highlighting potential new therapies for GI cancer.

Article Abstract

The production and secretion of extracellular vesicles (EVs) are common features of cells (including various normal cells, neoplastic cell lines as well as bacteria) that span all domains of life. Tumor-derived exosomes are enriched with kinds of tumorigenesis mediators which are derived from the cytoplasm of cancer cells and fully reflect the tumor conditions. Indeed, the major topics and challenges on current oncological research are the identification of tumorigenic and metastatic molecules in tumor-cell-derived exosomes as well as elucidating the pathways that guarantee these components to be included in exosomes. The bacterial EVs have also been implicated in the pathogenesis of gastrointestinal (GI) tumors and chronic inflammatory diseases; however, the possible function of outer membrane vesicles (OMVs) in tumorigenesis remains largely underestimated. We suggest that EVs from both eukaryotic cells and different microbes in GI tract act as regulators of intracellular and cross-species communication, thus particularly facilitate tumor cell survival and multi-drug resistance. Therefore, our review introduces comprehensive knowledge on the promising role of EVs (mainly exosomes and OMVs) production of GI cancer development and gut microbiome, as well as its roles in developing novel therapeutic strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085842PMC

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