Evidence map›Paper›PMID 39853696›Full record

ArticleMolecular oncology2025

Inhibition of acyl-CoA synthetase long-chain isozymes decreases multiple myeloma cell proliferation and causes mitochondrial dysfunction.

Connor S Murphy, Heather Fairfield, Victoria E DeMambro, Samaa Fadel, Carlos A Gartner, Michelle Karam, Christian Potts, Princess Rodriguez, Ya-Wei Qiang, Habib Hamidi and 3 more

Abstract read
In one paragraph

Article in Molecular oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Connor S MurphyCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Heather FairfieldCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Victoria E DeMambroCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Samaa FadelCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Carlos A GartnerCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Michelle KaramCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Christian PottsCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Princess RodriguezVermont Integrative Genomics Resource DNA Facility, University of Vermont, Burlington, VT, USA.
Ya-Wei QiangCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Habib HamidiGenentech, Inc., San Francisco, CA, USA.
Xiangnan GuanGenentech, Inc., San Francisco, CA, USA.
Calvin P H VaryCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.
Michaela R ReaganCenter for Molecular Medicine, MaineHealth Institute for Research, Scarborough, ME, USA.ORCID https://orcid.org/0000-0003-2884-6481

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI CLIFFORD JAMES ROSEN, Gary S. Stein · 2017 to 2026
$51.6M
The role of night shift work in metabolic disorders during and after pregnancyP20GM121301 · NIGMS · MAINEHEALTH · PI Elizabeth Scharnetzki · 2017 to 2026
$25.1M
Interdisciplinary Study of Marrow Adiposity, Mineral Metabolism & Energy BalanceR24DK092759 · NIDDK · MAINEHEALTH · PI HOROWITZ, MARK C, MACDOUGALD, ORMOND A · 2011 to 2019
$13.0M
Defining the Roles of Bone Marrow Adipocytes and FABP4/5 Signaling in Multiple Myeloma Drug Resistance - Diversity SupplementR37CA245330 · NCI · MAINEHEALTH · PI REAGAN, MICHAELA R. · 2020 to 2025
$2.8M
Research Specialist Support for Defining the Roles of Bone Marrow Adipocytes and FABP4/5 Signaling in Multiple MyelomaR50CA265331 · NCI · MAINEHEALTH · PI Heather F Campbell · 2022 to 2026
$498k
Lipid Metabolism-driven Drug Resistance in Multiple MyelomaF31CA257695 · NCI · MAINEHEALTH · PI MURPHY, CONNOR · 2021 to 2023
$96k
American Cancer Society RSG-19-037-01-LIBArthur Gary Family FoundationLeukemia and Lymphoma Society Michaela R. Reagan Scholar AwardNCI NIH HHS F31 CA257695NCI NIH HHS F31CA257695NCI NIH HHS R37 CA245330NCI NIH HHS R37CA245330NCI NIH HHS R50 CA265331NCI NIH HHS R50CA265331NIDDK NIH HHS R24 DK092759NIDDK NIH HHS R24DK092759NIGMS NIH HHS P20 GM121301NIGMS NIH HHS P20GM121301NIGMS NIH HHS U54 GM115516NIGMS NIH HHS U54GM115516Tallen and Kane Foundation
6 · The paper itself

Abstract

Multiple myeloma (MM) is an incurable cancer of plasma cells with a 5-year survival rate of 59%. Dysregulation of fatty acid (FA) metabolism is associated with MM development and progression; however, the underlying mechanisms remain unclear. Herein, we explore the roles of long-chain fatty acid coenzyme A ligase (ACSL) family members in MM. ACSLs convert free long-chain fatty acids into fatty acyl-CoA esters and play key roles in catabolic and anabolic fatty acid metabolism. Analysis of the Multiple Myeloma Research Foundation (MMRF) CoMMpass

Indexed as

Coenzyme A LigasesEnzyme InhibitorsMitochondriaMultiple MyelomaApoptosisCell Line, TumorCell ProliferationCell SurvivalHumansLong-Chain-Fatty-Acid-CoA LigaseTriazenesCoenzyme A LigasesEnzyme InhibitorsLong-Chain-Fatty-Acid-CoA Ligasetriacsin CTriazenesACSLcell metabolismfatty acidhematological malignanciesmultiple myelomaTriacsin C

Identifiers

PMID39853696
PMCPMC12161464

What Socratic 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 Socratic graph.