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Article: The Anticancer Effect of a Novel Quinoline Derivative 91b1 through Downregulation of Lumican

TitleThe Anticancer Effect of a Novel Quinoline Derivative 91b1 through Downregulation of Lumican
Authors
Keywordsanticancer
Lumican
microarray
quinoline
Issue Date29-Oct-2022
PublisherMultidisciplinary Digital Publishing Institute (MDPI)
Citation
International Journal of Molecular Sciences, 2022, v. 23, n. 21 How to Cite?
AbstractQuinoline derivatives have been reported to possess a wide range of pharmaceutical activities. Our group previously synthesized a series of quinoline compounds, in which compound 91b1 showed a significant anticancer effect. The purpose of this study was to evaluate the anticancer activity of compound 91b1 in vitro and in vivo, and screen out its regulated target. A series of cancer cell lines and nontumor cell lines were treated with compound 91b1 by MTS cytotoxicity assay and cell-cycle assay. In vivo anticancer activity was evaluated by a xenografted model on nude mice. Target prediction of 91b1 was assessed by microarray assay and confirmed by pancancer analysis. Relative expression of the target gene Lumican was measured by qRT-PCR. 91b1 significantly reduced tumor size in the nude mice xenograft model. Lumican was downregulated after 91b1 treatment. Lumican was proven to increase tumorigenesis in vivo, as well as cancer cell migration, invasion, and proliferation in vitro. The results of this study suggest that the anticancer activity of compound 91b1 probably works through downregulating the gene Lumican.
Persistent Identifierhttp://hdl.handle.net/10722/354908
ISSN
2023 Impact Factor: 4.9
2023 SCImago Journal Rankings: 1.179

 

DC FieldValueLanguage
dc.contributor.authorZhou, Yuanyuan-
dc.contributor.authorZhou, Zhongguo-
dc.contributor.authorChan, Dessy-
dc.contributor.authorChung, Po yee-
dc.contributor.authorWang, Yongqi-
dc.contributor.authorChan, Albert Sun chi-
dc.contributor.authorLaw, Simon-
dc.contributor.authorLam, Kim hung-
dc.contributor.authorTang, Johnny Cheuk On-
dc.date.accessioned2025-03-15T00:35:17Z-
dc.date.available2025-03-15T00:35:17Z-
dc.date.issued2022-10-29-
dc.identifier.citationInternational Journal of Molecular Sciences, 2022, v. 23, n. 21-
dc.identifier.issn1661-6596-
dc.identifier.urihttp://hdl.handle.net/10722/354908-
dc.description.abstractQuinoline derivatives have been reported to possess a wide range of pharmaceutical activities. Our group previously synthesized a series of quinoline compounds, in which compound 91b1 showed a significant anticancer effect. The purpose of this study was to evaluate the anticancer activity of compound 91b1 in vitro and in vivo, and screen out its regulated target. A series of cancer cell lines and nontumor cell lines were treated with compound 91b1 by MTS cytotoxicity assay and cell-cycle assay. In vivo anticancer activity was evaluated by a xenografted model on nude mice. Target prediction of 91b1 was assessed by microarray assay and confirmed by pancancer analysis. Relative expression of the target gene Lumican was measured by qRT-PCR. 91b1 significantly reduced tumor size in the nude mice xenograft model. Lumican was downregulated after 91b1 treatment. Lumican was proven to increase tumorigenesis in vivo, as well as cancer cell migration, invasion, and proliferation in vitro. The results of this study suggest that the anticancer activity of compound 91b1 probably works through downregulating the gene Lumican.-
dc.languageeng-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.relation.ispartofInternational Journal of Molecular Sciences-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectanticancer-
dc.subjectLumican-
dc.subjectmicroarray-
dc.subjectquinoline-
dc.titleThe Anticancer Effect of a Novel Quinoline Derivative 91b1 through Downregulation of Lumican-
dc.typeArticle-
dc.identifier.doi10.3390/ijms232113181-
dc.identifier.pmid36361971-
dc.identifier.scopuseid_2-s2.0-85141619818-
dc.identifier.volume23-
dc.identifier.issue21-
dc.identifier.eissn1422-0067-
dc.identifier.issnl1422-0067-

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