Evidence map›Paper›PMID 37189352›Full record

ReviewBiomolecules2023

Is It Still Possible to Think about HSP70 as a Therapeutic Target in Onco-Hematological Diseases?

Nayla Mouawad, Guido Capasso, Edoardo Ruggeri, Leonardo Martinello, Filippo Severin, Andrea Visentin, Monica Facco, Livio Trentin, Federica Frezzato

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Biological and Medicinal Properties ofInternational journal of molecular sciences · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Bioinformatics analysis and alternative polyadenylation in Heat Shock Proteins 70 (HSP70) family members.International journal of physiology, pathophysiology and pharmacology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. 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

9 authors at 1 institution in 1 country.

Nayla MouawadHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.
Guido CapassoHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.ORCID 0000-0002-4932-4917
Edoardo RuggeriHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.ORCID 0000-0002-9439-4121
Leonardo MartinelloHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.ORCID 0000-0003-0877-1099
Filippo SeverinHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.ORCID 0000-0001-8712-9656
Andrea VisentinHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.ORCID 0000-0003-0271-7200
Monica FaccoHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.ORCID 0000-0003-0100-5789
Livio TrentinHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.ORCID 0000-0003-1222-6149
Federica FrezzatoHematology and Clinical Immunology Unit, Department of Medicine, University of Padova, 35128 Padua, Italy.ORCID 0000-0001-7093-2493
University of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The search for molecules to be targeted that are involved in apoptosis resistance/increased survival and pathogenesis of onco-hematological malignancies is ongoing since these diseases are still not completely understood. Over the years, a good candidate has been identified in the Heat Shock Protein of 70kDa (HSP70), a molecule defined as "the most cytoprotective protein ever been described". HSP70 is induced in response to a wide variety of physiological and environmental insults, allowing cells to survive lethal conditions. This molecular chaperone has been detected and studied in almost all the onco-hematological diseases and is also correlated to poor prognosis and resistance to therapy. In this review, we give an overview of the discoveries that have led us to consider HSP70 as a therapeutic target for mono- or combination-therapies in acute and chronic leukemias, multiple myeloma and different types of lymphomas. In this

Indexed as

Heat-Shock ProteinsMultiple MyelomaApoptosisHSP70 Heat-Shock ProteinsHumansMolecular ChaperonesTranscription FactorsHeat-Shock ProteinsHSP70 Heat-Shock ProteinsMolecular ChaperonesTranscription FactorsHeat Shock ProteinsHSP70leukemialymphomamyelomatherapeutics

Identifiers

PMID37189352
PMCPMC10135835
OpenAlexW4361222754

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.