Basic Information
LncRNA/CircRNA Name | HOXD-AS1 |
Synonyms | HAGLR, HOXD-AS1, Mdgt |
Region | GRCh38_2:176164051-176188958 |
Ensemble | ENSG00000224189 |
Refseq | NR_033979 |
Classification Information
Regulatory Mechanism | Biological Function | Clinical Application | |||
---|---|---|---|---|---|
TF | Immune | Survival | |||
Enhancer | Apoptosis | apoptosis | Drug | Cisplatin | |
Variant | Cell Growth | Circulating | |||
MiRNA | EMT | Metastasis | |||
Methylation | Coding Ability | Recurrence |
Cancer&Entry Information
Cancer Name | cervical cancer |
ICD-0-3 | C53 |
Methods | qPCR, Western blot, Luciferase reporter assay, in vitro knockdown |
Sample | cervical cancer tissues, cell lines (CaSki and HeLa) |
Expression Pattern | up-regulated |
Function Description | qRT-PCR indicated that HOXD-AS1 was overexpressed in CC tissues and cisplatin-resistant CC cells. Loss-of-function assays showed that downregulation of HOXD-AS1 expression suppressed chemoresistance of cisplatin-resistant CC cells. HOXD-AS1 targeted miR-130a-3p, and in gain-of-function assays miR-130a-3p could reverse cisplatin resistance of CC cells. miR-130a-3p in turn targeted zinc finger E-box homeobox 1 (ZEB1). These results collectively show that HOXD-AS1 can act as a competing endogenous RNA to upregulate ZEB1 expression via miR-130a-3p. Fruits of colony formation assays displayed that proliferation was inhibited in HOXD-AS1 down-regulated cells (CaSki-DDP and HeLa-DDP), and we could observe that cells with higher concentrations of cisplatin have weaker proliferation ability. Knock down of HOXD-AS1 led to enhanced apoptosis in CaSki-DDP and HeLa-DDP cells in contrast with the NC group when exposed to cisplatin and such effect was greater with increasing concentration of cisplatin. |
Pubmed ID | 29896986 |
Year | 2018 |
Title | HOXD-AS1 Exerts Oncogenic Functions and Promotes Chemoresistance in Cisplatin-Resistant Cervical Cancer Cells |
External Links
Links for HOXD-AS1 | GenBank HGNC NONCODE |
Links for cervical cancer | OMIM COSMIC |