[1] PubMed ID: | 32985327 |
Disease Name: | Uterine Cervical Neoplasms |
Sample: | cervical cancer cells |
Dysfunction Pattern: | regulation[ARAP1-AS1/EZH2/DUSP5 axis ] |
Validated Method: | CCK8//qRT-PCR//Colony Formation Assay//EdU Staining//Transwell Assay |
Description: | In the current research, ARAP1-AS1 was discovered to exhibit a high level in cervical cancer cells. Finally, rescue assays certified the oncogenic function of ARAP1-AS1/EZH2/DUSP5 axis in cervical cancer. |
Causality: | Yes |
Causal Description: | Besides, the knockdown of ARAP1-AS1 repressed cell proliferative and migratory capacities in cervical cancer, as detected by loss-of-function assays including CCK-8, EdU, colony formation, and transwell assays. |
Clinical-realted Application: | |
[2] PubMed ID: | 31953923 |
Disease Name: | Uterine Cervical Neoplasms |
Sample: | cervical cancer (CC) tissues, cell lines and serum |
Dysfunction Pattern: | Expression[highly expressed] |
Validated Method: | RNA Pull-Down//ChIP//Western Blot//CCK8//qRT-PCR//RIP//Luciferase Report Assay//Transwell Assay |
Description: | Here, we focused on an oncogenic lncRNA, ARAP1 antisense RNA 1 (ARAP1-AS1), which was notably upregulated in cervical cancer (CC) tissues, cell lines and serum. |
Causality: | Yes |
Causal Description: | In vitro and in vivo assays showed that knockdown of ARAP1-AS1 inhibited, while overexpression of ARAP1-AS1 promoted CC cell growth and dissemination. |
Clinical-realted Application: | High ARAP1-AS1 expression was closely associated with larger tumor size, advanced FIGO stage as well as lymph node metastasis. |
[3] PubMed ID: | 33965958 |
Disease Name: | Uterine Cervical Neoplasms |
Sample: | CC samples |
Dysfunction Pattern: | Interaction(miR-149-3p and POU2F2) |
Validated Method: | In Vivo Experiment//IHC//Western Blot//Transfection//CCK8//qRT-PCR//Flow Cytometry//RIP//Luciferase Report Assay//Colony Formation Assay//Transwell Assay |
Description: | The expression of ARAP1-AS1 was enhanced in CC samples, while miR-149-3p was markedly suppressed. ARAP1-AS1 downregulated miR-149-3p via sponging it. ARAP1-AS1 and miR-149-3p exhibited a negative correlation in CC samples. On the other hand, ARAP1-AS1 enhanced the expression of POU2F2, which was validated as a target gene of miR-149-3p. |
Causality: | Yes |
Causal Description: | Additionally, ARAP1-AS1 overexpression enhanced the viability, migration, and invasion of CC cells. |
Clinical-realted Application: | |
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