Evidence map›Paper›PMID 37750732›Full record

ArticleMicrobiology spectrum2023

Proteasome inhibition as a therapeutic target for the fungal pathogen

Mélissa Caza, Daniel Assis Santos, Elizabeth Burden, Anna Brisland, Guanggan Hu, James W Kronstad

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

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

6 authors at 2 institutions in 2 countries.

Mélissa CazaDepartment of Microbiology and Immunology, Michael Smith Laboratories, University of British Columbia , Vancouver, British Columbia, Canada.
Daniel Assis SantosDepartment of Microbiology, Universidade Federal de Minas Gerais , Belo Horizonte, Minas Gerais, Brazil.
Elizabeth BurdenDepartment of Microbiology and Immunology, Michael Smith Laboratories, University of British Columbia , Vancouver, British Columbia, Canada.
Anna BrislandDepartment of Microbiology and Immunology, Michael Smith Laboratories, University of British Columbia , Vancouver, British Columbia, Canada.
Guanggan HuDepartment of Microbiology and Immunology, Michael Smith Laboratories, University of British Columbia , Vancouver, British Columbia, Canada.
James W KronstadDepartment of Microbiology and Immunology, Michael Smith Laboratories, University of British Columbia , Vancouver, British Columbia, Canada.ORCID 0000-0003-4240-6976
University of British Columbia · CAUniversidade Federal de Minas Gerais · BR

Funding

Rapid production of SARS-CoV-2 molecular clones using CRISPR-based yeast recombineeringR01AI100272 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MADHANI, HITEN D · 2012 to 2025
$11.3M
Comparative and functional genomics of C. neoformansR01AI053721 · NIAID · UNIVERSITY OF BRITISH COLUMBIA · PI KRONSTAD, JAMES W · 2003 to 2024
$5.4M
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Gouvernement du Canada | Canadian Institutes of Health Research (IRSC) PJT-166043HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) RO1 AI053721NIAID NIH HHS R01 AI053721NIAID NIH HHS R01 AI100272
6 · The paper itself

Abstract

importanceFungal diseases of humans are difficult to treat, and there is a clear need for additional antifungal drugs, better diagnostics, effective vaccines, and new approaches to deal with emerging drug resistance. Fungi are challenging to control because they share many common biochemical functions with their mammalian hosts and it is therefore difficult to identify fungal-specific targets for drug development. One approach is to employ existing antifungal drugs in combination with agents that target common cellular processes at levels that are (ideally) not toxic for the host. We pursued this approach in this study by examining the potential of the clinically approved proteasome inhibitor bortezomib to influence the proliferation and virulence of

Indexed as

bortezomibchemical genetic screenfungal pathogenesisHIV/AIDS

Identifiers

PMID37750732
PMCPMC10580939
OpenAlexW4387033262

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.