Evidence map›Paper›PMID 39348999›Full record

ArticleAnticancer research2024

Antitumor Potential of Guttiferone E Combined With Carboplatin Against Osimertinib-resistant H1975 Lung Cancer Through Apoptosis.

Aakash Nathani, Islauddin Khan, Matheus Hikaru Tanimoto, Jennyfer Andrea Aldana Mejía, Aline Mayrink DE Miranda, Arun Rishi, Satyanarayan Dev, Jairo Kenupp Bastos, Mandip Singh

Abstract read
In one paragraph

Article in Anticancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Frontiers in pharmacology · 2025
    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

9 authors.

Aakash Nathani *College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, FL, U.S.A.
Islauddin Khan *College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, FL, U.S.A.
Matheus Hikaru Tanimoto *School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.
Jennyfer Andrea Aldana MejíaSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.
Aline Mayrink DE MirandaSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.
Arun RishiDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI, U.S.A.
Satyanarayan DevBiological Systems Engineering, College of Agriculture and Food Sciences, Florida A&M University, Tallahassee, FL, U.S.A.
Jairo Kenupp BastosSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil; jkbastos@fcfrp.usp.br.
Mandip SinghCollege of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, FL, U.S.A.; mandip.sachdeva@famu.edu.

Funding

Research Project-3: Effectiveness of an eHealth intervention for uptake of cervical cancer screening in Hispanic womenU54MD007582 · NIMHD · FLORIDA AGRICULTURAL AND MECHANICAL UNIV · PI Sandra G Suther · 2019 to 2026
$28.1M
NIMHD NIH HHS U54 MD007582
6 · The paper itself

Abstract

BACKGROUND/

aimLow selectivity and high frequency of side-effects are the major problems of currently used chemotherapeutics. Among natural compounds, the polyprenylated acylphloroglucinol, guttiferone E, isolated from Brazilian red propolis, has attracted attention due to its marked anticancer properties and was evaluated here for its role against osimertinib-resistant H1975 cells (with double mutations of epidermal growth factor receptor: EGFR L858R/T790M). MATERIALS AND

methodsGuttiferone E was obtained from red propolis using established extraction procedures. Guttiferone E was tested using the H1975 cell line in in vitro (2D and 3D) cell cultures and in vivo in BALB/c athymic nude mice. Live/dead assay was also performed to support the results. Tumor tissues obtained from in vivo studies were used for western blotting. Guttiferone E reduced H1975 cell viability in a concentration-dependent manner. The IC

conclusionOur results show guttiferone E to be a promising, novel and potent antitumor drug candidate for osimertinib-resistant lung cancer with EGFR L858R/T790M mutations.

Indexed as

AcrylamidesAniline CompoundsApoptosisDrug Resistance, NeoplasmLung NeoplasmsMice, NudeXenograft Model Antitumor AssaysAnimalsAntineoplastic Combined Chemotherapy ProtocolsBenzophenonesCell Line, TumorCell SurvivalErbB ReceptorsHumansIndolesMiceAcrylamidesAniline CompoundsBenzophenonesEGFR protein, humanErbB ReceptorsIndolesosimertinibPyrimidinesapoptosiscarboplatinGuttiferone EPARPPD-L1SIRT1

Identifiers

PMID39348999
PMCPMC11863775

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.