New wirings in the survivin networks
| dc.contributor.author | Altieri, Dario C. | |
| dc.date | 2022-08-11T08:09:37.000 | |
| dc.date.accessioned | 2022-08-23T16:37:42Z | |
| dc.date.available | 2022-08-23T16:37:42Z | |
| dc.date.issued | 2008-10-22 | |
| dc.date.submitted | 2009-10-15 | |
| dc.identifier.citation | <p>Oncogene. 2008 Oct 20;27(48):6276-84. <a href="http://dx.doi.org/10.1038/onc.2008.303">Link to article on publisher's site</a></p> | |
| dc.identifier.issn | 1476-5594 (Electronic) | |
| dc.identifier.doi | 10.1038/onc.2008.303 | |
| dc.identifier.pmid | 18931693 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14038/39083 | |
| dc.description.abstract | A little over 10 years after its discovery in 1997, the small inhibitor of apoptosis (IAP) protein, survivin, continues to generate intense interest and keen attention from disparate segments of basic and disease-related research. Part of this interest reflects the intricate biology of this multifunctional protein that intersects fundamental networks of cellular homeostasis. Part is because of the role of survivin as a cancer gene, which touches nearly every aspect of the disease, from onset to outcome. And part is due to the potential value of survivin for novel cancer diagnostics and therapeutics, which have already reached the clinic, and with some promise. Grappling with emerging new signaling circuits in survivin biology, and their implications in cancer, will further our understanding of this nodal protein, and open fresh opportunities for translational oncology research. | |
| dc.language.iso | en_US | |
| dc.relation | <p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=18931693&dopt=Abstract">Link to Article in PubMed</a></p> | |
| dc.relation.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683067/ | |
| dc.subject | Humans | |
| dc.subject | Microtubule-Associated Proteins | |
| dc.subject | Neoplasm Proteins | |
| dc.subject | Neoplasms | |
| dc.subject | Signal Transduction | |
| dc.subject | Subcellular Fractions | |
| dc.subject | Life Sciences | |
| dc.subject | Medicine and Health Sciences | |
| dc.title | New wirings in the survivin networks | |
| dc.type | Journal Article | |
| dc.source.journaltitle | Oncogene | |
| dc.source.volume | 27 | |
| dc.source.issue | 48 | |
| dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/1901 | |
| dc.identifier.contextkey | 1036644 | |
| html.description.abstract | <p>A little over 10 years after its discovery in 1997, the small inhibitor of apoptosis (IAP) protein, survivin, continues to generate intense interest and keen attention from disparate segments of basic and disease-related research. Part of this interest reflects the intricate biology of this multifunctional protein that intersects fundamental networks of cellular homeostasis. Part is because of the role of survivin as a cancer gene, which touches nearly every aspect of the disease, from onset to outcome. And part is due to the potential value of survivin for novel cancer diagnostics and therapeutics, which have already reached the clinic, and with some promise. Grappling with emerging new signaling circuits in survivin biology, and their implications in cancer, will further our understanding of this nodal protein, and open fresh opportunities for translational oncology research.</p> | |
| dc.identifier.submissionpath | oapubs/1901 | |
| dc.contributor.department | Department of Cancer Biology and the Cancer Center | |
| dc.source.pages | 6276-84 |