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Article

Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient

  • Authors:
    • Mitsuru Chiba
    • Shiori Kubota
    • Ayaka Sakai
    • Satoru Monzen
  • View Affiliations / Copyright

    Affiliations: Department of Bioscience and Laboratory Medicine, Graduate School of Health Sciences, Hirosaki University, Hirosaki, Aomori 036‑8564, Japan, Department of Medical Technology, Graduate School of Health Sciences, Hirosaki University, Hirosaki, Aomori 036‑8564, Japan, Department of Radiation Science, Graduate School of Health Sciences, Hirosaki University, Hirosaki, Aomori 036‑8564, Japan
  • Pages: 3989-3996
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    Published online on: August 9, 2018
       https://doi.org/10.3892/mmr.2018.9376
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Abstract

Despite existing multimodal therapies, pancreatic cancer exhibits high metastatic capability and poor prognosis. Extracellular vesicles (EVs) are nanoparticles comprising lipid bilayers and various other components, such as protein and nucleic acids, derived from secreted cells. Recent research has demonstrated the involvement of EVs released from cancer cells in the metastasis of cancer cells to distant organs. However, the effects of EVs released from pancreatic cancer cells on other pancreatic cancer cells in a tumor microenvironment remain unclear. The present study aimed to elucidate that EVs released from PK‑45H pancreatic cancer cells are taken up by PK‑45P pancreatic cancer cells derived from the same patient through dynamin‑related endocytosis. Additionally, EVs released from PK‑45H cells augment the phosphorylation of classical mitogen‑activated protein kinase (MAPK) pathways in PK‑45P cells. The uptake of EVs released from PK‑45H cells by PK‑45P cells stimulates cell migration through the classical MAPK‑dependent pathway, suggesting that EVs released from one pancreatic cancer cell are taken up by other surrounding pancreatic cancer cells and could be critical inducers of cancer metastasis in the tumor microenvironment.
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Copy and paste a formatted citation
Spandidos Publications style
Chiba M, Kubota S, Sakai A and Monzen S: Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient. Mol Med Rep 18: 3989-3996, 2018.
APA
Chiba, M., Kubota, S., Sakai, A., & Monzen, S. (2018). Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient. Molecular Medicine Reports, 18, 3989-3996. https://doi.org/10.3892/mmr.2018.9376
MLA
Chiba, M., Kubota, S., Sakai, A., Monzen, S."Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient". Molecular Medicine Reports 18.4 (2018): 3989-3996.
Chicago
Chiba, M., Kubota, S., Sakai, A., Monzen, S."Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient". Molecular Medicine Reports 18, no. 4 (2018): 3989-3996. https://doi.org/10.3892/mmr.2018.9376
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Spandidos Publications style
Chiba M, Kubota S, Sakai A and Monzen S: Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient. Mol Med Rep 18: 3989-3996, 2018.
APA
Chiba, M., Kubota, S., Sakai, A., & Monzen, S. (2018). Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient. Molecular Medicine Reports, 18, 3989-3996. https://doi.org/10.3892/mmr.2018.9376
MLA
Chiba, M., Kubota, S., Sakai, A., Monzen, S."Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient". Molecular Medicine Reports 18.4 (2018): 3989-3996.
Chicago
Chiba, M., Kubota, S., Sakai, A., Monzen, S."Cell‑to‑cell communication via extracellular vesicles among human pancreatic cancer cells derived from the same patient". Molecular Medicine Reports 18, no. 4 (2018): 3989-3996. https://doi.org/10.3892/mmr.2018.9376
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