<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tawara M</submitter><funding>the Japan Agency for Medical Research and Development</funding><funding>Japan Society for the Promotion of Science</funding><pagination>9170</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12470293</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(18)</volume><pubmed_abstract>CD44 variants (CD44v) play essential roles in the promotion of tumor metastasis, maintenance of cancer stem cell properties, and resistance to treatments. Therefore, the development of anti-CD44v mAbs is essential for targeting CD44v-positive tumor cells. An anti-CD44v9 mAb, C&lt;sub>44&lt;/sub>Mab-1 (mouse, IgG&lt;sub>1&lt;/sub>, kappa), was previously established. C&lt;sub>44&lt;/sub>Mab-1 recognizes the variant exon 9-encoded region and applies to multiple research techniques. A mouse IgG&lt;sub>2a&lt;/sub> version of C&lt;sub>44&lt;/sub>Mab-1 (C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub>) was generated to evaluate the in vitro and in vivo antitumor activities using gastric and colorectal cancer cell lines. C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub> showed a reactivity to CD44v3-10-overexpressed Chinese hamster ovary-K1 (CHO/CD44v3-10), gastric cancer MKN45, and colorectal cancer COLO205 in flow cytometry. C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub> exhibited both antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) against CHO/CD44v3-10, MKN45, and COLO205. Furthermore, administration of C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub> significantly suppressed CHO/CD44v3-10, MKN45, and COLO205 xenograft tumor growth compared with control mouse IgG&lt;sub>2a&lt;/sub>. These results indicated that C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub>, which possesses ADCC/CDC activities, could be applied to the mAb-based therapy against CD44v9-positive carcinomas.</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Antitumor Activity by an Anti-CD44 Variant 9 Monoclonal Antibody in Gastric and Colorectal Cancer Xenograft Models.</pubmed_title><pmcid>PMC12470293</pmcid><funding_grant_id>25K10553 (to Y.K.)</funding_grant_id><funding_grant_id>JP25am0521010 (to Y.K.), JP25ama121008 (to Y.K.), JP25ama221339 (to Y.K.), and JP25bm1123027 (to Y.K.)</funding_grant_id><pubmed_authors>Kaneko MK</pubmed_authors><pubmed_authors>Kato Y</pubmed_authors><pubmed_authors>Tawara M</pubmed_authors><pubmed_authors>Suzuki H</pubmed_authors><pubmed_authors>Ohishi T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antitumor Activity by an Anti-CD44 Variant 9 Monoclonal Antibody in Gastric and Colorectal Cancer Xenograft Models.</name><description>CD44 variants (CD44v) play essential roles in the promotion of tumor metastasis, maintenance of cancer stem cell properties, and resistance to treatments. Therefore, the development of anti-CD44v mAbs is essential for targeting CD44v-positive tumor cells. An anti-CD44v9 mAb, C&lt;sub>44&lt;/sub>Mab-1 (mouse, IgG&lt;sub>1&lt;/sub>, kappa), was previously established. C&lt;sub>44&lt;/sub>Mab-1 recognizes the variant exon 9-encoded region and applies to multiple research techniques. A mouse IgG&lt;sub>2a&lt;/sub> version of C&lt;sub>44&lt;/sub>Mab-1 (C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub>) was generated to evaluate the in vitro and in vivo antitumor activities using gastric and colorectal cancer cell lines. C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub> showed a reactivity to CD44v3-10-overexpressed Chinese hamster ovary-K1 (CHO/CD44v3-10), gastric cancer MKN45, and colorectal cancer COLO205 in flow cytometry. C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub> exhibited both antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) against CHO/CD44v3-10, MKN45, and COLO205. Furthermore, administration of C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub> significantly suppressed CHO/CD44v3-10, MKN45, and COLO205 xenograft tumor growth compared with control mouse IgG&lt;sub>2a&lt;/sub>. These results indicated that C&lt;sub>44&lt;/sub>Mab-1-mG&lt;sub>2a&lt;/sub>, which possesses ADCC/CDC activities, could be applied to the mAb-based therapy against CD44v9-positive carcinomas.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-03T03:16:59.015Z</modification><creation>2026-05-03T03:11:29.769Z</creation></dates><accession>S-EPMC12470293</accession><cross_references><pubmed>41009730</pubmed><doi>10.3390/ijms26189170</doi></cross_references></HashMap>