Evidence map›Paper›PMID 34360606›Full record

ArticleInternational journal of molecular sciences2021

Metabolomic Identification of Anticancer Metabolites of Australian Propolis and Proteomic Elucidation of Its Synergistic Mechanisms with Doxorubicin in the MCF7 Cells.

Muhammad A Alsherbiny, Deep J Bhuyan, Ibrahim Radwan, Dennis Chang, Chun-Guang Li

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Green Synthesis ofBiomolecules · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Research Progress on Therapeutic Effect and Mechanism of Propolis on Wound Healing.Evidence-based complementary and alternative medicine : eCAM · 2022
    Review
  16. Review
  17. Article
  18. 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

5 authors at 3 institutions in 2 countries.

Muhammad A AlsherbinyNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.ORCID 0000-0001-9337-2441
Deep J BhuyanNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.ORCID 0000-0002-9736-0197
Ibrahim RadwanFaculty of Science and Technology, University of Canberra, Canberra, ACT 2617, Australia.ORCID 0000-0002-8170-5058
Dennis ChangNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.
Chun-Guang LiNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.
Western Sydney University · AUCairo University · EGUniversity of Canberra · AU

Funding

Maxwell Family Foundation N/ANICM Health Research Institute N/AWestern Sydney University N/A
6 · The paper itself

Abstract

The combination of natural products with standard chemotherapeutic agents offers a promising strategy to enhance the efficacy or reduce the side effects of standard chemotherapy. Doxorubicin (DOX), a standard drug for breast cancer, has several disadvantages, including severe side effects and the development of drug resistance. Recently, we reported the potential bioactive markers of Australian propolis extract (AP-1) and their broad spectrum of pharmacological activities. In the present study, we explored the synergistic interactions between AP-1 and DOX in the MCF7 breast adenocarcinoma cells using different synergy quantitation models. Biochemometric and metabolomics-driven analysis was performed to identify the potential anticancer metabolites in AP-1. The molecular mechanisms of synergy were studied by analysing the apoptotic profile via flow cytometry, apoptotic proteome array and measuring the oxidative status of the MCF7 cells treated with the most synergistic combination. Furthermore, label-free quantification proteomics analysis was performed to decipher the underlying synergistic mechanisms. Five prenylated stilbenes were identified as the key metabolites in the most active AP-1 fraction. Strong synergy was observed when AP-1 was combined with DOX in the ratio of 100:0.29 (

Indexed as

Drug SynergismAntibiotics, AntineoplasticAnti-Infective AgentsApoptosisBreast NeoplasmsCell ProliferationDoxorubicinDrug Therapy, CombinationFemaleHumansMCF-7 CellsMetabolomePropolisProteomeAntibiotics, AntineoplasticAnti-Infective AgentsDoxorubicinPropolisProteomeapoptosisbreast adenocarcinomabreast cancerdoxorubicinMCF7metabolomicspropolisproteomicssynergy

Identifiers

PMID34360606
PMCPMC8346082
OpenAlexW3186629832

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.