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抗Human SPRY1 抗体:
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Human Monoclonal SPRY1 Primary Antibody for IHC (p), ELISA - ABIN564437
Moghaddam, Amini, Wei, Pourgholami, Morris: Initial report on differential expression of sprouty proteins 1 and 2 in human epithelial ovarian cancer cell lines. in Journal of oncology 2012
Show all 2 Pubmed References
Human Polyclonal SPRY1 Primary Antibody for ELISA, WB - ABIN564436
Mekkawy, De Bock, Lin, Morris, Wang, Pourgholami: Novel protein interactors of urokinase-type plasminogen activator receptor. in Biochemical and biophysical research communications 2010
Human Polyclonal SPRY1 Primary Antibody for ELISA, IHC - ABIN4355747
Hanafusa, Torii, Yasunaga, Matsumoto, Nishida: Shp2, an SH2-containing protein-tyrosine phosphatase, positively regulates receptor tyrosine kinase signaling by dephosphorylating and inactivating the inhibitor Sprouty. in The Journal of biological chemistry 2004
Although the expression of SPRY1 was low when compared with other tumors, SPRY1 was variably expressed in primary Ewing sarcoma tumors and higher expression levels were significantly associated with improved outcome in a large patient cohort.
SPRY1 and SPRY2 (显示 SPRY2 抗体) mRNA transcripts were significantly upregulated in human CRC (显示 CALR 抗体). Suppression of SPRY2 (显示 SPRY2 抗体) repressed AKT2 (显示 AKT2 抗体) and EMT (显示 ITK 抗体)-inducing transcription factors and significantly increased E-cadherin (显示 CDH1 抗体) expression. Concurrent downregulation of SPRY1 and SPRY2 (显示 SPRY2 抗体) also increased E-cadherin (显示 CDH1 抗体) and suppressed mesenchymal markers in colon cancer cells.
Spry1 plays a selective role in at least a subset of triple-negative breast cancer to promote the malignant phenotype via enhancing EGF (显示 EGF 抗体)-mediated mesenchymal phenotype.
Suppression of SPRY1 by age-associated methylation inhibits the replenishment of the muscle stem cell pool.
Cosuppression of Sprouty and Sprouty-related negative regulators of FGF signalling in prostate cancer
There is an inverse correlation between the expression of Spry1 and growth, proliferation, invasion and migration of ovarian cancer cells.
A random population of LNCaP prostate cancer cells comprises a heterogeneous group of cells with different androgen-deprivation sensitivities and potential for invasiveness; expression levels of 2 genes known to be regulated by miR (显示 MLXIP 抗体)-21, an androgen-regulated microRNA, SPRY1 and JAG1 (显示 JAG1 抗体) were lower in an androgen insensitive clone, than an androgen sensitive clone.
The Spry1 acts as a sensor of mitogenic activity that not only attenuates RTK signaling but also induces a cellular senescence response to avoid uncontrolled proliferation.
Spry1 and Spry4 (显示 SPRY4 抗体) have opposing roles in VSMC phenotypic modulation, and Spry1 maintains the VSMC differentiation phenotype in vitro in part through an Akt (显示 AKT1 抗体)/FoxO (显示 FOXO3 抗体)/myocardin (显示 MYOCD 抗体) pathway.
Re-expression of SPRY1, a repressed target of BCL11B (显示 BCL11B 抗体), limits the transformation capacity of Ewing sarcoma cells.
Here, we present a novel mouse model of pheochromocytoma consisting of double-heterozygous mice for Pten (显示 PTEN 抗体) and Sprouty1 (Spry1), which leads to pheochromocytomas that appear at earlier onset and grow at a higher rate than those from Pten (显示 PTEN 抗体)+/- mice.
Sprouty gain of function disrupts lens cellular processes and growth by restricting receptor tyrosine kinase (显示 ERBB3 抗体) signaling.
In vivo analysis of thyroid glands from Spry1 knockout mice reveals that Spry1 induces a senescence-associated secretory phenotype via activation of the NFkappaB pathway.
showed that hSpry1 overexpression prevents VEGF secretion
Spry1 and Spry2 (显示 SPRY2 抗体) coordination is required for normal development of the external genitalia in mice
conjunctival epithelial Spry1 and Spry2 (显示 SPRY2 抗体) redundantly promote eyelid closure.
Findings demonstrate that Pokemon (显示 ZBTB7A 抗体) suppresses Sprouty1 expression through a miR (显示 MLXIP 抗体)-21-mediated mechanism, affecting the growth and proliferation of liver cancer cells.
ISG15 mRNA expression and IFN-dependent antiviral responses are enhanced in Spry1,2,4 triple knock-out mouse embryonic fibroblasts, consistent with negative feedback regulatory roles for Spry proteins in IFN-mediated signaling.
When Spry1 and Spry2 (显示 SPRY2 抗体) loss-of-function occurs in the context of heterozygosity for a null allele of the tumor suppressor gene Pten (显示 PTEN 抗体), there is a striking increase in prostatic intraepithelial neoplasia and evidence of neoplastic invasion.
May function as an antagonist of fibroblast growth factor (FGF) pathways and may negatively modulate respiratory organogenesis.
protein sprouty homolog 1
, sprouty, Drosophila, homolog of, 1 (antagonist of FGF signaling)
, sprouty 1 protein
, sprouty homolog 1, antagonist of FGF signaling (Drosophila)
, sprouty homolog 1, antagonist of FGF signaling
, sprouty 1
, sprouty homolog 1a, antagonist of FGF signaling
, sprouty homolog 1b, antagonist of FGF signaling
, inhibitor of receptor tyrosine kinases