Evidence map›Paper›PMID 35205675›Full record

ArticleCancers2022

Bone Marrow Stroma-Induced Transcriptome and Regulome Signatures of Multiple Myeloma.

Sebastian A Dziadowicz, Lei Wang, Halima Akhter, Drake Aesoph, Tulika Sharma, Donald A Adjeroh, Lori A Hazlehurst, Gangqing Hu

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  5. The influence of interleukin-27 on metabolic fitness in a murine neonatal model of bacterial sepsis.American journal of physiology. Endocrinology and metabolism · 2025
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  11. Code Interpreter for Bioinformatics: Are We There Yet?Annals of biomedical engineering · 2024
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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

8 authors at 1 institution in 1 country.

Sebastian A DziadowiczDepartment of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
Lei WangDepartment of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
Halima AkhterDepartment of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
Drake AesophDepartment of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
Tulika SharmaDepartment of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
Donald A AdjerohLane Department of Computer Science & Electrical Engineering, West Virginia University, Morgantown, WV 26506, USA.
Lori A HazlehurstWVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.ORCID 0000-0001-7040-4084
Gangqing HuDepartment of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.ORCID 0000-0001-5453-6888
West Virginia University · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI JUDITH FEINBERG · 2012 to 2026
$81.0M
WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI GARY O RANKIN · 2012 to 2026
$61.1M
WVU Flow Cytometry and Single Cell Core Facility (FCSCCF)P20GM121322 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Karen H Martin · 2018 to 2026
$22.4M
NIGMS NIH HHS 1P20 GM121322NIGMS NIH HHS 2U54GM104942-03NIGMS NIH HHS P20 GM103434NIGMS NIH HHS P20 GM103434-21S1NIGMS NIH HHS P20 GM121322NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

Multiple myeloma (MM) is a hematological cancer with inevitable drug resistance. MM cells interacting with bone marrow stromal cells (BMSCs) undergo substantial changes in the transcriptome and develop de novo multi-drug resistance. As a critical component in transcriptional regulation, how the chromatin landscape is transformed in MM cells exposed to BMSCs and contributes to the transcriptional response to BMSCs remains elusive. We profiled the transcriptome and regulome for MM cells using a transwell coculture system with BMSCs. The transcriptome and regulome of MM cells from the upper transwell resembled MM cells that coexisted with BMSCs from the lower chamber but were distinctive to monoculture. BMSC-induced genes were enriched in the JAK2/STAT3 signaling pathway, unfolded protein stress, signatures of early plasma cells, and response to proteasome inhibitors. Genes with increasing accessibility at multiple regulatory sites were preferentially induced by BMSCs; these genes were enriched in functions linked to responses to drugs and unfavorable clinic outcomes. We proposed JUNB and ATF4::CEBPβ as candidate transcription factors (TFs) that modulate the BMSC-induced transformation of the regulome linked to the transcriptional response. Together, we characterized the BMSC-induced transcriptome and regulome signatures of MM cells to facilitate research on epigenetic mechanisms of BMSC-induced multi-drug resistance in MM.

Indexed as

ATF4::CEBPβbone marrow stromal cellsde novo drug resistanceepigenetic regulationJUNBmultiple myelomapioneer factorsregulometranscriptometranscriptome and regulome signatures

Identifiers

PMID35205675
PMCPMC8870223
OpenAlexW4212886551

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.