Evidence map›Paper›PMID 34986757›Full record

ArticleBioengineered2022

Repressing phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma by microRNA-142-3p restrains the progression of hepatocellular carcinoma.

Chuanli Zeng, Gang Yuan, Yaoren Hu, Donghui Wang, Xiaojun Shi, Dedong Zhu, Airong Hu, Yina Meng, Jialin Lu

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Bioengineered, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. The Role of PI3K/AKT/mTOR Signaling in Hepatocellular Carcinoma Metabolism.International journal of molecular sciences · 2023
    Review
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Chuanli ZengDepartment of Severe Liver Disease, Ningbo HuaMei Hospital, University of Chinese Academy of Science, Ningbo, Zhejiang, China.
Gang YuanDepartment of Acute Infection, Ningbo Huamei Hospital, University of Chinese Academy of Science, Ningbo, Zhejiang, China.
Yaoren HuDepartment of Hepatology, Ningbo Huamei Hospital, University of Chinese Academy of Science, Ningbo, Zhejiang, China.
Donghui WangDepartment of Acute Infection, Ningbo Huamei Hospital, University of Chinese Academy of Science, Ningbo, Zhejiang, China.
Xiaojun ShiDepartment of Hepatology, Ningbo Huamei Hospital, University of Chinese Academy of Science, Ningbo, Zhejiang, China.
Dedong ZhuDepartment of Hepatology, Ningbo Huamei Hospital, University of Chinese Academy of Science, Ningbo, Zhejiang, China.
Airong HuInstitute of Liver Disease, Ningbo Huamei Hospital, University of Chinese Academy of Sciences, Ningbo, Zhejiang, China.
Yina MengMedical School of Ningbo University, Ningbo, Zhejiang, China.
Jialin LuMedical School of Ningbo University, Ningbo, Zhejiang, China.
Ningbo No. 2 Hospital · CNNingbo University · CNBlood Center of Zhejiang Province · CNUniversity of Chinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This paper probes the mechanisms underlying miR-142-3p's modulation of hepatocellular carcinoma (HCC) invasion and apoptosis. Quantitative real-time PCR and Western blot monitored the miR-142-3p profile in HCC tissues and non-tumor tissues. The correlation between miR-142-3p expression and HCC patients' clinicopathological indicators was analyzed. miR-142-3p overexpression and knockdown models were established in HCC cell lines. Cell proliferation was gauged by the colony formation assay and BrdU staining. For measuring apoptosis, flow cytometry and Western blot were implemented. Transwell assay tested cell migration and invasion. miR-142-3p mimics or inhibitors were transfected in Huh7 and HCCLM3 cells. The targeting association between miR-142-3p and PIK3CG was predicted through bioinformatics and further verified by related experiments. The influence of PIK3CG overexpression on miR-142-3p's role in HCC was assayed. A xenografted tumor model was built in mice to validate miR-142-3p knockdown's influence on HCC

Indexed as

AnimalsApoptosisCarcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationClass Ib Phosphatidylinositol 3-KinaseFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansLiver NeoplasmsMaleMiceMicroRNAsRNA, Small InterferingClass Ib Phosphatidylinositol 3-KinaseMicroRNAsMIRN142 microRNA, humanPIK3CG protein, humanRNA, Small Interferingapoptosishepatocellular carcinomaMir-142-3ppik3cg

Identifiers

PMID34986757
PMCPMC8805872
OpenAlexW4205549585

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.