Evidence map›Paper›PMID 31564215›Full record

ArticleTechnology in cancer research & treatment2019

MiR-122 Promotes the Development of Colon Cancer by Targeting

Hong Li, Xinhua Zhang, Zhao Jin, Tao Yin, Chuanyi Duan, Junwei Sun, Rui Xiong, Zilin Li

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Technology in cancer research & treatment, 2019. 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 It has been retracted, and should not be counted.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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. The Impact of miR-122 on Cancer.Current pharmaceutical biotechnology · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Low miR-1273a expression predicts poor prognosis of colon cancer and facilitates tumor cell proliferation, migration, and invasion.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
    Article
4 · The record

Corrections and comments

  • Retraction · 2023-04-19Duplication of/in Image · Lack of IRB/IACUC Approval and/or Compliance · Results Not Reproducible · Unreliable Results and/or Conclusions · · see also: https://pubpeer.com/publications/9A56A5A1B43D233A79E2AD7E52E365?utm_source=Chrome%26utm_medium=BrowserExtension%26utm_campaign=Chrome
  • Retracted
5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Hong LiHubei Cancer Hospital, Wuhan, Hubei, China.
Xinhua ZhangHubei Cancer Hospital, Wuhan, Hubei, China.
Zhao JinZhongnan Hospital of Wuhan University.
Tao YinHubei Cancer Hospital, Wuhan, Hubei, China.
Chuanyi DuanHubei Cancer Hospital, Wuhan, Hubei, China.
Junwei SunHubei Cancer Hospital, Wuhan, Hubei, China.
Rui XiongHubei Cancer Hospital, Wuhan, Hubei, China.
Zilin LiHubei Cancer Hospital, Wuhan, Hubei, China.
Hubei Cancer Hospital · CNZhongnan Hospital of Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-coding RNAs, originally considered junk gene products, have taken center stage in view of their significant involvement in a spectrum of biological processes during human development, thereby offering novel therapeutic targets for improvement of treatment options. Accumulating evidence has demonstrated non-coding RNA dysfunction across various human cancers. In particular, microRNAs have emerged as key regulatory molecules in cancer biology. MicroRNAs are noninvasive, readily accessible biomarkers that can be effectively applied for diagnosis and prognosis of different tumor types, including colon cancer. In this study, we reanalyzed the available data with bioinformatics tools to identify differentially expressed microRNAs in colon cancer cells. The top 3 upregulated microRNAs (miR-10, miR-199, and miR-122) in colon cancer cells were further validated in tissues of clinical patients via reverse transcription-quantitative polymerase chain reaction. Our results showed that miR-122 significantly promotes the proliferation and invasion ability of SW480 and SW620 cells through inhibition of Aldolase, Fructose-Bisphosphate A (

Indexed as

ApoptosisCarcinogenesisCell Line, TumorCell MovementCell ProliferationColonic NeoplasmsFemaleFructose-Bisphosphate AldolaseGene Expression Regulation, NeoplasticHumansMaleMicroRNAsNeoplasm InvasivenessALDOA protein, humanFructose-Bisphosphate AldolaseMicroRNAsMIRN122 microRNA, humanALDOAcolon cancerinvasion abilitymiR-10miR-122miR-199

Identifiers

PMID31564215
PMCPMC6767722
OpenAlexW2977373416

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.