Panpan Tan, Yuchen Du, Ruijuan He, Zhan Shi, Shanshan Xie, Yuanyuan Zhao, Baitao Wang, Baoqin Ping, Zhe Fang, Yu Zhang, Ao Liu, Yanwei Sun, Yun Song
{"title":"Circ_0007429通过miR-377-3p/THBS1轴促进肝细胞癌对索拉非尼的耐药性。","authors":"Panpan Tan, Yuchen Du, Ruijuan He, Zhan Shi, Shanshan Xie, Yuanyuan Zhao, Baitao Wang, Baoqin Ping, Zhe Fang, Yu Zhang, Ao Liu, Yanwei Sun, Yun Song","doi":"10.62347/GUJU9257","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To elucidate the function of circ_0007429 in hepatocellular carcinoma (HCC) chemoresistance, with a focus on its regulatory mechanisms via the miR-377-3p/THBS1 (Thrombospondin 1) axis.</p><p><strong>Methods: </strong>The expression levels of circ_0007429, miR-377-3p, and THBS1 mRNA were quantified using quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR). Cell viability was assessed with the CCK-8 assay, and THBS1 protein expression was evaluated by western blotting. The interactions between miR-377-3p and circ_0007429 or THBS1 were confirmed using luciferase reporter assays.</p><p><strong>Results: </strong>Circ_0007429 expression was substantially upregulated in sorafenib-resistant (SR) HCC cells. Knockdown of circ_0007429 accelerated sorafenib sensitivity by suppressing cell survival. Mechanistically, circ_0007429 acted as a molecular sponge for miR-377-3p, whose activity was increased upon circ_0007429 silencing. THBS1 was recognized as a downstream target of miR-377-3p, and its expression was suppressed by miR-377-3p. Circ_0007429 is a ceRNA for miR-377-3p, thus controlling THBS1 translation and contributing to sorafenib resistance.</p><p><strong>Conclusion: </strong>Circ_0007429 silencing enhances sorafenib sensitivity in HCC through the miR-377-3p/THBS1 axis. circ_0007429 may be a biomarker and therapeutic target for overcoming chemoresistance in HCC.</p>","PeriodicalId":7731,"journal":{"name":"American journal of translational research","volume":"17 6","pages":"4148-4158"},"PeriodicalIF":1.7000,"publicationDate":"2025-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261140/pdf/","citationCount":"0","resultStr":"{\"title\":\"Circ_0007429 promotes hepatocellular carcinoma resistance to sorafenib through the miR-377-3p/THBS1 axis.\",\"authors\":\"Panpan Tan, Yuchen Du, Ruijuan He, Zhan Shi, Shanshan Xie, Yuanyuan Zhao, Baitao Wang, Baoqin Ping, Zhe Fang, Yu Zhang, Ao Liu, Yanwei Sun, Yun Song\",\"doi\":\"10.62347/GUJU9257\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To elucidate the function of circ_0007429 in hepatocellular carcinoma (HCC) chemoresistance, with a focus on its regulatory mechanisms via the miR-377-3p/THBS1 (Thrombospondin 1) axis.</p><p><strong>Methods: </strong>The expression levels of circ_0007429, miR-377-3p, and THBS1 mRNA were quantified using quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR). Cell viability was assessed with the CCK-8 assay, and THBS1 protein expression was evaluated by western blotting. The interactions between miR-377-3p and circ_0007429 or THBS1 were confirmed using luciferase reporter assays.</p><p><strong>Results: </strong>Circ_0007429 expression was substantially upregulated in sorafenib-resistant (SR) HCC cells. Knockdown of circ_0007429 accelerated sorafenib sensitivity by suppressing cell survival. Mechanistically, circ_0007429 acted as a molecular sponge for miR-377-3p, whose activity was increased upon circ_0007429 silencing. THBS1 was recognized as a downstream target of miR-377-3p, and its expression was suppressed by miR-377-3p. Circ_0007429 is a ceRNA for miR-377-3p, thus controlling THBS1 translation and contributing to sorafenib resistance.</p><p><strong>Conclusion: </strong>Circ_0007429 silencing enhances sorafenib sensitivity in HCC through the miR-377-3p/THBS1 axis. circ_0007429 may be a biomarker and therapeutic target for overcoming chemoresistance in HCC.</p>\",\"PeriodicalId\":7731,\"journal\":{\"name\":\"American journal of translational research\",\"volume\":\"17 6\",\"pages\":\"4148-4158\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-06-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261140/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of translational research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.62347/GUJU9257\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of translational research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.62347/GUJU9257","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
Circ_0007429 promotes hepatocellular carcinoma resistance to sorafenib through the miR-377-3p/THBS1 axis.
Objective: To elucidate the function of circ_0007429 in hepatocellular carcinoma (HCC) chemoresistance, with a focus on its regulatory mechanisms via the miR-377-3p/THBS1 (Thrombospondin 1) axis.
Methods: The expression levels of circ_0007429, miR-377-3p, and THBS1 mRNA were quantified using quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR). Cell viability was assessed with the CCK-8 assay, and THBS1 protein expression was evaluated by western blotting. The interactions between miR-377-3p and circ_0007429 or THBS1 were confirmed using luciferase reporter assays.
Results: Circ_0007429 expression was substantially upregulated in sorafenib-resistant (SR) HCC cells. Knockdown of circ_0007429 accelerated sorafenib sensitivity by suppressing cell survival. Mechanistically, circ_0007429 acted as a molecular sponge for miR-377-3p, whose activity was increased upon circ_0007429 silencing. THBS1 was recognized as a downstream target of miR-377-3p, and its expression was suppressed by miR-377-3p. Circ_0007429 is a ceRNA for miR-377-3p, thus controlling THBS1 translation and contributing to sorafenib resistance.
Conclusion: Circ_0007429 silencing enhances sorafenib sensitivity in HCC through the miR-377-3p/THBS1 axis. circ_0007429 may be a biomarker and therapeutic target for overcoming chemoresistance in HCC.