Evidence map›Paper›PMID 37432498›Full record

ArticleMedical oncology (Northwood, London, England)2023

Auraptene-induced cytotoxic effects in acute myeloid leukemia cell lines.

Majid Ghorbani, Mohammad Soukhtanloo, Amir Salek Farrokhi, Seyed Mahdi Hassanian, Fatemeh Ghorbani, Amir Reza Afshari, Mohsen Taherian, Mohammad Hadi Sadeghian

RetractedErratum issuedAbstract readRetracted Publication
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2023. 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 It has been retracted, and should not be counted.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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Majid GhorbaniDepartment of Hematology and Blood Banking, Cancer Molecular Pathology Research Center, Mashhad University of Medical Sciences, P.O. Box: 1316943551, Mashhad, Iran.
Mohammad SoukhtanlooDepartment of Medical Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Amir Salek FarrokhiDepartment of Immunology, Pasteur Institute of Iran, Tehran, Iran.
Seyed Mahdi HassanianDepartment of Medical Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Fatemeh GhorbaniDepartment of Immunology, Semnan University of Medical Sciences, Semnan, Iran.
Amir Reza AfshariDepartment of Physiology and Pharmacology, Faculty of Medicine, North Khorasan University of Medical Sciences, Bojnurd, Iran.
Mohsen TaherianIslamic Azad University, Semnan, Iran.
Mohammad Hadi SadeghianDepartment of Hematology and Blood Banking, Cancer Molecular Pathology Research Center, Mashhad University of Medical Sciences, P.O. Box: 1316943551, Mashhad, Iran. sadeghianmh@mums.ac.ir.
Mashhad University of Medical Sciences · IRIslamic Azad University Semnan · IRNorth Khorasan University of Medical Sciences · IRPasteur Institute of Iran · IRSemnan University of Medical Sciences · IR

Funding

Mashhad University of Medical Sciences 985254
6 · The paper itself

Abstract

Acute myeloid leukemia is one of the most commonly identified hematological malignancies with poor prognosis. This research was planned to identify the cytotoxic effects of Auraptene on HL60 and U937 cell lines. The cytotoxic effects of Auraptene were measured by AlamarBlue assay (Resazurin) after 24- and 48-h treatments with different doses of Auraptene. The inductive effects of Auraptene on cellular oxidative stress were investigated by determining cellular ROS levels. The cell cycle progression and cell apoptosis were also evaluated by flow cytometry method. Our findings revealed that Auraptene decreased HL60 and U937 cellular proliferation by downregulation of Cyclin D1. Auraptene also induces cellular oxidative stress by upregulation of cellular ROS levels. Auraptene induces cell cycle arrest the early and late phases of apoptosis by upregulation of Bax and p53 proteins. Our data suggest that the anti-tumor function of Auraptene can be mediated by promoting apoptosis and cell cycle arrest and inducing cellular oxidative stress in HL60 and U937 cell lines. These results support that Auraptene may be used as a potent anti-tumor agent against hematologic malignancies in the further studies.

Indexed as

Antineoplastic AgentsHematologic NeoplasmsLeukemia, Myeloid, AcuteCell LineCoumarinsHumansReactive Oxygen SpeciesU937 CellsAntineoplastic AgentsauraptenCoumarinsReactive Oxygen SpeciesAMLApoptosisAurapteneCell cycleCytotoxic effect

Identifiers

PMID37432498
OpenAlexW4383872718

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.