posted on 2018-10-15, 14:46authored byVeronica Gatti, Claudia Fierro, Mirco Compagnone, Federica Giangrazi, Elke Katrin Markert, Lucilla Bongiorno-Borbone, Gerry Melino, Angelo Peschiaroli
Triple negative breast cancers (TNBC) represent the most aggressive and clinically relevant breast carcinomas. On the basis of specific molecular signature, the majority of TNBC can be classified as basal-like breast carcinoma. Here, we report data showing that in basal-like breast carcinoma cells ΔNp63 is capable of sustaining the production of the hyaluronic acid (HA), one of the major component of the extracellular matrix (ECM). At molecular level, we found that ΔNp63 regulates the expression of HA-related genes, such as the HA synthase HAS3, the hyaluronidase HYAL-1 and CD44, the major HA cell membrane receptor. By controlling this pathway, ∆Np63 contributes to maintain the self-renewal of breast cancer stem cells. Importantly, high HAS3 expression is a negative prognostic factor of TNBC patients. Our data suggest that in basal-type breast carcinoma ∆Np63 might favor a HA-rich microenviroment, which can sustain tumor proliferation and stemness.
Funding
This work has been supported by the MFAG AIRC #15523 grant awarded to A.P. Partial support has been also provided by the Medical Research Council (UK) and AIRC Grant IG-20473 to G.M.