|Forever young? Exploring the link between rapamycin, longevity and cancer.|
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|PMID: 23152185 Owner: NLM Status: MEDLINE|
|Michael Van Meter; Andrei Seluanov; Vera Gorbunova|
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|Type: Editorial Date: 2012-11-14|
|Title: Cell cycle (Georgetown, Tex.) Volume: 11 ISSN: 1551-4005 ISO Abbreviation: Cell Cycle Publication Date: 2012 Dec|
|Created Date: 2012-12-10 Completed Date: 2013-05-17 Revised Date: 2013-07-11|
Medline Journal Info:
|Nlm Unique ID: 101137841 Medline TA: Cell Cycle Country: United States|
|Languages: eng Pagination: 4296-7 Citation Subset: IM|
|APA/MLA Format Download EndNote Download BibTex|
Antineoplastic Agents / therapeutic use*
Neoplasms / drug therapy*, metabolism, pathology
Sirolimus / therapeutic use*
TOR Serine-Threonine Kinases / antagonists & inhibitors, metabolism
Tumor Suppressor Protein p53 / deficiency, genetics, metabolism
|F31 AG041603/AG/NIA NIH HHS; R01 AG027237/AG/NIA NIH HHS|
|0/Antineoplastic Agents; 0/Tumor Suppressor Protein p53; 53123-88-9/Sirolimus; EC 220.127.116.11/TOR Serine-Threonine Kinases|
Journal ID (nlm-ta): Cell Cycle
Journal ID (iso-abbrev): Cell Cycle
Journal ID (publisher-id): CC
Publisher: Landes Bioscience
Copyright © 2012 Landes Bioscience
Print publication date: Day: 01 Month: 12 Year: 2012
pmc-release publication date: Day: 01 Month: 12 Year: 2012
Volume: 11 Issue: 23
First Page: 4296 Last Page: 4297
PubMed Id: 23152185
Publisher Id: 2012CC11-23-Van Meter
Publisher Item Identifier: 22868
|Forever young? Exploring the link between rapamycin, longevity and cancer|
|Michael Van Meter|
|Department of Biology; University of Rochester; Rochester, NY USA
|*Correspondence to: Andrei Seluanov, Email: email@example.com and Vera Gorbunova, Email: firstname.lastname@example.org
There are a very few drug candidates that either extend lifespan or prevent a broad spectrum of age-related diseases. Of the few drug candidates that have exhibited preclinical success, rapamycin is the best characterized and perhaps shows the most promise for use in a clinical setting. Rapamycin inhibits the mTOR pathway, which integrates signals about nutrient availability, oxygen tension, ATP levels and mitogens to regulate protein synthesis, ribosome biogenesis, cell proliferation, angiogenesis and survival in response to stress.1 Multiple studies conducted using mouse models have demonstrated that rapamycin can extend murine lifespan by upwards of 15%,2,3 and additional studies have indicated that rapamycin can delay or mitigate the effects of a range of age-related pathologies. Currently, a large body of research is dedicated toward understanding precisely how rapamycin extends lifespan, and whether the drug may be clinically relevant in the treatment of one of the most prevalent and deadly age-related diseases, cancer. Two new studies from the Gudkov and the Antoch laboratories and their collaborators provide insight into the molecular mechanisms of rapamycin's effect on lifespan and its anti-tumorigenic potential.4,5 A large-scale 2009 study from The National Institute on Aging Interventions Testing Program demonstrated that rapamycin extended lifespan in mice;2 intriguingly, the rapamycin-fed cohort experienced the same number of cancer-related mortalities as the control group; however, cancer-related deaths were postponed by rapamycin treatment.2,3
The notion that rapamycin may be useful in the context of cancer therapy stems from the observation that the mTOR pathway integrates signaling from several proto-oncogenes, such as PI3K, Akt and eIF4E. Moreover, mTOR signling is often hyperactivated in a broad range of cancers. While these observations seem to suggest that mTOR signaling would be a prime target for cancer therapy, studies in mice and human patients have had mixed success, suggesting that our understanding of the mTOR pathway and the molecular mechanism of rapamycin-based therapies is incomplete. In two new studies, rapamycin was applied to highly tumor-prone p53+/− and p53−/− mice. Interestingly, rapamycin extended the lifespan of these tumor-prone mice and delayed tumorigenesis. A question that comes to mind is why did not rapamycin work well as an anticancer treatment?
Komarova et al. fed rapamycin to heterozygous p53+/− mice, and found that while rapamycin treatment extended lifespan, it appeared to only postpone carcinogenesis. Interestingly, the authors observed that mice that began rapamycin treatment early in life (before 5 mo of age) lived longer and were able to delay tumor formation until later in life than mice that did not begin rapamycin treatment until late in life (after 5 mo of age).4 One interpretation of these results is that rapamycin may function to prevent tumor initiation, but may have little effect on established tumor bodies.
Comas et al. pursued this hypothesis, that inhibition of mTOR signaling might delay oncogenesis.5 The authors synthesized highly soluble, nanoformulated micelles of rapamycin, dubbed Rapatar, for oral delivery to the highly tumorigenic homozygous p53−/− mice. Rapatar demonstrated increased bioavailabilty over conventional rapamycin treatment and displayed no additional toxicity. Rapatar treatment extended the lifespan of the p53−/− mice by 30% compared with control animals. Consistent with previous studies, however, the Rapatar-treated mice developed a similar tumor spectrum as control animals; carcinogenesis was merely delayed until later in life.
A critical question regarding rapamycin is the mechanism by which treatment extends lifespan in mice. There are at least two possibilities, (1) mice are tumor-prone animals, and rapamycin is toxic to cancer cells and can therefore extend murine lifespan, or (2) rapamycin slows aging through other processes and, as a result, cancer develops later in life (Fig. 1). The clinical implications of these two models are quite different: the first model suggests that rapamycin would be an effective anti-tumor therapy and could be prescribed acutely to treat neoplasms; in contrast, the second model suggests that rapamycin prevents tumor initiation and, therefore, that rapamycin needs to be taken before tumor development to prevent carcinogenesis. In these newest studies, it is interesting to note that the survival curves of the rapamycin-treated mice were shifted to the right, but ran parallel to the survival curves of the control animals. This favors the second possibility, and suggests that intervention with rapamycin delayed the onset of aging. If rapamycin were acting by inhibiting carcinogenesis, the rapamycin-treated mice would likely exhibit different aging kinetics, and the shoulder of their survival curve would be steeper, indicating a longer healthspan.
While more research is required to fully differentiate between these possibilities, evidence from the clinic also lends credence to the second possibility. To date, most clinical trials utilizing rapamycin as an anti-tumor therapy have disappointed clinicians; the most successful results came in patients who presented with tumors that were addicted to mTOR signaling, suggesting that rapamycin may only have narrow applications for the treatment of developed tumors.6-8 While there have not yet been clinical trials to assess the efficacy of rapamycin as a tumor-preventative agent, evidence from the early 2000s suggests that rapamycin may have this effect: in 1999, the FDA approved rapamycin for use as an immunosuppressant to promote renal engraftment after transplantation. Patients who received cyclosporine as the primary means of immunosuppression developed malignancies at a high rate due to poor immunosurveillance; in contrast, patients taking rapamycin experienced a lower rate of lymphoproliferative disorders post-transplant.9 This suggests that tumor initiation was delayed in these patients receiving rapamycin, underscoring the drug’s potential as a tumor-preventative medicine. These newest studies4,5 represent important steps toward understanding the mechanism by which rapamycin impacts on aging and age-related diseases. While more work is needed to fully understand the mechanism by which rapamycin works, as well as its clinical potential, these studies underscore the potential of the drug and provide hope that we will one day be able to develop a successful anti-aging medication.
Previously published online: www.landesbioscience.com/journals/cc/article/22868
|1.||Zoncu R,et al. Nat Rev Mol Cell BiolYear: 201112213510.1038/nrm302521157483|
|2.||Harrison DE,et al. NatureYear: 2009460392519587680|
|3.||Miller RA,et al. J Gerontol A Biol Sci Med SciYear: 20116619120110.1093/gerona/glq17820974732|
|4.||Komarova EA,et al. Aging (Albany NY)Year: 201247192723123616|
|5.||Comas M,et al. Aging (Albany NY)Year: 201247283523241754|
|6.||Efeyan A,et al. Curr Opin Cell BiolYear: 2010221697610.1016/j.ceb.2009.10.00719945836|
|7.||Mosley JD,et al. Mol Cancer TherYear: 2007621889710.1158/1535-7163.MCT-07-023517699716|
|8.||Cloughesy TF,et al. PLoS MedYear: 20085e810.1371/journal.pmed.005000818215105|
|9.||Mathew T,et al. Clin TransplantYear: 200418446910.1111/j.1399-0012.2004.00188.x15233824|
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