Evidence map›Paper›PMID 34499008›Full record

ArticleBioengineered2021

The tumor-suppressive effects of alpha-ketoglutarate-dependent dioxygenase FTO via N6-methyladenosine RNA methylation on bladder cancer patients.

Wenfa Yi, Yong Yu, Yafei Li, Juan Yang, Shuying Gao, Lingfen Xu

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. 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
1.1field-weighted citation impact, top 22% 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, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. FTO-mediated mTranslational cancer research · 2025
    Article
  6. Review
  7. RNA NNature reviews. Urology · 2024
    Review
  8. Article
  9. Review
  10. Review
  11. Recent Advances in RNA mCancer treatment and research · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. 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

6 authors at 1 institution in 1 country.

Wenfa YiDepartment Of Urology, Qinghai Provincial People's Hospital, Xining, Qinghai Province, China.
Yong YuDepartment Of Urology, Qinghai Provincial People's Hospital, Xining, Qinghai Province, China.
Yafei LiDepartment Of Urology, Qinghai Provincial People's Hospital, Xining, Qinghai Province, China.
Juan YangDepartment Of Oncology, Qinghai Provincial People's Hospital, Xining, Qinghai Province, China.
Shuying GaoDepartment Of Endoscopy Room, Qinghai Provincial People's Hospital, Xining, Qinghai Province, China.
Lingfen XuDepartment Of General Practice, Qinghai Provincial People's Hospital, Xining, Qinghai Province, China.
Qinghai Provincial Peoples Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N6-methyladenosine (m6A) methylation participates in the progression of bladder cancer (BCa). Nevertheless, the regulatory mechanism of alpha-ketoglutarate-dependent dioxygenase FTO influencing the BCa progression has still remained elusive. In this study, to investigate the tumor-suppressive effects of FTO via m6A RNA methylation on BCa patients, a total of 15 cancer tissues and adjacent normal tissues (ANTs) were collected from BCa patients who received tumor resection in our hospital from September 2015 to December 2019. We found that the FTO expression was significantly reduced in cancer tissues compared with that in ANTs, which indicated a lower malignant potential and a higher overall survival rate. It was revealed that overexpression of FTO in two human urinary BCa cell lines (HT-1197 and HT-1376) significantly decreased the cell proliferation and invasion abilities compared with the negative controls, whereas the cell apoptosis was markedly enhanced. In addition, we noted that the changes in m6A methylation level mainly appeared at 5' untranslated region (5' UTR) of MALAT1 and NOTCH1 transcripts, and at 3' UTR of CSNK2A2 and ITGA6 transcripts, responding to the overexpression of FTO. Mechanistically, we found that the splicing factor, proline- and glutamine-rich (SFPQ) could influence the FTO-mediated m6A RNA demethylation, eventually affecting the gene expression. This study provided a new insight into the relationship between the FTO expression and the m6A RNA methylation, assisting scholars to better understand the pathogenesis of BCa.

Indexed as

MethylationUrinary Bladder NeoplasmsAdenosineAgedAlpha-Ketoglutarate-Dependent Dioxygenase FTOCell Line, TumorFemaleHumansMaleMiddle AgedPTB-Associated Splicing FactorRNA, MessengerAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanN-methyladenosinePTB-Associated Splicing FactorRNA, Messengerbladder cancerFTOm6A rna methylationsfpq

Identifiers

PMID34499008
PMCPMC8806820
OpenAlexW3196681785

What OpenQuestion holds

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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.