Mustard NPR1, a mammalian IκB homologue inhibits NF-κB activation in human GBM cell lines
Mustard NPR1, a mammalian IκB homologue inhibits NF-κB activation in human GBM cell lines
| dc.contributor.author | Kesanakurti, Divya | |
| dc.contributor.author | Sareddy, Gangadhara Reddy | |
| dc.contributor.author | Babu, Phanithi Prakash | |
| dc.contributor.author | Kirti, Pulugurtha Bharadwaja | |
| dc.date.accessioned | 2022-03-27T05:16:32Z | |
| dc.date.available | 2022-03-27T05:16:32Z | |
| dc.date.issued | 2009-12-18 | |
| dc.description.abstract | NF-κB activity is tightly regulated by IκB class of proteins. IκB proteins possess ankyrin repeats for binding to and inhibiting NF-κB. The regulatory protein, NPR1 from Brassica juncea possesses ankyrin repeats with sequence similarity to IκBα subgroup. Therefore, we examined whether stably expressed BjNPR1 could function as IκB in inhibiting NF-κB in human glioblastoma cell lines. We observed that BjNPR1 bound to NF-κB and inhibited its nuclear translocation. Further, BjNPR1 expression down-regulated the NF-κB target genes iNOS, Cox-2, c-Myc and cyclin D1 and reduced the proliferation rate of U373 cells. Finally, BjNPR1 decreased the levels of pERK, pJNK and PKCα and increased the Caspase-3 and Caspase-8 activities. These results suggested that inhibition of NF-κB activation by BjNPR1 can be a promising therapy in NF-κB dependent pathologies. © 2009 Elsevier Inc. All rights reserved. | |
| dc.identifier.citation | Biochemical and Biophysical Research Communications. v.390(3) | |
| dc.identifier.issn | 0006291X | |
| dc.identifier.uri | 10.1016/j.bbrc.2009.09.046 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0006291X09018488 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/7673 | |
| dc.subject | IκB | |
| dc.subject | Mustard | |
| dc.subject | NF-κB | |
| dc.subject | NPR1 | |
| dc.subject | p50 | |
| dc.subject | p65 | |
| dc.subject | U373 | |
| dc.title | Mustard NPR1, a mammalian IκB homologue inhibits NF-κB activation in human GBM cell lines | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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