Basic Information
LncRNA/CircRNA Name | SNHG7 |
Synonyms | NA |
Region | GRCh38_9:136721366-136728184 |
Ensemble | ENSG00000233016 |
Refseq | NR_003672 |
Classification Information
Regulatory Mechanism | Biological Function | Clinical Application | |||
---|---|---|---|---|---|
TF | Immune | Survival | |||
Enhancer | Apoptosis | apoptosis | Drug | ||
Variant | Cell Growth | Circulating | 2 | ||
MiRNA | EMT | Metastasis | |||
Methylation | Coding Ability | Recurrence |
Cancer&Entry Information
Cancer Name | colorectal cancer |
ICD-0-3 | C19.9 |
Methods | Microarray, qPCR, Western blot, Luciferase reporter assay, in vitro knockdown, RIP |
Sample | colorectal cancer,cell lines (caco2, SW480, SW620, Hct116, and LoVo) |
Expression Pattern | up-regulated |
Function Description | SNHG7 expression showed a high fold (SW620/SW480) in CRC microarrays. The CRC patients with high expression of SNHG7 had a significantly poor prognosis. High level of lncRNA-SNHG7 was correlated with tumor size, lymphatic metastasis, distant metastasis, and tumor stage. Furthermore, SNHG7 promoted CRC cell proliferation, metastasis, mediated cell cycle, and inhibited apoptosis. SNHG7 and GALNT7 were observed for co-expression by CNC analysis, and a negative correlation of SNHG7 and miR-34a were found by competing endogenous RNA (ceRNA) analysis. Further results indicated that SNHG7 facilitated the proliferation and metastasis as a competing endogenous RNA to regulate GALNT7 expression by sponging miR-34a in CRC cell lines. SNHG7 also played the oncogenic role in regulating PI3K/Akt/mTOR pathway by competing endogenous miR-34a and GALNT7. |
Pubmed ID | 29970122 |
Year | 2018 |
Title | Long Non-Coding RNA-SNHG7 Acts as a Target of miR-34a to Increase GALNT7 Level and Regulate PI3K/Akt/mTOR Pathway in Colorectal Cancer Progression |
External Links
Links for SNHG7 | GenBank HGNC NONCODE |
Links for colorectal cancer | OMIM COSMIC |