Evidence map›Paper›PMID 29017057›Full record

ArticleCancer cell2017

A p53 Super-tumor Suppressor Reveals a Tumor Suppressive p53-Ptpn14-Yap Axis in Pancreatic Cancer.

Stephano S Mello, Liz J Valente, Nitin Raj, Jose A Seoane, Brittany M Flowers, Jacob McClendon, Kathryn T Bieging-Rolett, Jonghyeob Lee, Danton Ivanochko, Margaret M Kozak and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
8.7field-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

114 citing papers in PubMed, 186 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 3 institutions in 2 countries.

Stephano S MelloDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Liz J ValenteDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Nitin RajDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Jose A SeoaneDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Brittany M FlowersDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Jacob McClendonDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Kathryn T Bieging-RolettDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Jonghyeob LeeDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Danton IvanochkoPrincess Margaret Cancer Centre, Structural Genomics Consortium and Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Margaret M KozakDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Daniel T ChangDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Teri A LongacreStanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Albert C KoongDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Cheryl H ArrowsmithPrincess Margaret Cancer Centre, Structural Genomics Consortium and Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Seung K KimDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Hannes VogelStanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Laura D WoodDepartment of Pathology, The Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Ralph H HrubanDepartment of Pathology, The Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Christina CurtisDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Laura D AttardiDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: attardi@stanford.edu.
Stanford University · USCancer Research Center · USPrincess Margaret Cancer Centre · CA

Funding

Integrative approaches to elucidate p53 transcriptional networks during carcinogenesisR35CA197591 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI · 2015 to 2026
$11.6M
Mouse Models to Dissect p53 Tumor Suppressor FunctionR01CA140875 · NCI · STANFORD UNIVERSITY · PI ATTARDI, LAURA D · 2011 to 2015
$1.7M
Elucidating p53 transcriptional networks involved in pancreatic cancer suppressioR21CA169673 · NCI · STANFORD UNIVERSITY · PI ATTARDI, LAURA D · 2012 to 2013
$368k
NCI NIH HHS R01 CA140875NCI NIH HHS R21 CA169673NCI NIH HHS R35 CA197591
6 · The paper itself

Abstract

The p53 transcription factor is a critical barrier to pancreatic cancer progression. To unravel mechanisms of p53-mediated tumor suppression, which have remained elusive, we analyzed pancreatic cancer development in mice expressing p53 transcriptional activation domain (TAD) mutants. Surprisingly, the p53

Indexed as

AnimalsCell Cycle ProteinsCell ProliferationCell Transformation, NeoplasticGene Expression ProfilingHumansMiceMutationNuclear ProteinsPancreatic NeoplasmsProtein Tyrosine Phosphatases, Non-ReceptorSignal TransductionTranscription FactorsTumor Suppressor Protein p53Cell Cycle ProteinsNuclear ProteinsProtein Tyrosine Phosphatases, Non-ReceptorPTPN14 protein, humanTP53 protein, humanTranscription FactorsTumor Suppressor Protein p53YY1AP1 protein, humanHippo pathwaymouse modelp53pancreas cancerPtpn14transactivation domaintumor suppressorYAP

Identifiers

PMID29017057
PMCPMC5659188
OpenAlexW2761908907

What OpenQuestion holds

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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.