Furthermore, using flow cytometry, Costa et al. showed that fibroblasts in breast cancer could be divided into four populations (CAF-S1 to S4), according to the expression of commonly used markers such as FAPα, αSMA, FSP1, PDGFRβ and Caveolin, demonstrating an immunosuppressive role of CAF-S1 in the TME [37]. The gene discussed is ACTA1; the disease is breast cancer.