Evidence map›Paper›PMID 31020046›Full record

ArticleJournal of cancer metastasis and treatment2019

Metabolic alterations and the potential for targeting metabolic pathways in the treatment of multiple myeloma.

Dustin Rizzieri, Barry Paul, Yubin Kang

Open access · diamondAbstract read
In one paragraph

Article in Journal of cancer metastasis and treatment, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
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  19. Lipid metabolic vulnerabilities of multiple myeloma.Clinical and experimental medicine · 2023
    Review
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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

3 authors at 1 institution in 1 country.

Dustin RizzieriDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC 27710, USA.
Barry PaulDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC 27710, USA.
Yubin KangDivision of Hematological Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC 27710, USA.
Duke University · US

Funding

Sample Engineering CoreU19AI067773 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FORNACE, ALBERT J · 2005 to 2024
$105.4M
TRANSFUSION MEDICINE AND RELATED AREAST32HL007057 · NHLBI · DUKE UNIVERSITY · PI Gowthami M Arepally · 1985 to 2026
$10.6M
Clinical Trial of ABC294640 in Patients with Refractory Multiple MyelomaR44CA199767 · NCI · APOGEE BIOTECHNOLOGY CORPORATION · PI SMITH, CHARLES D · 2015 to 2017
$2.0M
Targeting sphingosine kinase 2 for the treatment of multiple myelomaR01CA197792 · NCI · DUKE UNIVERSITY · PI KANG, YUBIN · 2015 to 2019
$1.8M
Plerixafor for allogeneic hematopoietic stem cell transplantationK08HL103780 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KANG, YUBIN · 2011 to 2015
$649k
Effects of PPAR agonists on response to immunomodulatory agents in patients with multiple myelomaR21CA234701 · NCI · DUKE UNIVERSITY · PI KANG, YUBIN · 2019 to 2020
$385k
NCI NIH HHS R01 CA197792NCI NIH HHS R21 CA234701NCI NIH HHS R44 CA199767NHLBI NIH HHS K08 HL103780NHLBI NIH HHS T32 HL007057NIAID NIH HHS U19 AI067773
6 · The paper itself

Abstract

Metabolism is defined as the collection of complex biochemical processes that living cells use to generate energy and maintain their growth and survival. Metabolism encompasses the synthesis and breakdown of glucose, fatty acids, and amino acids; the generation of energy (ATP); and oxidative phosphorylation. In cancer cells, metabolism can be commandeered to promote tumor growth and cellular proliferation. These alterations in metabolism have emerged as an additional hallmark of various cancers. In this review we focus on metabolic alterations in multiple myeloma (MM) - a malignancy of plasma cells - including derangements in glycolysis, gluconeogenesis, the tricarboxylic acid cycle, oxidative phosphorylation, and fatty acid/amino acid synthesis and degradation. Particular focus is given to metabolic alterations that contribute to myeloma cell growth, proliferation and drug resistance. Finally, novel approaches that target metabolic pathways for the treatment of MM are discussed.

Indexed as

alterationsMetabolismmultiple myelomatreatment

Identifiers

PMID31020046
PMCPMC6476731
OpenAlexW2930384550

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.