ATP2A2 Antibody

1. SGK3 a kinase transcriptionally regulated by estrogen receptor alpha (ERalpha) in breast cancer, sustains ERalpha signaling and drives the acquired aromatase inhibitors resistance by protecting against endoplasmic reticulum (EnR) stress-induced ERalpha downregulation and cell death through preserving SERCA2b function. PMID: 28174265
2. Darier disease (DD) is a rare autosomal dominant skin disorder due to mutations in the ATP2A2 gene. PMID: 29142187
3. SERCA2a gene transfer significantly improves left ventricle function and dimensions in doxorubicin-induced cardiomyopathy, suggesting LV-SERCA2a gene transfer an attractive treatment modality for doxorubicin-induced heart failure. PMID: 27203155
4. Studies indicate that Darier disease (DD) is caused by mutations in the ATP2A2 gene, whereas the ATP2C1 gene is associated with Hailey-Hailey disease (HHD). PMID: 28035777
5. Taken together, these results suggest that SERCA2 contributes to the migration of CCL21-activated Dendritic Cells as an important feature of the adaptive immune response and provide novel insights regarding the role of SERCA2 in Dendritic Cells functions. PMID: 27538371
6. Novel mutations in Darier disease and association to self-reported disease severity PMID: 29028823
7. VMP1 modulates SERCA2 activity to control endoplasmic reticulum contacts for autophagosome formation. PMID: 28890335
8. The left atrium / right atrium expression ratio was significantly increased in Atrial fibrillation for SERCA2 - gene related to calcium uptake and release, and located on the sarcoplasmic reticulum membrane. PMID: 27494721
9. Loss of SERCA2 impairs ER-to-Golgi transport of nascent DC. PMID: 28156030
10. We propose that the increased SERCA1a expression indicates the existence and location of compensating mechanisms in ischemic muscle. PMID: 28648117
11. Results show that ATP2A2 is variably expressed in astrocytoma tissues and its expression correlates with tumor grade. Its overexpression suppresses growth of astrocytoma cells. PMID: 28339043
12. study identifies a novel splice acceptor site mutation in the ATP2A2 gene, in a family showing Darier disease PMID: 27595213
13. Data suggest that mutations of the sarcoplasmic/endoplasmic reticulum calcium ATPase 2 (ATP2A2) gene may lead to the occurrence of Darier disease (DD) in both familial and sporadic cases with DD. PMID: 27577212
14. Phospholamban and sarcolipin are membrane proteins that differentially regulate SERCA function. (Review) PMID: 26743715
15. High SERCA2 expression is associated with colorectal cancer. PMID: 26608678
16. Quantification of SERCA2 mRNA or protein expression levels revealed no differences in airway smooth muscle cells obtained from subjects with asthma compared to non-asthmatic controls. PMID: 25880173
17. Inhibition of SERCA2 activity by curcumin disrupts the Ca(2+) homeostasis and thereby promotes apoptosis in ovarian cancer cells. PMID: 26607901
18. The association between Darier disease and bipolar disorder is manifest also in the population, and data suggest that genetic variability within the ATP2A2 gene that causes Darier disease also confers susceptibility for bipolar disorder. PMID: 25213221
19. ATP2A2 mutation was found in patients diagnosed with Darier disease. PMID: 26051059
20. Two novel missense mutations, p.R603I and p.G749V, in the ATP2A2 gene in two families containing individuals diagnosed with Darier disease. PMID: 25872913
21. study identified two heterozygous mutations in exon 12 of the ATP2A2 gene in two different Darier disease families PMID: 24552170
22. Case Report: ATP2A2 missense mutation at one of the calcium-binding residues causing Darier's disease. PMID: 24979555
23. We report here two Chinese Han patients with sporadic Darier disease; mutation analysis of ATP2A2 supported the genetic diagnosis. PMID: 25283811
24. SPCA1 and sarco/endoplasmic reticulum Ca(2+) ATPase2 (SERCA2) encoded by ATP2A2 are two essential calcium pumps needed for Ca(2+) homeostasis maintenance in keratinocytes. PMID: 25256005
25. SERCA and PMCA pump activities are strongly affected by the localization of F508del-CFTR protein. PMID: 25661196
26. Evidence obtained from different diabetes models has suggested a role for advanced glycation end products formation, oxidative stress and increased O-GlcNAcylation in the lowered SERCA2 expression observed in diabetic cardiomyopathy PMID: 25270119
27. Gene therapy in heart failure. SERCA2a as a therapeutic target. PMID: 25327883
28. PDE3A is part of a SERCA2 signaling complex in cardiac myocytes. PMID: 25593322
29. ERK activation is sufficient to reduce SERCA2 mRNA. PMID: 25008120
30. A large Chinese family have a novel missense mutation in Darier disease. PMID: 23621824
31. Exposure of normal keratinocytes to the SERCA2 inhibitor thapsigargin recapitulated these abnormalities, supporting the role of loss of SERCA2 function in impaired desmosome and adherens junction formation. PMID: 24390139
32. a novel role of SERCA2b in facilitating the blockade of human liposarcoma differentiation PMID: 24508653
33. palmitoylated calnexin interacts with sarcoendoplasmic reticulum Ca(2+) transport ATPase 2b and this interaction determines endoplasmic reticulum Ca(2+) content and the regulation of endoplasmic reticulum-mitochondria Ca(2+) crosstalk. PMID: 23843619
34. I-1 and sarco/endoplasmic reticulum Ca2+ -ATPase synergistically induce the vascular smooth muscle cell contractile phenotype. PMID: 24249716
35. the protective effect of hepatic stimulator substance against endoplasmic reticulum stress may be associated with the removal of reactive oxygen species to restore the activity of the sarco-endoplasmic reticulum Ca(2+)-ATPase. PMID: 24284796
36. Novel ATP2A2 mutations in a large sample of individuals with Darier disease. PMID: 23356892
37. The results demonstrate that (*)NO-mediated activation of SERCA2b via S-glutathiolation of cysteine-674 is required for VEGF-induced EC Ca(2+) influx and migration, and establish redox regulation of SERCA2b as a key component in angiogenic signaling. PMID: 22472004
38. Downregulation of SERCA2a plays a critical role in modulating vascular and right ventricular phenotype associated with pulmonary arterial hypertension. PMID: 23804254
39. The gene encodes a calcium-ATPase type 2 in the sarco-/endoplasmic reticulum (SERCA2), which belongs to the large family of P-type cation pumps. PMID: 23337962
40. By introducing SERCA2 gene to an experimental heart failure model, cardiac functions and prognosis were improved and cardiac remodelling suppressed. SERCA2 is believed to be an important key to correct molecular network in heart failure. PMID: 23229631
41. The protein SERCA2 expression was decreased and 43 miRNAs were deregulated in infarcted myocardium compared to corresponding remote myocardium. PMID: 23066896
42. Shared histopathological features of acrokeratosis verruciformis of Hopf with Darier disease suggest that they are allelic disorders with variable expression of the same disease. Identical mutations in ATP2A2 in both diseases were not reported to date. PMID: 22814319
43. we report one novel heterozygous splice site mutation of ATP2A2 gene and one previously described nonsense mutation. PMID: 22909361
44. a higher Ca(2+) affinity of SERCA2b relative to other SERCA isoforms, not only on the cytosolic side, but also on the luminal side. PMID: 23024360
45. SERCA2 dysregulation is a pathogenic event in 22q11 deletion syndrome (22q11DS) and schizophrenia. PMID: 23055483
46. We report two novel mutations of the ATP2A2 gene in two Chinese families with Darier disease. PMID: 22329366
47. Review article highlights the regulatory mechanisms of cardiac contractility by way of the multimeric SERCA/phospholamban (PLN)-ensemble. PMID: 22679139
48. functional interactions of SERCA2b and Bcl-2 in the cell may be modulated by HSP70 and other chaperones and stress-regulated proteins. PMID: 22360692
49. Loss of SERCA2 expression is observed in human diabetes and occurs within the context of PPAR-gamma phosphorylation and CDK5 activation. PMID: 22240811
50. SERCA2-controlled Ca(2)+-dependent keratinocyte adhesion and differentiation is mediated via the sphingolipid pathway. PMID: 22277942

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HGNC: 812

OMIM: 101900

KEGG: hsa:488

STRING: 9606.ENSP00000440045

UniGene: Hs.506759