Evidence map›Paper›PMID 34013357›Full record

ArticleInternational journal of oncology2021

The inhibitory effect of CTAB on human osteosarcoma through the PI3K/AKT signaling pathway.

Wacili Da, Lin Tao, Yue Zhu

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  4. Review
  5. Microcystins can be extracted from Microcystis aeruginosa using amino acid-derived biosurfactants.Environmental science and pollution research international · 2022
    Article
  6. Article
  7. Article
  8. International journal of immunopathology and pharmacology
    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

3 authors at 2 institutions in 1 country.

Wacili DaDepartment of Orthopedics, The First Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China.
Lin TaoDepartment of Orthopedics, The First Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China.
Yue ZhuDepartment of Orthopedics, The First Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China.
First Hospital of China Medical University · CNChina Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) metastasis and recurrence and multidrug resistance are three major obstacles in the clinic. New highly effective and low toxicity drugs for osteosarcoma are needed. The antitumoral efficacy of cetrimonium bromide (CTAB), a quaternary ammonium compound, is gradually being investigated. The aim of the present study was to investigate the effects of CTAB on OS cells and the underlying mechanisms. CTAB inhibited the proliferation of osteosarcoma cells in a concentration‑ and time‑dependent manner, resulting in cell cycle arrest in G1 phase. CTAB also suppressed the migration and invasion of HOS and MG63 cells at a low concentration without inhibiting the growth of human osteoblasts. Moreover, CTAB promoted caspase‑mediated apoptosis of osteosarcoma cells through the PI3K/AKT cascade, and this effect was accompanied by obvious mitochondrial toxicity.

Indexed as

AnimalsAntinematodal AgentsApoptosisBone NeoplasmsCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationCetrimoniumHumansMaleMembrane Potential, MitochondrialMiceMice, NudeOsteosarcomaPhosphatidylinositol 3-KinasesAntinematodal AgentsCetrimoniumPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktapoptosisCTABinvasionmigrationosteosarcomaPI3K/AKTproliferation

Identifiers

PMID34013357
PMCPMC8131084
OpenAlexW3161651970

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.