PTPRR and breast cancer: Furthermore, by subdividing basal cells into BC-ES, BC-AS1, and BC-AS2 based on pseudotime, we were able to elucidate how BC-ES cells transition in different directions and how they interact with neighboring subpopulations (SC and IFI27+) via multiple signaling pathways—such as NOTCH, PTPR, and PERIOSTIN—which exhibit distinct characteristics along each branch.