{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["2020"],"submitter":["Li Y"],"pubmed_abstract":["<h4>Background</h4>Tissue-resident macrophages can be educated to tumor-associated macrophages (TAMs) by the tumor microenvironment and many types of macrophages express erythropoietic receptor (EPOR); However, little is known about the expression of EPOR on TAMs and the identity of EPOR<sup>+</sup> TAMs in osteosarcoma lung metastasis has thus far remained elusive.<h4>Methods</h4>EPOR-eGFPcre mice were used to determine the expression of EPOR on lung tissue-resident macrophages. Flow cytometry, RT-PCR, and Western blot were examined to define the identity of EPOR<sup>+</sup> TAMs in 106 osteosarcoma lung metastasis specimens. Moreover, the clinicopathologic factors and prognosis of patients with CD163<sup>+</sup>EPOR<sup>+</sup> macrophages were compared.<h4>Results</h4>We found that a subpopulation of mouse lung tissue-resident macrophages express EPOR and EPO enhances the proliferation of EPOR<sup>+</sup> macrophages in mouse lung. A subpopulation of CD163<sup>+</sup> macrophages expresses EPOR in human osteosarcoma lung metastasis specimens. CD163<sup>+</sup>EPOR<sup>+</sup>TAMs increase 2.5 times in human osteosarcoma lung metastasis tissues; CD206, CD163, and PD1, which are known to have a significant role in TAM function had high expression in CD163<sup>+</sup>EPOR<sup>+</sup> TAMs compared with CD163<sup>+</sup>EPOR<sup>-</sup> TAMs. Furthermore, CD163<sup>+</sup>EPOR<sup>+</sup> TAMs had higher M2 marker and cytokine expression in osteosarcoma tissues compared with para-osteosarcoma tissues. EPO enhanced the expression of M2 cytokines in primary CD163<sup>+</sup>EPOR<sup>+</sup> TAMs. Importantly, the percentage of CD163<sup>+</sup>EPOR<sup>+</sup> TAMs had a positive linear association with malignant phenotypes as well as poor disease-free survival and overall survival time.<h4>Conclusions</h4>We have characterized TAMs expressing EPOR and CD163<sup>+</sup>EPOR<sup>+</sup> macrophages as TAMs in osteosarcoma lung metastasis patients, which are highly associated with tumor aggressiveness."],"journal":["Journal of immunology research"],"pagination":["9374240"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7450330"],"repository":["biostudies-literature"],"pubmed_title":["Identification and Functional Analysis of EPOR<sup>+</sup> Tumor-Associated Macrophages in Human Osteosarcoma Lung Metastasis."],"pmcid":["PMC7450330"],"pubmed_authors":["Wu J","Li Y","Wei R","Li M"],"additional_accession":[]},"is_claimable":false,"name":"Identification and Functional Analysis of EPOR<sup>+</sup> Tumor-Associated Macrophages in Human Osteosarcoma Lung Metastasis.","description":"<h4>Background</h4>Tissue-resident macrophages can be educated to tumor-associated macrophages (TAMs) by the tumor microenvironment and many types of macrophages express erythropoietic receptor (EPOR); However, little is known about the expression of EPOR on TAMs and the identity of EPOR<sup>+</sup> TAMs in osteosarcoma lung metastasis has thus far remained elusive.<h4>Methods</h4>EPOR-eGFPcre mice were used to determine the expression of EPOR on lung tissue-resident macrophages. Flow cytometry, RT-PCR, and Western blot were examined to define the identity of EPOR<sup>+</sup> TAMs in 106 osteosarcoma lung metastasis specimens. Moreover, the clinicopathologic factors and prognosis of patients with CD163<sup>+</sup>EPOR<sup>+</sup> macrophages were compared.<h4>Results</h4>We found that a subpopulation of mouse lung tissue-resident macrophages express EPOR and EPO enhances the proliferation of EPOR<sup>+</sup> macrophages in mouse lung. A subpopulation of CD163<sup>+</sup> macrophages expresses EPOR in human osteosarcoma lung metastasis specimens. CD163<sup>+</sup>EPOR<sup>+</sup>TAMs increase 2.5 times in human osteosarcoma lung metastasis tissues; CD206, CD163, and PD1, which are known to have a significant role in TAM function had high expression in CD163<sup>+</sup>EPOR<sup>+</sup> TAMs compared with CD163<sup>+</sup>EPOR<sup>-</sup> TAMs. Furthermore, CD163<sup>+</sup>EPOR<sup>+</sup> TAMs had higher M2 marker and cytokine expression in osteosarcoma tissues compared with para-osteosarcoma tissues. EPO enhanced the expression of M2 cytokines in primary CD163<sup>+</sup>EPOR<sup>+</sup> TAMs. Importantly, the percentage of CD163<sup>+</sup>EPOR<sup>+</sup> TAMs had a positive linear association with malignant phenotypes as well as poor disease-free survival and overall survival time.<h4>Conclusions</h4>We have characterized TAMs expressing EPOR and CD163<sup>+</sup>EPOR<sup>+</sup> macrophages as TAMs in osteosarcoma lung metastasis patients, which are highly associated with tumor aggressiveness.","dates":{"release":"2020-01-01T00:00:00Z","publication":"2020","modification":"2024-02-14T23:49:08.987Z","creation":"2020-09-12T07:07:03Z"},"accession":"S-EPMC7450330","cross_references":{"pubmed":["32908942"],"doi":["10.1155/2020/9374240"]}}