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- Publisher Website: 10.1038/sj.onc.1203739
- Scopus: eid_2-s2.0-0034680008
- PMID: 10962553
- WOS: WOS:000088825300002
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Article: The conserved PI3'K/PTEN/AKt signaling pathway regulates both cell size and survival in Drosophila
Title | The conserved PI3'K/PTEN/AKt signaling pathway regulates both cell size and survival in Drosophila |
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Authors | |
Keywords | PTEN PI3K Drosophila Cell size PKB Cell survival |
Issue Date | 2000 |
Citation | Oncogene, 2000, v. 19, n. 35, p. 3971-3977 How to Cite? |
Abstract | Akt (or PKB) is an oncogene involved in the regulation of cell survival. Akt is regulated by phosphatidylinositol 3-OH kinase (PI3'K) signaling and has shown to be hyperactivated through the loss of the PTEN tumor suppressor. In Drosophila, insulin signaling as studied using the Drosophila IRS-4 homolog (Chico) has been shown to be a crucial regulator of cell size. We have studied Drosophila Akt (Dakt1) and have shown that it is also involved in the regulation of cell size. Furthermore we have performed genetic epistasis tests to demonstrate that in Drosophila, PI3'K, PTEN and Akt comprise a signaling cassette that is utilized during multiple stages of development. In addition, we show that this signaling cassette is also involved in the regulation of cell survival during embryogenesis. This study therefore establishes the evolutionary conservation of this signaling pathway in Drosophila. |
Persistent Identifier | http://hdl.handle.net/10722/291544 |
ISSN | 2023 Impact Factor: 6.9 2023 SCImago Journal Rankings: 2.334 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Scanga, Sam E. | - |
dc.contributor.author | Ruel, Laurent | - |
dc.contributor.author | Binari, Richard C. | - |
dc.contributor.author | Snow, Brian | - |
dc.contributor.author | Stambolic, Vuk | - |
dc.contributor.author | Bouchard, Denis | - |
dc.contributor.author | Peters, Malte | - |
dc.contributor.author | Calvieri, Batista | - |
dc.contributor.author | Mak, Tak W. | - |
dc.contributor.author | Woodgett, James R. | - |
dc.contributor.author | Manoukian, Armen S. | - |
dc.date.accessioned | 2020-11-17T14:54:36Z | - |
dc.date.available | 2020-11-17T14:54:36Z | - |
dc.date.issued | 2000 | - |
dc.identifier.citation | Oncogene, 2000, v. 19, n. 35, p. 3971-3977 | - |
dc.identifier.issn | 0950-9232 | - |
dc.identifier.uri | http://hdl.handle.net/10722/291544 | - |
dc.description.abstract | Akt (or PKB) is an oncogene involved in the regulation of cell survival. Akt is regulated by phosphatidylinositol 3-OH kinase (PI3'K) signaling and has shown to be hyperactivated through the loss of the PTEN tumor suppressor. In Drosophila, insulin signaling as studied using the Drosophila IRS-4 homolog (Chico) has been shown to be a crucial regulator of cell size. We have studied Drosophila Akt (Dakt1) and have shown that it is also involved in the regulation of cell size. Furthermore we have performed genetic epistasis tests to demonstrate that in Drosophila, PI3'K, PTEN and Akt comprise a signaling cassette that is utilized during multiple stages of development. In addition, we show that this signaling cassette is also involved in the regulation of cell survival during embryogenesis. This study therefore establishes the evolutionary conservation of this signaling pathway in Drosophila. | - |
dc.language | eng | - |
dc.relation.ispartof | Oncogene | - |
dc.subject | PTEN | - |
dc.subject | PI3K | - |
dc.subject | Drosophila | - |
dc.subject | Cell size | - |
dc.subject | PKB | - |
dc.subject | Cell survival | - |
dc.title | The conserved PI3'K/PTEN/AKt signaling pathway regulates both cell size and survival in Drosophila | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1038/sj.onc.1203739 | - |
dc.identifier.pmid | 10962553 | - |
dc.identifier.scopus | eid_2-s2.0-0034680008 | - |
dc.identifier.volume | 19 | - |
dc.identifier.issue | 35 | - |
dc.identifier.spage | 3971 | - |
dc.identifier.epage | 3977 | - |
dc.identifier.isi | WOS:000088825300002 | - |
dc.identifier.issnl | 0950-9232 | - |