Evidence map›Paper›PMID 31942187›Full record

ArticleJournal of Cancer2020

Identifying Predictive Factors of Recurrence after Radical Resection in Gastric Cancer by RNA Immune-oncology Panel.

Yuehong Cui, Shan Yu, Mengxuan Zhu, Xi Cheng, Yiyi Yu, Zhaoqing Tang, Xuefei Wang, Jun Hou, Yingyong Hou, Dandan Ren and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2020. 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
1.0field-weighted citation impact, top 20% 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, 11 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

13 authors at 3 institutions in 1 country.

Yuehong CuiDepartment of medical oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Shan YuDepartment of medical oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Mengxuan ZhuDepartment of medical oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xi ChengDepartment of medical oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yiyi YuDepartment of medical oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Zhaoqing TangDepartment of general surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Xuefei WangDepartment of general surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Jun HouDepartment of pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yingyong HouDepartment of pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Dandan RenGenecast Precision Medicine Technology Institute, Beijing, China.
Beibei MaoGenecast Precision Medicine Technology Institute, Beijing, China.
Rashid KhalidDepartment of medical oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Tianshu LiuDepartment of medical oncology, Zhongshan Hospital, Fudan University, Shanghai, China.
Shanghai Medical College of Fudan University · CNSun Yat-sen University · CNGenecast (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aiming to identify novel immunotargets for gastric cancer (GC), we retrospectively analyzed the formalin-fixed paraffin embedded (FFPE) samples of gastric cancer tissues from postoperative patients who relapsed or metastasized within (early recurrence, n=25) or after two years (late recurrence, n=23). RNA immune-oncology panel (RIOP) including 398 immune-related genes was used to detect the RNA expression level. Disease free survival (DFS) time in early and late recurrent group was 7.52±0.72 and 28.49±0.81 months, respectively. 18 genes were significantly different between the early and late recurrent groups, and the expression of ITK, EBI3, CX3CL1, MYC, EOMES, CA4, TAGAP, MMP2, HAVCR2, FCGR1 and SNAI2 were verified to be associated with the DFS time. We also found that 18 genes were differentially expressed in diffusal type and non-diffusal type of GC. Leukocyte-inhibition, Leukocyte-migration, and Lymphocyte-infiltrate signal/functional pathways were activated in diffusal type of GC by cluster analysis. Our data uncovered the gene set consisted of ITK, EBI3, and CX3CL1 as a potential tool for prediction of early recurrence or poor prognosis in GC, which could be used as novel immunotargets and prognostic markers for the management of GC.

Identifiers

PMID31942187
PMCPMC6959033
OpenAlexW2994416619

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.