2022
DOI: 10.1016/j.phrs.2022.106196
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The miR-145–MMP1 axis is a critical regulator for imiquimod-induced cancer stemness and chemoresistance

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Cited by 7 publications
(5 citation statements)
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“…The gene silencing caused by aberrant promoter methylation has been demonstrated in oncogenesis and progression, which showed the potential as a prognostic or therapeutic biomarker. [25][26][27] The present study identified that the promoter methylation levels of CSF3R…”
Section: Discussionmentioning
confidence: 50%
“…The gene silencing caused by aberrant promoter methylation has been demonstrated in oncogenesis and progression, which showed the potential as a prognostic or therapeutic biomarker. [25][26][27] The present study identified that the promoter methylation levels of CSF3R…”
Section: Discussionmentioning
confidence: 50%
“… 40 , 49 Moreover, LGR6 contributes to CSC properties in ovarian, breast, and cervical cancers. 22 , 23 , 24 In our study, when comparing LGR6 expression between spheroid and adherent components of A427 cells harboring a CTNNB1 exon 3 mutation, LGR6 was predominantly expressed in the component of spheroids, which is a CSC‐related characteristic, 38 accompanied by upregulation of several stem cell‐associated pathways and genes, including MMP1 , 50 CPA4 , 51 and SRPX2 . 52 These findings support the idea that Wnt/β‐catenin pathway activation, mediated by CTNNB1 exon 3 mutations, induces LGR6 overexpression, which in turn confers cancer stemness properties via Wnt pathway activation.…”
Section: Discussionmentioning
confidence: 66%
“…The neuronal marker genes NES, MAP2, PTK2B, CHN1, DNM1, NRSN2, FBLN2, and SCAMP1 [ 24 , [28] , [29] , [30] , [31] , [32] , [33] , [34] ] gradually increased with the induction time, while TMEM59L, SLC1A1, DLG4, CDK5, and ENO2 [ [35] , [36] , [37] , [38] , [39] ] peaked in the induction 5h cell cluster but significantly decreased in the induction 8h cell cluster. However, the expression of CCND1, IL1B, MMP1, MMP3, MYO10, and BMP2 [ [40] , [41] , [42] , [43] , [44] , [45] , [46] ], stem cell marker genes, were highest in the ADSC cluster and significantly decreased in their differentiated cell clusters with increasing induction time. Meanwhile, the BP functions related to neuronal differentiation and development, such as neuronal differentiation and projection and apoptosis, dendritic morphogenesis, axonogenesis, guidance, extension, protein transport and damage response and regeneration, synaptic assembly, cell transport and regulation of endocytosis in their differentiated cell clusters were significantly up-regulated with longer induction time.…”
Section: Discussionmentioning
confidence: 99%