TUSC7

gene
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Also known as LINC00902LOC285194

Summary

TUSC7 (tumor suppressor candidate 7, HGNC:27701) is a long non-coding RNA gene on chromosome 3q13.31.

At a glance

  • Gene type: non-coding (lncRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:27701
Approved symbolTUSC7
Nametumor suppressor candidate 7
Location3q13.31
Locus typeRNA, long non-coding
StatusApproved
AliasesLINC00902, LOC285194
Ensembl geneENSG00000243197
Ensembl biotypelncRNA
OMIM616057
Entrez285194
RNAcentralURS00026A1F84 — lncRNA, 2107 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 9 — 9 lncRNA

ENST00000466156, ENST00000466856, ENST00000477539, ENST00000477805, ENST00000496154, ENST00000496242, ENST00000609361, ENST00000660554, ENST00000665622

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000466156 — 4 exons

ExonStartEnd
ENSE00001862911116712355116712599
ENSE00001895289116716188116716431
ENSE00001929387116714039116714150
ENSE00001941677116709969116710421

Expression profiles

Bgee: expression breadth broad, 85 present calls, max score 85.17.

Top tissues by expression

85 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
corpus callosumUBERON:000233685.17gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047384.68gold quality
left testisUBERON:000453381.18gold quality
testisUBERON:000047381.08gold quality
right testisUBERON:000453479.80gold quality
adrenal tissueUBERON:001830375.61gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099174.34gold quality
sural nerveUBERON:001548861.42silver quality
stomachUBERON:000094559.52gold quality
urinary bladderUBERON:000125559.34silver quality
uterine cervixUBERON:000000259.28gold quality
bloodUBERON:000017856.28gold quality
multicellular organismUBERON:000046855.72gold quality
monocyteCL:000057654.52gold quality
calcaneal tendonUBERON:000370154.11gold quality
superior frontal gyrusUBERON:000266153.83gold quality
prefrontal cortexUBERON:000045153.51gold quality
lungUBERON:000204852.92gold quality
adrenal glandUBERON:000236952.58gold quality
endometriumUBERON:000129552.48silver quality
kidneyUBERON:000211352.46gold quality
primary visual cortexUBERON:000243652.41gold quality
intestineUBERON:000016051.98gold quality
cortex of kidneyUBERON:000122550.94silver quality
pancreasUBERON:000126450.24silver quality
heartUBERON:000094850.09gold quality
liverUBERON:000210749.46silver quality
prostate glandUBERON:000236749.15gold quality
tibial nerveUBERON:000132349.04gold quality
gastrocnemiusUBERON:000138848.49gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes4.40

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 25)

  • The results suggest that loc285194 is a p53-regulated tumor suppressor, which acts in part through repression of miR-211. (PMID:23558749)
  • LOC285194 might be a novel prognostic indicator in colorectal cancer. (PMID:23680400)
  • Decreased expression of LOC285194 could serve as a molecular marker to predict the clinical outcome of Esophageal squamous cell carcinoma patients after surgery, and select patients who would benefit from preoperative Chemoradiotherapy. (PMID:25169763)
  • Low expression of TUSC7 is associated with osteosarcoma. (PMID:26781978)
  • A three-lncRNA signature (LOC285194, RP11-462C24.1 and Nbla12061) identified via stepwise regression analysis showed potential as a diagnostic marker for colorectal cancer. (PMID:27683121)
  • Ectopic expression of TUSC7 in HCT116 and SW480 cells significantly inhibited cell proliferation rate. There were 2 binding sites of miR-211-3p within the sequence of TUSC7 and TUSC7 expression level was negatively correlated with miR-211-3p. (PMID:28214867)
  • long non-coding RNA TUSC7 was underexpressed in endometrial carcinoma, especially in endometrial carcinoma chemotherapy-resistant tissues and cell lines and acted as a potential tumor suppressor gene to inhibit cell growth as well as advance the chemotherapy sensitivity through targeted silencing of miR-23b, which might provide a new therapeutic target to endometrial carcinoma (PMID:28653877)
  • TUSC7 was an independent prognostic indicator for overall survival and disease free survival. (PMID:28925483)
  • Low expression of TUSC7 is associated with temozolomide resistance in glioblastoma. (PMID:29397407)
  • These findings suggested TUSC7 suppressed chemotherapy resistance of ESCC by downregulating miR-224 to modulate DESC1/EGFR/AKT pathway. (PMID:29530057)
  • Study results revealed that the expression of LOC285194 was significantly lower in non-small cell lung cancer (NSCLC) tumor tissues when compared with the corresponding non-tumor tissues. Its expression was correlated with the tumor size, disease-free survival, and overall survival rates. RNA protein interaction analysis revealed that p53 was the direct binding target of LOC285194 in NSCLC. (PMID:30542733)
  • overexpression of TUSC7 inhibited Colorectal cancer (CRC) cell proliferation, metastasis, invasion and epithelialmesenchymal transition These findings indicated that TUSC7 is involved in CRC development. (PMID:31002365)
  • This study demonstrated that decreased level of lncRNA loc285194 was associated with poor clinical outcomes for patients with different types of cancer, supporting a promising potential biomarker for prognosis and metastasis in human cancers.[systematic review and meta-analysis] (PMID:31054796)
  • TUSC7 was downexpressed in EC tissues and cell lines, and TUSC7 upregulation could remarkably inhibit cell proliferation, cycle progression and metastasis in EC cells. (PMID:31200002)
  • TUSC-7 was proved to be one strong suppressive lnc-RNA in lung adenocarcinoma stem cells, functioning through inactivating NOTCH signaling, and the turbulence on division modes precisely pointed to the key mechanisms of stem cells’ renewal. (PMID:31279783)
  • Decreased expression of long non-coding LOC285194 predicts tumour progression and poor prognosis of hepatocellular carcinoma after curative hepatectomy. (PMID:31494574)
  • Long non-coding RNA TUSC7 suppresses osteosarcoma by targeting miR-211. (PMID:31652435)
  • Long non-coding RNA LOC285194 in cancer. (PMID:31837299)
  • LncRNA LOC285194 modulates gastric carcinoma progression through activating Wnt/beta-catenin signaling pathway. (PMID:31991056)
  • LOC285194 inhibits proliferation of human keratinocytes through regulating miR-616/GATA3 pathway. (PMID:32439362)
  • Downregulation of long noncoding RNA TUSC7 promoted cell growth, invasion and migration through sponging with miR-616-5p/GSK3beta pathway in ovarian cancer. (PMID:32706063)
  • [Serum level of lncRNA TUSC7 in patients with esophageal squamous cell carcinoma and its role in promoting tumor cell migration and invasion]. (PMID:32897196)
  • Long non-coding RNA TUSC7 suppressed colorectal cancer progression via regulation of miR-23b/PDE7A Axis. (PMID:33370523)
  • lncRNA TUSC7 inhibits osteosarcoma progression through the miR181a/RASSF6 axis. (PMID:33416181)
  • A Proposed TUSC7/miR-211/Nurr1 ceRNET Might Potentially be Disturbed by a cer-SNP rs2615499 in Breast Cancer. (PMID:35296964)

Cross-species orthologs

0 orthologs

Protein

Non-coding RNA — no protein product; not a drug target.

Function

No curated pathway, Gene-Ontology, or interaction data.

Disease & clinical

No curated disease, variant, or cancer-driver associations.

Drugs & pharmacology

No drug or pharmacology data — not an established drug target.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.