<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR241/000/SRR24149800/SRR24149800.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR241/099/SRR24149799/SRR24149799.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>OBGYN, UCLA</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA954837</full_dataset_link><scientific_name>Mus musculus</scientific_name><tag>xref:PubMed:38360876</tag><long_description>Effective targeting of cancer-associated fibroblasts (CAFs) is hindered by the lack of specific biomarkers and a poor understanding of the mechanisms by which different populations of CAFs contribute to cancer progression. While the role of TGFβ in CAFs is well-studied, less attention has been focused on a structurally and functionally similar protein, Activin A (encoded by INHBA), which is typically associated with poor survival and advanced stage in ovarian cancer. Here, we identified INHBA(+) CAFs as key players in tumor promotion and immune evasion. In syngeneic ovarian cancer mouse models, intraperitoneal injection of the Activin A neutralizing antibody attenuated tumor progression and infiltration with the host INHBA(+) CAFs and M2 macrophages. Collectively, our study identified an INHBA(+) subset of pro-tumoral CAFs as a potential therapeutic target in ovarian cancer. Overall design: To facilitate uniform recruitment of host fibroblasts to the tumor, we used the peritoneal abrasion-facilitated C57BL/6 p53/myc/Hras model in which peritoneal wound healing facilitates the recruitment of fibroblasts into the tumor. C57BL/6 mice with peritoneal abrasion were injected i.p. with syngeneic p53/myc/Hras ovarian cancer cells (genotype: p53-/-, myc, Hras). One day after cancer cell injection, the mice received daily i.p. injections of the Activin A neutralizing antibody (n=8) or control IgG (n=7). After 10 days of treatment, mice were euthanized to assess the intraperitoneal tumor burden. Mice treated with the Activin A neutralizing antibody had smaller tumor lesions at the site of peritoneal abrasion.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Gene expression profile at single cell level of syngeneic ovarian tumors from mice treated with inhibitory Activin-A antibody or control IgG</name><description>Gene expression profile at single cell level of syngeneic ovarian tumors from mice treated with inhibitory Activin-A antibody or control IgG</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-05-02</first_public></dates><accession>PRJNA954837</accession><cross_references><GEO>GSE229529</GEO><taxon>10090</taxon><PubMed>38360876</PubMed></cross_references></HashMap>