Evidence map›Paper›PMID 34657551›Full record

ArticleBioengineered2021

MiR-130a-3p suppresses colorectal cancer growth by targeting Wnt Family Member 1 (WNT1).

Guang-Lin Song, Ming Xiao, Xiao-Ya Wan, Jun Deng, Jun-Da Ling, Ying-Guo Tian, Min Li, Jie Yin, Ren-Ying Zheng, Yi Tang and 1 more

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 26 citations in OpenAlex.

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  11. Exploring the Key Signaling Pathways and ncRNAs in Colorectal Cancer.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Article
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  15. Article
  16. Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer.Journal of cancer research and clinical oncology · 2023
    Article
  17. Article
  18. Review
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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

11 authors at 3 institutions in 1 country.

Guang-Lin SongDepartment of Oncology, People's Hospital of Yuechi County, Yuechi County, Sichuan Province, China.
Ming XiaoDepartment of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, China.
Xiao-Ya WanDepartment of Oncology, People's Hospital of Yuechi County, Yuechi County, Sichuan Province, China.
Jun DengDepartment of Oncology, People's Hospital of Yuechi County, Yuechi County, Sichuan Province, China.
Jun-Da LingDepartment of Oncology, People's Hospital of Yuechi County, Yuechi County, Sichuan Province, China.
Ying-Guo TianDepartment of Oncology, People's Hospital of Yuechi County, Yuechi County, Sichuan Province, China.
Min LiDepartment of Oncology, People's Hospital of Yuechi County, Yuechi County, Sichuan Province, China.
Jie YinDepartment of Oncology, People's Hospital of Yuechi County, Yuechi County, Sichuan Province, China.
Ren-Ying ZhengDepartment of Oncology, People's Hospital of Yuechi County, Yuechi County, Sichuan Province, China.
Yi TangDepartment of Pathology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, China.
Gui-Yuan LiuDepartment of General Surgery, The Affiliated Hospital of Chongqing Three Gorges, Chongqing, China.
Yueqing People's Hospital · CNChongqing Medical University · CNChongqing Three Gorges Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The microRNA miR-130a-3p (miR-130a-3p) has anti-tumor activity against numerous cancer types. Further, miR-130a-3p may target Wnt signaling, which is a critical pathway regulating tumorigenesis. Functions of miR-130a-3p in colorectal cancer (CRC) and contributions of Wnt1 pathway modulation, however, have not been examined, hence the exploration on these two aspects. In this study, in comparison with normal controls, both CRC tissue and multiple CRC cell lines showed downregulated miR-130a-3p. MiR-130a-3p overexpression contributed to a decrease in CRC cell proliferation. Additionally, its overexpression also caused reduced expression of WNT Family Member 1 (WNT1) and downstream WNT pathway factors c-myc and cyclin D1. Dual-luciferase assay revealed WNT1 as a direct target of miR-130a-3p, and further the inhibitory effect of miR-130a-3p on c-myc and cyclin D1 was proved to be reversed by overexpressed WNT1. Collectively, miR-130a-3p inhibits CRC growth by directly targeting WNT1, and miR-130a-3p and WNT1 pathway-associated factors are defined as potential targets for CRC treatment.

Indexed as

Down-Regulation3' Untranslated RegionsAnimalsCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsCyclin D1FemaleGene Expression Regulation, NeoplasticHCT116 CellsHumansMiceMicroRNAsNeoplasm TransplantationProto-Oncogene Proteins c-myc3' Untranslated RegionsCCND1 protein, humanCyclin D1MicroRNAsMIRN130 microRNA, humanMYC protein, humanProto-Oncogene Proteins c-mycWnt1 ProteinWNT1 protein, humanColorectal cancermiR-130a-3ptumor suppressionWNT1Wnt signaling pathway

Identifiers

PMID34657551
PMCPMC8806712
OpenAlexW3206972099

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.