Evidence map›Paper›PMID 31102318›Full record

ArticleFEBS open bio2019

Low expression of WWC1, a tumor suppressor gene, is associated with aggressive breast cancer and poor survival outcome.

Zhanwei Wang, Dionyssios Katsaros, Nicoletta Biglia, Yi Shen, Yuanyuan Fu, Maarit Tiirikainen, Herbert Yu

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 15 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

7 authors at 4 institutions in 2 countries.

Zhanwei WangUniversity of Hawaii Cancer Center, Honolulu, HI, USA.
Dionyssios KatsarosDepartment of Surgical Sciences, Gynecology, AOU Città della Salute, University of Turin, Italy.
Nicoletta BigliaDepartment of Surgical Science, Division of Obstetrics and Gynecology, Mauriziano Hospital, University of Torino School of Medicine, Turin, Italy.
Yi ShenUniversity of Hawaii Cancer Center, Honolulu, HI, USA.
Yuanyuan FuUniversity of Hawaii Cancer Center, Honolulu, HI, USA.
Maarit TiirikainenUniversity of Hawaii Cancer Center, Honolulu, HI, USA.
Herbert YuUniversity of Hawaii Cancer Center, Honolulu, HI, USA.
University of Hawaii Cancer CenterUniversity of Hawaii System · USCancer Center of Hawaii · USUniversity of Turin · IT

Funding

University of Hawaii Cancer Center CCSGP30CA071789 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI GERTRAUD MASKARINEC · 1996 to 2026
$56.2M
RESEARCH DESIGN AND BIOSTATISTICS COREU54MD007584 · NIMHD · UNIVERSITY OF HAWAII AT MANOA · PI MOKUAU, NOREEN, SHIRAMIZU, BRUCE T · 2012 to 2018
$21.1M
NCI NIH HHS P30 CA071789NIMHD NIH HHS U54 MD007584
6 · The paper itself

Abstract

The WW and C2 domain containing 1 (WWC1) gene encodes a protein named WWC1 (or KIBRA), which is involved in the Hippo signaling pathway. WWC1 is often lost in triple-negative breast cancer and has been shown to suppress tumor metastasis. In this study, 470 breast cancer patients were recruited and WWC1 expression in the tumor samples was measured with quantitative reverse transcriptase PCR. Associations of WWC1 expression with breast cancer survival were analyzed using the Cox proportional hazards regression model and Kaplan-Meier survival analysis. The relationship between WWC1 expression and methylation was evaluated in a dataset from The Cancer Genome Atlas. Using our microarray data on gene expression and the Ingenuity Pathway Analysis, we predicted the WWC1-associated signaling pathways in breast cancer. Our results showed that low expression of WWC1 was significantly associated with advanced-stage diseases, high-grade tumors, and estrogen receptor- or progesterone receptor-negative status. Compared to those with high expression, patients with low WWC1 had higher risk of breast cancer relapse [hazard ratio (HR) = 2.06, 95% confidence interval (CI): 1.26-3.37] and higher risk of death (HR = 2.76, 95% CI: 1.51-5.03). The association with relapse-free survival remained significant after adjustment for disease stage, tumor grade, and hormone receptor status and was replicated in a public dataset. Analysis of high-throughput gene expression data indicated that WWC1 was involved in the Hippo signaling pathway. Online data also suggested that DNA methylation was inversely associated with WWC1 expression. The study confirmed that low WWC1 expression was associated with aggressive breast cancer and poor survival outcomes.

Indexed as

Biomarkers, TumorBreast NeoplasmsDatabases, GeneticDisease-Free SurvivalDNA MethylationFemaleGene ExpressionGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansIntracellular Signaling Peptides and ProteinsKaplan-Meier EstimateNeoplasm GradingNeoplasm Recurrence, LocalPrognosisProportional Hazards ModelsBiomarkers, TumorIntracellular Signaling Peptides and ProteinsWWC1 protein, humanbreast cancermethylationoverall survivalrelapse-free survivalWWC1

Identifiers

PMID31102318
PMCPMC6609559
OpenAlexW2945927973

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LicenceCC BY
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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.