Evidence mapPaperPMID 40296192Full record

ReviewStem cells (Dayton, Ohio)2025

Inflammatory pathways and the bone marrow microenvironment in inherited bone marrow failure syndromes.

Nicholas Neoman, Hye Na Kim, Jacob Viduya, Anju Goyal, Y Lucy Liu, Kathleen M Sakamoto

Abstract readReview
In one paragraph

Review in Stem cells (Dayton, Ohio), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

6 authors.

Nicholas NeomanDivision of Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305-5162, United States.ORCID 0009-0002-2393-321X
Hye Na KimDivision of Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305-5162, United States.
Jacob ViduyaDivision of Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305-5162, United States.
Anju GoyalDivision of Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305-5162, United States.
Y Lucy LiuDivision of Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305-5162, United States.
Kathleen M SakamotoDivision of Hematology/Oncology/Stem Cell Transplantation and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305-5162, United States.

Funding

Investigating and targeting the translational landscape of DBAR01DK136961 · STANFORD UNIVERSITY · 2025 to 2025
$673k
Increasing Interest in Hematology Research: Training for Promising StudentsR25DK130827 · STANFORD UNIVERSITY · 2025 to 2025
$106k
NIDDK NIH HHS R01 DK107286NIDDK NIH HHS R01 DK136961NIDDK NIH HHS R25 DK130827NIDDK NIH HHS R56 DK136961NIH HHS DK130827NIH HHS DK136961NIH HHS R01 DK107286
6 · The paper itself

Abstract

Inherited bone marrow failure syndromes (IBMFS) are a diverse group of genetic disorders characterized by insufficient hematopoietic cell production due to blood stem cell dysfunction. The most common syndromes are Fanconi Anemia, Diamond-Blackfan Anemia, and Shwachman-Diamond Syndrome. These conditions share a theme of chronically producing pro-inflammatory cytokines such as TNF-α, IL-1β, IL-6, TGF-β, IFN-I, and IFN-γ. Each of these cytokines can impact the bone marrow microenvironment and drive the pathophysiology of IBMFS. This review aims to provide the latest progress in the field regarding the mechanistic underpinnings of inflammation in these IBMFS, as well as the effect of inflammation on the bone marrow microenvironment. A comprehensive understanding of the inflammation in IBMFS will open new avenues for intervention to restore bone marrow stability and improve patient prognosis. Future research must include targeting these mechanisms to develop novel therapies that can potentially mitigate the effects of chronic inflammation in IBMFS.

Indexed as

Bone MarrowBone Marrow DiseasesCellular MicroenvironmentHemoglobinuria, ParoxysmalInflammationAnimalsBone Marrow Failure DisordersCytokinesHumansCytokinesbone marrow microenvironmentinflammationinherited bone marrow failure syndromesmesenchymal stromal cellspro-inflammatory cytokines

Identifiers

PMID40296192
PMCPMC12121359

What Socratic holds

Textmetadata
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 Socratic graph.