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. Author manuscript; available in PMC: 2020 May 15.
Published in final edited form as: Cancer Res. 2019 Oct 1;79(22):5826–5838. doi: 10.1158/0008-5472.CAN-19-1058

Figure 2.

Figure 2.

Murine and human cancers increase circulating pre-B-like cells, as revealed by FACS phenotyping in the indicated tissues and primary tumors of BALB/c mice with 4T1 cancer (n=14–32; shown frequency, A, and absolute numbers, B, of CD25+ Pre-B-like cells ) and C57BL/6 mice with spontaneous ovarian cancer (n=6–13, mogp, C). Mice with EMT6 cells, despite having a larger tumor than 4T1 cells (D), inefficiently increased CD25+pre-B-like cells (E, n=5, the result was reproduced twice). Compared with healthy people (HD, n=18), peripheral blood of humans with breast cancer markedly increased the frequency of CD10+CD19+ B cells (BC, n=85, F). RT/PCR assay confirmed expression of RAG1, RAG2, and VPREB in tumor infiltrating B cells in humans with BC (TIL-B, n=5, relative to GAPDH, G). Controls were tonsils (n=2, G). AF, each symbol is for a single mouse or human and G shows mean ± SD. *p < 0.05, **p < 0.01, ***p < 0.001; ns, not significant in Mann-Whitney Wilcoxon t-test (AF).