Evidence map›Paper›PMID 34462526›Full record

ReviewLeukemia2021

Lysosomes in acute myeloid leukemia: potential therapeutic targets?

Sreoshee Rafiq, Sharon L McKenna, Sylviane Muller, Mario P Tschan, Magali Humbert

Open access · hybridAbstract readReview
In one paragraph

Review in Leukemia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.2field-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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  9. Article
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  11. Review
  12. Article
  13. Targeting regulated cell death pathways in acute myeloid leukemia.Cancer drug resistance (Alhambra, Calif.) · 2023
    Review
  14. Article
  15. Article
  16. The dual role of autophagy in acute myeloid leukemia.Journal of hematology & oncology · 2022
    Review
  17. Review
  18. Review
  19. 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

5 authors at 4 institutions in 4 countries.

Sreoshee RafiqDivision of Experimental Pathology, Institute of Pathology, Bern, Switzerland.
Sharon L McKennaCancer Research, UCC, Western Gateway Building, University College Cork, Cork, Ireland.
Sylviane MullerTRANSAUTOPHAGY: European Network for Multidisciplinary Research and Translation of Autophagy Knowledge, COST Action CA15138, Barcelona, Spain.
Mario P TschanDivision of Experimental Pathology, Institute of Pathology, Bern, Switzerland.ORCID http://orcid.org/0000-0001-5897-3647
Magali HumbertDivision of Experimental Pathology, Institute of Pathology, Bern, Switzerland. magali.humbert@yahoo.fr.ORCID http://orcid.org/0000-0003-3820-0297
University of Bern · CHCentre National de la Recherche Scientifique · FRCharles Humbert 8 · CHUniversity College Cork · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lysosomes, since their discovery, have been primarily known for degrading cellular macromolecules. However, in recent studies, they have begun to emerge as crucial regulators of cell homeostasis. They are at the crossroads of catabolic and anabolic pathways and are intricately involved in cellular trafficking, nutrient signaling, energy metabolism, and immune regulation. Their involvement in such essential cellular functions has renewed clinical interest in targeting the lysosome as a novel way to treat disease, particularly cancer. Acute myeloid leukemia (AML) is an aggressive blood cancer with a low survival probability, particularly in older patients. The genomic landscape of AML has been extensively characterized but few targeted therapies (with the exception of differentiation therapy) can achieve a long-term cure. Therefore, there is an unmet need for less intensive and more tolerable therapeutic interventions. In this review, we will give an overview on the myriad of functions performed by lysosomes and their importance in malignant disease. Furthermore, we will discuss their relevance in hematopoietic cells and different ways to potentially target them in AML.

Indexed as

AnimalsHumansLeukemia, Myeloid, AcuteLysosomesMolecular Targeted TherapySignal Transduction

Identifiers

PMID34462526
PMCPMC8478647
OpenAlexW3198170042

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.