ZFHX3 Antibody

1. alterations in the expression and subcellular localization of ATBF1, as a result of posttranscriptional modifications, are associated with malignant features of colon tumours. PMID: 28713972
2. Study identified DNA methylation (DNAm) site cg07786668 in ZFHX3 that is independently and significantly associated with myocardial infarction (MI) along with DNAm cg17218495 in SMARCA4. These results suggest that the development of MI might be influenced by changes in DNAm at these sites via a pathway that differs from that affected by cardiovascular disease-associated SNPs in these genes. PMID: 28515798
3. using in vitro prolactin induced lactogenic differentiation in an HC11 mouse cell model and an in vivo conditional knockout mouse model we showed that mouse Zfhx3 is essential for mouse mammary epithelial cell differentiation and mouse mammary gland development at the lactation stage through regulation of prolactin receptor expression and the downstream Jak2-Stat5 signaling pathway. PMID: 27129249
4. Increasing experimental data support that ZFHX3 gene plays a critical role in the pathogenesis of atrial fibrillation where it was found up-regulated. [review] PMID: 29126922
5. We showed that the ZFHX3 polymorphism, rs2106261 (A allele), was a risk marker for atrial fibrillation (A)F and AF-related phenotypes. PMID: 28007413
6. Nuclear localization of AT-motif binding factor 1 (ATBF1) indicates better prognosis of urothelial carcinoma. PMID: 27756245
7. Cellular localization of ATBF1 is correlated with its function in breast cancer. Nuclear ATBF1 was co-localized with chromosome during mitosis normally. Estrogen induced translocation of cytoplasmic ATBF1 to nuclei in MCF7. PMID: 28624455
8. The results suggest an additive effect of ZFHX3 and PTEN deletions on the development and progression of prostate neoplasia PMID: 26233892
9. Both ZFHX3 and PITX2c regulate expression of NPPA, TBX5 and NKX2.5. PMID: 26267381
10. In a Caucasian population, genetic variant rs7193343 SNP in ZFHX3 gene is associated with risk of atrial fibrillation. PMID: 26112950
11. The CAA repeat polymorphism in exon 9 of the ZFHX3 gene contributes to the Coronary heart disease susceptibility in the Chinese population. PMID: 25797214
12. ZFHX3 defects are associated with poor outcome in endometroid endometrial cancer. PMID: 26330387
13. Two SNPs (rs2106261, rs6499600) located in gene ZFHX3 showed significant associations with atrial fibrillation in a Chinese Han population. PMID: 24983873
14. ZFHX3 transcription is regulated in a transcript-specific fashion by independent cis-acting transcribed polymorphisms. PMID: 25539802
15. A missense mutation in ZFHX3 results in damage to the ZFHX3 protein structure in patients with extreme atrial fibrillation. PMID: 25391453
16. nuclear localization and SUMOylation are important for the transcription factor function of ATBF1, and that ATBF1 could cooperate with PML NBs to regulate protein SUMOylation in different biological processes. PMID: 24651376
17. Nuclear localization of ATBF1 is frequently interrupted in HNSCC, and the interruption is significantly associated with the progression of HNSCC PMID: 22791392
18. based on observations, nuclear ATBF1 staining was associated with low malignancy profiles of skin cancer PMID: 23317484
19. A polymorphism in the ZFHX3 gene, encoding a cardiac transcription factor, was associated with increased AF risk in HF patients, and the genetic association with AF was more pronounced in HF patients than in the general population. PMID: 23132824
20. findings indicate that Atbf1 plays a role in the development of pubertal mammary gland likely by modulating the function of estrogen-ER signaling in luminal cells and by modulating gene expression in basal cells PMID: 23251482
21. These findings suggest that ATBF1 plays a crucial role in the Progesterone-progesterone receptors signaling pathway in mammary epithelial cells. PMID: 23159610
22. Suppression of ZFHX3 expression in tumor cells decreases the survival rate among patients with NSCLC. PMID: 23144151
23. 3 loci from related cardiovascular genomewide studies were significant: PHACTR1 in large-vessel disease (P=2.63e(-6)), PITX2 in cardioembolic stroke (P=4.78e(-8)), and ZFHX3 in cardioembolic stroke (P=5.50e(-7)). PMID: 23042660
24. Levels of ATBF1 protein in breast tumors are positively correlated with the levels of estrogen-responsive finger protein (EFP). PMID: 22452784
25. gen up-regulates ATBF1 transcription but causes its protein degradation in estrogen receptor-alpha-positive breast cancer cells PMID: 21367855
26. Our results indicate that the s2106261 SNP in ZFHX3 confers a significant risk of atrial fibrillation in a Chinese Han population. PMID: 21107608
27. A novel signaling pathway that links ATM via CREB to the transcription factor ZFHX3, which in turn promotes survival of neurons by inducing expression of platelet-derived growth factor receptor beta, is reported. PMID: 20876357
28. Using DirectDNA sequencing analysis, we detected ATBF1, CYLD, PARK2 and WNT9A mutations in stomach and colorectal cancers PMID: 20854080
29. ATBF1 associates with RUNX3 and translocates to the nucleus in response to TGF-beta signal transduction and might function in the nucleus as tumor suppressor and transcriptional regulator. PMID: 20599712
30. Aberrant expression of ATBF1 induces the expression of various factors that are otherwise suppressed, and this somehow determines the biological features of Alpha-fetoprotein producing gastric cancer. PMID: 14654895
31. In conclusion, ATBF1 can suppress the IL-6-mediated cellular response by acting together with PIAS3. PMID: 14715251
32. ATBF1-A mRNA has a role in lymph node metastasis of breast neoplasms PMID: 15671546
33. Somatic mutations of the transcription factor ATBF1 is associated with human prostate cancer PMID: 15750593
34. Two somatic mutations (shortening of a polypyrimidine tract [Poly(T)n] and a deletion beginning at codon 3381 (3381del)) were each observed in multiple prostate cancer samples and both appear to have an impact on ATBF1 gene function and expression. PMID: 16637072
35. ATBF1 plays a role in breast cancer through transcriptional downregulation rather than mutations. PMID: 16932943
36. Results indicate that ATBF1 in the nucleus negatively regulates the MUC5AC gene in gastric cancer by binding to an AT motif-like element in the MUC5AC promoter. PMID: 17330845
37. Genetic alterations of the ATBF1 gene is associated with gastric cancer PMID: 17671116
38. The ATBF1 gene may contribute to the development of hepatocellular carcinomas via transcriptional down-regulation of mRNA expression, but not by genetic or epigenetic alterations. PMID: 18312352
39. ATBF1 and NQO1 as candidate targets for allelic loss at chromosome arm 16q in breast cancer: absence of somatic ATBF1 mutations and no role for the C609T NQO1 polymorphism. PMID: 18416817
40. ATBF1-A mRNA levels are regulated at the transcriptional stage, but not by genetic mechanisms, deletions (LOH), or mutations. PMID: 18796146
41. Prostate cancer linkage to the same region of 16q23 has been observed by others and the region contains several strong candidate genes including the known prostate cancer tumor suppressor genes ATBF1 and WWOX. PMID: 19035517
42. A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with atrial fibrillation (odds ratio OR = 1.21, P = 1.4 x 10(-10)). PMID: 19597491
43. Meta-analyses of 896 prevalent (15,768 referents) and 2,517 incident (21,337 referents) atrial fibrillation (AF) cases identified a new locus for AF (ZFHX3, rs2106261, risk ratio RR = 1.19; P = 2.3 x 10(-7)). PMID: 19597492

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HGNC: 777

OMIM: 104155

KEGG: hsa:463

STRING: 9606.ENSP00000268489

UniGene: Hs.598297