Evidence map›Paper›PMID 32757436›Full record

ArticleJournal of cellular and molecular medicine2020

Quantitative proteomics identified 3 oxidative phosphorylation genes with clinical prognostic significance in gastric cancer.

Fei Su, Fen-Fang Zhou, Tao Zhang, Dan-Wen Wang, Da Zhao, Xiao-Ming Hou, Mao-Hui Feng

Abstract readComparative Study
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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  6. Energy metabolism in health and diseases.Signal transduction and targeted therapy · 2025
    Review
  7. Energy metabolism: a new target for gastric cancer treatment.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
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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

7 authors.

Fei SuDepartment of Oncology, The First Hospital of Lanzhou University, Lanzhou, China.
Fen-Fang ZhouDepartment of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, China.
Tao ZhangDepartment of Oncology, The First Hospital of Lanzhou University, Lanzhou, China.
Dan-Wen WangCenter for Clinical Medicine of Peritoneal Cancer of Wuhan, Wuhan, China.
Da ZhaoDepartment of Oncology, The First Hospital of Lanzhou University, Lanzhou, China.
Xiao-Ming HouDepartment of Oncology, The First Hospital of Lanzhou University, Lanzhou, China.ORCID 0000-0002-8521-749X
Mao-Hui FengCenter for Clinical Medicine of Peritoneal Cancer of Wuhan, Wuhan, China.ORCID 0000-0002-3559-5513

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to explore the underlying mechanisms involved in gastric cancer (GC) formation using data-independent acquisition (DIA) quantitative proteomics analysis. We identified the differences in protein expression and related functions involved in biological metabolic processes in GC. Totally, 745 differentially expressed proteins (DEPs) were found in GC tissues vs. gastric normal tissues. Despite enormous complexity in the details of the underlying regulatory network, we find that clusters of proteins from the DEPs were mainly involved in 38 pathways. All of the identified DEPs involved in oxidative phosphorylation were down-regulated. Moreover, GC possesses significantly altered biological metabolic processes, such as NADH dehydrogenase complex assembly and tricarboxylic acid cycle, which is mostly consistent with that in KEGG analysis. Furthermore the higher expression of UQCRQ, NDUFB7 and UQCRC2 were positively correlated with a better prognosis, implicating these proteins may as novel candidate diagnostic and prognostic biomarkers.

Indexed as

Gene Expression Regulation, NeoplasticOxidative PhosphorylationAdenocarcinomaAdultAgedBiomarkers, TumorDown-RegulationFemaleGastric MucosaGene Regulatory NetworksHumansKaplan-Meier EstimateMaleMetabolic Networks and PathwaysMiddle AgedNeoplasm ProteinsBiomarkers, TumorNeoplasm ProteinsRNA, MessengerRNA, NeoplasmbiomarkersDIAgastric cancermetabolic network

Identifiers

PMID32757436
PMCPMC7521272

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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.