<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(3)</volume><submitter>Peng L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Combining Endostar (ES) with radiotherapy (RT) has shown a promising therapeutic effect on non-small cell lung carcinoma with brain metastases (BMs) in clinical practice. However, the specific mechanism is not yet fully understood. The present study aimed to investigate the effects of ES on blood vessels, tumor-associated macrophages (TAMs), and T cells in a tumor microenvironment treated with RT.&lt;h4>Methods&lt;/h4>BM models were established by stereotactic and intracarotid injection of luciferase-Lewis lung cancer (LLC) cells into female C57BL mice. The animals were randomly divided into 4 groups: normal saline (NS), ES, RT, and ES plus radiotherapy (ES + RT) groups. Tumor size was determined with the IVIS imaging system. Tumor specimens were stained with CD34 and α-SMA to</pubmed_abstract><journal>Translational lung cancer research</journal><pagination>745-760</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7354151</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The effect of combining Endostar with radiotherapy on blood vessels, tumor-associated macrophages, and T cells in brain metastases of Lewis lung cancer.</pubmed_title><pmcid>PMC7354151</pmcid><pubmed_authors>Fei S</pubmed_authors><pubmed_authors>Dong X</pubmed_authors><pubmed_authors>Wei C</pubmed_authors><pubmed_authors>Ma H</pubmed_authors><pubmed_authors>Peng L</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Tong F</pubmed_authors><pubmed_authors>Wu G</pubmed_authors></additional><is_claimable>false</is_claimable><name>The effect of combining Endostar with radiotherapy on blood vessels, tumor-associated macrophages, and T cells in brain metastases of Lewis lung cancer.</name><description>&lt;h4>Background&lt;/h4>Combining Endostar (ES) with radiotherapy (RT) has shown a promising therapeutic effect on non-small cell lung carcinoma with brain metastases (BMs) in clinical practice. However, the specific mechanism is not yet fully understood. The present study aimed to investigate the effects of ES on blood vessels, tumor-associated macrophages (TAMs), and T cells in a tumor microenvironment treated with RT.&lt;h4>Methods&lt;/h4>BM models were established by stereotactic and intracarotid injection of luciferase-Lewis lung cancer (LLC) cells into female C57BL mice. The animals were randomly divided into 4 groups: normal saline (NS), ES, RT, and ES plus radiotherapy (ES + RT) groups. Tumor size was determined with the IVIS imaging system. Tumor specimens were stained with CD34 and α-SMA to</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2025-06-01T00:33:27.264Z</modification><creation>2024-11-13T05:22:27.322Z</creation></dates><accession>S-EPMC7354151</accession><cross_references><pubmed>32676336</pubmed><doi>10.21037/tlcr-20-500</doi></cross_references></HashMap>