Evidence map›Paper›PMID 36980800›Full record

ArticleCancers2023

A Novel Family of Lysosomotropic Tetracyclic Compounds for Treating Leukemia.

José M Carbó, Josep M Cornet-Masana, Laia Cuesta-Casanovas, Jennifer Delgado-Martínez, Antònia Banús-Mulet, Lise Clément-Demange, Carme Serra, Juanlo Catena, Amadeu Llebaria, Jordi Esteve and 1 more

Open access · goldFull text read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

11 authors at 3 institutions in 1 country.

José M CarbóJosep Carreras Leukaemia Research Institute (IJC), 08916 Barcelona, Spain.
Josep M Cornet-MasanaJosep Carreras Leukaemia Research Institute (IJC), 08916 Barcelona, Spain.
Laia Cuesta-CasanovasJosep Carreras Leukaemia Research Institute (IJC), 08916 Barcelona, Spain.
Jennifer Delgado-MartínezJosep Carreras Leukaemia Research Institute (IJC), 08916 Barcelona, Spain.ORCID 0000-0002-5962-3064
Antònia Banús-MuletJosep Carreras Leukaemia Research Institute (IJC), 08916 Barcelona, Spain.
Lise Clément-DemangeLeukos Biotech, 08021 Barcelona, Spain.ORCID 0000-0002-9360-1344
Carme SerraMCS, Laboratory of Medicinal Chemistry and Synthesis, Institute of Advanced Chemistry of Catalonia (IQAC-CSIC), 08034 Barcelona, Spain.ORCID 0000-0001-6643-3077
Juanlo CatenaMCS, Laboratory of Medicinal Chemistry and Synthesis, Institute of Advanced Chemistry of Catalonia (IQAC-CSIC), 08034 Barcelona, Spain.ORCID 0000-0002-2423-5926
Amadeu LlebariaMCS, Laboratory of Medicinal Chemistry and Synthesis, Institute of Advanced Chemistry of Catalonia (IQAC-CSIC), 08034 Barcelona, Spain.ORCID 0000-0002-8200-4827
Jordi EsteveJosep Carreras Leukaemia Research Institute (IJC), 08916 Barcelona, Spain.
Ruth M RisueñoJosep Carreras Leukaemia Research Institute (IJC), 08916 Barcelona, Spain.ORCID 0000-0003-4048-9536
Josep Carreras Leukaemia Research Institute · ESInstitute of Advanced Chemistry of Catalonia · ESUniversitat Autònoma de Barcelona · ES

Funding

Agency for Administration of University and Research PRODUCTEFundació Marató TV3 201930-30Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona Caixaimpulse
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogeneous hematological cancer characterized by poor prognosis and frequent relapses. Aside from specific mutation-related changes, in AML, the overall function of lysosomes and mitochondria is drastically altered to fulfill the elevated biomass and bioenergetic demands. On the basis of previous results, in silico drug discovery screening was used to identify a new family of lysosome-/mitochondria-targeting compounds. These novel tetracyclic hits, with a cationic amphiphilic structure, specifically eradicate leukemic cells by inducing both mitochondrial damage and apoptosis, and simultaneous lysosomal membrane leakiness. Lysosomal leakiness does not only elicit canonical lysosome-dependent cell death, but also activates the terminal differentiation of AML cells through the Ca

Indexed as

apoptosisautophagydrug discoveryleukemialysosomenew chemical entity

Identifiers

PMID36980800
PMCPMC10047683
OpenAlexW4360616269

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read38
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.