Evidence map›Paper›PMID 33414893›Full record

ArticleOxidative medicine and cellular longevity2020

MiR-429 Involves in the Pathogenesis of Colorectal Cancer via Directly Targeting LATS2.

Xia Chen, Ai-Li Wang, Yuan-Yuan Liu, Chen-Xi Zhao, Xue Zhou, Hai-Long Liu, Mo-Bin Lin

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Biomedicines · 2026
    Article
  2. Article
  3. Review
  4. Exploring the Key Signaling Pathways and ncRNAs in Colorectal Cancer.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. 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

7 authors at 1 institution in 1 country.

Xia ChenCenter for Clinical Research and Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.ORCID https://orcid.org/0000-0002-7222-1166
Ai-Li WangCenter for Clinical Research and Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.ORCID https://orcid.org/0000-0002-0854-5369
Yuan-Yuan LiuCenter for Clinical Research and Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.ORCID https://orcid.org/0000-0003-2976-9561
Chen-Xi ZhaoCenter for Clinical Research and Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.ORCID https://orcid.org/0000-0002-1286-4696
Xue ZhouCenter for Clinical Research and Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.ORCID https://orcid.org/0000-0003-2593-016X
Hai-Long LiuCenter for Clinical Research and Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.ORCID https://orcid.org/0000-0003-3826-0476
Mo-Bin LinCenter for Clinical Research and Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.ORCID https://orcid.org/0000-0002-0686-688X
Tongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a leading cause of cancer-related death around the world whose recurrence and metastasis rate is high. Due to the underlying unclear pathogenesis, it is hard so far to predict the tumorigenesis and prevent its recurrence. YAP/TAZ has been reported to be activated and functioned as a potential oncogene in multiple cancer types and proved to be essential for the carcinogenesis of most solid tumors. In the present study, we found that YAP/TAZ was markedly upregulated in CRC tissues comparing with the adjacent noncancerous tissues due to the downregulation of LATS2, the main upstream regulator. We further identified miR-429 as a direct regulator of LATS2-YAP/TAZ activation, suggesting that the miR-429-LATS2-YAP/TAZ might be novel effective diagnostic axis and therapeutic targets for CRC.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell Line, TumorColorectal NeoplasmsDown-RegulationFemaleHCT116 CellsHumansIntracellular Signaling Peptides and ProteinsMiceMice, Inbred BALB CMice, NudeMicroRNAsNeoplasm MetastasisNeoplasm Recurrence, LocalProtein Serine-Threonine KinasesAdaptor Proteins, Signal TransducingIntracellular Signaling Peptides and ProteinsLATS2 protein, humanLATS2 protein, mouseMicroRNAsMIRN429 microRNA, humanMIRN429 microRNA, mouseProtein Serine-Threonine KinasesTranscriptional Coactivator with PDZ-Binding Motif ProteinsTranscription FactorsTumor Suppressor ProteinsWWTR1 protein, humanWwtr1 protein, mouseYAP1 protein, humanYap1 protein, mouseYAP-Signaling Proteins

Identifiers

PMID33414893
PMCPMC7769676
OpenAlexW3116400448

What OpenQuestion holds

Textmetadata
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.