Physical nanoscale conduit-mediated communication between tumour cells and the endothelium modulates endothelial phenotype.
Yamicia ConnorSarah TekleabShyama NandakumarCherelle WallsYonatan TekleabAmjad HusainOr GadishVenkata SabbisettiShelly KaushikSeema SehrawatAshish KulkarniHarold DvorakBruce ZetterElazer R EdelmanShiladitya SenguptaPublished in: Nature communications (2015)
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.
Keyphrases
- nitric oxide
- atomic force microscopy
- squamous cell carcinoma
- small cell lung cancer
- papillary thyroid
- physical activity
- mental health
- endothelial cells
- high speed
- induced apoptosis
- single cell
- single molecule
- stem cells
- risk factors
- type diabetes
- mesenchymal stem cells
- coronary artery disease
- drug delivery
- childhood cancer
- lymph node metastasis
- cancer therapy
- stress induced