Evidence map›Paper›PMID 30555158›Full record

ArticleBritish journal of cancer2019

(Pro)renin receptor promotes colorectal cancer through the Wnt/beta-catenin signalling pathway despite constitutive pathway component mutations.

Juan Wang, Yuki Shibayama, Anqi Zhang, Hiroyuki Ohsaki, Eisuke Asano, Yasuyuki Suzuki, Yoshio Kushida, Hideki Kobara, Tsutomu Masaki, Zhiyu Wang and 1 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-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

26 citing papers in PubMed, 50 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

11 authors at 4 institutions in 2 countries.

Juan WangDepartment of Medical Oncology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, 310009, Zhejiang Province, China.
Yuki ShibayamaDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, 761-0793, Japan.
Anqi ZhangDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, 761-0793, Japan.
Hiroyuki OhsakiDepartment of Medical Biophysics, Kobe University Graduate School of Health Sciences, Kobe, 650-0017, Japan.
Eisuke Asano
Yasuyuki SuzukiDepartment of Gastroenterological Surgery, Faculty of Medicine, Kagawa University, Kagawa, 761-0793, Japan.
Yoshio KushidaDepartment of Diagnostic Pathology, Faculty of Medicine, Kagawa University, Kagawa, 761-0793, Japan.
Hideki KobaraDepartment of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, 761-0793, Japan.
Tsutomu MasakiDepartment of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, 761-0793, Japan.
Zhiyu WangDepartment of Immuno-oncology, Fourth Affiliated Hospital of Hebei Medical University, Shijiazhuang, 050000, Hebei Province, China.
Akira NishiyamaDepartment of Pharmacology, Faculty of Medicine, Kagawa University, Kagawa, 761-0793, Japan. akira@med.kagawa-u.ac.jp.
Kagawa University · JPFourth Hospital of Hebei Medical University · CNHebei Medical University · CNKobe University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough constitutive activating mutations in the Wnt/β-catenin signalling pathway are important for colorectal cancer development, canonical signalling through Wnt ligands is essential for β-catenin activation. Here, we investigated the role of (pro)renin receptor ((P)RR), a component of the Wnt receptor complex, in the pathogenesis of colorectal cancer.

methods(P)RR silencing was performed in human colorectal cancer cells containing constitutive activating mutations in the Wnt/β-catenin pathway. (P)RR overexpression was induced in normal colon epithelial cells. Protein and mRNA levels of pathway components were detected, and Wnt signalling activity was measured using a β-catenin reporter. Cell proliferative activity and apoptosis were evaluated using WST-1 assay and flow cytometry. Xenografts were induced in nude mice.

results(P)RR expression was greater in colorectal cancer tissues and cells than in normal colorectal samples. Patients with strong (P)RR expression took more proportion in groups with poorly-differentiated, advanced and rapidly-progressing cancers. (P)RR silencing attenuated the pathway in colorectal cancer cells, impaired their proliferation in vitro and vivo. (P)RR overexpression enhanced the pathway and proliferation of normal colon epithelial cells.

conclusionsAberrant (P)RR expression promotes colorectal cancer through the Wnt/β-catenin signalling pathway despite constitutive pathway-activating mutations. (P)RR is a potential diagnostic and therapeutic target for colorectal cancer.

Indexed as

AnimalsApoptosisbeta CateninCell Line, TumorCell ProliferationColorectal NeoplasmsGene Expression Regulation, NeoplasticHumansMiceMutationProrenin ReceptorReceptors, Cell SurfaceReninVacuolar Proton-Translocating ATPasesWnt Signaling PathwayXenograft Model Antitumor AssaysATP6AP2 protein, humanbeta CateninCTNNB1 protein, humanProrenin ReceptorReceptors, Cell SurfaceReninVacuolar Proton-Translocating ATPases

Identifiers

PMID30555158
PMCPMC6342928
OpenAlexW2903797246

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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.