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GENE:

INPP5J (Inositol Polyphosphate-5-Phosphatase J)

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Other names: Inositol Polyphosphate-5-Phosphatase J, PIPP, Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase A, PIB5PA, INPP5, Phosphatidylinositol (4,5) Bisphosphate 5-Phosphatase, A, Inositol Polyphosphate 5-Phosphatase J, INPP5J
Associations
Trials
1year
Alterations in Blood and Hippocampal mRNA and miRNA Expression, Along with Fat Deposition in Female B6C3F1 Mice Continuously Exposed to Prenatal Low-Dose-Rate Radiation and Their Comparison with Male Mice. (PubMed, Cells)
These gene expression changes may be associated with the increased fat deposition observed following chronic low-dose-rate gamma irradiation exposure. This study underscores the importance of investigating sex-specific biological responses to prenatal gamma irradiation and highlights potential molecular pathways linked to observed physiological changes.
Clinical • Preclinical • Journal
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CD74 (CD74 Molecule) • INPP5J (Inositol Polyphosphate-5-Phosphatase J)
almost2years
PELI1 overexpression contributes to pancreatic cancer progression through upregulating ubiquitination-mediated INPP5J degradation. (PubMed, Cell Signal)
In conclusion, the results suggest that INPP5J, decreased by PELI1 through ubiquitination, may promote PC progression. The PELI1-INPP5J axis represents a potential therapeutic targetable node for PC.
Journal
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INPP5J (Inositol Polyphosphate-5-Phosphatase J) • UBR5 (Ubiquitin Protein Ligase E3 Component N-Recognin 5)
almost3years
Identification of potential tumor antigens and immune subtypes for lung adenocarcinoma. (PubMed, Med Oncol)
the three subtypes were significantly positively correlated with the turquoise module gene list, indicating a good prognosis with high scores. We hope that the identified tumor antigens and immune subtypes can be used for immunotherapy and prognosis in LUAD patients.
Journal • IO biomarker
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CD4 (CD4 Molecule) • INPP5J (Inositol Polyphosphate-5-Phosphatase J)
over3years
A Distinct Glucose Metabolism Signature of Lung Adenocarcinoma With Prognostic Value. (PubMed, Front Genet)
Notably, the low-risk group is more likely to respond to immunotherapy. Overall, this study systematically explored the prognostic value of glucose metabolism and generated a prognostic risk signature with favorable efficacy and accuracy, which help select candidate patients and explore potential therapeutic approaches targeting the reprogrammed glucose metabolism in LUAD.
Journal • IO biomarker
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PRKCB (Protein Kinase C Beta) • INPP5J (Inositol Polyphosphate-5-Phosphatase J)
4years
Predicting signaling pathways regulating demyelination in a rat model of lithium-pilocarpine-induced acute epilepsy: A proteomics study. (PubMed, Int J Biol Macromol)
These findings suggest that the actin cytoskeleton, Tβ4, and MAPK signaling pathways regulate the decrease in pMBP in the hippocampus in a rat model of epilepsy. Our results indicate that regulating the actin cytoskeleton, Tβ4, and MAPK signaling pathways may facilitate the prevention of demyelination in IE.
Preclinical • Journal
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INPP5J (Inositol Polyphosphate-5-Phosphatase J) • MAPK8 (Mitogen-activated protein kinase 8)