Evidence map›Paper›PMID 28939850›Full record

ArticleScientific reports2017

Glutaminase 2 expression is associated with regional heterogeneity of 5-aminolevulinic acid fluorescence in glioblastoma.

Sojin Kim, Ja Eun Kim, Yong Hwy Kim, Taeyoung Hwang, Sung Kwon Kim, Wen Jun Xu, Jong-Yeon Shin, Jong-Il Kim, Hyoungseon Choi, Hee Chan Kim and 13 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
1.2field-weighted citation impact, top 23% 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, 30 citations in OpenAlex.

  1. Article
  2. Targeting Glutaminase Isoforms GLS and GLS2 in Luminal Breast Cancer.International journal of molecular sciences · 2026
    Article
  3. Review
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  10. Electrotherapies for Glioblastoma.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  11. Review
  12. Experience Profiling of Fluorescence-Guided Surgery I: Gliomas.Brain tumor research and treatment · 2019
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
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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

23 authors at 7 institutions in 3 countries.

Sojin KimDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Ja Eun KimCell and Gene Therapy Products Division, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju, Korea.
Yong Hwy KimDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Taeyoung HwangDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sung Kwon KimDepartment of Neurosurgery, Gyeongsang National University School of Medicine, Gyeongsang National University Hospital, Jinju, Korea.
Wen Jun XuCollege of Pharmacy, Natural Product Research Institute, Seoul National University, Seoul, Korea.
Jong-Yeon ShinGenomic Medicine Institute, Medical Research Center, Seoul National University, Seoul, Korea.
Jong-Il KimDepartment of Biochemical and Molecular Biology, Seoul National University College of Medicine, Seoul, Korea.ORCID 0000-0002-7240-3744
Hyoungseon ChoiDMC R&D center, Samsung Electronics Co., Ltd., Seoul, Korea.
Hee Chan KimDepartment of Biomedical Engineering, College of Medicine and Institute of Medical and Biological Engineering, Medical Research Center, Seoul National University, Seoul, Korea.
Hye Rim ChoDepartment of Radiology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Anna ChoiDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Tamrin ChowdhuryDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-6747-6316
Youngbeom SeoDepartment of Neurosurgery, Yeungnam University College of Medicine, Daegu, Korea.
Yun-Sik DhoDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Jin Wook KimDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Dong Gyu KimDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Sung-Hye ParkDepartment of Pathology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-8681-1597
Hyeonjin KimDepartment of Radiology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Seung Hong ChoiDepartment of Radiology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Sunghyouk ParkCollege of Pharmacy, Natural Product Research Institute, Seoul National University, Seoul, Korea.
Se-Hoon LeeDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Chul-Kee ParkDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea. nsckpark@snu.ac.kr.ORCID 0000-0002-2350-9876
Seoul National University Hospital · KRSeoul National University · KRMinistry of Food and Drug Safety · KRJohns Hopkins University · USSamsung Medical Center · KRSamsung (South Korea) · KRYeungnam University College

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescence-guided surgery using 5-aminolevulinic acid (5-ALA) is now a widely-used modality for glioblastoma (GBM) treatment. However, intratumoral heterogeneity of fluorescence intensity may reflect different onco-metabolic programs. Here, we investigated the metabolic mechanism underlying the heterogeneity of 5-ALA fluorescence in GBM. Using an in-house developed fluorescence quantification system for tumor tissues, we collected 3 types of GBM tissues on the basis of their fluorescence intensity, which was characterized as strong, weak, and none. Expression profiling by RNA-sequencing revealed 77 genes with a proportional relationship and 509 genes with an inverse relationship between gene expression and fluorescence intensity. Functional analysis and in vitro experiments confirmed glutaminase 2 (GLS2) as a key gene associated with the fluorescence heterogeneity. Subsequent metabolite profiling discovered that insufficient NADPH due to GLS2 underexpression was responsible for the delayed metabolism of 5-ALA and accumulation of protoporphyrin IX (PpIX) in the high fluorescence area. The expression level of GLS2 and related NADPH production capacity is associated with the regional heterogeneity of 5-ALA fluorescence in GBM.

Indexed as

Aminolevulinic AcidBrain NeoplasmsCell Line, TumorFluorescenceFluorescent DyesGene Expression ProfilingGlioblastomaGlutaminaseHumansLevulinic AcidsNADPProspective StudiesProtoporphyrinsSurgery, Computer-AssistedAminolevulinic AcidFluorescent DyesGLS2 protein, humanGlutaminaseLevulinic AcidsNADPprotoporphyrin IXProtoporphyrins

Identifiers

PMID28939850
PMCPMC5610329
OpenAlexW2754397116

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.