KIAA1524

Protein CIP2A also known as cancerous inhibitor of PP2A (CIP2A) is a protein that in humans is encoded by the KIAA1524 gene.[5][6]

CIP2A
Identifiers
Aliases	CIP2A, C330027C09Rik, AA408511, AU018569, Cip2a, Kiaa1524, p90, KIAA1524, cell proliferation regulating inhibitor of protein phosphatase 2A, cellular inhibitor of PP2A
External IDs	OMIM: 610643 MGI: 2146335 HomoloGene: 10842 GeneCards: CIP2A
Gene location (Human) Chr. Chromosome 3 (human)[1] Band 3q13.13 Start 108,549,864 bp[1] End 108,589,644 bp[1]
Gene location (Mouse) Chr. Chromosome 16 (mouse)[2] Band 16|16 B5 Start 48,994,185 bp[2] End 49,019,709 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • GO:0001948 protein binding • cadherin binding • protein homodimerization activity Cellular component • integral component of membrane • cell membrane • membrane • cytoplasm • cytosol Biological process • positive regulation of neural precursor cell proliferation • spermatogenesis Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	57650	224171
Ensembl	ENSG00000163507	ENSMUSG00000033031
UniProt	Q8TCG1	Q8BWY9
RefSeq (mRNA)	NM_020890	NM_172616
RefSeq (protein)	NP_065941	NP_766204
Location (UCSC)	Chr 3: 108.55 – 108.59 Mb	Chr 16: 48.99 – 49.02 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Function

Protein phosphatase 2A (PP2A) is a trimeric serine-threonine phosphatase consisting of a catalytic C-subunit (PP2Ac), a scaffolding A-subunit and various regulatory B-subunits. Importantly, it has been estimated that collectively PP2A complexes can dephosphorylate a vast majority of all cellular serine/threonine phosphorylated proteins including large number of phosphoproteins involved in cancer maintenance and progression. The functional role of PP2A as a human tumor suppressor was validated by studies initiated by the Weinberg laboratory, which demonstrated that normal human cells immortalized by overexpression of TERT and inhibition of p53 and Rb, could not be transformed by oncogenic forms of H-Ras without simultaneous inhibition of PP2A activity. These studies established the paradigm that increased activity of oncogenic kinases is not sufficient to drive human cell transformation if PP2A activity is not simultaneously inhibited. In striking contrast to the tumor suppressor p53, which in human tumors is mainly inactivated by mutations, PP2A complex proteins are mutated at low frequency (http://www.cbioportal.org) and rather seem to be inhibited by overexpression of PP2A inhibitor proteins such as CIP2A, PME-1 and SET.

CIP2A inhibits PP2A tumor suppressor activity in human malignancies.[7] More specifically, CIP2A was demonstrated to inhibit PP2A activity towards oncogenic transcription factor c-Myc, and thereby prevent c-Myc proteolytic degradation. Moreover, CIP2A is required for the malignant cellular growth and for in vivo tumor formation. In accordance with the oncogenic role of CIP2A, overexpression of CIP2A promotes Ras-elicited cell growth and transforms immortalized human cells (HEK-TERVs). More recently CIP2A has been shown to regulate phosphorylation and activity of many other oncoproteins and to drive malignant cell growth and tumorigenesis in various human cancer types. Importantly, CIP2A deficient mice are viable, suggesting that targeting of oncogenic function of CIP2A would not results in serious side-effects.

Clinical significance

CIP2A is over-expressed in several common human malignancies including, human head and neck squamous cell carcinoma (HNSCC), colon cancer, gastric cancer, breast cancer, prostate cancer and lung cancer. Notably, in these cancer types CIP2A over-expression is observed with very high frequency; in breast cancer around 40% of cancer patients are over-expressing CIP2A whereas in all other studied cancer types the frequency is between 65-87 percent. In breast cancer CIP2A expression correlates with disease aggressivity whereas in gastric and lung cancer CIP2A expression predicts for poor patient survival.[8][9] To date high CIP2A expression has been observed to predict poor patient prognosis in more than dozen human cancer types, which makes it one of the most frequently altered human oncoprotein with clinical relevance.

CIP2A is also over expressed in prostate cancer,[10] lung cancer,[11] oral squamous cell carcinoma,[12] and gastric cancer.[8] Furthermore, the expression of CIP2A correlates with breast cancer aggressivity.[13] It is also implicated in some Chronic Myeloid Leukemia (CML) resistance to imatinib (Gleevec).

References

1. GRCh38: Ensembl release 89: ENSG00000163507 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000033031 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Nagase T, Kikuno R, Ishikawa K, Hirosawa M, Ohara O (Sep 2000). "Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Res. 7 (2): 143–50. doi:10.1093/dnares/7.2.143. PMID 10819331.
6. "Entrez Gene: KIAA1524 KIAA1524".
7. Junttila MR, Puustinen P, Niemelä M, et al. (2007). "CIP2A inhibits PP2A in human malignancies". Cell. 130 (1): 51–62. doi:10.1016/j.cell.2007.04.044. PMID 17632056. S2CID 7748174.
8. Khanna A, Böckelman C, Hemmes A, Junttila MR, Wiksten JP, Lundin M, Junnila S, Murphy DJ, Evan GI, Haglund C, Westermarck J, Ristimäki A (June 2009). "MYC-dependent regulation and prognostic role of CIP2A in gastric cancer". J. Natl. Cancer Inst. 101 (11): 793–805. doi:10.1093/jnci/djp103. PMID 19470954.
9. Soo Hoo L, Zhang JY, Chan EK (2002). "Cloning and characterization of a novel 90 kDa 'companion' auto-antigen of p62 over-expressed in cancer". Oncogene. 21 (32): 5006–15. doi:10.1038/sj.onc.1205625. PMID 12118381.
10. Vaarala MH, Väisänen MR, Ristimäki A (2010). "CIP2A expression is increased in prostate cancer". J. Exp. Clin. Cancer Res. 29 (1): 136. doi:10.1186/1756-9966-29-136. PMC 2984408. PMID 20964854.
11. Dong QZ, Wang Y, Dong XJ, Li ZX, Tang ZP, Cui QZ, Wang EH (September 2010). "CIP2A is Overexpressed in Non-Small Cell Lung Cancer and Correlates with Poor Prognosis". Ann Surg Oncol. 18 (3): 857–865. doi:10.1245/s10434-010-1313-8. PMID 20842459. S2CID 10445927.
12. Basile JR, Czerninski R (November 2010). "The role of CIP2A in oral squamous cell carcinoma". Cancer Biol. Ther. 10 (7): 700–2. doi:10.4161/cbt.10.7.13151. PMID 20729627.
13. Côme C, Laine A, Chanrion M, Edgren H, Mattila E, Liu X, Jonkers J, Ivaska J, Isola J, Darbon JM, Kallioniemi O, Thézenas S, Westermarck J (August 2009). "CIP2A is associated with human breast cancer aggressivity". Clin. Cancer Res. 15 (16): 5092–100. doi:10.1158/1078-0432.CCR-08-3283. PMID 19671842.

• IL-10 promotes tumor aggressiveness via upregulation of CIP2A transcription in lung adenocarcinoma. Sung WW et al.,. Clin Cancer Res. 2013 Aug 1;19(15):4092-103
• Senescence sensitivity of breast cancer cells is defined by positive feedback loop between CIP2A and E2F1. Laine A et al., Cancer Discov.2013 Feb;3(2):182-97
• CIP2A is a target of bortezomib in human triple negative breast cancer cells. Tseng LM et al. Breast Cancer Res. 2012 Apr 26;14(2):R68
• CIP2A promotes proliferation of spermatogonial progenitor cells and spermatogenesis in mice. Ventelä S et al., PLoS One.2012;7(3):e33209
• Cancerous inhibitor of PP2A (CIP2A) at diagnosis of chronic myeloid leukemia is a critical determinant of disease progression. Lucas CM et al., Blood. 2011 Jun 16;117(24):6660-8
• The dependence receptor UNC5H2/B triggers apoptosis via PP2A-mediateddephosphorylation of DAP kinase. Guenebeaud C, et al., Mol Cell. 2010 Dec 22;40(6):863-76
• CIP2A mediates effects of bortezomib on phospho-Akt and apoptosis in hepatocellular carcinoma cells. Chen KF et al.,. Oncogene 2010 Nov 25;29(47):6257-66
• CIP2A is associated with human breast cancer aggressivity. Côme C, et al., Clin Cancer Res. 2009 Aug15;15(16):5092-100
• MYC-dependent regulation and prognostic role of CIP2A in gastric cancer. Khanna A, et al., J Natl Cancer Inst .2009 Jun 3;101(11):793-805
• CIP2A inhibits PP2A in human malignancies. Junttila MR, et al., Cell. 2007 Jul 13;130(1):51-62

Further reading

• Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination". Genome Res. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948. PMID 11076863.
• Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
• Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Rep. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614.
• Soo Hoo L, Zhang JY, Chan EK (2002). "Cloning and characterization of a novel 90 kDa 'companion' auto-antigen of p62 overexpressed in cancer". Oncogene. 21 (32): 5006–15. doi:10.1038/sj.onc.1205625. PMID 12118381.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930. PMID 15489336.
• Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006". Nucleic Acids Res. 34 (Database issue): D415–8. doi:10.1093/nar/gkj139. PMC 1347501. PMID 16381901.
• Junttila MR, Puustinen P, Niemelä M, et al. (2007). "CIP2A inhibits PP2A in human malignancies". Cell. 130 (1): 51–62. doi:10.1016/j.cell.2007.04.044. PMID 17632056. S2CID 7748174.