Evidence map›Paper›PMID 26745603›Full record

ArticleOncotarget2016

MiR-let-7a inhibits cell proliferation, migration, and invasion by down-regulating PKM2 in gastric cancer.

Ran Tang, Chao Yang, Xiang Ma, Younan Wang, Dakui Luo, Chi Huang, Zekuan Xu, Ping Liu, Li Yang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 99 citations in OpenAlex.

  1. Trial
  2. Review
  3. Emerging Roles of ncRNAs Regulating PKM2 in Cancer Progression.Current pharmaceutical biotechnology · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. New Insights into the Link Between Melanoma and Obesity.Advances in experimental medicine and biology · 2024
    Review
  8. Review
  9. Development of 5-FU-modified tumor suppressor microRNAs as a platform for novel microRNA-based cancer therapeutics.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Cancers · 2021
    Article
  17. Article
  18. Review
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Ran TangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chao YangLiver Transplantation Center of the First Affiliated Hospital and Key Laboratory on Living Donor Liver Transplantation, Ministry of Health, Nanjing Medical University, Nanjing, China.
Xiang MaDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Younan WangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Dakui LuoDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chi HuangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Zekuan XuDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ping LiuDepartment of Oncology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Li YangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNJiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In contrast to normal differentiated cells that depend on aerobicoxidation for energy production, cancer cells use aerobic glycolysis as the main source (Warburg's effect). The M2 splice isoform of pyruvate kinase (PKM2) is the key regulator for the aerobic glycolysis, high expression of PKM2 contributes to the aerobic glycolysis, promotes the growth of tumors. In the present study, we found that PKM2 was highly expressed in gastric cancer (GC) tissues and had a strongly inverse correlation with the expression of microRNA-let-7a (miR-let-7a). Furthermore, we found that the overexpression of miR-let-7a markedly suppressed the proliferation, migration, and invasion of GC cells by down-regulating the expression of PKM2. MicroRNAs (miRNAs) are important regulators play key roles in tumorigenesis and tumor progression. Although previous reports showed that let-7 family members act as tumor suppressors in many cancers. The specific regulatory mechanism of miR-let-7a to PKM2 in gastric cancer is still unclear. In this study, we revealed that miR-let-7a function as the antitumor and gene regulatory effects of PKM2 in GC cells.

Indexed as

Carrier ProteinsCell DifferentiationCell MovementCell ProliferationDown-RegulationFemaleHumansMaleMembrane ProteinsMicroRNAsMiddle AgedPyruvate KinaseStomach NeoplasmsThyroid Hormone-Binding ProteinsThyroid HormonesTransfectionCarrier ProteinsMembrane ProteinsMicroRNAsmirnlet7 microRNA, humanPyruvate KinaseThyroid Hormone-Binding ProteinsThyroid Hormonesgastric cancermicroRNA-let-7aPKM2

Identifiers

PMID26745603
PMCPMC4868734
OpenAlexW2235523043

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.