Evidence map›Paper›PMID 37287867›Full record

ArticleFASEB bioAdvances2023

GPX2 promotes EMT and metastasis in non-small cell lung cancer by activating PI3K/AKT/mTOR/Snail signaling axis.

Fang Peng, Qiushi Xu, Xiaomeng Jing, Xinming Chi, Zheming Zhang, Xiangpeng Meng, Xinyuan Liu, Jiao Yan, Xuefeng Liu, Shujuan Shao

Open access · goldAbstract read
In one paragraph

Article in FASEB bioAdvances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  18. Review
  19. Glutathione-Dependent Pathways in Cancer Cells.International journal of molecular sciences · 2024
    Review
  20. 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

10 authors at 2 institutions in 2 countries.

Fang PengLiaoning Key Laboratory of Proteomics Dalian Medical University Dalian China.
Qiushi XuDepartment of Neurosurgery Dalian Municipal Central Hospital Dalian China.
Xiaomeng JingDepartment of Pathology Second Affiliated Hospital of Dalian Medical University Dalian China.
Xinming ChiLiaoning Key Laboratory of Proteomics Dalian Medical University Dalian China.
Zheming ZhangLiaoning Key Laboratory of Proteomics Dalian Medical University Dalian China.
Xiangpeng MengLiaoning Key Laboratory of Proteomics Dalian Medical University Dalian China.
Xinyuan LiuLiaoning Key Laboratory of Proteomics Dalian Medical University Dalian China.
Jiao YanLiaoning Key Laboratory of Proteomics Dalian Medical University Dalian China.
Xuefeng LiuInstitute of Cancer Stem Cell Dalian Medical University Dalian China.
Shujuan ShaoLiaoning Key Laboratory of Proteomics Dalian Medical University Dalian China.ORCID https://orcid.org/0000-0002-7314-8319
Dalian Medical University · CNDalian Municipal Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer, with non-small cell lung cancer (NSCLC) being the main subtype, is the leading cause of cancer death worldwide, which is mainly due to the cancer metastasis. Glutathione peroxidase 2 (GPX2), an antioxidant enzyme, is involved in tumor progression and metastasis. Nevertheless, the role of GPX2 in NSCLC metastasis has not been clarified. In this study, we found that GPX2 expression was elevated in NSCLC tissues and high GPX2 expression was correlated with poor prognosis in patients with NSCLC. In addtion, GPX2 expression was related to the patient's clinicopathological features, including lymph node metastasis, tumor size, and TNM stage. Overexpression of GPX2 promoted epithelial-mesenchymal transition (EMT), migration, and invasion of NSCLC cells in vitro. Knockdown of GPX2 showed the opposite effects in vitro and inhibited the metastasis of NSCLC cells in nude mice. Furthermore, GPX2 reduced reactive oxygen species (ROS) accumulation and activated the PI3K/AKT/mTOR/Snail signaling axis. Therefore, our results indicate that GPX2 promotes EMT and metastasis of NSCLC cells by activating the PI3K/AKT/mTOR/Snail signaling axis via the removal of ROS. GPX2 may be an effective diagnostic and prognostic biomarker for NSCLC.

Indexed as

diagnosisEMTGPX2IHCmetastasisNSCLCprognosis

Identifiers

PMID37287867
PMCPMC10242197
OpenAlexW4323317271

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.