dc.contributor.author |
INCHANALKAR, SIDDHI |
en_US |
dc.contributor.author |
BALASUBRAMANIAN, NAGARAJ |
en_US |
dc.date.accessioned |
2022-03-01T04:00:24Z |
|
dc.date.available |
2022-03-01T04:00:24Z |
|
dc.date.issued |
2021-05 |
en_US |
dc.identifier.citation |
Journal of Biosciences, 46, 46 |
en_US |
dc.identifier.issn |
0250-5991 |
en_US |
dc.identifier.issn |
0973-7138 |
en_US |
dc.identifier.uri |
https://doi.org/10.1007/s12038-021-00164-4 |
en_US |
dc.identifier.uri |
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6604 |
|
dc.description.abstract |
Aurora kinases despite their similarity have distinct roles in the cell cycle, which is regulated by cell-matrix adhesion and growth factors. This study reveals loss of adhesion and re-adhesion to differentially regulate Aurora kinases. AURKB activation that drops on the loss of adhesion recovers on re-adhesion in serum-deprived conditions but not in the presence of serum growth factors. A rapid 30 min serum treatment of serum-deprived cells blocks the adhesion-dependent recovery of AURKB, which negatively correlates with Erk activation. AZD mediated inhibition of AURKB in serum-deprived re-adherent cells promotes Erk activation and membrane ruffling, comparable to presence of serum. These studies thus define a novel adhesion-growth factor-dependent regulation of AURKB that controls adhesion-dependent Erk activation in re-adherent fibroblasts. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Indian Academy of Sciences |
en_US |
dc.subject |
Adhesion |
en_US |
dc.subject |
AURKA |
en_US |
dc.subject |
AURKB |
en_US |
dc.subject |
Erk |
en_US |
dc.subject |
Growth factors |
en_US |
dc.subject |
2021 |
en_US |
dc.title |
Adhesion-growth factor crosstalk regulates AURKB activation and ERK signalling in re-adherent fibroblasts |
en_US |
dc.type |
Article |
en_US |
dc.contributor.department |
Dept. of Biology |
en_US |
dc.identifier.sourcetitle |
Journal of Biosciences |
en_US |
dc.publication.originofpublisher |
Indian |
en_US |