Evidence map›Paper›PMID 31040181›Full record

ArticleThe Journal of biological chemistry2019

Dual inhibition of glutaminase and carnitine palmitoyltransferase decreases growth and migration of glutaminase inhibition-resistant triple-negative breast cancer cells.

Larissa Menezes Dos Reis, Douglas Adamoski, Rodolpho Ornitz Oliveira Souza, Carolline Fernanda Rodrigues Ascenção, Krishina Ratna Sousa de Oliveira, Felipe Corrêa-da-Silva, Fábio Malta de Sá Patroni, Marília Meira Dias, Sílvio Roberto Consonni, Pedro Manoel Mendes de Moraes-Vieira and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

63 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Targeting the Glutaminolysis Pathway in Glaucoma-Associated Fibrosis.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Article
  11. Mitochondrial CaJournal of cellular physiology · 2025
    Review
  12. Review
  13. Targeting glutamine metabolism as a potential target for cancer treatment.Journal of experimental & clinical cancer research : CR · 2025
    Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Journal of cardiovascular development and disease · 2024
    Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Larissa Menezes Dos ReisFrom the Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil.ORCID 0000-0003-1597-0176
Douglas AdamoskiFrom the Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil.ORCID 0000-0001-5062-2586
Rodolpho Ornitz Oliveira Souzathe Laboratory of Biochemistry of Tryps, Department of Parasitology, Institute of Biomedical Science, University of São Paulo, 05508-000 São Paulo, São Paulo, Brazil.
Carolline Fernanda Rodrigues AscençãoFrom the Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil.
Krishina Ratna Sousa de OliveiraFrom the Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil.
Felipe Corrêa-da-Silvathe Graduate Program in Genetics and Molecular Biology, Institute of Biology, University of Campinas, 13083-970 Campinas, São Paulo, Brazil.
Fábio Malta de Sá PatroniFrom the Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil.ORCID 0000-0003-0221-8380
Marília Meira DiasFrom the Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil.
Sílvio Roberto Consonnithe Department of Biochemistry and Tissue Biology, Laboratory of Cytochemistry and Immunocytochemistry, Institute of Biology, University of Campinas, 13083-970 Campinas, São Paulo, Brazil.
Pedro Manoel Mendes de Moraes-Vieirathe Department of Genetics, Evolution, Microbiology, and Immunology, Laboratory of Immunometabolism, Institute of Biology, University of Campinas, 13083-970 Campinas, São Paulo, Brazil, and.ORCID 0000-0002-8263-786X
Ariel Mariano Silberthe Laboratory of Biochemistry of Tryps, Department of Parasitology, Institute of Biomedical Science, University of São Paulo, 05508-000 São Paulo, São Paulo, Brazil.
Sandra Martha Gomes DiasFrom the Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil, sandra.dias@lnbio.cnpem.br.ORCID 0000-0002-1589-7856
Universidade Estadual de Campinas (UNICAMP) · BRBrazilian Center for Research in Energy and Materials · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancers (TNBCs) lack progesterone and estrogen receptors and do not have amplified human epidermal growth factor receptor 2, the main therapeutic targets for managing breast cancer. TNBCs have an altered metabolism, including an increased Warburg effect and glutamine dependence, making the glutaminase inhibitor CB-839 therapeutically promising for this tumor type. Accordingly, CB-839 is currently in phase I/II clinical trials. However, not all TNBCs respond to CB-839 treatment, and the tumor resistance mechanism is not yet fully understood. Here we classified cell lines as CB-839-sensitive or -resistant according to their growth responses to CB-839. Compared with sensitive cells, resistant cells were less glutaminolytic and, upon CB-839 treatment, exhibited a smaller decrease in ATP content and less mitochondrial fragmentation, an indicator of poor mitochondrial health. Transcriptional analyses revealed that the expression levels of genes linked to lipid metabolism were altered between sensitive and resistant cells and between breast cancer tissues (available from The Cancer Genome Atlas project) with low

Indexed as

BenzeneacetamidesCarnitine O-PalmitoyltransferaseCell MovementCell ProliferationDrug Resistance, NeoplasmFemaleGlutaminaseGlutamineHumansOxidation-ReductionThiadiazolesTriple Negative Breast NeoplasmsTumor Cells, CulturedBenzeneacetamidesCarnitine O-PalmitoyltransferaseCB-839CPT1A protein, humanGlutaminaseGlutamineThiadiazolesbreast cancercancer therapyCB-839CPT1CPT2energy metabolismetomoxirglutaminaseβ-oxidation

Identifiers

PMID31040181
PMCPMC6579458
OpenAlexW2943489129

What OpenQuestion holds

Textmetadata
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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.