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Physical nanoscale conduit-mediated communication between tumour cells and the endothelium modulates endothelial phenotype

Author

Listed:
  • Yamicia Connor

    (Harvard-MIT Division of Health Sciences and Technology
    Massachusetts Institute of Technology
    Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA
    Harvard Medical School)

  • Sarah Tekleab

    (Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA)

  • Shyama Nandakumar

    (Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA)

  • Cherelle Walls

    (Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA)

  • Yonatan Tekleab

    (Massachusetts Institute of Technology)

  • Amjad Husain

    (Harvard Medical School
    Beth Israel Deaconess Medical Center)

  • Or Gadish

    (Harvard-MIT Division of Health Sciences and Technology
    Massachusetts Institute of Technology)

  • Venkata Sabbisetti

    (Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA
    Harvard Medical School)

  • Shelly Kaushik

    (India Innovation Research Center)

  • Seema Sehrawat

    (Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA)

  • Ashish Kulkarni

    (Harvard-MIT Division of Health Sciences and Technology
    Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA
    Harvard Medical School)

  • Harold Dvorak

    (Harvard Medical School
    Beth Israel Deaconess Medical Center)

  • Bruce Zetter

    (Harvard Medical School
    Children’s Hospital, Boston, Massachusetts 02115, USA
    Dana Farber Cancer Institute)

  • Elazer R. Edelman

    (Harvard-MIT Division of Health Sciences and Technology
    Massachusetts Institute of Technology
    Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA
    Harvard Medical School)

  • Shiladitya Sengupta

    (Harvard-MIT Division of Health Sciences and Technology
    Brigham and Women’s Hospital, 65 Landsdowne Street, Room 317, Boston, Massachusetts 02115, USA
    Harvard Medical School
    Dana Farber Cancer Institute)

Abstract

Metastasis is a major cause of mortality and remains a hurdle in the search for a cure for cancer. Not much is known about metastatic cancer cells and endothelial cross-talk, which occurs at multiple stages during metastasis. Here we report a dynamic regulation of the endothelium by cancer cells through the formation of nanoscale intercellular membrane bridges, which act as physical conduits for transfer of microRNAs. The communication between the tumour cell and the endothelium upregulates markers associated with pathological endothelium, which is reversed by pharmacological inhibition of these nanoscale conduits. These results lead us to define the notion of ‘metastatic hijack’: cancer cell-induced transformation of healthy endothelium into pathological endothelium via horizontal communication through the nanoscale conduits. Pharmacological perturbation of these nanoscale membrane bridges decreases metastatic foci in vivo. Targeting these nanoscale membrane bridges may potentially emerge as a new therapeutic opportunity in the management of metastatic cancer.

Suggested Citation

  • Yamicia Connor & Sarah Tekleab & Shyama Nandakumar & Cherelle Walls & Yonatan Tekleab & Amjad Husain & Or Gadish & Venkata Sabbisetti & Shelly Kaushik & Seema Sehrawat & Ashish Kulkarni & Harold Dvora, 2015. "Physical nanoscale conduit-mediated communication between tumour cells and the endothelium modulates endothelial phenotype," Nature Communications, Nature, vol. 6(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms9671
    DOI: 10.1038/ncomms9671
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    Cited by:

    1. Sarah Renaud & Anthony Lefebvre & Olivier Moralès & Nadira Delhem, 2019. "Mini Review - Exosomes from Discovery to Isolation," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 15(2), pages 11286-11293, February.

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