2026-10-16T01:19:27Z https://data.mendeley.com/oai

oai:data.mendeley.com/5ttrnmvjjx.4 2022-04-14T14:35:15Z

Jia, Qingzhu Tumors hijack erythropoiesis for myelopoiesis and immunosuppression Mendeley Data Despite the unprecedented success of immune checkpoint inhibitors (ICIs) as anti-cancer therapy, it remains a prevailing clinical need to identify additional mechanisms underlying ICIs therapeutic efficacy and potential drug resistance. Here, using lineage tracking in cancer patients and tumor-bearing mice, we demonstrate that erythroid progenitor cells lose their developmental potential and switch to the myeloid lineage. Single-cell transcriptome analyses reveal that, notwithstanding quantitative differences in erythroid gene expression, erythroid differentiated myeloid cells (EDMCs) are transcriptionally indistinguishable from their myeloid-originated counterparts. EDMCs possess multifaceted machinery to curtail T cell-mediated anti-tumor responses. Consequently, the EDMCs content within tumor tissues is negatively associated with T cell inflammation for the majority of solid cancers; moreover, EDMCs enrichment, in accordance with anemia manifestation, is predictive of poor prognosis in various cohorts of patients undergoing ICIs therapy. Together, our findings reveal a feed-forward mechanism by which tumors exploit anemia-triggered erythropoiesis for myeloid transdifferentiation and immunosuppression. RNA Sequencing Dataset doi:10.17632/5ttrnmvjjx.4 oai:data.mendeley.com/5ttrnmvjjx.4 Creative Commons Attribution 4.0 International http://creativecommons.org/licenses/by/4.0 https://data.mendeley.com/datasets/5ttrnmvjjx 2022-04-14T14:35:15Z 2022-05-11T23:59:59Z