Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12935-020-01683-0
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dc.titleSKP1 promotes YAP-mediated colorectal cancer stemness via suppressing RASSF1
dc.contributor.authorTian, C.
dc.contributor.authorLang, T.
dc.contributor.authorQiu, J.
dc.contributor.authorHan, K.
dc.contributor.authorZhou, L.
dc.contributor.authorMin, D.
dc.contributor.authorZhang, Z.
dc.contributor.authorQi, D.
dc.date.accessioned2021-08-25T14:01:12Z
dc.date.available2021-08-25T14:01:12Z
dc.date.issued2020
dc.identifier.citationTian, C., Lang, T., Qiu, J., Han, K., Zhou, L., Min, D., Zhang, Z., Qi, D. (2020). SKP1 promotes YAP-mediated colorectal cancer stemness via suppressing RASSF1. Cancer Cell International 20 (1) : 579. ScholarBank@NUS Repository. https://doi.org/10.1186/s12935-020-01683-0
dc.identifier.issn14752867
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/199264
dc.description.abstractBackground: Cancer stem cells (CSCs) have been recognized as an important drug target, however, the underlying mechanisms have not been fully understood. SKP1 is a traditional drug target for cancer therapy, while, whether SKP1 promotes colorectal cancer (CRC) stem cells (CRC-SCs) and the underlying mechanisms have remained elusive. Methods: Human CRC cell lines and primary human CRC cells were used in this study. Gene manipulation was performed by lentivirus system. The mRNA and protein levels of target genes were examined by qRT-PCR and western blot. The sphere-forming and in vitro migration capacities were determined by sphere formation and transwell assay. The self-renewal was determined by limiting dilution assay. The tumorigenicity and metastasis of cancer cells were examined by xenograft model. The promoter activity was examined by luciferase reporter assay. Nuclear run-on and Chromatin immunoprecipitation-PCR (ChIP-PCR) assay were employed to examine the transcription and protein-DNA interaction. Co-immunoprecipitation assay was used to test protein–protein interaction. The relationship between gene expression and survival was analyzed by Kaplan–meier analysis. The correlation between two genes was analyzed by Spearman analysis. Data are represented as mean ± SD and the significance was determined by Student’s t test. Results: SKP1 was upregulated in CRC-SCs and predicted poor prognosis of colon cancer patients. Overexpression of SKP1 promoted the stemness of CRC cells reflected by increased sphere-forming, migration and self-renewal capacities as well as the expression of CSCs markers. In contrast, SKP1 depletion produced the opposite effects. SKP1 strengthened YAP activity and knockdown of YAP abolished the effect of SKP1 on the stemness of CRC cells. SKP1 suppressed RASSF1 at both mRNA and protein level. Overexpression of RASSF1 abolished the effect of SKP1 on YAP activity and CRC stemness. Conclusion: Our results demonstrated that SKP1 suppresses RASSF1 at both mRNA and protein level, attenuates Hippo signaling, activates YAP, and thereby promoting the stemness of CRC cells. © 2020, The Author(s).
dc.publisherBioMed Central Ltd
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2020
dc.subjectColorectal cancer
dc.subjectRASSF1
dc.subjectSKP1
dc.subjectStemness
dc.subjectYAP
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/s12935-020-01683-0
dc.description.sourcetitleCancer Cell International
dc.description.volume20
dc.description.issue1
dc.description.page579
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