Difference between revisions of "CCAT2"
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<ref name="ref1"> Ling H, Spizzo R, Atlasi Y, Nicoloso M, Shimizu M, Redis RS, et al. CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer[J]. Genome research. 2013,23(9):1446-61. | <ref name="ref1"> Ling H, Spizzo R, Atlasi Y, Nicoloso M, Shimizu M, Redis RS, et al. CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer[J]. Genome research. 2013,23(9):1446-61. | ||
</ref>(1) | </ref>(1) | ||
− | <ref name=" | + | <ref name="ref2"> Qiu M, Xu Y, Yang X, Wang J, Hu J, Xu L, et al. CCAT2 is a lung adenocarcinoma-specific long non-coding RNA and promotes invasion of non-small cell lung cancer[J]. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 2014,35(6):5375-80. |
</ref>(2) | </ref>(2) | ||
</references> | </references> | ||
[[Category: Antisense]] | [[Category: Antisense]] |
Revision as of 12:28, 2 April 2015
CCAT2, a novel long noncoding RNA transcript (lncRNA) harboring a single nucleotide polymorphism rs6983267 SNP, promotes tumor growth, metastasis, and chromosomal instability, including colon cancer[1] and non-small cell lung cancer [2]
Contents
Annotated Information
Name
CCAT2, colon cancer-associated transcript 2 (CCAT2) (HGNC nomenclature)
Characteristics
CCAT2 is transcribed from chromosome 8q24, a very conserved region harboring a single nucleotide polymorphism rs6983267, which has been identified in various genome-wide association studies . [2]
Function
CCAT2 promotes cancer growth and metastasis and induces chromosomal instability. CCAT2 can regulates MYC transcription. CCAT2 responds to WNT signaling. [1] CCAT2 is a lung adenocarcinoma-specific lncRNA and promotes invasion of NSCLC and highlight its potential as a biomarker for lymph node metastasis.[2]
Regulation
rs6983267 status affects the CCAT2 expression, providing an additional mechanism linking the risk allele of rs6983267 with higher CRC risk. CCAT2 shows significant association with MYC expression levels, suggesting that the SNP status may also affect CCAT2 function as an RNA transcript. [1]
Diseases
Expression
CCAT2 is expressed at high levels in MSS CRC tumor tissues and influences MYC levels, but has very low-level expression in normal colon tissues. [1]
PCR Primers | Sequence |
---|---|
CCAT2 F1 | CCCTGGTCAAATTGCTTAACCT[1] |
CCAT2 R1 | TTATTCGTCCCTCTGTTTTATGGAT[1] |
CCAT2 F2 | CCGAGGTGATCAGGTGGACTTTC[1] |
CCAT2 R2 | GTCTTCTGGGCTGATGTTGC[1] |
siRNA | Target Sequence |
CCAT2 siRNA 1 | TTAACCTCTTCCTATCTCA[1] |
CCAT2 siRNA 2 | AGGTGTAGCCAGAGTTAAT[1] |
CCAT2 siRNA 3 | CGAATAAACTCTCCTCCTA[1] |
shRNA | Sequences cloned into pRS vector |
CCAT2 shRNA1 | GATCCCCAATTGCTTAACCTCTTCCTTTCAAGAGAAGGAAGAGGTTAAGCAATTTTTTTA[1] |
CCAT2 shRNA2 | GATCCCCGATGAAAGGCACTGAGAAATTCAAGAGATTTCTCAGTGCCTTTCATCTTTTTA[1] |
CCAT2 shRNA3 | GATCCCCTTAACCTCTTCCTATCTCATTCAAGAGATGAGATAGGAAGAGGTTAATTTTTA[1] |
Sequence
>gi|565671809|ref|NR_109834.1| Homo sapiens colon cancer associated transcript 2 (non-protein coding) (CCAT2), long non-coding RNA
000081 AGAAAGCTAG TATGAGACTA CCAAATGATC ATCAGACATT TCTTGAACAC CAATTAAATT GCTAGGTATG CTAAAGTTTG 000160
000161 CAAAACTGGT ATAGACACCA AGAGGGAGGT ATCAACAGAG ACTCCCCAAG AGCTAAGAGG AAACCACCTT GGACTGGAAG 000240
000241 TCAAGAGCCA AAATTCTAGA CTCTACTCTG TAATTAACTA CCTATTTGAA TTTGGAAAAA TCACCATCAA CTTTCCCAGC 000320
000321 CTCGTTCTCT GCATCTGGGA AATGAAGGCG TCGTCCAAAT GATTACAAGC TTCTTTTCCT GCTCTTATTG CATGATTCCA 000400
000401 CTTCCACAGC CCTCCAGCAT TTTTTAGCAG CTGCATCGCT CCATAGAGCC TGCAGAGGGC ACTAGACTGG GAATTAGAAA 000480
000481 ACCTGATTTC CCTTCCAGCT CCACCTCTGA CCAATTGCCT GACCCTGGTC AAATTGCTTA ACCTCTTCCT ATCTCAGCTC 000560
000561 CCTATCCATA AAACAGAGGG ACGAATAAAC TCTCCTCCTA CCACTAAGAG GTGTAGCCAG AGTTAATACC CTCATCGTCC 000640
000641 TTTGAGCTCA GCAGATGAAA GGCACTGAGA AAAGTACAAA GAATTTTTAT GTGCTATTGA CTTTATTTTA TTTTATGTGG 000720
000721 GGGAGGGAGC CGGCCCCAGC TGGAAAGCTG CTTTCTCTGA ATCAAAGGGC AGGAACCCAG CAAGTTTCTC AGGATTGGGG 000800
000801 CCTTAGACTG GGCTGTGTAT ACAGACAGTG CCAGCCAACC CCACAGTTCA GTTTCCTTTA ACCTGGTGCT CCAGGCAATA 000880
000881 ACTGTGCAAC TCTGCAATTT AACAATGTGT TCTTTGTCCC ACAACTGTTC TCGTTTCTCA ACTGCCCAGG TAATATGTTT 000960
000961 GGGCCTGTAG GAAGAGTCAA ATAGTTAATA AGGGAAGGGT TTGGCATGCC CTACGTAAGT TCTACCAGCA AGTCCCAACA 001040
001041 AGAAGGCATT CTGTGTCTCC TGATTCCTGA CCTACCCCCA AAATGTACAA ATGTACAAGG AATGAGCCCA CTTTCCCAGC 001120
001121 AGGCTGTAAT ACCAGTTTGG CCTATATCAA TGCATTGGTG AGCTGTGTTT TGTTTATGGT TTTATGCCAT CTATTTTCCC 001200
001201 ATGGATATTA TGTTTTCTAA AGAGCCCTTA AGTTTACGTC AGCTTTTAAA GCTACCAGCA GCACCATTTC AGTTCATATT 001280
001281 AAGCCCTTAA TATGGTATGA ATAGGAGAGC TATTAGACTA AAGAGCCATA ATCATCCCTG AGGAAAACAT CCATCACCAA 001360
001361 CATTTATGTG GTCCCTGAAC TTCTAAAAGG TGTCATCTCT CTGGGGTGTA TCTGGTGAGA GCTTTCTCTG GGAGATGCCA 001440
001441 AAAAGCCAAT GCATTAGATG AAGCTTAGAA GGGCATTTTC TAACCATTAC AAATTGCCTA GTCTAGCATC TCAATTTCAT 001520
001521 CTACGTGAAG AGCCTTAATT AAATTTGTTG GGGTTTGATC CTTTATCCCC AGATGTGGCG CTGACAGAGA TTGCTTACAT 001600
001601 AAATAATGTG TGCTCCAAGT GCTTGCCAGG CTCCTGGCTC AGCTGGGACA GCTGTAGCTT TTTGAATGTC ATTCCCAAGA 001680
001681 TATCCTGCAG GTGTTCAGCT TCCCCTGTTC TACTCTGGGA AGAGAGCCGT GGGCAACATC AGCCCAGAAG AC
Labs working on this lncRNA
- Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA; [1]
- Jiangsu Key Laboratory of Molecular and Translational Cancer Research, Nanjing Medical University Affiliated Cancer Hospital, Cancer Institute of Jiangsu Province, Nanjing, 210009, China [2].
References
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 1.16 Ling H, Spizzo R, Atlasi Y, Nicoloso M, Shimizu M, Redis RS, et al. CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer[J]. Genome research. 2013,23(9):1446-61.
- ↑ 2.0 2.1 2.2 2.3 2.4 Qiu M, Xu Y, Yang X, Wang J, Hu J, Xu L, et al. CCAT2 is a lung adenocarcinoma-specific long non-coding RNA and promotes invasion of non-small cell lung cancer[J]. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 2014,35(6):5375-80.