Evidence map›Paper›PMID 39769262›Full record

ArticleInternational journal of molecular sciences2024

Galectin Plasmatic Levels Reveal a Cluster Associated with Disease Aggressiveness and Kidney Damage in Multiple Myeloma Patients.

Lidiane Vasconcelos do Nascimento Carvalho, Reijane Alves Assis, Claudio Montenegro, Michelle Melgarejo da Rosa, Michelly Cristiny Pereira, Maira Galdino da Rocha Pitta, Moacyr Jesus Barreto de Melo Rêgo

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Acridine-Based Chalcone 1C and ABC Transporters.International journal of molecular sciences · 2025
    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

7 authors.

Lidiane Vasconcelos do Nascimento CarvalhoResearch Center for Therapeutic Innovation (NUPIT-SG), Federal University of Pernambuco, Recife 50670-901, PE, Brazil.
Reijane Alves AssisHematology Service of the Hospital de Câncer de Pernambuco, Cabugá/ 50040-000, Recife 50040-000, PE, Brazil.
Claudio MontenegroResearch Center for Therapeutic Innovation (NUPIT-SG), Federal University of Pernambuco, Recife 50670-901, PE, Brazil.
Michelle Melgarejo da RosaResearch Center for Therapeutic Innovation (NUPIT-SG), Federal University of Pernambuco, Recife 50670-901, PE, Brazil.ORCID 0000-0002-0163-3833
Michelly Cristiny PereiraResearch Center for Therapeutic Innovation (NUPIT-SG), Federal University of Pernambuco, Recife 50670-901, PE, Brazil.ORCID 0000-0002-1672-8202
Maira Galdino da Rocha PittaResearch Center for Therapeutic Innovation (NUPIT-SG), Federal University of Pernambuco, Recife 50670-901, PE, Brazil.
Moacyr Jesus Barreto de Melo RêgoResearch Center for Therapeutic Innovation (NUPIT-SG), Federal University of Pernambuco, Recife 50670-901, PE, Brazil.ORCID 0000-0002-1883-6012

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico n/aCoordenação de Aperfeiçoamento de Pessoal de Nível Superior n/a
6 · The paper itself

Abstract

Multiple myeloma (MM) is a malignant disease characterized by the proliferation of plasma cells, primarily in the bone marrow. It accounts for approximately 1% of all cancers and 10% of hematologic malignancies. Clinical manifestations include hypercalcemia, anemia, renal failure, and bone lesions. The pathogenesis of MM involves complex interactions between myeloma cells and their microenvironment. Galectins, a family of β-galactoside-binding proteins, particularly galectin-1, -3, -4, -7, and -9, have been implicated in MM development. This study aimed to assess the plasma levels of these galectins in newly diagnosed MM patients and explore their correlation with clinical parameters. Peripheral blood samples were collected from patients at the Oncohematology Service of the Hospital de Câncer de Pernambuco, and galectin levels were measured using ELISA. Plasma levels of galectins-3, -7, and -9 were significantly higher in MM patients compared to the control group. Three clusters of MM patients were identified based on galectin plasma levels, with cluster 3, characterized by high levels of galectin-1, -4, and -7, being associated with a worse prognosis. A strong positive correlation was found between galectin-1, -4, and -7 levels and markers of kidney function (urea, creatinine, and β2-microglobulin), while negative correlations were observed with hematocrit and hemoglobin. Additionally, galectin-9 showed high accuracy in distinguishing MM patients from healthy controls (AUC = 0.931). Elevated galectin levels were indicative of disease aggressiveness and renal impairment in MM patients. Overall, our findings suggest that galectins-1, -4, -7, and -9 could serve as potential biomarkers for MM progression and severity, warranting further investigation into their utility in MM diagnosis and treatment.

Indexed as

GalectinsMultiple MyelomaAdultAgedAged, 80 and overBiomarkers, TumorFemaleHumansKidneyMaleMiddle AgedPrognosisBiomarkers, TumorGalectinsgalectin 1galectin 3galectin 7galectin 9hematologymultiple myeloma

Identifiers

PMID39769262
PMCPMC11676459

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Registered trials

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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.