Defining the role of mTOR in cancer
What this study shows
Comprehensive review arguing mTOR signaling is commonly deregulated in human cancers, laying out the rationale for rapalog trials in oncology.
At a glance
| Evidence type | R Review — secondary literature, not a new result Marked R because it is a review or synthesis of existing evidence rather than a new primary result; that is a different form of writing, not a weaker one. |
| Study type | Narrative Review |
| Model system | Review article |
| Journal | Cancer Cell |
| Year | 2007 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1016/j.ccr.2007.05.008 · PMID 17613433 |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | Not applicable (review) |
| Target | mTOR |
| Model | Review |
| Effect | Reviews the role of mTOR in cancer and the rationale for rapalog therapy |
In the Atlas
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- Randomized phase II study of multiple dose levels of CCI-779, a novel mammalian target of rapamycin kinase inhibitor, in patients with advanced refractory renal cell carcinoma (2004)
- Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma (2007)
- Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial (2008)
- Circadian regulation of mTOR by the ubiquitin pathway in renal cell carcinoma (2013)
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