Evidence map›Paper›PMID 38731863›Full record

ReviewInternational journal of molecular sciences2024

Characterization of Human B Cell Hematological Malignancies Using Protein-Based Approaches.

Cristina Jiménez, Alba Garrote-de-Barros, Carlos López-Portugués, María Hernández-Sánchez, Paula Díez

Registry-linked trialAbstract readReview
In one paragraph

Review 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. It is linked to trial NCT07515313 (Expression of CD274), which is not on this map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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.

NCT07515313 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Expression of CD274 (PD-L1) and CD276 in B-cell Malignancies: A Study by Flowcyometry

TypeobservationalSponsorAssiut UniversityRan2026 to 2030Enrolled159ConditionsB-cell Malignancies
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. 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.

Cristina JiménezHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007 Salamanca, Spain.ORCID 0000-0002-5543-5154
Alba Garrote-de-BarrosDepartment of Biochemistry and Molecular Biology, Pharmacy School, Universidad Complutense de Madrid, 28040 Madrid, Spain.ORCID 0009-0005-1151-9566
Carlos López-PortuguésDepartment of Physical and Analytical Chemistry Chemistry, Faculty of Chemistry, University of Oviedo, 33006 Oviedo, Spain.ORCID 0009-0001-6947-9887
María Hernández-SánchezDepartment of Biochemistry and Molecular Biology, Pharmacy School, Universidad Complutense de Madrid, 28040 Madrid, Spain.ORCID 0000-0001-9968-2782
Paula DíezDepartment of Physical and Analytical Chemistry Chemistry, Faculty of Chemistry, University of Oviedo, 33006 Oviedo, Spain.ORCID 0000-0003-2150-6898

Funding

CRIS contra el Cáncer 2024/27Fundación Española de Hematología y Hemoterapia FEHHJAN23/001HInstituto de Salud Carlos III CD22/00009Instituto de Salud Carlos III PI21/00568Spanish Ministry for Science and Innovation PID2022-137222OB-I00Spanish Ministry for Science and Innovation PREP2022-000180
6 · The paper itself

Abstract

The maturation of B cells is a complex, multi-step process. During B cell differentiation, errors can occur, leading to the emergence of aberrant versions of B cells that, finally, constitute a malignant tumor. These B cell malignancies are classified into three main groups: leukemias, myelomas, and lymphomas, the latter being the most heterogeneous type. Since their discovery, multiple biological studies have been performed to characterize these diseases, aiming to define their specific features and determine potential biomarkers for diagnosis, stratification, and prognosis. The rise of advanced -omics approaches has significantly contributed to this end. Notably, proteomics strategies appear as promising tools to comprehensively profile the final molecular effector of these cells. In this narrative review, we first introduce the main B cell malignancies together with the most relevant proteomics approaches. Then, we describe the core studies conducted in the field and their main findings and, finally, we evaluate the advantages and drawbacks of flow cytometry, mass cytometry, and mass spectrometry for the profiling of human B cell disorders.

Indexed as

B-LymphocytesHematologic NeoplasmsProteomicsBiomarkers, TumorFlow CytometryHumansMass SpectrometryBiomarkers, TumorB cell disorderflow cytometryleukemialymphomamass cytometrymass spectrometrymultiple myelomaprotein

Identifiers

PMID38731863
PMCPMC11083628

What OpenQuestion holds

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Registered trials

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.