Evidence map›Paper›PMID 34826027›Full record

ArticleMolecular and cellular biochemistry2022

MiR-196a promotes the proliferation and migration of esophageal cancer via the UHRF2/TET2 axis.

Chang-Mei Hu, Jie Peng, Liang Lv, Xue-Hong Wang, Ji-Rong Huo, De-Liang Liu

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. The diverse role of RNA methylation in esophageal cancer.Acta biochimica et biophysica Sinica · 2023
    Review
  11. Article
  12. Article
  13. The Role of SUMO E3 Ligases in Signaling Pathway of Cancer Cells.International journal of molecular sciences · 2022
    Review
  14. Role of repressed microRNAs in endometriosis.Medical molecular morphology · 2022
    Review
  15. The UHRF protein family in epigenetics, development, and carcinogenesis.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2022
    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 1 institution in 1 country.

Chang-Mei HuDepartment of Gastroenterology, Second Xiangya Hospital, Central South University, No. 139, Mid RenMin Rd., Changsha, 410011, Hunan Province, People's Republic of China. channmeih13@163.com.ORCID http://orcid.org/0000-0002-9646-2589
Jie PengDepartment of Haematology, Xiangya Hospital, Central South University, Changsha, 410078, Hunan Province, People's Republic of China.
Liang LvDepartment of Gastroenterology, Second Xiangya Hospital, Central South University, No. 139, Mid RenMin Rd., Changsha, 410011, Hunan Province, People's Republic of China.
Xue-Hong WangDepartment of Gastroenterology, Second Xiangya Hospital, Central South University, No. 139, Mid RenMin Rd., Changsha, 410011, Hunan Province, People's Republic of China.
Ji-Rong HuoDepartment of Gastroenterology, Second Xiangya Hospital, Central South University, No. 139, Mid RenMin Rd., Changsha, 410011, Hunan Province, People's Republic of China.
De-Liang LiuDepartment of Gastroenterology, Second Xiangya Hospital, Central South University, No. 139, Mid RenMin Rd., Changsha, 410011, Hunan Province, People's Republic of China.
Central South University · CN

Funding

natural science foundation of hunan province No. 2019JJ40416
6 · The paper itself

Abstract

The aim of this study was to investigate the functions and molecular mechanism of miR-196a in esophageal cancer (EC). miR-196a as well as UHRF2 and TET2 mRNA and protein levels in EC tissues and cells were detected using quantitative real-time PCR or western blot, respectively. Cell proliferation was evaluated via MTT assay. Transwell assays were used to detect cell migration. In addition, the targeted relationship between miR-196a and UHRF2 was assessed through a dual luciferase reporter assay. Enzyme-linked immunosorbent assay was performed to detect the levels of the cytosine intermediates 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC). We found increased miR-196a expression in EC tissues and cells but decreased UHRF2 and TET2 expression. Next, functional experiments showed that knockdown of miR-196a or UHRF2 overexpression suppress EC cell proliferation and migration. miR-196a negatively regulates TET2 expression by directly targeting UHRF2. UHRF2 overexpression decreased 5mC levels but increased 5hmC levels. Furthermore, TET2 downregulation reversed the functions of miR-196a inhibition on EC cell proliferation and migration. Collectively, our study suggested that miR-196a was closely related to the progression of EC possibly by regulating the UHRF2/TET2 axis. Thus, miR-196a represents a potential new EC therapeutic target.

Indexed as

Cell MovementCell ProliferationSignal TransductionCell Line, TumorDioxygenasesDNA-Binding ProteinsEsophageal NeoplasmsHumansMicroRNAsNeoplasm ProteinsRNA, NeoplasmUbiquitin-Protein LigasesDioxygenasesDNA-Binding ProteinsMicroRNAsMIRN196 microRNA, humanNeoplasm ProteinsRNA, NeoplasmTET2 protein, humanUbiquitin-Protein LigasesUHRF2 protein, humanEsophageal cancermiR-196aProliferation and migrationTET2UHRF2

Identifiers

PMID34826027
OpenAlexW3216932357

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.