Evidence map›Paper›PMID 24867265›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2014

PLCE1 mRNA and protein expression and survival of patients with esophageal squamous cell carcinoma and gastric adenocarcinoma.

Wen-Qing Li, Nan Hu, Victoria H Burton, Howard H Yang, Hua Su, Catherine M Conway, Lemin Wang, Chaoyu Wang, Ti Ding, Yi Xu and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  11. Remote modulation of lncRNAScience advances · 2020
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  15. Differentially expressed genesOncology letters · 2019
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  16. BioMed research international · 2019
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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

15 authors at 5 institutions in 2 countries.

Wen-Qing Li *Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Nan Hu *Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Victoria H Burton *Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Howard H YangOffice of the Director, Center for Cancer Research, NCI, Bethesda, MD.
Hua SuDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Catherine M ConwayTissue Array Research Program, Laboratory of Pathology, National Cancer Institute, Bethesda, MD.
Lemin WangDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Chaoyu WangDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Ti DingShanxi Cancer Hospital, Taiyuan, Shanxi, PR China.
Yi XuShanxi Cancer Hospital, Taiyuan, Shanxi, PR China.
Carol GiffenInformation Management Services, Inc., Silver Spring, MD.
Christian C AbnetDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Alisa M GoldsteinDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Stephen M HewittTissue Array Research Program, Laboratory of Pathology, National Cancer Institute, Bethesda, MD.
Philip R TaylorDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, MD 20852.
Division of Cancer Epidemiology and GeneticsCancer Genetics (United States) · USShanxi Provincial Cancer Hospital · CNCenter for Cancer Research · USInformation Management Services · US

Funding

UGI Cancer Genetic StudiesZIACP000150 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI TAYLOR, PHILIP · 2009 to 2011
$4.1M
UGI Cancer Genetic StudiesZ01CP000150 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI TAYLOR, PHILIP · 2005 to 2008
$1.8M
Applied Molecular Pathology LaboratoryZICBC011257 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HEWITT, STEPHEN · 2010 to 2014
$1.2M
Intramural NIH HHS Z01 CP000150Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA CP000150
6 · The paper itself

Abstract

backgroundGermline genetic variants in PLCE1 (10q23) have demonstrated consistent associations with risk of esophageal squamous cell carcinoma (ESCC) and gastric cancer among Chinese. We evaluated PLCE1 mRNA and protein expression in paired tumor-normal tissues, and their relationship with survival.

methodsPLCE1 mRNA was profiled using three probes in the Affymetrix GeneChip U133 for paired tumor-normal tissues of ESCC (n = 132), gastric cardia adenocarcinoma (GCA, n = 62), and gastric noncardia adenocarcinoma (GNCA, n = 72). We used immunohistochemistry to detect PLCE1 protein on slides from tissue microarrays in paired tumor-normal tissues of ESCC (n = 303), and tumors of GCA (n = 298) and GNCA (n = 124).

resultsCompared with normal tissues, PLCE1 mRNA expression was significantly reduced in ESCC tumors (P = 0.03, probe_205112_at), as well as in GCA and GNCA tumors (P < 0.0001, each probe). Protein expression was nonsignificantly reduced in ESCC tumors (P = 0.51). Increased tumor-normal mRNA fold change (probe_205112_at) was associated with longer survival in ESCC (9.6 months for highest vs. lowest quartile; Ptrend = 0.02). Increased mRNA tumor-normal fold change (probe_205111_at) was associated with longer survival for GCA (10.7 months for highest quartile; Ptrend = 0.04), but not for GNCA cases (P = 0.72). Similar to mRNA, elevated tumor-normal fold change for protein in ESCC was also associated with improved survival (8.1 months for highest quartile; Ptrend = 0.04).

conclusionsDysregulated PLCE1 mRNA expression was observed for both ESCC (one probe only) and GCA tumors, and the altered PLCE1 expression seems to be associated with cancer prognosis. IMPACT: A potential role for PLCE1 in the early detection and/or therapy of ESCC and GCA warrants further investigation.

Indexed as

AdenocarcinomaBiomarkers, TumorCarcinoma, Squamous CellEsophageal NeoplasmsHumansImmunohistochemistryKaplan-Meier EstimateOligonucleotide Array Sequence AnalysisPhosphoinositide Phospholipase CPolymorphism, Single NucleotideProportional Hazards ModelsRNA, MessengerStomach NeoplasmsTissue Array AnalysisBiomarkers, TumorPhosphoinositide Phospholipase Cphospholipase C epsilonRNA, Messenger

Identifiers

PMID24867265
PMCPMC4207376
OpenAlexW2159929630

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Registered trials

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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.