<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(24)</volume><submitter>Wang F</submitter><pubmed_abstract>In this study, we comprehensively charted the cellular landscape of colorectal cancer (CRC) and well-matched liver metastatic CRC using single-cell and spatial transcriptome RNA sequencing. We generated 41,892 CD45&lt;sup>-&lt;/sup> nonimmune cells and 196,473 CD45&lt;sup>+&lt;/sup> immune cells from 27 samples of six CRC patients, and found that CD8_CXCL13 and CD4_CXCL13 subsets increased significantly in liver metastatic samples that exhibited high proliferation ability and tumor-activating characterization, contributing to better prognosis of patients. Distinct fibroblast profiles were observed in primary and liver metastatic tumors. &lt;i>F3&lt;/i>&lt;sup>+&lt;/sup> fibroblasts enriched in primary tumors contributed to worse overall survival by expressing protumor factors. However, &lt;i>MCAM&lt;/i>&lt;sup>+&lt;/sup> fib</pubmed_abstract><journal>Science advances</journal><pagination>eadf5464</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10275599</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Single-cell and spatial transcriptome analysis reveals the cellular heterogeneity of liver metastatic colorectal cancer.</pubmed_title><pmcid>PMC10275599</pmcid><pubmed_authors>Huang C</pubmed_authors><pubmed_authors>Long J</pubmed_authors><pubmed_authors>Cao J</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Da TT</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Wang XQ</pubmed_authors><pubmed_authors>Yao XQ</pubmed_authors><pubmed_authors>Lian ZX</pubmed_authors><pubmed_authors>Jiang YH</pubmed_authors><pubmed_authors>Ma HQ</pubmed_authors><pubmed_authors>Zhao ZB</pubmed_authors><pubmed_authors>Wu ZX</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell and spatial transcriptome analysis reveals the cellular heterogeneity of liver metastatic colorectal cancer.</name><description>In this study, we comprehensively charted the cellular landscape of colorectal cancer (CRC) and well-matched liver metastatic CRC using single-cell and spatial transcriptome RNA sequencing. We generated 41,892 CD45&lt;sup>-&lt;/sup> nonimmune cells and 196,473 CD45&lt;sup>+&lt;/sup> immune cells from 27 samples of six CRC patients, and found that CD8_CXCL13 and CD4_CXCL13 subsets increased significantly in liver metastatic samples that exhibited high proliferation ability and tumor-activating characterization, contributing to better prognosis of patients. Distinct fibroblast profiles were observed in primary and liver metastatic tumors. &lt;i>F3&lt;/i>&lt;sup>+&lt;/sup> fibroblasts enriched in primary tumors contributed to worse overall survival by expressing protumor factors. However, &lt;i>MCAM&lt;/i>&lt;sup>+&lt;/sup> fib</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2026-05-28T18:43:50.41Z</modification><creation>2025-04-03T22:51:03.928Z</creation></dates><accession>S-EPMC10275599</accession><cross_references><pubmed>37327339</pubmed><doi>10.1126/sciadv.adf5464</doi></cross_references></HashMap>