- Symbol
- Pawr
- Aliases
- PAR4; Par-4; 2310001G03Rik
- Name
- PRKC, apoptosis, WT1, regulator
- Organism
- Mus musculus (AnAge)
- Known functions and activities
- Tumor-suppressor protein that induces apoptosis in cancer cells, but not in normal/immortalized cells
- Observations
- Par4-null mice are prone to develop tumours, both spontaneously and on carcinogenic treatment. The endometrium and prostate of Par4-null mice were
particularly sensitive to the development of proliferative lesions. Most (80%) Par4-null females presented endometrial hyperplasia by 9 months of age, and a significant proportion (36%) developed endometrial adenocarcinomas after 1 year of age. Similarly, Par4- null males showed a high incidence of prostate hyperplasia and prostatic intraepithelial neoplasias, and were extraordinarily sensitive to testosterone-induced prostate hyperplasia. 25% reduction in mean LS was observed compared to WT and 20% reduction in MLS. Heterozygote KOLS did not differ significantly from the WT.
- % change in max lifespan
- Maximum lifespan is 20% lower.
- % change in avg or median lifespan
- Average lifespan is 25% lower.
- Lifespan Effect
- Decrease
- Genetic Manipulation
- Deletion
- Longevity Category
- Pro-Longevity
- Primary reference
-
- Observations
- Mice overexpressing the pro-apoptotic protein domain were resistant to tumours. Transgenic animals showed normal fertility, viability, and ageing, though they were slightly longer-lived possibly because of the cancer-resistance.
- Lifespan Effect
- Increase
- Genetic Manipulation
- Overexpression
- Longevity Category
- Pro-Longevity
- Primary reference
-
- Danio rerio
- pawr
- Homo sapiens
- PAWR
- Rattus norvegicus
- Pawr
- Mouse Genome Informatics
- Search
- Ensembl
- Search
- Entrez Gene
- View on Entrez Gene database (114774)
- Homologues
- Search HomoloGene
- UniProt
- Search
- Internet
- Search Google or Search Google Scholar