Evidence map›Paper›PMID 35196196›Full record

ArticleCell cycle (Georgetown, Tex.)2022

miR-4461 inhibits the progression of Gallbladder carcinoma via regulating EGFR/AKT signaling.

Xingzhou Yan, Pinghua Yang, Hu Liu, Yongyang Zhao, Zhixiong Wu, Baohua Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Non-coding RNAs as potential biomarkers of gallbladder cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  5. Article
  6. 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

6 authors at 2 institutions in 1 country.

Xingzhou YanDepartment of Biliary Tract Surgery, Third Affiliated Hospital of Second Military Medical University, Shanghai, China.
Pinghua YangDepartment of Biliary Tract Surgery, Third Affiliated Hospital of Second Military Medical University, Shanghai, China.
Hu LiuDepartment of Biliary Tract Surgery, Third Affiliated Hospital of Second Military Medical University, Shanghai, China.
Yongyang ZhaoDepartment of Biliary Tract Surgery, Third Affiliated Hospital of Second Military Medical University, Shanghai, China.
Zhixiong WuDepartment of Critical Care Medicine, Huadong Hospital, Shanghai, China.
Baohua ZhangDepartment of Biliary Tract Surgery, Third Affiliated Hospital of Second Military Medical University, Shanghai, China.
Second Military Medical University · CNHuadong Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence has demonstrated that microRNAs (miRNAs) participated in the tumorigenesis, progression and recurrence of various malignancies including Gallbladder carcinoma (GBC). miR-4461 was reported to work as a tumor suppressor gene in renal cell carcinoma. However, the role of miR-4461 in GBC remains unknown. Herein, we show that miR-4461 is downregulated in gallbladder cancer stem cells (CSCs). Forced miR-4461 expression attenuates the self-renewal, tumorigenicity of gallbladder CSCs, and inhibits proliferation and metastasis of GBC cells. Conversely, miR-4461 knockdown promotes the self-renewal of gallbladder CSCs, and facilities proliferation and metastasis of GBC cells. Mechanistically, miR-4461 inhibits GBC progression via downregulating EGFR/AKT pathway. Special EGFR siRNA or AKT overexpression virus abolishes the discrepancy of self-renewal, tumorigenesis, growth, and metastasis between miR-4461 overexpression GBC cells and their control cells. In conclusion, miR-4461 suppresses GBC cells self-renewal, tumorigenicity, proliferation, and metastasis by inactivating EGFR/AKT signaling, and may therefore prove to be a potential therapeutic target for GBC patients.

Indexed as

Gallbladder NeoplasmsMicroRNAsProto-Oncogene Proteins c-aktCarcinogenesisCell Line, TumorCell ProliferationCell Transformation, NeoplasticErbB ReceptorsHumansEGFR protein, humanErbB ReceptorsMicroRNAsMIRN4461 microRNA, humanProto-Oncogene Proteins c-aktAKTcancer stem cellEGFRGallbladder carcinomamiR-4461

Identifiers

PMID35196196
PMCPMC9103642
OpenAlexW4213434720

What OpenQuestion holds

Textmetadata
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.