Evidence map›Paper›PMID 32564009›Full record

ArticleAging2020

FAM83H and SCRIB stabilize β-catenin and stimulate progression of gastric carcinoma.

Usama Khamis Hussein, Sang Hoon Ha, Asmaa Gamal Ahmed, Kyoung Min Kim, See-Hyoung Park, Chan Young Kim, Keun Sang Kwon, Zhongkai Zhang, Sang-A Lee, Ho Sung Park and 6 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.3field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 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

16 authors at 4 institutions in 2 countries.

Usama Khamis HusseinDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Sang Hoon HaDivision of Biotechnology, Jeonbuk National University, Iksan, Republic of Korea.
Asmaa Gamal AhmedDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Kyoung Min KimDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
See-Hyoung ParkDepartment of Bio and Chemical Engineering, Hongik University, Sejong, Republic of Korea.
Chan Young KimResearch Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju, Republic of Korea.
Keun Sang KwonDepartment of Preventive Medicine, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Zhongkai ZhangDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Sang-A LeeDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Ho Sung ParkDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Byung-Hyun ParkDepartment of Biochemistry, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Ho LeeDepartment of Forensic Medicine, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Myoung Ja ChungDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Woo Sung MoonDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Myoung Jae KangDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Kyu Yun JangDepartment of Pathology, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Jeonbuk National University · KRJeonbuk National University Hospital · KRBeni-Suef University · EGHongik University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FAM83H primarily is known for its function in tooth development. Recently, a role for FAM83H in tumorigenesis, conjunction with MYC and β-catenin, has been suggested. Analysis of public data indicates that FAM83H expression is closely associated with SCRIB expression in human gastric cancers. Therefore, this study investigated the roles of FAM83H and SCRIB in 200 human gastric cancers and gastric cancer cells. In human gastric carcinomas, both the individual and combined expression patterns of the nuclear FAM83H and SCRIB were independent indicators of shorter survival of gastric carcinoma patients. In MKN-45 and NCI-N87 gastric cancer cells, the expression of FAM83H and SCRIB were associated with proliferation and invasiveness of cells. FAM83H-mediated

Indexed as

Animalsbeta CateninCarcinogenesisCarcinomaCell Line, TumorCell ProliferationDisease-Free SurvivalDisease ProgressionFemaleGastrectomyGastric MucosaGene Knockdown TechniquesHumansKaplan-Meier EstimateMaleMembrane Proteinsbeta CateninCTNNB1 protein, humanFAM83H protein, humanMembrane ProteinsProteasome Endopeptidase ComplexProteinsSCRIB protein, humanTumor Suppressor ProteinscancerFAM83HSCRIBstomachβ-catenin

Identifiers

PMID32564009
PMCPMC7343515
OpenAlexW3036249641

What OpenQuestion holds

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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.