Evidence map›Paper›PMID 35508523›Full record

ArticleCell death & disease2022

SP1-mediated up-regulation of lncRNA TUG1 underlines an oncogenic property in colorectal cancer.

Wei Liu, Jin Meng, Rongjun Su, Changjun Shen, Shuai Zhang, Yantao Zhao, Wenqi Liu, Jiang Du, Shuai Zhu, Pan Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 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
2.0field-weighted citation impact, top 12% 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, 23 citations in OpenAlex.

  1. Review
  2. Function ofOncology letters · 2025
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  4. Article
  5. Review
  6. Article
  7. Wnt/β-catenin-driven EMT regulation in human cancers.Cellular and molecular life sciences : CMLS · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Specificity Proteins (Sp) and Cancer.International journal of molecular sciences · 2023
    Review
  12. Review
  13. Review
  14. Review
  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

12 authors at 2 institutions in 1 country.

Wei LiuDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Jin MengDepartment of Fifth Treatment Areas of Anorectal Disease, Shenyang Coloproctology Hospital, Shenyang, 110002, P.R. China.
Rongjun SuDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Changjun ShenDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Shuai ZhangDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Yantao ZhaoDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Wenqi LiuDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Jiang DuDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Shuai ZhuDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Pan LiDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China.
Zhigang WangDepartment of Fifth Treatment Areas of Anorectal Disease, Shenyang Coloproctology Hospital, Shenyang, 110002, P.R. China.
Xiaoxia LiDepartment of General Surgery, Yan'an People's Hospital, Yan'an, 716000, P.R. China. xxli63@cmu.edu.cn.ORCID 0000-0003-3972-9715
Yan'an University · CNShenyang Anorectal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The long non-coding RNA (lncRNA) taurine up-regulated gene 1 (TUG1) acts as tumor-promoting factor in colorectal cancer (CRC). We aimed to elucidate the mechanism by which the transcription factor specificity protein 1 (SP1) regulates TUG1 and microRNAs (miRs)/mRNAs in the context of CRC, which has not been fully studied before. Expression patterns of TUG1 and SP1 were determined in clinical CRC samples and cells, followed by identification of their interaction. Next, the functional significance of TUG1 in CRC was investigated. An in vivo CRC model was established to validate the effect of TUG1. The results demonstrated that TUG1 and SP1 were highly-expressed in CRC, wherein SP1 bound to the TUG1 promoter and consequently, positively regulated its expression. Silencing of TUG1 caused suppression of CRC cell growth and promotion of cell apoptosis. TUG1 could bind to miR-421 to increase KDM2A expression, a target gene of miR-421. TUG1 could activate the ERK pathway by impairing miR-421-targeted inhibition of KDM2A. Additionally, SP1 could facilitate the tumorigenesis of CRC cells in vivo by regulating the TUG1/miR-421/KDM2A/ERK axis. Altogether, the current study emphasizes the oncogenic role of TUG1 in CRC, and illustrates its interactions with the upstream transcription factor SP1 and the downstream modulatory axis miR-421/KDM2A/ERK, thus offering novel insights into the cancerogenic mechanism in CRC.

Indexed as

Colorectal NeoplasmsF-Box ProteinsMicroRNAsRNA, Long NoncodingCarcinogenesisCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansJumonji Domain-Containing Histone DemethylasesSp1 Transcription FactorTranscription FactorsUp-RegulationF-Box ProteinsJumonji Domain-Containing Histone DemethylasesKDM2A protein, humanMicroRNAsMIRN421 microRNA, humanRNA, Long NoncodingSP1 protein, humanSp1 Transcription FactorTranscription Factors

Identifiers

PMID35508523
PMCPMC9068916
OpenAlexW4229025722

What OpenQuestion holds

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LicenceCC BY
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.