<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hu R</submitter><funding>Natural Science Foundation of Liaoning Province</funding><funding>National Natural Science Foundation of China</funding><pagination>48</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10949598</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Breast cancer stem cell (CSC) expansion results in tumor progression and chemoresistance; however, the modulation of CSC pluripotency remains unexplored. Transmembrane protein 120B (TMEM120B) is a newly discovered protein expressed in human tissues, especially in malignant tissues; however, its role in CSC expansion has not been studied. This study aimed to determine the role of TMEM120B in transcriptional coactivator with PDZ-binding motif (TAZ)-mediated CSC expansion and chemotherapy resistance.&lt;h4>Methods&lt;/h4>Both bioinformatics analysis and immunohistochemistry assays were performed to examine expression patterns of TMEM120B in lung, breast, gastric, colon, and ovarian cancers. Clinicopathological factors and overall survival were also evaluated. Next, colony formati</pubmed_abstract><journal>Breast cancer research : BCR</journal><pubmed_title>TMEM120B strengthens breast cancer cell stemness and accelerates chemotherapy resistance via β1-integrin/FAK-TAZ-mTOR signaling axis by binding to MYH9.</pubmed_title><pmcid>PMC10949598</pmcid><funding_grant_id>82002890</funding_grant_id><funding_grant_id>2021-MS-163</funding_grant_id><funding_grant_id>2020- MS-183</funding_grant_id><funding_grant_id>2020-MS-173</funding_grant_id><pubmed_authors>Deng N</pubmed_authors><pubmed_authors>Yang K</pubmed_authors><pubmed_authors>Fan M</pubmed_authors><pubmed_authors>Ma X</pubmed_authors><pubmed_authors>Ying J</pubmed_authors><pubmed_authors>Zhao T</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Hou Y</pubmed_authors><pubmed_authors>Guan M</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Hu R</pubmed_authors></additional><is_claimable>false</is_claimable><name>TMEM120B strengthens breast cancer cell stemness and accelerates chemotherapy resistance via β1-integrin/FAK-TAZ-mTOR signaling axis by binding to MYH9.</name><description>&lt;h4>Background&lt;/h4>Breast cancer stem cell (CSC) expansion results in tumor progression and chemoresistance; however, the modulation of CSC pluripotency remains unexplored. Transmembrane protein 120B (TMEM120B) is a newly discovered protein expressed in human tissues, especially in malignant tissues; however, its role in CSC expansion has not been studied. This study aimed to determine the role of TMEM120B in transcriptional coactivator with PDZ-binding motif (TAZ)-mediated CSC expansion and chemotherapy resistance.&lt;h4>Methods&lt;/h4>Both bioinformatics analysis and immunohistochemistry assays were performed to examine expression patterns of TMEM120B in lung, breast, gastric, colon, and ovarian cancers. Clinicopathological factors and overall survival were also evaluated. Next, colony formati</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-01T17:24:12.078Z</modification><creation>2025-04-06T07:45:26.224Z</creation></dates><accession>S-EPMC10949598</accession><cross_references><pubmed>38504374</pubmed><doi>10.1186/s13058-024-01802-z</doi></cross_references></HashMap>