Human Glia-derived nexin(SERPINE2) ELISA kit

1. Study identified a secreted protein, SerpinE2 or glia-derived nexin, as causative for the highly invasive potential of slow-cycling melanoma cells. PMID: 28925403
2. miR-199a-3p overexpression inhibited the expression of the extracellular serine protease inhibitor E2 (SerpinE2). PMID: 28677735
3. The role of PN-1 in the pathogenesis of intervertebral disk degeneration PMID: 27460424
4. SerpinE2 is required in the extracellular milieu of breast tumors where it acts in multiple ways to regulate tumor matrix deposition, thereby controlling tumor cell dissemination. PMID: 27793045
5. Single nucleotide polymorphisms in EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population. PMID: 27193053
6. high expression of SerpinE2 in osteosarcoma stimulates cell proliferation, promotes drugresistance, and results in poor survival by regulating CDK4 and cyclin D1. PMID: 27221371
7. The results indicate that SERPINE2 and SLPI play a significant role in the development of papillary thyroid cancer and imply that the evaluation of serum concentrations of both anticoagulant molecules may be considered as additional marker for the differentiation of malignancies during the preoperative diagnosis of patients with thyroid gland tumors. PMID: 28255192
8. We filtered four OSCC genes including SERPINB9, SERPINE2, GAK, and HSP90B1 through the gene global prioritization score (P < 0.005). PMID: 26318431
9. together, these data demonstrate that SERPINE2 might prevent cartilage catabolism by inhibiting the expression of MMP-13, one of the most relevant collagenases, involved in cartilage breakdown in OA. PMID: 26305372
10. The results suggest that the rs3795879 polymorphism of SERPINE2 is not a risk factor for chronic obstructive pulmonary disease. PMID: 26214473
11. aberrant Serpine2/Pn-1 is required for proliferation of human and mouse medulloblastoma cells. PMID: 25901736
12. Our findings indicate that upregulated SERPINE2 may contribute to the aggressive phenotype of gastric cancer and suggest that SERPINE2 can be used as a novel prognostic factor and anticancer target in patients with gastric cancer. PMID: 25359682
13. MAGI2, SERPINE2, and NT5C3B expression levels are associated with airway wall thickening and additionally with bronchial inflammation, emphysema, and lung function, respectively, all features of chronic obstructive pulmonary disease. PMID: 25517131
14. Haplotypes carrying major alleles of rs729631 (C), rs975278 (G), rs7583463 (C) of SERPINE2 had protective effect on lung function amongst South Indian male smokers with COPD. PMID: 24587150
15. role in lung homeostasis and pulmonary fibrosis PMID: 25199049
16. SERPINE2 and PLAU are involved in cumulus expansion and oocyte maturation. PMID: 24023701
17. Studies suggest that protease nexin 1 as a marker of prostate cancer. PMID: 23385179
18. PN1 regulates Hh signaling by decreasing protein levels of the Hh ligand Sonic (SHH) and its downstream effectors. PMID: 23041623
19. crystal structures of PN1 in complex with heparin and catalytically inert thrombin suggest a unique 2-step mechanism of thrombin recognition involving rapid electrostatics-driven association PMID: 22618708
20. PN-1 has direct antiangiogenic properties and is a yet-unrecognized player in the angiogenic balance PMID: 22331468
21. Data suggested that there was no significant association between SERPINE2 polymorphism and COPD susceptibility in the Chinese Han population. PMID: 22028159
22. SERPINE2 gene is a chronic obstructive pulmonary disease susceptibility gene, and block 1 of SERPINE2 appears to be the genetic variant region that affects the Han Chinese. PMID: 21611750
23. The variant allele of the rs729631 SNP was found to pose over two-fold risk for overall panlobular changes and over four-fold risk for pathological panlobular changes. PMID: 22145704
24. Results weakly support SERPINE2 as a Dutch hypothesis candidate gene through nominally significant associations with asthma and related traits. PMID: 21436250
25. data identify the temporal and spatial SERPINE2 distribution in the human placenta and suggest its possible role in modulating tissue remodeling of extravillous trophoblasts in the placenta during pregnancy. PMID: 21806836
26. SERPINE2 protein is highly expressed in the endometrium during the secretory phase, indicating that it may participate in tissue remodeling involved in implantation. PMID: 21426587
27. platelet PN-1 can be considered as a new important regulator of thrombolysis in vivo PMID: 21403095
28. In cerebellum, thrombin can activate PAR-1 expression after ICH, and PN-1 appears quickly after Intracerebral hemorrhage in order to control the deleterious effect of thrombin. PMID: 20819545
29. data indicate that serpinE2 is up-regulated by oncogenic activation of Ras, BRAF and MEK1 and contributes to pro-neoplastic actions of ERK signaling in intestinal epithelial cells. PMID: 20942929
30. SERPINE2 may be a risk factor for the development of emphysema and its association with emphysema may be stronger in smokers. PMID: 21067581
31. SERPINE2 was overexpressed in the ER-negative breast cancer group. PMID: 20805453
32. human astrocytes express Pn-1 and astrocytic expression is regulated in a dynamic manner by injury-related factors PMID: 20623540
33. SERPINE2, was previously identified as a COPD susceptibility gene in the chromosome 2q linkage region. Using independent genotyping data in 2 smaller studies in Boston and Norway the results were replicated. PMID: 20463177
34. SERPINE2 was identified as a possible promoter of testicular germ cell tumors lymph node metastasis. PMID: 20035713
35. Results suggest that the SERPINE2 gene contributes to the susceptibility to COPD. PMID: 19949669
36. Platelet PN-1 is a key player in the thrombotic process, whose negative regulatory role has been, up to now, markedly underestimated. PMID: 19855083
37. Elevated levels of GDN/PN1 and XIP mRNAs induced by Allitridi provide valuable molecular evidence for elucidating garlic's efficacies against neurodegenerative and inflammatory diseases. PMID: 11925594
38. PN1 may play a much larger role in the modeling and remodeling of brain tissues during development and is not simply an extravasated thrombin clearance mechanism as previously suggested PMID: 12356769
39. the 4G/4G-PAI-1 genotype might be a protective factor against atherothrombotic cerebral infarction (ACI), whereas the factor V point mutation (1691G-A) and the factor VII Arg/Gln353 gene polymorphism have not proved to be risk factors for ACI PMID: 12859287
40. The pericyte expression of protease nexin 1 may provide endogenous anticoagulant activity. PMID: 16015279
41. Arg15, Phe34, Pro13, and Arg20 are important for FXIa inhibition by PN2 Kunitz protease inhibitor domain PMID: 16085935
42. SERPINE2 is a COPD-susceptibility gene and is likely influenced by gene-by-smoking interaction. PMID: 16358219
43. This study shows that syndecan-1-mediated internalization of protease nexin-1 stimulated the Ras-ERK signaling pathway. PMID: 16741952
44. Expression array analysis demonstrated association and repication of SERPINE2 as a potential COPD susceptibility gene. PMID: 16921128
45. Protease nexin-1 forms complexes with thrombomodulin and modulates its anticoagulant activity. PMID: 17379830
46. provides support for SERPINE2 as a COPD susceptibility gene PMID: 17446335
47. Co-injection of pancreatic stellate cells and tumor cells dramatically enhances the invasive potential of SERPINE2-expressing SUIT-2 cells in nude mice. PMID: 17703087
48. Macrophages and platelets are the major source of protease nexin-1 in human atherosclerotic plaque. PMID: 18617644
49. in severe COPD, SNPs in EPHX1 and SERPINE2 were associated with hypoxemia PMID: 19017876
50. Here, we report that nexin-1 inhibits trypsin-4, and forms stable complexes only with this trypsin-isoenzyme. This result suggests that nexin-1 could modulate trypsin activity in brain where both nexin-1 and trypsin-4 are expressed. PMID: 19249338

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HGNC: 8951

OMIM: 177010

KEGG: hsa:5270

STRING: 9606.ENSP00000415786

UniGene: Hs.38449