Evidence map›Paper›PMID 34336555›Full record

ArticleAnalytical cellular pathology (Amsterdam)2021

miR-142-3p Modulates Cell Invasion and Migration via PKM2-Mediated Aerobic Glycolysis in Colorectal Cancer.

JunYu Ren, Wenliang Li, Guoqing Pan, Fengchang Huang, Jun Yang, Hongbin Zhang, Ruize Zhou, Ning Xu

Open access · goldAbstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Emerging Roles of ncRNAs Regulating PKM2 in Cancer Progression.Current pharmaceutical biotechnology · 2025
    Review
  6. Review
  7. Review
  8. Review
  9. Regulatory role of the miR-142-3p/Translational lung cancer research · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
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

8 authors at 1 institution in 1 country.

JunYu RenDepartment of Oncological Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Wenliang LiDepartment of Oncological Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.ORCID https://orcid.org/0000-0002-4990-5607
Guoqing PanDepartment of Pathology, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Fengchang HuangDepartment of Oncological Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Jun YangDepartment of Oncological Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Hongbin ZhangDepartment of Oncological Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Ruize ZhouDepartment of Oncological Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Ning XuDepartment of Oncological Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Kunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decreased expression of miR-142-3p was observed in human cancers. However, the function and mechanism of miR-142-3p in human colorectal cancer remain obscure. The expressions of miR-142-3p in human colorectal cancer tissues and cell lines were measured by RT-qPCR. The effects of miR-142-3p on cell invasion and migration were detected by transwell assays. The efficiency of aerobic glycolysis was determined by glucose consumption and lactate production. Dual-luciferase reporter assays were performed to confirm the correlation between miR-142-3p and pyruvate kinase isozyme M2 (PKM2). The level of PKM2 was assessed by western blotting. Our results showed that the expression of miR-142-3p was decreased both in human colorectal cancer tissues and in cells. Overexpression of miR-142-3p in cell line attenuated colorectal cancer cell invasion and migration. About the underlying mechanism, we found that miR-142-3p modulated aerobic glycolysis via targeting pyruvate kinase M2 (PKM2). In addition, we demonstrated PKM2 and PKM2-mediated aerobic glycolysis contributes to miR-142-3p-mediated colorectal cancer cell invasion and migration. Hence, these data suggested that miR-142-3p was a potential therapeutic target for the treatment of human colorectal cancer.

Indexed as

Colorectal NeoplasmsMicroRNAsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticGlycolysisHumansPyruvate KinaseMicroRNAsMIRN142 microRNA, humanPyruvate Kinase

Identifiers

PMID34336555
PMCPMC8294993
OpenAlexW3177808425

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.