CASC2
gene geneOn this page
Summary
CASC2 (cancer susceptibility 2, HGNC:22933) is a long non-coding RNA gene on chromosome 10q26.11. May act as a potential tumor suppressor.
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:22933 |
| Approved symbol | CASC2 |
| Name | cancer susceptibility 2 |
| Location | 10q26.11 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Ensembl gene | ENSG00000177640 |
| Ensembl biotype | lncRNA |
| OMIM | 608598 |
| Entrez | 255082 |
| RNAcentral | URS000075B07A — lncRNA, 3284 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 26 — 26 lncRNA
ENST00000414722, ENST00000426021, ENST00000435944, ENST00000439517, ENST00000454781, ENST00000454857, ENST00000614455, ENST00000622752, ENST00000657543, ENST00000665675, ENST00000781591, ENST00000781592, ENST00000781593, ENST00000781594, ENST00000781595, ENST00000781596, ENST00000781597, ENST00000781598, ENST00000781599, ENST00000781600, ENST00000781601, ENST00000781602, ENST00000781603, ENST00000781604, ENST00000781605, ENST00000781606
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000414722 — 4 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001644747 | 118206522 | 118206659 |
| ENSE00001653241 | 118046279 | 118046647 |
| ENSE00001672903 | 118052131 | 118052196 |
| ENSE00001765675 | 118049512 | 118049617 |
Expression profiles
Bgee: expression breadth ubiquitous, 167 present calls, max score 85.58.
FANTOM5 (CAGE): breadth ubiquitous, TPM avg 2.7300 / max 108.5483, expressed in 958 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 107286 | 2.7300 | 958 |
Top tissues by expression
243 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 85.58 | gold quality |
| right uterine tube | UBERON:0001302 | 85.55 | gold quality |
| sural nerve | UBERON:0015488 | 80.71 | gold quality |
| oviduct epithelium | UBERON:0004804 | 77.90 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 77.38 | gold quality |
| bronchial epithelial cell | CL:0002328 | 76.51 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 75.83 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 74.99 | gold quality |
| bronchus | UBERON:0002185 | 74.89 | gold quality |
| spinal cord | UBERON:0002240 | 74.04 | gold quality |
| bone marrow cell | CL:0002092 | 73.13 | silver quality |
| colonic epithelium | UBERON:0000397 | 73.08 | silver quality |
| buccal mucosa cell | CL:0002336 | 71.95 | silver quality |
| islet of Langerhans | UBERON:0000006 | 71.28 | gold quality |
| caudate nucleus | UBERON:0001873 | 71.18 | gold quality |
| nucleus accumbens | UBERON:0001882 | 71.12 | gold quality |
| fallopian tube | UBERON:0003889 | 71.09 | gold quality |
| prefrontal cortex | UBERON:0000451 | 71.08 | gold quality |
| hypothalamus | UBERON:0001898 | 70.97 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 70.61 | gold quality |
| testis | UBERON:0000473 | 69.57 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 69.34 | gold quality |
| putamen | UBERON:0001874 | 69.28 | gold quality |
| amygdala | UBERON:0001876 | 69.10 | gold quality |
| left testis | UBERON:0004533 | 68.79 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 68.06 | gold quality |
| adenohypophysis | UBERON:0002196 | 67.96 | gold quality |
| right testis | UBERON:0004534 | 67.93 | gold quality |
| thyroid gland | UBERON:0002046 | 67.68 | gold quality |
| right frontal lobe | UBERON:0002810 | 67.49 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 5.25 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 40)
- Identification of CASC2, in a region of common allelic loss at chromosome 10q26 in endometrial cancer. (PMID:15024726)
- CASC2 plays a tumor suppressive role in glioma via negative regulation of miR-21, which may be a novel therapeutic target for treating gliomas. (PMID:25446261)
- CASC2 is involved in the development and progression of NSCLC. (PMID:26790438)
- Study in clinical samples and colorectal cancer (CRC) cell lines demonstrates that CASC2 is downregulated, and the downregulation of CASC2 is significantly associated with advanced pathological stage in patients with CRC. Overexpression of CASC2 is able to inhibit cell proliferation and tumor growth. These findings suggest that CASC2 plays a critical role in the modulation of CRC progression. (PMID:27198161)
- CASC2 acts as a tumor suppressor gene in RCC. CASC2 is directly targeted by miR21, and ectopic CASC2 expression inhibits proliferation and migration of RCC cells. (PMID:27222255)
- LncRNA CASC2 Interacts With miR-181a to Modulate Glioma Growth and Resistance to TMZ Through PTEN Pathway (PMID:28121023)
- lncRNA CASC2 plays an pivotal role in bladder tumorigenesis and progression and may act as a potential biomarker for the treatment of bladder cancer. (PMID:28199978)
- Patients who possessed both low CASC2c and high miR-101 had a longer survival. (PMID:28252647)
- Our findings demonstrate that CASC2 could be a useful tumour suppressor factor and a promising therapeutic target for hepatocellular carcinoma. (PMID:28621238)
- CASC2 may be a potential prognostic marker and therapeutic target. (PMID:28654795)
- FBXW7 was a downstream target of miR-367 and CASC2 prohibited epithelial-to-mesenchymal transition progression and subsequently exerted its anti-metastatic effects via CASC2/miR-367/FBXW7 axis in hepatocellular carcinoma cells. (PMID:28716020)
- the present study indicated the important roles and underlying molecular mechanisms of long noncoding RNAs CASC2 on gastric cancer. (PMID:28849111)
- these findings will shed light on the role and mechanism of HNF1A/CASC2 in regulating pancreatic cancer cells proliferation through PTEN/Akt signaling. (PMID:28865121)
- LncRNA CASC2 inhibited the viability and induced the apoptosis of HCC cells through regulating miR-24-3p. (PMID:29091305)
- CASC2 is downregulated in gliomas, resulting in increased miR-193a-5p level and a decrease in mTOR expression, which further induces protective autophagy, leading to temozolomide resistance. (PMID:29136760)
- Downregulation of lncRNA cancer susceptibility candidate 2 facilitates osteosarcoma growth and invasion through miR-181a (PMID:29194827)
- The present study reported that CASC2 may inhibit osteosarcoma development. Osteosarcoma tissues demonstrated reduced CASC2 expression compared with normal adjacent tissues. In addition, CASC2 transduction may decrease proliferation, migration and invasion of osteosarcoma cell lines whereas knockdown of CASC2 displayed opposing effects. (PMID:29257211)
- Investigated RNA-binding region-containing protein 1 (RNPC1) action on signal pathways and disease progression in lung cancer samples and cells. Found RNPC1 acts to downregulate the miR-181a mediated inhibition of cancer susceptibility 2 (CASC2) expression in lung cancer. Results show RNPC1 inhibits NSCLC progression in a miR-181a/CASC2 axis-dependent manner. (PMID:29288351)
- We therefore investigated the effects of CASC2 expression on NF-kappaB pathway activity. Ultimately, we determined that CASC2 regulates hepatocellular carcinoma cell activity by targeting miR-362-5p and thus inhibiting the NF-kappaB pathway (PMID:29319182)
- CASC2 competes with SPRY2 for miR-183 binding to rescue the expression of SPRY2 in PC cells, thus enhancing the sensitivity of PC cells to docetaxel through SPRY2 downstream ERK signaling pathway (PMID:29373811)
- Upregulated CASC2 may inhibit cell proliferation, migration, and invasion through regulating miR-18a-5p and its target gene RUNX1 in MM. (PMID:29422114)
- a CASC2/miR-24/miR-221 axis, which can affect the TRAIL resistance of hepatocellular carcinoma through regulating caspase 3/8, is reported. (PMID:29476051)
- Results indicate that long non-coding RNA (lncRNA) CASC2 can promote PLXNC1 expression by sponging miR-181a, thereby inhibiting the proliferation and invasion of melanoma cells. (PMID:29514220)
- lncRNA CASC2 was a key factor in the tumorigenesis. (PMID:29523222)
- Long Non-Coding RNA CASC2 Improves Diabetic Nephropathy by Inhibiting JNK Pathway. (PMID:29890555)
- LncRNA CASC2 inhibited breast cancer cell growth and metastasis through the regulation of the miR-96-5p/SYVN1 signaling pathway.LncRNA CASC2 expression is downregulated in breast cancer tissues. (PMID:30106139)
- The low CASC2 expression was correlated with advanced clinicopathological characteristics of cancer tumors, and CASC2 may thus be a potential prognostic biomarker in human cancer. However, more studies are needed to further corroborate these findings. (PMID:30144439)
- Compared with healthy controls, expression of lncRNA CASC2 in serum and renal tissue was specifically downregulated in patients with type 2 diabetes combined with chronic renal failure but not in type 2 diabetic patients combined with other complications. (PMID:30171178)
- Overexpression of CASC2 promoted cell apoptosis and suppressed cell growth and metastasis in hepatocellular carcinoma. (PMID:30362539)
- CASC2 overexpression overcame cisplatin resistance in gastric cancer by sponging miR-19a. (PMID:30372881)
- In this study, the expression of lncRNA CASC2 in tumor tissues, adjacent healthy tissues, and plasma of 122 oral squamous cell carcinoma (OSCC) patients as well as in plasma of 52 healthy controls was detected by RT-qPCR. We conclude that downregulation of lncRNA CASC2 may participate in the postoperative local recurrence of early OSCC through miRNA-21. (PMID:30467776)
- CASC2 downregulation promoted proliferation and inhibited apoptotic cell death in nasopharyngeal carcinoma (NPC) cells. In contrast, CASC2 upregulation inhibited proliferation and increased apoptosis. There were putative binding sites of miR18a5p in the promoter of CASC2. The level of miR18a5p was upregulated in NPC tissues and cells. CASC2 could directly bind with miR18a5p and inhibit miR18a5p expression. (PMID:30569153)
- Low CASC2 expression is associated with papillary thyroid carcinoma. (PMID:30609134)
- LncRNA CASC2 was upregulated in cells treated with berberine, and knockdown of lncRNA CASC2 reversed the berberine-induced apoptosis. (PMID:30681073)
- CASC2c may serve as a new biomarker and therapeutic target in the diagnosis and treatment of non-small cell lung cancer (PMID:31300295)
- data demonstrated that E2F6 could regulate the proliferation, invasion and apoptosis of gastric carcinoma (GC) cells via inhibiting the expression of CASC2, suggesting that E2F6/CASC2 axis is another regulator of GC progression (PMID:31301415)
- lncRNA CASC2 activated paclitaxel resistance in breast cancer through regulation of miR-18a-5p/CDK19 (PMID:31352515)
- Long noncoding RNA CASC2c inhibited cell proliferation in hepatocellular carcinoma by inactivated ERK1/2 and Wnt/beta-catenin signaling pathway. (PMID:31625123)
- Overexpression of CASC2 overcame cisplatin resistance in hepatocellular carcinoma (HCC) by regulating miR-222 expression, thereby providing a potential therapeutic strategy for overcoming HCC cell chemoresistance. (PMID:31633393)
- Long noncoding RNA CASC2 suppresses pancreatic cancer cell growth and progression by regulating the miR24/MUC6 axis. (PMID:31894271)
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.