Evidence map›Paper›PMID 39563886›Full record

ReviewAdvances in hematology2024

Advancements in B-Cell Non-Hodgkin's Lymphoma: From Signaling Pathways to Targeted Therapies.

Abdullah Alfaifi, Salem Bahashwan, Mohammed Alsaadi, Ali H Ageel, Hamzah H Ahmed, Kaneez Fatima, Hafiz Malhan, Ishtiaq Qadri, Hussein Almehdar

Abstract readReview
In one paragraph

Review in Advances in hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. PAX Family, Master Regulator in Cancer.Diagnostics (Basel, Switzerland) · 2025
    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

9 authors.

Abdullah AlfaifiDepartment of Biological Science, Faculty of Science, King AbdulAziz University, Jeddah 21589, Saudi Arabia.ORCID https://orcid.org/0000-0002-0747-9451
Salem BahashwanHematology Research Unit, King Fahad Medical Research Center, King AbdulAziz University, Jeddah 21589, Saudi Arabia.
Mohammed AlsaadiHematology Research Unit, King Fahad Medical Research Center, King AbdulAziz University, Jeddah 21589, Saudi Arabia.ORCID https://orcid.org/0000-0002-2976-2696
Ali H AgeelEradah Hospital, Ministry of Health, Jazan 82943, Saudi Arabia.
Hamzah H AhmedDepartment of Radiologic Sciences, Faculty of Applied Medical Sciences, King AbdulAziz University, Jeddah 21589, Saudi Arabia.
Kaneez FatimaIQ Institute of Infection and Immunity, Lahore, Punjab, Pakistan.
Hafiz MalhanPrince Mohammed Bin Nasser Hospital, Ministry of Health, Jazan 82943, Saudi Arabia.
Ishtiaq QadriDepartment of Biological Science, Faculty of Science, King AbdulAziz University, Jeddah 21589, Saudi Arabia.
Hussein AlmehdarDepartment of Biological Science, Faculty of Science, King AbdulAziz University, Jeddah 21589, Saudi Arabia.ORCID https://orcid.org/0009-0002-1744-8250

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphoma is the sixth most prevalent cancer globally. Non-Hodgkin's lymphomas are the majority group of lymphomas, with B cells accounting for approximately 95% of these lymphomas. A key feature of B-cell lymphoma is the functional perturbations of essential biological pathways caused by genetic aberrations. These lead to atypical gene expression, providing cells with a selective growth advantage. Molecular analysis reveals that each lymphoma subtype has unique molecular mutations, which pose challenges in disease management and treatment. Substantial efforts over the last decade have led to the integration of this information into clinical applications, resulting in crucial insights into clinical diagnosis and targeted therapies. However, with the growing need for more effective medication development, we anticipate a deeper understanding of signaling pathways and their interactions to emerge. This review aims to demonstrate how the BCR, specific signaling pathways like PI3K/AKT/mTOR, NF-kB, and JAK/STAT are diverse in common types of B-cell lymphoma. Furthermore, it offers a detailed examination of each pathway and a synopsis of the approved or in-development targeted therapies. In conclusion, finding the activated signaling pathways is crucial for developing effective treatment plans to improve the prognosis of patients with relapsed or refractory lymphoma.

Indexed as

B-cell lymphomaBCRJAK/STATNF-kBPI3K/AKT/mTORsignaling pathwaystargeted therapy

Identifiers

PMID39563886
PMCPMC11576080

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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.