Evidence map›Paper›PMID 33521927›Full record

ArticleInternational journal of cancer2021

Oxidatively modified low-density lipoproteins are potential mediators of proteasome inhibitor resistance in multiple myeloma.

Srikanth R Polusani, Valerie Cortez, Javier Esparza, Huynh Nga Nguyen, Hongxin Fan, Gopalrao V N Velagaleti, Matthew J Butler, Marsha C Kinney, Babatunde O Oyajobi, Samy L Habib and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of cancer, 2021. 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
0.3field-weighted citation impact, top 45% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Srikanth R PolusaniDivision of Hematopathology, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Valerie CortezDivision of Hematopathology, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Javier EsparzaDivision of Hematopathology, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Huynh Nga NguyenDepartment of Biochemistry and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Hongxin FanDivision of Hematopathology, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Gopalrao V N VelagaletiDivision of Hematopathology, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Matthew J ButlerDivision of Hematology and Medical Oncology, Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Marsha C KinneyDivision of Hematopathology, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Babatunde O OyajobiDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, Texas, USA.
Samy L HabibDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, Texas, USA.
Reto AsmisDepartment of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Edward A MedinaDivision of Hematopathology, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.ORCID 0000-0002-1305-4046
The University of Texas Health Science Center at San Antonio · USWake Forest University · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
San Antonio Biomedical Education and ResearchK12GM111726 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LECHLEITER, JAMES D, OYAJOBI, BABATUNDE OLUKAYODE · 2015 to 2024
$7.6M
Atheroprotective Mechanisms of Ursolic Acid and Related PhytochemicalsR01AT006885 · NCCIH · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ASMIS, RETO H.R. · 2013 to 2017
$1.8M
Role of OxLDL in metabolic syndrome-associated resistance of myeloma to proteasome inhibitorsR21CA227414 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MEDINA, EDWARD A. · 2018 to 2019
$360k
NCATS NIH HHS UL1 TR001120NCCIH NIH HHS R01 AT006885NCCIH NIH HHS RO1 AT006885NCI NIH HHS P30 CA054174NCI NIH HHS R21 CA227414NIGMS NIH HHS K12 GM111726NIGMS NIH HHS K12GM 111726
6 · The paper itself

Abstract

Proteasome inhibitor (PI) therapy has improved the survival of multiple myeloma (MM) patients. However, inevitably, primary or acquired resistance to PIs leads to disease progression; resistance mechanisms are unclear. Obesity is a risk factor for MM mortality. Oxidized LDL (OxLDL), a central mediator of atherosclerosis that is elevated in metabolic syndrome (co-occurrence of obesity, insulin resistance, dyslipidemia and hypertension), has been linked to an increased risk of solid cancers and shown to stimulate pro-oncogenic/survival signaling. We hypothesized that OxLDL is a mediator of chemoresistance and evaluated its effects on MM cell killing by PIs. OxLDL potently suppressed the ability of the boronic acid-based PIs bortezomib (BTZ) and ixazomib, but not the epoxyketone-based PI carfilzomib, to kill human MM cell lines and primary cells. OxLDL suppressed BTZ-induced inhibition of proteasome activity and induction of pro-apoptotic signaling. These cytoprotective effects were abrogated when lipid hydroperoxides (LOOHs) associated with OxLDL were enzymatically reduced. We also demonstrated the presence of OxLDL in the MM bone marrow microenvironment as well as numerous granulocytes and monocytes capable of cell-mediated LDL oxidation through myeloperoxidase. Our findings suggest that OxLDL may be a potent mediator of boronic acid-based PI resistance, particularly for MM patients with metabolic syndrome, given their elevated systemic levels of OxLDL. LDL cholesterol-lowering therapy to reduce circulating OxLDL, and pharmacologic targeting of LOOH levels or resistance pathways induced by the modified lipoprotein, could deepen the response to these important agents and offer clinical benefit to MM patients with metabolic syndrome.

Indexed as

Drug Resistance, NeoplasmBoron CompoundsBortezomibCell Line, TumorGlycineGranulocytesHumansLipid PeroxidesLipoproteins, LDLMonocytesMultiple MyelomaOligopeptidesProteasome InhibitorsBoron CompoundsBortezomibcarfilzomibGlycineixazomibLipid PeroxidesLipoproteins, LDLOligopeptidesoxidized low density lipoproteinProteasome Inhibitorsmetabolic syndromemultiple myelomaobesityoxidized LDLproteasome inhibitor resistance

Identifiers

PMID33521927
PMCPMC9107792
OpenAlexW3128762320

What OpenQuestion holds

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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.