Evidence map›Paper›PMID 32356270›Full record

ArticleAnnals of surgical oncology2020

High RAD18 Expression is Associated with Disease Progression and Poor Prognosis in Patients with Gastric Cancer.

Seded Baatar, Tuya Bai, Takehiko Yokobori, Navchaa Gombodorj, Nobuhiro Nakazawa, Yasunari Ubukata, Akiharu Kimura, Norimichi Kogure, Akihiko Sano, Makoto Sohda and 6 more

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Article in Annals of surgical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
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, 21 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 1 institution in 2 countries.

Seded BaatarDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Tuya BaiDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Takehiko YokoboriDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan. bori45@gunma-u.ac.jp.
Navchaa GombodorjResearch Program for Omics-Based Medical Science, Division of Integrated Oncology Research, Gunma University Initiative for Advanced Research (GIAR), Maebashi, Japan.
Nobuhiro NakazawaDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Yasunari UbukataDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Akiharu KimuraDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Norimichi KogureDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Akihiko SanoDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Makoto SohdaDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Makoto SakaiDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Amartuvshin TumenjargalDepartment of Bioimaging and Information Analysis, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Kyoichi OgataDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Hiroyuki KuwanoDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Ken ShirabeDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Hiroshi SaekiDepartment of General Surgical Science, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Gunma University · JP

Funding

Japan Society for the Promotion of Science (JSPS) 17K19893Japan Society for the Promotion of Science (JSPS) 18H02877Japan Society for the Promotion of Science (JSPS) 18K07665
6 · The paper itself

Abstract

backgroundRAD18 plays an important role in DNA damage repair by inducing monoubiquitinated PCNA (mUB-PCNA) in both cancer and normal tissues. Previous studies have not determined the significance of RAD18 expression in clinical gastric cancer (GC) samples. Thus, this study aimed to clarify the expression and functional significance of RAD18 in GC.

methodsOverall, 96 resected GC samples were subjected to an immunohistochemical analysis of RAD18. GC cell lines were also subjected to functional RNA interference analyses of RAD18.

resultsRAD18 expression was predominantly nuclear and was observed at higher levels in GC tissues than in normal tissues. In GC tissues, strong RAD18 expression was associated with progression of lymph node metastasis (p = 0.0001), lymphatic invasion (p = 0.0255), venous invasion (p < 0.0001), recurrence (p = 0.028), and disease stage (p = 0.0253). Moreover, GC patients with high tumor RAD18 expression had shorter overall survival (p = 0.0061) and recurrence-free survival durations (p = 0.035) than those with low tumor RAD18 expression. RAD18 knockdown inhibited GC proliferation and invasiveness and increased chemosensitivity by suppressing mUB-PCNA.

conclusionsRAD18 expression may be a useful marker of progression and poor prognosis of GC. Moreover, therapeutic strategies that target RAD18 might be a novel chemosensitizer to eradicate the refractory GC.

Indexed as

DNA-Binding ProteinsStomach NeoplasmsUbiquitin-Protein LigasesBiomarkers, TumorCell Line, TumorDisease ProgressionHumansNeoplasm InvasivenessPrognosisBiomarkers, TumorDNA-Binding ProteinsRAD18 protein, humanUbiquitin-Protein Ligases

Identifiers

PMID32356270
OpenAlexW3021878945

What OpenQuestion holds

Textmetadata
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.