<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang S</submitter><funding>National High-level Personnel of Special Support Program</funding><funding>Science and Technology Program of Guangzhou</funding><funding>Basic and Applied Basic Research Foundation of Guangdong Province</funding><funding>National Natural Science Foundation of China</funding><funding>China Postdoctoral Science Foundation</funding><funding>The Fundamental Research Funds for The Central Universities</funding><funding>Chinese National Postdoctoral Program for Innovative Talents</funding><funding>Postdoctoral Fellowship Program of CPSF</funding><pagination>81-93</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12703295</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>75(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Circulating tumour cell (CTC)-neutrophil clusters represent a key driver and a hallmark of tumour metastasis; however, efficient approaches for their elimination are still lacking.&lt;h4>Objective&lt;/h4>This study sought to elucidate the location and mechanisms of CTC-neutrophil cluster formation and develop more effective antimetastasis strategies.&lt;h4>Design&lt;/h4>Immunofluorescence staining of clinical colorectal cancer (CRC) samples was performed to identify the location of CTC-neutrophil clusters. The correlation between the expression of nicotinamide N-methyltransferase (NNMT) in pericytes and patient prognosis, as well as its association with CTC-neutrophil cluster formation, was assessed using clinical specimens and public CRC datasets. The formation process of CTC-neutr</pubmed_abstract><journal>Gut</journal><pubmed_title>Pericyte drives the formation of circulating tumour cell-neutrophil clusters to promote colorectal cancer metastasis.</pubmed_title><pmcid>PMC12703295</pmcid><funding_grant_id>82304526</funding_grant_id><funding_grant_id>BX20230144</funding_grant_id><funding_grant_id>2023M731323</funding_grant_id><funding_grant_id>82404673</funding_grant_id><funding_grant_id>82273941</funding_grant_id><funding_grant_id>2023A1515110210</funding_grant_id><funding_grant_id>82473950</funding_grant_id><funding_grant_id>U24A20815</funding_grant_id><funding_grant_id>82403529</funding_grant_id><funding_grant_id>Dongmei Zhang and Minfeng Chen</funding_grant_id><funding_grant_id>21624103</funding_grant_id><funding_grant_id>2025A04J3400</funding_grant_id><funding_grant_id>2023M741391</funding_grant_id><funding_grant_id>GZB20230268</funding_grant_id><funding_grant_id>2025A04J5158</funding_grant_id><funding_grant_id>82204428</funding_grant_id><funding_grant_id>82293681(82293680)</funding_grant_id><funding_grant_id>82430108</funding_grant_id><funding_grant_id>2024A1515013086</funding_grant_id><funding_grant_id>2024B1515020098</funding_grant_id><funding_grant_id>2023B1515120023</funding_grant_id><pubmed_authors>Deng R</pubmed_authors><pubmed_authors>Qi M</pubmed_authors><pubmed_authors>Huang D</pubmed_authors><pubmed_authors>Zhang D</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Huang M</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Ye W</pubmed_authors><pubmed_authors>Shuai H</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Qiu S</pubmed_authors><pubmed_authors>Cheng M</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Yuan X</pubmed_authors><pubmed_authors>Tan L</pubmed_authors><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Chu X</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Pan J</pubmed_authors><pubmed_authors>Lin C</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Shi C</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Ye G</pubmed_authors><pubmed_authors>Zeng H</pubmed_authors><pubmed_authors>Xu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pericyte drives the formation of circulating tumour cell-neutrophil clusters to promote colorectal cancer metastasis.</name><description>&lt;h4>Background&lt;/h4>Circulating tumour cell (CTC)-neutrophil clusters represent a key driver and a hallmark of tumour metastasis; however, efficient approaches for their elimination are still lacking.&lt;h4>Objective&lt;/h4>This study sought to elucidate the location and mechanisms of CTC-neutrophil cluster formation and develop more effective antimetastasis strategies.&lt;h4>Design&lt;/h4>Immunofluorescence staining of clinical colorectal cancer (CRC) samples was performed to identify the location of CTC-neutrophil clusters. The correlation between the expression of nicotinamide N-methyltransferase (NNMT) in pericytes and patient prognosis, as well as its association with CTC-neutrophil cluster formation, was assessed using clinical specimens and public CRC datasets. The formation process of CTC-neutr</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-07T05:00:09.832Z</modification><creation>2026-06-07T03:06:32.652Z</creation></dates><accession>S-EPMC12703295</accession><cross_references><pubmed>40701795</pubmed><doi>10.1136/gutjnl-2024-334618</doi></cross_references></HashMap>