anti-Paternally Expressed 10 (PEG10) Antibodies

Human Paternally Expressed 10 (PEG10) interaction partners

1. PEG10 knockdown inhibited cell viability, migration and invasion, induced cell apoptosis through miR-506 upregulation, as well as inactivation of Raf/MEK/ERK and JAK1/STAT3 signal pathways in human glioma cell line U251 cells

2. USP11 depletion suppresses cell proliferation and wound healing in lung epithelial cells, and these effects are reversed by E2F1 and PEG10 overexpression.

3. lncRNA PEG10 functioned as an oncogene in bladder cancer by sponging miR-134.

4. PEG10 repressed TGF-beta and BMP signaling in chondrosarcoma cells. PEG10 knockdown increased the level of phosphorylated SMAD3 and SMAD1/5/9.

5. PEG10 might be a molecular target for suppressing the aggressive phenotypes of chondrosarcoma cells.

6. PEG10 expression is associated with advanced clinicopathological characteristics and can be used as a prognostic biomarker in patients with solid tumors.

7. Results demonstrated that an increased expression of PEG10 is associated vessel invasion, and the overall survival time of PC patients. E2F-1 mediated PEG10 overexpression promotes pancreatic cancer (PC) cell proliferation via accelerating cell cycle progression and increase migration and invasion through ERK/MMP7 pathway. These results suggest that PEG10 may serve as an oncogene in PC pathogenesis.

8. miR-122 suppresses PEG10 expression via direct binding to the 3'-UTR of the PEG10 transcript.

9. PEG10 expression associates with the lymph node metastasis and overall survival of hepatocellular carcinoma patients.PEG10 expression level is essential for TGF-beta1 induced epithelialmesenchymal transition.

10. Knockdown of PEG10 expression by siRNA could lead to growth arrest and cell apoptosis in diffuse large B cell lymphoma cells in vitro.

11. PEG10 protein could be a potential biomarker predicting early recurrence and recurrence-free survival in HCC patients after curative resection, even in those with normal serum alpha-fetoprotein levels.

12. Study shows that expression level of PEG10 was significantly elevated in breast cancer tissues and associated with distant metastasis and poor clinical outcome and provides evidence that PEG10 is a crucial oncogene.

13. important role in trophoblast proliferation and promotes trophoblast invasion through TIMP-1

14. Results revealed that PEG10 high expression was closely associated with the TNM classification in lung cancer and is a critical indicator for poor prognosis. Also, It promotes significantly proliferation, migration and invasion of A549 lung cancer cells.

15. The downregulated expression of the imprinted gene PEG10 may be an important reason for the occurrence of preeclampsia.

16. elevated expression of PEG10 is likely to be involved in the pathophysiology of preeclampsia

17. promotes migration of Burkitt's lymphoma cells via upregulation of matrix metalloproteinase-2 and -9

18. Overexpression of PEG10 and TSG101 was detected in gallbladder adenocarcinoma.

19. PEG10 imprinting is lost in a majority of hepatocellular carcinomas and no correlation exists between the imprinting status of PEG10 and its expression in HCC tissues.

20. the mRNA expression level of PEG10 were significantly up-regulated in tumorous liver tissues compared with corresponding nontumorous counterparts.

Mouse (Murine) Paternally Expressed 10 (PEG10) interaction partners

1. Loss of DNA methylation at the Peg10 imprinted gDMD associated with decreased embryonic viability and decreased labyrinthine volume.

2. Knockdown of Syncytin-A demonstrated a functional regulation of cell-cell fusion, where knockdown of Peg10 showed no involvement in cell fusion

3. Programmed -1 ribosomal frameshifting in mouse and human Peg10 genes.

4. It is a retrotransposon-derived imprinted gene and plays a essential role in placental formation.(review)

5. Peg10 gene is imprinted, with preferential expression from the paternal allele, and its deletion results in early embryonic lethality.

6. Results indicate that the induction of the imprinted gene paternally expressed 10 (PEG10) may play an important role during liver regeneration or carcinogenesis of the hepatocyte.

7. These findings strongly indicate that peg10 plays a crucial role at the immediate early stage of adipocyte differentiation.

8. the ORF1-2 protein of PEG10, synthesized utilizing the most efficient -1 frameshift mechanism yet documented in vivo, will have an essential function that is intrinsic to the importance of PEG10 in mammals

Cow (Bovine) Paternally Expressed 10 (PEG10) interaction partners

1. the abnormal DNA methylation epigenetic reprogramming of imprinting PEG10 gene in placenta may be one of the main causes of the abnormal development and death of the transgenic cloned cattle.

Pig (Porcine) Paternally Expressed 10 (PEG10) interaction partners

1. polymorphisms in PEG10 and PPP1R9A were associated with fat deposition and carcass traits

2. A transition SNP was identified by microarray expression profiling and confirmed by pyrosequencing in Meishan and white composite swine breeds.

3. The imprinting status of PEG10 is conserved in swine as paternal expression was demonstrated by quantitative allelic sequencing of reciprocal crosses in fetal tissues of whole brain, carcass, liver and placentae.

4. The expression patterns of PLAGL1 and PEG10 genes in two breeds of swine are reported.

5. Gene is monoallelically expressed and may be imprinted in porcine placentas on days 75 and 90 of gestation.