Browse our anti-ATF2 (ATF2) Antibodies

Human Activating Transcription Factor 2 (ATF2) interaction partners

1. Analgesic effect of fentanyl in the cold pressor-induced pain test was significantly associated with rs7583431 SNP in the ATF2 region.

2. beta-catenin-independent regulation of Wnt target genes by RoR2 and ATF2/ATF4 in colon cancer cells

3. Demonstration of an interaction between PCSK9 and ATF-2, which reduces ATF-2/c-Jun dimerization and ATF-2/c-Jun binding to the IFNbeta enhancer. This novel function of PCSK9 should have important implications in optimizing the clinical use of PCSK9 inhibitors.

4. ARHGEF39 promotes tumor growth and invasion by activating the Rac1-P38-ATF2 signaling pathway, as well as increasing the expression of Cyclin A2, Cyclin D1, and MMP2 in NSCLC cells.

5. Our study found that miR-451 regulates the drug resistance of renal cell carcinoma by targeting ATF-2

6. deregulation of the miR-144-5p/ATF2 axis plays an important role in non-small-cell lung cancer cell radiosensitivity.

7. p38alpha and ATF2 expression play a crucial role in the malignant phenotypes of ovarian tumor cells and are a markers of poor prognosis in patients with ovarian serous adenocarcinomas.

8. activation of JNK was found to be dependent on muscarinic acid receptor induced Ca(2+)/CAMKII as well as ROS. JNK dependent phosphorylation of ATF2/c-Jun transcription factors resulted in TGF-beta transcription and its signaling.

9. ATF2 regulated by miR-204 might also play an important role in the regulation of malignant behavior of glioblastoma.

10. We further demonstrated the suppressive function of lncRNA#32 in hepatitis B virus and hepatitis C virus infection. lncRNA#32 bound to activating transcription factor 2 (ATF2) and regulated ISG expression. Our results reveal a role for lncRNA#32 in host antiviral responses.

11. Results show that ATF2 is highly expressed in renal cell carcinoma (RCC) tissues and promotes RCC cell proliferation, migration and invasion. The study suggests that ATF2 exerts an oncogenic role in RCC.

12. These findings point to an oncogenic function for ATF2 in melanoma development that appears to be independent of its transcriptional activity.

13. this study demonstrates that CPEB2 alternative splicing is a major regulator of key cellular pathways linked to anoikis resistance and metastasis.

14. Noxin facilitated the expression of Cyclin D1 and Cyclin E1 through activating P38-activating transcription factor 2 signaling pathway, thus enhanced cell growth of breast cancer

15. these observations suggest that CD99 is involved in the regulation of CD1a transcription and expression by increasing ATF-2.

16. This review provides an overview of the currently known upstream regulators and downstream targets of ATF2. [review]

17. TNF induces the binding of ATF2 to the TNF-responsive element.

18. miR-204 may act as a tumor suppressor by directly targeting ATF2 in non-small cell lung cancer

19. the variant alleles of TSG101 rs2292179 and ATF2 rs3845744 were associated with a reduced risk of breast cancer, particularly for subjects with BMI <24 (kg/m(2)) and postmenopausal women, respectively

20. Results reveal that mitochondrial ATF2 is associated with the induction of apoptosis and BRAF inhibitor resistance through Bim activation.

Fruit Fly (Drosophila melanogaster) Activating Transcription Factor 2 (ATF2) interaction partners

1. This study reveals that Drosophila ATF-2 (dATF-2) is required for heterochromatin assembly, whereas the stress-induced phosphorylation of dATF-2, via Mekk1-p38, disrupts heterochromatin.

2. ATF-2 is critical for regulation of fat metabolism.

3. dATF-2 is activated by the locomotor while it increases sleep, suggesting a role for dATF-2 as a regulator to connect sleep with locomotion.

Cow (Bovine) Activating Transcription Factor 2 (ATF2) interaction partners

1. The current data shows a timely GFP translation in bovine embryos depending on sequences in the 3'UTR of ATF1/2, and indicates a difference between short and long isoforms.

2. Ang II increases endothelial arginase activity/expression through a p38 MAPK/ATF-2 pathway leading to reduced endothelial NO production

3. Data indicate that Ser738/742-to-glutamate protein kinase D mutant increased AngII-induced CREB protein and activating transcription factor 2 phosphorylation, and phospho-CREB binding to the steroidogenic acute regulatory protein promoter.

Mouse (Murine) Activating Transcription Factor 2 (ATF2) interaction partners

1. Phosphorylation of ATF2 at Thr-52 was reduced in the hippocampus of PKCepsilon null mice, suggesting that ATF2 is a phosphorylation substrate of PKCepsilon. PKCepsilon protein concentrations were significantly reduced 4, 24, 48 and 72 h after transient global cerebral ischemia, resulting in translocation of nuclear ATF2 to the mitochondria. Degenerating neurons staining positively with Fluoro-Jade C exhibited cytoplasm...

2. The up-regulation of HMGB1 was thought to be modified by dual channels: in the transcriptional level, it was regulated by JNK1/JNK2-ATF2 axis; post-transcriptionally, it was regulated by the microRNA (miR)-200 family, especially miR-429. miR-429 liver conditional knockout mice (miR-429(Deltahep)), fed either a normal diet or an HFD, showed severe liver inflammation and dysfunction, accompanied by greater expression of ...

3. These findings point to an oncogenic function for ATF2 in melanoma development that appears to be independent of its transcriptional activity.

4. adiponectin inhibited endoplasmic reticulum stress and apoptosis of adipocyte in vivo and in vitro by activating the AMPK/PPARalpha/ATF2 pathway.

5. Quantitative real-time polymerase chain reaction (qRT-PCR) and Western blotting were used to detect the mRNA and protein expressions of p-p38MAPK, AAT, signal transducer and activator of transcription 1 (STAT1) and activating transcription factor2 (ATF2)

6. increased expression of the gene encoding PKCepsilon and abundance of phosphorylated, transcriptionally active ATF2 were observed in advanced-stage melanomas and correlated with decreased FUK expression

7. These data identified a role for ATF2 in regulating melanocyte responses.

8. suppression of tumorigenesis by JNK requires ATF2.

9. Taken together, our observations indicated that SOCS2 could suppress myotube formation, act as an anti-regulator of mitochondria biogenesis via inhibiting p38 MAPK signal pathway.

10. ATF2 is an important transcriptional factor relating to inflammation through the suppression of ATF3 in M1 macrophages of White adipose tissue.

11. ATF-2 plays critical roles for proper expression of tyrosine hydroxylase gene and for neurite extension of catecholaminergic neurons, possibly through repressor-like action.

12. these studies show that the IL-1beta-induced increase in intestinal tight junction permeability was regulated by p38 kinase activation of ATF-2 and by ATF-2 regulation of MLCK gene activity

13. The ATF2 represses renin expression by drifting the transcriptional control of renin gene away from CRE-binding protein (CREB).

14. ATF2 has a critical role in limiting the activities of stress kinases JNK and p38 which are potent inducers of cell death in the CNS

15. ATF2 interacts with beta-cell-enriched transcription factors, MafA, Pdx1, and beta2, and activates insulin gene transcription.

16. MITF is downregulated by ATF2 in the skin of Atf2-/- mice, in primary human melanocytes, and in melanoma cell lines.

17. Growth factor-independent signaling pathways converge in the formation of an active c-Jun.AFT2 dimer, which induces the expression of the anti-apoptotic factor Bcl-X(L) that mediates a pro-survival response.

18. Data show that ATF-2 was rapidly phosphorylated and recruited to the Tnfa promoter following ligation of TLR2.

19. ATF-2 plays an important regulatory role in MAG expression at a specific stage of shi/shi oligodendrocyte differentiation.

20. P38 and this protein are involved in osteoblast osmotic response to elevated extracellular glucose

Xenopus laevis Activating Transcription Factor 2 (ATF2) interaction partners

1. ATF2-based luciferase reporter to monitor non-canonical Wnt signaling in Xenopus embryos.