Heat stress stimulates colon cancer cells to secret specific population of extracellular nanovesicles enriched by HSP70 and microRNAs

Background. Heat stress (Hs) induces the cellular secretion of heat shock proteins (Hsp) and extracellular nanovesicles (eNVs). the biological link between these phenomena is poorly understood. in the case of colorectal cancer (cRc) cells, the secretion of Hsps and eNV may be involved in the clinical response to intraperitoneal therapy of peritoneal carcinomatosis. material and methods. established colon cancer cell lines colo320, Hct116, Ht29 and dld1 were used. eNVs were isolated from culture media by differential ultra-centrifugation and analyzed by dynamic light scattering, nanoparticle tracking analysis, atomic force microscopy and flow cytometry. super-paramagnetic particles (spmp) covered by antibodies to the membrane form of Hsp70 were used for isolation and quantification of Hsp70(+) eNVs. Vesicular microRNa was assayed by Rt-qpcR. Results. Hs induces the secretion of eNVs by cRc cells, the resistance to Hs correlates with the activity of Hs-induced eNVs secretion. Hs induces the secretion of a specific population of eNVs enriched by membrane form Hsp70 (mHsp70). the microRNa content of mHsp70(+) eNVs has qualitative and quantitative features. the concentration of miR-126-3p, -181-5p, -155-5p, -223 is increased in mHsp70(+) eNVs secreted by three cRc cell lines. conclusion. Hs induces the secretion of mHsp70(+) eNVs by cRc cells. this phenomenon may be involved in a clinical response to intraperitoneal chemo-hyperthermic perfusion therapy of peritoneal carcinomatosis.