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| Content Provider | PubMed Central |
|---|---|
| Author | Hatchi, Elodie Rodier, Geneviève Sardet, Claude Cam, Laurent Le |
| Copyright Year | 2011 |
| Abstract | The multifunctional E4F1 protein was originally identified as a cellular target of the E1A adenoviral oncoprotein. Although E4F1 is implicated in several key oncogenic pathways, its roles in tumorigenesis remain unclear. Using a genetically engineered mouse model of myeloid leukemia (histiocytic sarcomas, HS) based on the genetic inactivation of the tumor suppressor Ink4a/Arf locus, we have recently unraveled an unsuspected function of E4F1 in the survival of leukemic cells. In vivo, genetic ablation of E4F1 in established myeloid tumors results in tumor regression. E4F1 inactivation results in a cascade of alterations originating from dysfunctional mitochondria that induce increased reactive oxygen species (ROS) levels and ends in massive autophagic cell death in HS transformed, but not normal myeloid cells. E4F1 depletion also induces cell death in various human myeloid leukemic cell lines, including acute myeloid leukemic (AML) cell lines. Interestingly, the E4F1 protein is overexpressed in a large proportion of human AML samples. These data provide new insights into E4F1-associated survival functions implicated in tumorigenesis and could open the path for new therapeutic strategies. |
| Related Links | http://dx.doi.org/10.4161/auto.7.12.17991 |
| Ending Page | 1567 |
| Page Count | 2 |
| Starting Page | 1566 |
| File Format | |
| ISSN | 15548627 |
| e-ISSN | 15548635 |
| Journal | Autophagy |
| Issue Number | 12 |
| Volume Number | 7 |
| Language | English |
| Publisher | Landes Bioscience |
| Publisher Date | 2011-12-01 |
| Access Restriction | Open |
| Rights Holder | Landes Bioscience |
| Subject Keyword | Cell Biology Molecular Biology Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Cell Biology Molecular Biology |
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