Evidence map›Paper›PMID 23332765›Full record

ArticleCell2013

Monitoring tumorigenesis and senescence in vivo with a p16(INK4a)-luciferase model.

Christin E Burd, Jessica A Sorrentino, Kelly S Clark, David B Darr, Janakiraman Krishnamurthy, Allison M Deal, Nabeel Bardeesy, Diego H Castrillon, David H Beach, Norman E Sharpless

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 262 papers.

0numbers the graph read from it
0cells of the map it votes in
262citing papers in PubMed
13.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

262 citing papers in PubMed, 405 citations in OpenAlex.

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  19. SARS-CoV-2 uptake and inflammatory response in senescent endothelial cells are regulated by the BSG/VEGFR2 pathway.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Article

202 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Christin E BurdDepartment of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC 27599-7264, USA.
Jessica A Sorrentino
Kelly S Clark
David B Darr
Janakiraman Krishnamurthy
Allison M Deal
Nabeel Bardeesy
Diego H Castrillon
David H Beach
Norman E Sharpless
UNC Lineberger Comprehensive Cancer CenterUniversity of North Carolina at Chapel Hill · USHarvard University · USQueen Mary University of London · GBThe University of Texas Southwestern Medical Center · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
TOXICOLOGYT32ES007126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ILONA JASPERS, Bernard E. Weissman · 1985 to 2026
$13.0M
The Role of p16INK4 in Mammalian AgingR01AG024379 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HE, SHENGHUI · 2004 to 2019
$4.6M
In vivo murine models of metastasis for therapeutic testingR01CA163896 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SHARPLESS, NORMAN E, WONG, KWOK KIN · 2012 to 2016
$2.0M
Mouse Models and Translational Studies of Endometrial CancerR01CA137181 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CASTRILLON, DIEGO H · 2010 to 2014
$1.8M
A Novel p16INK4a Reporter System to Assess Aging In VivoR00AG036817 · NIA · OHIO STATE UNIVERSITY · PI BURD, CHRISTIN E · 2013 to 2015
$721k
A Novel p16INK4a Reporter System to Assess Aging In VivoK99AG036817 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BURD, CHRISTIN E · 2010 to 2011
$147k
NCI NIH HHS CA137181NCI NIH HHS CA163896NCI NIH HHS P30 CA016086NCI NIH HHS R01 CA137181NCI NIH HHS R01 CA163896NIA NIH HHS AG024379NIA NIH HHS AG036817NIA NIH HHS K99 AG036817NIA NIH HHS R00 AG036817NIA NIH HHS R01 AG024379NIEHS NIH HHS T32 ES007126
6 · The paper itself

Abstract

Monitoring cancer and aging in vivo remains experimentally challenging. Here, we describe a luciferase knockin mouse (p16(LUC)), which faithfully reports expression of p16(INK4a), a tumor suppressor and aging biomarker. Lifelong assessment of luminescence in p16(+/LUC) mice revealed an exponential increase with aging, which was highly variable in a cohort of contemporaneously housed, syngeneic mice. Expression of p16(INK4a) with aging did not predict cancer development, suggesting that the accumulation of senescent cells is not a principal determinant of cancer-related death. In 14 of 14 tested tumor models, expression of p16(LUC) was focally activated by early neoplastic events, enabling visualization of tumors with sensitivity exceeding other imaging modalities. Activation of p16(INK4a) was noted in the emerging neoplasm and surrounding stromal cells. This work suggests that p16(INK4a) activation is a characteristic of all emerging cancers, making the p16(LUC) allele a sensitive, unbiased reporter of neoplastic transformation.

Indexed as

BiomarkersCell Transformation, NeoplasticAgingAnimalsCellular SenescenceCyclin-Dependent Kinase Inhibitor p16FemaleGene Knock-In TechniquesLuciferasesMiceNeoplasmsWounds and InjuriesBiomarkersCdkn2a protein, mouseCyclin-Dependent Kinase Inhibitor p16Luciferases

Identifiers

PMID23332765
PMCPMC3718011
OpenAlexW1988233144

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.