Ontology highlight
ABSTRACT: Objective
To investigate the clinical relevance of common myeloid progenitor (CMP) cells in breast tumor microenvironment (TME).Background
The role of rare cells in TME is less studied. In Silico transcriptomic analyses of real-world data enable us to detect and quantify rare cells, including CMP cells.Methods
A total of 5176 breast cancer (BC) patients from SCAN-B, METABRIC, and 5 single-cell sequence cohorts were analyzed using the xCell algorithm. The high group was defined as more than two-thirds of the CMP scores in each cohort.Results
CMP cells consist of 0.07% to 0.25% of bulk breast tumor cells, more in estrogen receptor-positive (ER+) compared with triple-negative (TN) subtype (0.1% to 0.75%, 0.18% to 0.33% of immune cells, respectively). CMP cells
SUBMITTER: Oshi M
PROVIDER: S-EPMC11797412 | biostudies-literature | 2024 Oct
REPOSITORIES: biostudies-literature