“…Mast cells (MCs) are a portion of innate immunity and their participation in the initiation of allergic reactions and the pathogenesis of allergic diseases has been well documented (Elieh Ali Komi & Bjermer, 2019). Their presence in TME gained attention for several reasons: (a) MCs express a wide range of receptors for cytokines, chemokines, complement, and immunoglobulins, that enables them to respond to various signals within TME (i.e., tumor cells produce stem cell factor, the key survival and growth factor of MCs, which acts through MC‐expressed c‐KIT) (Komi & Redegeld, 2020), (b) MCs upon activation degranulate and release three categories of mediators (preformed such as histamine, heparin, chymase, tryptase, de novo synthesized mediators, and later cytokines of which several are involved in tumor biology; Elieh Ali Komi et al, 2020), (c) promising results of tyrosine kinase inhibitors targeting C‐kit signaling and their effectiveness in different tumor types (Sheikh et al, 2022), (d) MCs accumulate in many tumors and their accumulation is associated to better or poor prognosis based on the tumor type (Dantas et al, 2017; Molin et al, 2002), (e) increased levels of MC specific mediators in serum of patients, which is associated to the prognosis or are suggested as markers for monitoring the chemotherapy (Goffredo et al, 2013; Ranieri et al, 2015; Sperr et al, 2009).…”