Evidence map›Paper›PMID 35091751›Full record

ArticleNeuro-oncology2022

Deuterium magnetic resonance spectroscopy enables noninvasive metabolic imaging of tumor burden and response to therapy in low-grade gliomas.

Céline Taglang, Georgios Batsios, Joydeep Mukherjee, Meryssa Tran, Anne Marie Gillespie, Donghyun Hong, Sabrina M Ronen, Hema Artee Luchman, Russell O Pieper, Pavithra Viswanath

Open access · bronzeAbstract read
In one paragraph

Article in Neuro-oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  19. Deuterium Metabolic Imaging Reports on TERT Expression and Early Response to Therapy in Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
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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

10 authors at 2 institutions in 2 countries.

Céline TaglangDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California, USA.ORCID 0000-0002-3927-6675
Georgios BatsiosDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California, USA.
Joydeep MukherjeeDepartment of Neurological Surgery, University of California, San Francisco, San Francisco, California, USA.
Meryssa TranDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California, USA.
Anne Marie GillespieDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California, USA.
Donghyun HongDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California, USA.
Sabrina M RonenDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California, USA.
Hema Artee LuchmanDepartment of Cell Biology and Anatomy, Hotchkiss Brain Institute and Arnie Charbonneau Cancer Institute, University of Calgary, Calgary, Alberta, Canada.
Russell O PieperDepartment of Neurological Surgery, University of California, San Francisco, San Francisco, California, USA.
Pavithra ViswanathDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California, USA.
University of California, San Francisco · USUniversity of Calgary · CA

Funding

Project 4: Multi-modality Metabolic Imaging for Monitoring Molecular Sub-types of GliomaP01CA118816 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Susan M Chang, Janine Marie Lupo · 2007 to 2026
$44.7M
Metabolic Reprogramming in Brain TumorsR01CA172845 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RONEN, SABRINA MIRIAM · 2013 to 2022
$6.3M
Metabolic Imaging of Brain Tumor Response to TherapyR01CA197254 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RONEN, SABRINA MIRIAM · 2016 to 2020
$3.2M
IMAGING TELOMERE MAINTENANCE MECHANISMS IN GLIOMASR01CA239288 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RONEN, SABRINA MIRIAM, VISWANATH, PAVITHRA · 2020 to 2024
$3.2M
Contributions of IDH1 mutation to alternative lengthening of telomeres in lower-grade gliomaR01NS105087 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PIEPER, RUSSELL O. · 2017 to 2021
$1.7M
NCI NIH HHS P01 CA118816NCI NIH HHS R01 CA172845NCI NIH HHS R01 CA197254NCI NIH HHS R01 CA239288NINDS NIH HHS R01 NS105087
6 · The paper itself

Abstract

backgroundThe alternative lengthening of telomeres (ALT) pathway is essential for tumor proliferation in astrocytomas. The goal of this study was to identify metabolic alterations linked to the ALT pathway that can be exploited for noninvasive magnetic resonance spectroscopy (MRS)-based imaging of astrocytomas in vivo.

methodsGenetic and pharmacological methods were used to dissect the association between the ALT pathway and glucose metabolism in genetically engineered and patient-derived astrocytoma models. 2H-MRS was used for noninvasive imaging of ALT-linked modulation of glycolytic flux in mice bearing orthotopic astrocytomas in vivo.

resultsThe ALT pathway was associated with higher activity of the rate-limiting glycolytic enzyme phosphofructokinase-1 and concomitantly elevated flux of glucose to lactate in astrocytoma cells. Silencing the ALT pathway or treating with the poly(ADP-ribose) polymerase inhibitor niraparib that induces telomeric fusion in ALT-dependent astrocytoma cells abrogated glycolytic flux. Importantly, this metabolic reprogramming could be non-invasively visualized by 2H-MRS. Lactate production from [6,6'-2H]-glucose was higher in ALT-dependent astrocytoma tumors relative to the normal brain in vivo. Furthermore, treatment of orthotopic astrocytoma-bearing mice with niraparib reduced lactate production from [6,6'-2H]-glucose at early timepoints when alterations in tumor volume could not be detected by anatomical imaging, pointing to the ability of [6,6'-2H]-glucose to report on pseudoprogression in vivo.

conclusionsWe have mechanistically linked the ALT pathway to elevated glycolytic flux and demonstrated the ability of [6,6'-2H]-glucose to non-invasively assess tumor burden and response to therapy in astrocytomas. Our findings point to a novel, clinically translatable method for metabolic imaging of astrocytoma patients.

Indexed as

AstrocytomaBrain NeoplasmsGliomaAnimalsDeuteriumGlucoseLactatesMagnetic Resonance ImagingMagnetic Resonance SpectroscopyMiceTumor BurdenDeuteriumGlucoseLactatesalternative lengthening of telomeresastrocytomasdeuterium metabolic imaginggliomasisocitrate dehydrogenase mutation

Identifiers

PMID35091751
PMCPMC9248401
OpenAlexW4206992752

What OpenQuestion holds

Textmetadata
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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.