Translational Medicine II. (Poster discussion will take place in the Aula during the Coffee Break)
Previous experiments demonstrated that 3 times Modulated Electro Hyperthermia Treatments (mEHT) of 4T1 Triple Negative Breast Cancer (TNBC) mouse model caused acute phase reaction (APR), optimization of the systemic innate immune response and inhibition of tumor growth. Besides, mEHT has elevated Cyclooxygenase2(COX2) and proinflammatory cytokines - IL1 beta and IL6 synthesis. Conversely, mEHT did not stimulate adaptive immune response and secondary immunogenic cell death in our TNBC (4T1, 4T07) models significantly. Descriptive effect of mEHT could be considered as a part of the inflammation, which might have multifaceted roles in tumorigenesis, including immunosurveillance or tumor promoting effects by supporting tumor favorable microenvironment (TME). We hypothesized, that anti-inflammatory therapy could enhance the effect of mEHT. Our group has already studied Acetylsalicylic acid (ASA) and mEHT synergistic effects on melanoma B16F10 cancer model in vivo. In our current research, we combined mEHT with selective (SC236) and non-selective (ASA) COX2 inhibitors on the 4T1 TNBC model, that demonstrated significant diminution of tumor growth and bigger tumor destruction ratio (TDR) compared to mEHT mono therapy. Tumor favorable microenvironment inhibition can be one of the probable explanations of the abovementioned synergism, which molecular mechanism is going to be investigated further.
Funding: EFOP-3.6.3-VEKOP-16-2017-00009