Evidence map›Paper›PMID 32605263›Full record

ArticleMetabolites2020

Metabolic Signatures of Tumor Responses to Doxorubicin Elucidated by Metabolic Profiling

Iman W Achkar, Sara Kader, Shaima S Dib, Kulsoom Junejo, Salha Bujassoum Al-Bader, Shahina Hayat, Aditya M Bhagwat, Xavier Rousset, Yan Wang, Jean Viallet and 2 more

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Frontiers in immunology · 2022
    Review
  15. Review
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

12 authors at 4 institutions in 2 countries.

Iman W AchkarDepartment of Physiology and Biophysics, Weill Cornell Medicine - Qatar, Doha 24144, Qatar.ORCID 0000-0003-3197-7108
Sara KaderDepartment of Physiology and Biophysics, Weill Cornell Medicine - Qatar, Doha 24144, Qatar.
Shaima S DibDepartment of Physiology and Biophysics, Weill Cornell Medicine - Qatar, Doha 24144, Qatar.
Kulsoom JunejoBreast Cancer Unit, Hamad General Hospital, Hamad Medical Corporation, Doha 3050, Qatar.
Salha Bujassoum Al-BaderDepartment of Medical Oncology, National Center of Cancer Care and Research, Hamad Medical Corporation, Doha 3050, Qatar.
Shahina HayatDepartment of Physiology and Biophysics, Weill Cornell Medicine - Qatar, Doha 24144, Qatar.
Aditya M BhagwatScientific Service Group of Biomolecular Mass Spectrometry, Max Planck Institute for Heart and Lung Research, D-61231 Bad Nauheim, Germany.
Xavier RoussetDepartment, INOVOTION SAS, 38700 La Tronche, France.
Yan WangDepartment, INOVOTION SAS, 38700 La Tronche, France.
Jean VialletDepartment, INOVOTION SAS, 38700 La Tronche, France.
Karsten SuhreDepartment of Physiology and Biophysics, Weill Cornell Medicine - Qatar, Doha 24144, Qatar.
Anna HalamaDepartment of Physiology and Biophysics, Weill Cornell Medicine - Qatar, Doha 24144, Qatar.ORCID 0000-0003-4910-6255
Weill Cornell Medical College in Qatar · QAHamad General Hospital · QAMax Planck Institute for Heart and Lung Research · DENational Center for Cancer Care and Research · QA

Funding

Qatar National Research Fund NPRP12S-0205-190042Qatar National Research Fund NPRP8-061-3-011
6 · The paper itself

Abstract

backgroundDysregulated cancer metabolism is associated with acquired resistance to chemotherapeutic treatment and contributes to the activation of cancer survival mechanisms. However, which metabolic pathways are activated following treatment often remains elusive. The combination of chicken embryo tumor models (

methodsMB-MDA-231 cells were grafted

resultsWe observed a significant suppression of tumor growth in the doxorubicin treated group. The metabolic profiles of doxorubicin and DMSO-treated tumors were clearly separated in a principle component analysis. Inhibition of glycolysis, nucleotide synthesis, and glycerophospholipid metabolism appear to be triggered by doxorubicin treatment, which could explain the observed suppressed tumor growth. In addition, metabolic cancer survival mechanisms could be supported by an acceleration of antioxidative pathways.

conclusionsMetabolomics in combination with

Indexed as

cancer survival mechanismchicken chorioallantoic membrane (CAM) system in ovo modeldoxorubicin treatmentlipidomicsmetabolomicstriple negative breast cancer

Identifiers

PMID32605263
PMCPMC7408021
OpenAlexW3037096916

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.