作者: Marco Cippitelli , Cinzia Fionda , Helena Stabile , Angela Santoni , Angela Gismondi
DOI: 10.3390/IJMS22031103
关键词: Cancer research 、 Cancer 、 Cancer cell 、 Immune system 、 Transcription factor 、 Biology 、 Cytotoxic T cell 、 Multiple myeloma 、 B cell 、 Lymphocyte
摘要: The Ikaros zing-finger family transcription factors (IKZF TFs) are important regulators of lymphocyte development and differentiation also highly expressed in B cell malignancies, including Multiple Myeloma (MM), where they required for cancer growth survival. Moreover, IKZF TFs negatively control the functional properties many immune cells. Thus, targeting these proteins has relevant therapeutic implications cancer. Indeed, accumulating evidence demonstrated that downregulation Aiolos, two members family, malignant plasma cells as well adaptative innate lymphocytes, is key anti-myeloma activity Immunomodulatory drugs (IMiDs). This review focused on TF-related pathways MM. In particular, we will address how depletion exerts cytotoxic effects MM cells, by reducing their survival proliferation, concomitantly potentiates antitumor response, thus contributing to efficacy IMiDs, a cornerstone treatment this neoplasia.