Evidence map›Paper›PMID 26553359›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

miR-198 targets SHMT1 to inhibit cell proliferation and enhance cell apoptosis in lung adenocarcinoma.

Shujun Wu, Guojun Zhang, Ping Li, Shanshan Chen, Furui Zhang, Juan Li, Chenyang Jiang, Xiaonan Chen, Yuanyuan Wang, Yuwen Du and 2 more

RetractedAbstract readRetracted Publication
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. MicroRNAs as Regulators of Cancer Cell Energy Metabolism.Journal of personalized medicine · 2022
    Review
  3. Article
  4. The promising role and prognostic value of miR-198 in human diseases.American journal of translational research · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Reprogramming of serine, glycine and one-carbon metabolism in cancer.Biochimica et biophysica acta. Molecular basis of disease · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. SHMT1 inhibits the metastasis of HCC by repressing NOX1-mediated ROS production.Journal of experimental & clinical cancer research : CR · 2019
    Article
  18. Metabolic Intermediates in Tumorigenesis and Progression.International journal of biological sciences · 2019
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Shujun WuDepartment of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People' s Republic of China.
Guojun ZhangDepartment of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People' s Republic of China. gjzhangzzu@126.com.
Ping LiDepartment of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People' s Republic of China.
Shanshan ChenDepartment of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People' s Republic of China.
Furui ZhangDepartment of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People' s Republic of China.
Juan LiDepartment of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People' s Republic of China.
Chenyang JiangDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, People' s Republic of China.
Xiaonan ChenSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 450001, People' s Republic of China.
Yuanyuan WangSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 450001, People' s Republic of China.
Yuwen DuSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 450001, People' s Republic of China.
Qianqian SunSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 450001, People' s Republic of China.
Guoqiang ZhaoSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 450001, People' s Republic of China. zhaogq@zzu.edu.cn.
Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MiR-198 is involved in tumorigenesis, migration, invasion, and metastasis of various malignant cancers. However, the exact expression levels of miR-198 and the molecular mechanism underlying its role in lung adenocarcinoma require further exploration. In this study, quantitative real-time PCR was applied to study miR-198 and serine hydroxymethyltransferase 1 (SHMT1) expression in 47 paired lung adenocarcinoma tissues and adjacent nontumor lung tissues. Clinicopathological characters were analyzed. Pearson's correlation analysis was used to detect the relationship between miR-198 and SHMT1 expression. The function of miR-198 was explored by measuring cell proliferation, cell apoptosis, and the cell-cycle in vitro and in vivo. The target gene of miR-198 was certified using dual luciferase report assay. We found that in lung adenocarcinoma, miR-198 was significantly downregulated and SHMT1 was inversely upregulated. A strong negative correlation was noticed between miR-198 and SHMT1 expression. Further analysis revealed that miR-198 expression was associated with TNM stage and lymph node metastasis. Upregulated miR-198 could inhibit cell proliferation, enhance cell apoptosis, and lead to cell-cycle arrest in lung adenocarcinoma, which showed a more effective alteration than SHMT1 siRNA. Moreover, we identified SHMT1 as a target gene of miR-198. In conclusion, miR-198 suppressed proliferation of lung adenocarcinoma cells both in vitro and in vivo by directly targeting SHMT1. miR-198 may be a potential therapeutic target for lung adenocarcinoma in the near future.

Indexed as

AdenocarcinomaAdenocarcinoma of LungAdultAgedApoptosisCarcinogenesisCell Cycle CheckpointsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticGlycine HydroxymethyltransferaseHumansLung NeoplasmsLymphatic MetastasisMaleGlycine HydroxymethyltransferaseMicroRNAsMIRN198 microRNA, humanSHMT protein, humanApoptosisLung adenocarcinomaMiR-198ProliferationSerine hydroxymethyltransferase 1

Identifiers

PMID26553359
OpenAlexW2119406817

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.