Evidence map›Paper›PMID 36306063›Full record

ArticleGenes & genomics2023

Knockdown of growth differentiation factor-15 inhibited nonsmall cell lung cancer through inactivating PTEN/PI3K/AKT signaling pathway.

Yongshi Liu, Jie Lei, Xiang Ji, Chunmei Li, Xiaoxia Chen, Juan Wang, Jiajia Dong, Hongpei Zhang, Yan Li

Abstract read
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In one paragraph

Article in Genes & genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. HNRNPA2B1-mediated mJournal of translational medicine · 2023
    Article
  8. 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 1 institution in 1 country.

Yongshi LiuDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China.
Jie LeiDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China.
Xiang JiDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China. b20160701128@stu.ccsu.edu.cn.
Chunmei LiDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China.
Xiaoxia ChenDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China.
Juan WangDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China.
Jiajia DongDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China.
Hongpei ZhangDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China.
Yan LiDepartment of thoracic surgery, Second Affiliated Hospital of Air Force Medical University, No. 1 Xinsi Road, 710038, Xi'an, China.
Air Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-small cell lung cancer (NSCLC) is characterized by high morbidity and mortality in the world. Growth and differentiation factor 15 (GDF15) has been proved to play an important role in regulating tumor progression. However, the influence of GDF15 on NSCLC remains unclear.

objectiveWe aimed to investigate the regulatory role of GDF15 in NSCLC.

methodsThe correlation between GDF15 expression and prognosis, stage of NSCLC was examined with bioinformatics method. The cell proliferation was detected with CCK8 and EdU staining. Wound healing, Transwell, flow cytometry assays were used to measure cell migration, invasion, and apoptosis, respectively.

resultsHigh expression of GDF15 is correlated with worse survival and malignant progression of NSCLC. Knockdown of GDF15 restrained the proliferation, invasion, migration, but accelerated apoptosis of lung cancer cells through regulating PTEN/PI3K/AKT signaling pathway. sh-GDF15 suppressed epithelial mesenchymal transition (EMT) process and promoted the chemotherapy sensitivity of lung cancer cells.

conclusionGDF15 plays an important role in NSCLC progression. GDF15 mediated PTEN/PI3K/AKT signaling pathway might be the potential therapeutic targets for the prevention and treatment of GDF15.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSignal TransductionPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanEMTGDF15NSCLCPTEN/PI3K/AKT

Identifiers

PMID36306063
OpenAlexW4307501955

What Socratic holds

Textmetadata
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.