Evidence map›Paper›PMID 28656962›Full record

ArticleNature communications2017

Negative regulation of EGFR signalling by the human folliculin tumour suppressor protein.

Laura A Laviolette, Julien Mermoud, Isabel A Calvo, Nicholas Olson, Myriam Boukhali, Ortrud K Steinlein, Elisabeth Roider, Elke C Sattler, Dachuan Huang, Bin Tean Teh and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

34 citing papers in PubMed, 49 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 3 countries.

Laura A LavioletteCenter for Cancer Research, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts 02139, USA.
Julien MermoudCenter for Cancer Research, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts 02139, USA.
Isabel A CalvoCenter for Cancer Research, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts 02139, USA.
Nicholas OlsonCenter for Cancer Research, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts 02139, USA.
Myriam BoukhaliCenter for Cancer Research, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts 02139, USA.
Ortrud K SteinleinInstitute of Human Genetics, University Hospital Munich, University of Munich, Munich 80336, Germany.
Elisabeth RoiderDepartment of Dermatology and Allergology, University Hospital, Ludwig Maximilian University Munich, Munich D-80337, Germany.
Elke C SattlerDepartment of Dermatology and Allergology, University Hospital, Ludwig Maximilian University Munich, Munich D-80337, Germany.
Dachuan HuangLaboratory of Cancer Epigenome, Division of Medical Sciences, National Cancer Centre Singapore, Singapore 169610, Singapore.
Bin Tean TehLaboratory of Cancer Epigenome, Division of Medical Sciences, National Cancer Centre Singapore, Singapore 169610, Singapore.
Mo MotamediCenter for Cancer Research, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts 02139, USA.
Wilhelm HaasCenter for Cancer Research, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts 02139, USA.
Othon IliopoulosCenter for Cancer Research, Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts 02139, USA.
Center for Cancer Research · USMassachusetts General Hospital · USHarvard University · USLudwig-Maximilians-Universität München · DEDuke-NUS Medical School · SGNational Cancer Centre Singapore · SG

Funding

Molecular targets of hypoxia in signaling cancerR01CA104574 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI ILIOPOULOS, OTHON · 2004 to 2007
$1.1M
NCI NIH HHS R01 CA104574
6 · The paper itself

Abstract

Germline mutations in the Folliculin (FLCN) tumour suppressor gene result in fibrofolliculomas, lung cysts and renal cancers, but the precise mechanisms of tumour suppression by FLCN remain elusive. Here we identify Rab7A, a small GTPase important for endocytic trafficking, as a novel FLCN interacting protein and demonstrate that FLCN acts as a Rab7A GTPase-activating protein. FLCN

Indexed as

AnimalsBirt-Hogg-Dube SyndromeCell Line, TumorEndosomesErbB ReceptorsFemaleHumansKidney NeoplasmsMaleMice, Inbred C57BLMice, TransgenicMutationProto-Oncogene Proteinsrab7 GTP-Binding Proteinsrab GTP-Binding ProteinsSchizosaccharomycesEGFR protein, humanErbB ReceptorsFLCN protein, humanProto-Oncogene Proteinsrab7 GTP-Binding Proteinsrab GTP-Binding ProteinsTumor Suppressor Proteins

Identifiers

PMID28656962
PMCPMC5493755
OpenAlexW2731594787

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.