Evidence map›Paper›PMID 32376548›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2020

[Recombinant methioninase regulates PI3K/Akt/Glut-1 pathway and inhibits aerobic glycolysis to promote apoptosis of gastric cancer cells].

Liqiang Zhou, Shihao Li, Li Liu, Qi Zhou, Yiwu Yuan, Lin Xin

Open access · greenAbstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. [Preliminary Investigation of the Molecular Mechanism of Empagliflozin Suppressing Gastric Cancer Through Mammalian Target of Rapamycin].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2023
    Article
  4. Review
  5. Article
  6. Review
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

6 authors at 2 institutions in 1 country.

Liqiang ZhouDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Shihao LiDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Li LiuDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Qi ZhouDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Yiwu YuanDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Lin XinDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Nanchang University · CNSecond Affiliated Hospital of Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the molecular mechanism of recombinant methioninase (rMETase) in promoting apoptosis of gastric cancer cells.

methodsGastric cancer SGC-7901 cells were treated with rMETase (final concentration of 1.25 and 2.50 mmmol/L) for 72 h, and the changes in the cell viability were detected using CCK-8 method and the cell morphology changes were observed under an inverted microscope. Plate colony formation assay was used to evaluate colony formation ability of the cells, and flow cytometry was performed to analyze the changes in cell apoptosis and cell cycles. Glucose and lactate levels in the culture medium were determined using a colorimetric method and ATP concentration was detected using a fluorescence microplate reader; Western blotting was used to assess the effect of rMETase on PI3K/Akt pathway, glucose transporter-1 (GLUT-1), glycolysis- related proteins and apoptotic proteins in SGC-7901 cells.

resultsrMETase significantly inhibited the proliferation and clonal formation, promoted cell apoptosis, and induced cell cycle arrest in S phase in SGC-7901 cells (

conclusionsrMETase can inhibit aerobic glycolysis, induce apoptosis and inhibit the proliferation of SGC-7901 cells by inhibiting the activity of PI3K/Akt/GLUT-1 pathway, suggesting its potential as a therapeutic agent for gastric cancer.

Indexed as

ApoptosisSignal TransductionCarbon-Sulfur LyasesCell Line, TumorCell ProliferationGlucose Transporter Type 1GlycolysisHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRecombinant ProteinsStomach NeoplasmsCarbon-Sulfur LyasesGlucose Transporter Type 1L-methionine gamma-lyasePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRecombinant ProteinsSLC2A1 protein, humanaerobic glycolysisAktgastric cancerglucose transporter-1phosphoinositide 3-kinaserecombinant methioninase

Identifiers

PMID32376548
PMCPMC7040764
OpenAlexW3009419837

What OpenQuestion holds

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Read underepoch 390

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.