<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tian J</submitter><funding>Research Project of Anhui Province of China</funding><funding>National Natural Science Foundation of China</funding><pagination>e0010661</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9362908</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(8)</volume><pubmed_abstract>Schistosomiasis is a serious and widespread parasitic disease caused by infection with Schistosoma. Because the parasite's eggs are primarily responsible for schistosomiasis dissemination and pathogenesis, inhibiting egg production is a potential approach to control the spread and severity of the disease. The bromodomain and extra-terminal (BET) proteins represent promising targets for the development of epigenetic drugs against Schistosoma. JQ-1 is a selective inhibitor of the BET protein family. In the present study, JQ-1 was applied to S. japonicum in vitro. By using laser confocal scanning microscopy and EdU incorporation assays, we showed that application of JQ-1 to worms in vitro affected egg laying and the development of both the male and female reproductive systems. JQ-1 also inhib</pubmed_abstract><journal>PLoS neglected tropical diseases</journal><pubmed_title>JQ-1 ameliorates schistosomiasis liver granuloma in mice by suppressing male and female reproductive systems and egg development of Schistosoma japonicum.</pubmed_title><pmcid>PMC9362908</pmcid><funding_grant_id>81271865</funding_grant_id><funding_grant_id>KJ2019A0223</funding_grant_id><pubmed_authors>Tian J</pubmed_authors><pubmed_authors>Ding H</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Shen J</pubmed_authors><pubmed_authors>Dai B</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Gong L</pubmed_authors><pubmed_authors>Xia S</pubmed_authors><pubmed_authors>Sun W</pubmed_authors><pubmed_authors>Ren C</pubmed_authors></additional><is_claimable>false</is_claimable><name>JQ-1 ameliorates schistosomiasis liver granuloma in mice by suppressing male and female reproductive systems and egg development of Schistosoma japonicum.</name><description>Schistosomiasis is a serious and widespread parasitic disease caused by infection with Schistosoma. Because the parasite's eggs are primarily responsible for schistosomiasis dissemination and pathogenesis, inhibiting egg production is a potential approach to control the spread and severity of the disease. The bromodomain and extra-terminal (BET) proteins represent promising targets for the development of epigenetic drugs against Schistosoma. JQ-1 is a selective inhibitor of the BET protein family. In the present study, JQ-1 was applied to S. japonicum in vitro. By using laser confocal scanning microscopy and EdU incorporation assays, we showed that application of JQ-1 to worms in vitro affected egg laying and the development of both the male and female reproductive systems. JQ-1 also inhib</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-19T22:58:29.955Z</modification><creation>2025-04-19T22:58:29.955Z</creation></dates><accession>S-EPMC9362908</accession><cross_references><pubmed>35943970</pubmed><doi>10.1371/journal.pntd.0010661</doi></cross_references></HashMap>