<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ray U</submitter><funding>American Cancer Society</funding><funding>NCI NIH HHS</funding><funding>DoD OCRP Ovarian Cancer Academy Award</funding><funding>NIH</funding><funding>ATCC</funding><pagination>1038-1054</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8930558</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>82(6)</volume><pubmed_abstract>Dissemination of ovarian cancer cells can lead to inoperable metastatic lesions in the bowel and omentum that cause patient death. Here we show that LRRC15, a type-I 15-leucine-rich repeat-containing membrane protein, highly overexpressed in ovarian cancer bowel metastases compared with matched primary tumors and acts as a potent promoter of omental metastasis. Complementary models of ovarian cancer demonstrated that LRRC15 expression leads to inhibition of anoikis-induced cell death and promotes adhesion and invasion through matrices that mimic omentum. Mechanistically, LRRC15 interacted with β1-integrin to stimulate activation of focal adhesion kinase (FAK) signaling. As a therapeutic proof of concept, targeting LRRC15 with the specific antibody-drug conjugate ABBV-085 in both early and late metastatic ovarian cancer cell line xenograft models prevented metastatic dissemination, and these results were corroborated in metastatic patient-derived ovarian cancer xenograft models. Furthermore, treatment of 3D-spheroid cultures of LRRC15-positive patient-derived ascites with ABBV-085 reduced cell viability. Overall, these data uncover a role for LRRC15 in promoting ovarian cancer metastasis and suggest a novel and promising therapy to target ovarian cancer metastases.Significance: This study identifies that LRRC15 activates β1-integrin/FAK signaling to promote ovarian cancer metastasis and shows that the LRRC15-targeted antibody-drug conjugate ABBV-085 suppresses ovarian cancer metastasis in preclinical models.</pubmed_abstract><journal>Cancer research</journal><pubmed_title>Targeting LRRC15 Inhibits Metastatic Dissemination of Ovarian Cancer.</pubmed_title><pmcid>PMC8930558</pmcid><funding_grant_id>OVCAR 7/5/10</funding_grant_id><funding_grant_id>P50 CA136393</funding_grant_id><funding_grant_id>TOV21G</funding_grant_id><funding_grant_id>W81XWH-15-0253</funding_grant_id><funding_grant_id>P30 CA015083</funding_grant_id><funding_grant_id>P50CA136393</funding_grant_id><funding_grant_id>RSG-21-019-01-CSM</funding_grant_id><pubmed_authors>Dasari S</pubmed_authors><pubmed_authors>Thirusangu P</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Roy B</pubmed_authors><pubmed_authors>Shridhar V</pubmed_authors><pubmed_authors>Jung DB</pubmed_authors><pubmed_authors>Staub JK</pubmed_authors><pubmed_authors>Hou X</pubmed_authors><pubmed_authors>Sarkar Bhattacharya S</pubmed_authors><pubmed_authors>Mitra AK</pubmed_authors><pubmed_authors>Ray U</pubmed_authors><pubmed_authors>Kannan N</pubmed_authors><pubmed_authors>Roy D</pubmed_authors><pubmed_authors>Bakkum-Gamez JN</pubmed_authors><pubmed_authors>Kaufmann SH</pubmed_authors><pubmed_authors>Purcell JW</pubmed_authors><pubmed_authors>Weroha SJ</pubmed_authors><pubmed_authors>Jin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting LRRC15 Inhibits Metastatic Dissemination of Ovarian Cancer.</name><description>Dissemination of ovarian cancer cells can lead to inoperable metastatic lesions in the bowel and omentum that cause patient death. Here we show that LRRC15, a type-I 15-leucine-rich repeat-containing membrane protein, highly overexpressed in ovarian cancer bowel metastases compared with matched primary tumors and acts as a potent promoter of omental metastasis. Complementary models of ovarian cancer demonstrated that LRRC15 expression leads to inhibition of anoikis-induced cell death and promotes adhesion and invasion through matrices that mimic omentum. Mechanistically, LRRC15 interacted with β1-integrin to stimulate activation of focal adhesion kinase (FAK) signaling. As a therapeutic proof of concept, targeting LRRC15 with the specific antibody-drug conjugate ABBV-085 in both early and late metastatic ovarian cancer cell line xenograft models prevented metastatic dissemination, and these results were corroborated in metastatic patient-derived ovarian cancer xenograft models. Furthermore, treatment of 3D-spheroid cultures of LRRC15-positive patient-derived ascites with ABBV-085 reduced cell viability. Overall, these data uncover a role for LRRC15 in promoting ovarian cancer metastasis and suggest a novel and promising therapy to target ovarian cancer metastases.Significance: This study identifies that LRRC15 activates β1-integrin/FAK signaling to promote ovarian cancer metastasis and shows that the LRRC15-targeted antibody-drug conjugate ABBV-085 suppresses ovarian cancer metastasis in preclinical models.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-05-09T13:28:03.627Z</modification><creation>2025-05-29T16:10:46.242Z</creation></dates><accession>S-EPMC8930558</accession><cross_references><pubmed>34654724</pubmed><doi>10.1158/0008-5472.CAN-21-0622</doi></cross_references></HashMap>