Evidence map›Paper›PMID 35011413›Full record

SynthesisMolecules (Basel, Switzerland)2021

In Vivo Anticancer Activity of AZD3965: A Systematic Review.

Ana Silva, Beatriz Antunes, Alberta Batista, Filipa Pinto-Ribeiro, Fátima Baltazar, Julieta Afonso

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

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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 1 institution in 1 country.

Ana SilvaLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.
Beatriz AntunesLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.
Alberta BatistaLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.
Filipa Pinto-RibeiroLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.ORCID 0000-0001-7574-6489
Fátima BaltazarLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.ORCID 0000-0002-1770-4544
Julieta AfonsoLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.ORCID 0000-0002-9748-3752
University of Minho · PT

Funding

Fundação para a Ciência e Tecnologia projects UIDB/50026/2020 and UIDP/50026/2020, fellowship SFRH/BPD/116784/2016Norte Portugal Regional Operational Programme (NORTE 2020) NORTE-01-0145-FEDER-000055
6 · The paper itself

Abstract

Proliferating cancer cells have high energy demands, which is mainly obtained through glycolysis. The transmembrane trafficking of lactate, a major metabolite produced by glycolytic cancer cells, relies on monocarboxylate transporters (MCTs). MCT1 optimally imports lactate, although it can work bidirectionally, and its activity has been linked to cancer aggressiveness and poor outcomes. AZD3965, a specific MCT1 inhibitor, was tested both in vitro and in vivo, with encouraging results; a phase I clinical trial has already been undertaken. Thus, analysis of the experimental evidence using AZD3965 in different cancer types could give valuable information for its clinical use. This systematic review aimed to assess the in vivo anticancer activity of AZD3965 either alone (monotherapy) or with other interventions (combination therapy). Study search was performed in nine different databases using the keywords "AZD3965 in vivo" as search terms. The results show that AZD3965 successfully decreased tumor growth and promoted intracellular lactate accumulation, which confirmed its effectiveness, especially in combined therapy. These results support the setup of clinical trials, but other important findings, namely AZD3965 enhanced activity when given in combination with other therapies, or MCT4-induced treatment resistance, should be further considered in the clinical trial design to improve therapy response.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorDisease ManagementDisease ProgressionDrug Evaluation, PreclinicalEnergy MetabolismGlycolysisHumansLactic AcidMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersNeoplasmsPyrimidinonesSignal TransductionSymportersAntineoplastic AgentsAZD3965Lactic AcidMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersPyrimidinonesSymportersThiophenesAZD3965cancerglycolysisin vivo modelslactatemonocarboxylate transporter 1

Identifiers

PMID35011413
PMCPMC8746498
OpenAlexW4200392910

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.