Evidence map›Paper›PMID 27821484›Full record

ArticleCancer research2017

PROTOCADHERIN 7 Acts through SET and PP2A to Potentiate MAPK Signaling by EGFR and KRAS during Lung Tumorigenesis.

Xiaorong Zhou, Barrett L Updegraff, Yabin Guo, Michael Peyton, Luc Girard, Jill E Larsen, Xian-Jin Xie, Yunyun Zhou, Tae Hyun Hwang, Yang Xie and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
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  3. A CpG Epigenetic Switch Reverts PFAS ToxicityAn In Vitro Study.Environment & health (Washington, D.C.) · 2025
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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

16 authors at 4 institutions in 3 countries.

Xiaorong ZhouDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, Texas.
Barrett L UpdegraffDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, Texas.
Yabin GuoDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, Texas.
Michael PeytonHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, Texas.
Luc GirardHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, Texas.
Jill E LarsenDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland.
Xian-Jin XieDepartment of Clinical Science, UT Southwestern Medical Center, Dallas, Texas.
Yunyun ZhouDepartment of Clinical Science, UT Southwestern Medical Center, Dallas, Texas.
Tae Hyun HwangDepartment of Clinical Science, UT Southwestern Medical Center, Dallas, Texas.
Yang XieDepartment of Clinical Science, UT Southwestern Medical Center, Dallas, Texas.
Jaime Rodriguez-CanalesDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pamela VillalobosDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Carmen BehrensDepartment of Thoracic Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ignacio I WistubaDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
John D MinnaHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, Texas.
Kathryn A O'DonnellDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, Texas. Kathryn.ODonnell@UTSouthwestern.edu.
Southwestern Medical Center · USThe University of Texas MD Anderson Cancer Center · USNantong University · CNQIMR Berghofer Medical Research Institute · AU

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
DIVISION OF CELL &MOLECULAR BIOLOGY TRAINING PROGRAMT32GM008203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1987 to 2018
$7.0M
Lung cancer oncogenotype-selective drug target discoveryU01CA176284 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MACMILLAN, JOHN B, MINNA, JOHN D. · 2013 to 2016
$2.8M
NCI NIH HHS P30 CA142543NCI NIH HHS P50 CA070907NCI NIH HHS U01 CA176284NIGMS NIH HHS T32 GM008203
6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) is the leading cause of cancer-associated deaths worldwide. Given the efficacy of membrane proteins as therapeutic targets in human malignancies, we examined cell-surface receptors that may act as drivers of lung tumorigenesis. Here, we report that the PROTOCADHERIN PCDH7 is overexpressed frequently in NSCLC tumors where this event is associated with poor clinical outcome. PCDH7 overexpression synergized with EGFR and KRAS to induce MAPK signaling and tumorigenesis. Conversely, PCDH7 depletion suppressed ERK activation, sensitized cells to MEK inhibitors, and reduced tumor growth. PCDH7 potentiated ERK signaling by facilitating interaction of protein phosphatase PP2A with its potent inhibitor, the SET oncoprotein. By establishing an oncogenic role for PCDH7 in lung tumorigenesis, our results provide a rationale to develop novel PCDH7 targeting therapies that act at the cell surface of NSCLC cells to compromise their growth. Cancer Res; 77(1); 187-97. ©2016 AACR.

Indexed as

AnimalsBlotting, WesternCadherinsCarcinoma, Non-Small-Cell LungCell Line, TumorCell Transformation, NeoplasticDNA-Binding ProteinsErbB ReceptorsHeterograftsHistone ChaperonesHumansImmunoprecipitationLung NeoplasmsMAP Kinase Signaling SystemMiceMice, Inbred NODCadherinsDNA-Binding ProteinsEGFR protein, humanErbB ReceptorsHistone ChaperonesKRAS protein, humanPCDH7 protein, humanProtein Phosphatase 2ProtocadherinsProto-Oncogene Proteins p21(ras)SET protein, humanTranscription Factors

Identifiers

PMID27821484
PMCPMC5410365
OpenAlexW2555005730

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.