دورية أكاديمية

L-type amino acid transporter (LAT) 1 expression in 18 F-FET-negative gliomas.

التفاصيل البيبلوغرافية
العنوان: L-type amino acid transporter (LAT) 1 expression in 18 F-FET-negative gliomas.
المؤلفون: Vettermann FJ; Department of Nuclear Medicine, University Hospital of Munich, LMU Munich, Munich, Germany. Franziska.vettermann@med.uni-muenchen.de., Diekmann C; Department of Nuclear Medicine, University Hospital of Munich, LMU Munich, Munich, Germany., Weidner L; Department of Neuropathology, Regensburg University Hospital, Regensburg, Germany., Unterrainer M; Department of Radiology, University Hospital of Munich, LMU Munich, Munich, Germany., Suchorska B; Department of Neurosurgery, University Hospital of Munich, LMU Munich, Munich, Germany.; Department of Neurosurgery, Sana Hospital, Duisburg, Germany., Ruf V; Center for Neuropathology, University Hospital of Munich, LMU Munich, Munich, Germany., Dorostkar M; Center for Neuropathology, University Hospital of Munich, LMU Munich, Munich, Germany., Wenter V; Department of Nuclear Medicine, University Hospital of Munich, LMU Munich, Munich, Germany., Herms J; Center for Neuropathology, University Hospital of Munich, LMU Munich, Munich, Germany., Tonn JC; Department of Neurosurgery, University Hospital of Munich, LMU Munich, Munich, Germany.; German Cancer Consortium (DKTK), Partner Site Munich, German Cancer Research Center (DKFZ), Heidelberg, Germany., Bartenstein P; Department of Nuclear Medicine, University Hospital of Munich, LMU Munich, Munich, Germany.; German Cancer Consortium (DKTK), Partner Site Munich, German Cancer Research Center (DKFZ), Heidelberg, Germany., Riemenschneider MJ; Department of Neuropathology, Regensburg University Hospital, Regensburg, Germany., Albert NL; Department of Nuclear Medicine, University Hospital of Munich, LMU Munich, Munich, Germany.; German Cancer Consortium (DKTK), Partner Site Munich, German Cancer Research Center (DKFZ), Heidelberg, Germany.
المصدر: EJNMMI research [EJNMMI Res] 2021 Dec 14; Vol. 11 (1), pp. 124. Date of Electronic Publication: 2021 Dec 14.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Springer Berlin Country of Publication: Germany NLM ID: 101560946 Publication Model: Electronic Cited Medium: Print ISSN: 2191-219X (Print) Linking ISSN: 2191219X NLM ISO Abbreviation: EJNMMI Res Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Heidelberg : Springer Berlin
مستخلص: Background: O-(2-[ 18 F]-fluoroethyl)-L-tyrosine ( 18 F-FET) is a highly sensitive PET tracer for glioma imaging, and its uptake is suggested to be driven by an overexpression of the L-type amino-acid transporter 1 (LAT1). However, 30% of low- and 5% of high-grade gliomas do not present enhanced 18 F-FET uptake at primary diagnosis (" 18 F-FET-negative gliomas") and the pathophysiologic basis for this phenomenon remains unclear. The aim of this study was to determine the expression of LAT1 in a homogeneous group of newly diagnosed 18 F-FET-negative gliomas and to compare them to a matched group of 18 F-FET-positive gliomas. Forty newly diagnosed IDH-mutant astrocytomas without 1p/19q codeletion were evaluated (n = 20 18 F-FET-negative (tumour-to-background ratio (TBR) < 1.6), n = 20 18 F-FET-positive gliomas (TBR > 1.6)). LAT1 immunohistochemistry (IHC) was performed using SLC7A5/LAT1 antibody. The percentage of LAT1-positive tumour cells (%) and the staining intensity (range 0-2) were multiplied to an overall score (H-score; range 0-200) and correlated to PET findings as well as progression-free survival (PFS).
Results: IHC staining of LAT1 expression was positive in both, 18 F-FET-positive as well as 18 F-FET-negative gliomas. No differences were found between the 18 F-FET-negative and 18 F-FET-positive group with regard to percentage of LAT1-positive tumour cells, staining intensity or H-score. Interestingly, the LAT1 expression showed a significant negative correlation with the PFS (p = 0.031), whereas no significant correlation was found for TBR max , neither in the overall group nor in the 18 F-FET-positive group only (p = 0.651 and p = 0.140).
Conclusion: Although LAT1 is reported to mediate the uptake of 18 F-FET into tumour cells, the levels of LAT1 expression do not correlate with the levels of 18 F-FET uptake in IDH-mutant astrocytomas. In particular, the lack of tracer uptake in 18 F-FET-negative gliomas cannot be explained by a reduced LAT1 expression. A higher LAT1 expression in IDH-mutant astrocytomas seems to be associated with a short PFS. Further studies regarding mechanisms influencing the uptake of 18 F-FET are necessary.
(© 2021. The Author(s).)
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فهرسة مساهمة: Keywords: FET PET; Glioma; LAT1; Molecular imaging
تواريخ الأحداث: Date Created: 20211214 Latest Revision: 20211218
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC8671595
DOI: 10.1186/s13550-021-00865-9
PMID: 34905134
قاعدة البيانات: MEDLINE
الوصف
تدمد:2191-219X
DOI:10.1186/s13550-021-00865-9