Evidence map›Paper›PMID 35284980›Full record

ArticleJournal of the Egyptian National Cancer Institute2022

Transcriptome analysis reveals SALL4 as a prognostic key gene in gastric adenocarcinoma.

Ranjan Jyoti Sarma, Sarathbabu Subbarayan, John Zohmingthanga, Saia Chenkual, Thomas Zomuana, Sailo Tlau Lalruatfela, Jeremy L Pautu, Arindam Maitra, Nachimuthu Senthil Kumar

Open access · diamondAbstract read
In one paragraph

Article in Journal of the Egyptian National Cancer Institute, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

9 authors at 4 institutions in 1 country.

Ranjan Jyoti SarmaDepartment of Biotechnology, Mizoram University, Aizawl, Mizoram, 796 004, India.
Sarathbabu SubbarayanDepartment of Biotechnology, Mizoram University, Aizawl, Mizoram, 796 004, India.
John ZohmingthangaDirector, Zoram Medical College, Falkawn, Mizoram, 796005, India.
Saia ChenkualDepartment of Surgery, Civil Hospital Aizawl, Aizawl, Mizoram, 796 001, India.
Thomas ZomuanaDepartment of Surgery, Civil Hospital Aizawl, Aizawl, Mizoram, 796 001, India.
Sailo Tlau LalruatfelaDepartment of Surgery, Civil Hospital Aizawl, Aizawl, Mizoram, 796 001, India.
Jeremy L PautuDepartment of Medical Oncology, Mizoram State Cancer Institute, Aizawl, Mizoram, 796017, India.
Arindam MaitraNational Institute of Biomedical Genomics, Kalyani, West Bengal, 741251, India. am1@nibmg.ac.in.
Nachimuthu Senthil KumarDepartment of Biotechnology, Mizoram University, Aizawl, Mizoram, 796 004, India. nskmzu@gmail.com.ORCID http://orcid.org/0000-0002-0192-2133
Aizawl Adventist Hospital · INMizoram University · INCancer Institute (WIA) · INNational Institute of Biomedical Genomics · IN

Funding

department of biotechnology , ministry of science and technology DBT- NER/Health/46/2015 and BT/551/NE/U-Excel/2014
6 · The paper itself

Abstract

backgroundStomach adenocarcinoma (STAD) dominates 80-90% of gastric cancer (GC). Over the years, it has been realized that the identification of the genes responsible for gastric carcinogenesis is essential to understand the biomarker discovery.

methodsThis study aims to identify candidate genes for biomarker discovery in STAD. RNA-Seq was performed on three paired tumor-normal and one unpaired tumor samples from four GC patients and investigated for differentially expressed genes (DEGs) using DESeq2. Gene set enrichment analysis were performed. The DEGs were compared with two STAD microarray datasets available on Gene Expression Omnibus (GEO) database. Survival study (OS) were performed using KM-Plotter on the common genes between all the datasets.

resultsTotally, 148 DEGs were identified, wherein 55 genes were upregulated and 93 genes were downregulated with |log2foldchange| > 1 and Benjamini-Hochberg (BH) Adjusted P value < 0.01. Cell adhesion molecule (CAM) Pathway was found to be the most significant among the upregulated genes. Gastric acid secretion and mineral absorption pathways were the most significant pathways among the downregulated genes. Comparison with two GEO datasets followed by OS analysis revealed two upregulating genes, APOC1 and SALL4 with prognostic significance.

conclusionUpregulation of APOC1 is associated with marginal overall survival (OS) and SALL4 over-expression was associated with the poor OS using KM-Plotter during 5 years data period. Our study suggests that SALL4 could be a promising biomarker candidate in STAD.

Indexed as

AdenocarcinomaStomach NeoplasmsGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPrognosisTranscription FactorsSALL4 protein, humanTranscription FactorsBiomarkerDifferentially expressed genesPoor survivalRNA-SeqStomach adenocarcinoma

Identifiers

PMID35284980
PMCPMC13314243
OpenAlexW4221011784

What Socratic 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 Socratic graph.