Evidence map›Paper›PMID 28589430›Full record

ReviewClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2017

SLC14A1: a novel target for human urothelial cancer.

R Hou, X Kong, B Yang, Y Xie, G Chen

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

22 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  8. Computational exploration ofBiochemistry and biophysics reports · 2024
    Article
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  10. Review
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  20. Sickle Cell Anemia: Variants in theFrontiers in pharmacology · 2020
    Article
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

5 authors at 4 institutions in 2 countries.

R HouDepartment of Urology, China Japan Union Hospital, Jilin University, Changchun, 130033, Jilin, China.
X KongDepartment of Urology, China Japan Union Hospital, Jilin University, Changchun, 130033, Jilin, China.
B YangDepartment of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Y XieRenal Division, Department of Medicine, Emory University School of Medicine, Atlanta, GA, 30322, USA.
G ChenRenal Division, Department of Medicine, Emory University School of Medicine, Atlanta, GA, 30322, USA. gchen3@emory.edu.
Jilin University · CNCentral South University · CNEmory University · USPeking University · CN

Funding

Small Proteins and Renal Urea Transport RegulationR01DK087838 · NIDDK · EMORY UNIVERSITY · PI CHEN, GUANGPING · 2011 to 2015
$1.7M
Foundation for the National Institutes of Health R01-DK087838NIDDK NIH HHS R01 DK087838
6 · The paper itself

Abstract

Urinary bladder cancer is the second commonly diagnosed genitourinary malignancy. Previously, bio-molecular alterations have been observed within certain locations such as chromosome 9, retinoblastoma gene and fibroblast growth factor receptor-3. Solute carrier family 14 member 1 (SLC14A1) gene encodes the type-B urea transporter (UT-B) which facilitates the passive movement of urea across cell membrane, and has recently been related with human malignancies, especially for bladder cancer. Herein, we discussed the SLC14A1 gene and UT-B protein properties, aiming to elucidate the expression behavior of SLC14A1 in human bladder cancer. Furthermore, by reviewing some well-established theories regarding the carcinogenesis of bladder cancer, including several genome wide association researches, we have bridged the mechanisms of cancer development with the aberrant expression of SLC14A1. In conclusion, the altered expression of SLC14A1 gene in human urothelial cancer may implicate its significance as a novel target for research.

Indexed as

Antineoplastic AgentsHumansMembrane Transport ProteinsPrognosisUrea TransportersUrinary Bladder NeoplasmsAntineoplastic AgentsMembrane Transport ProteinsUrea TransportersCancerGene expressionUrea transporterUrothelium

Identifiers

PMID28589430
PMCPMC5700210
OpenAlexW2623337525

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.