Evidence map›Paper›PMID 27224648›Full record

Trial reportPloS one2016

Overexpression of L-Type Amino Acid Transporter 1 (LAT1) and 2 (LAT2): Novel Markers of Neuroendocrine Tumors.

Susi Barollo, Loris Bertazza, Sara Watutantrige-Fernando, Simona Censi, Elisabetta Cavedon, Francesca Galuppini, Gianmaria Pennelli, Ambrogio Fassina, Marilisa Citton, Beatrice Rubin and 5 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 53 citations in OpenAlex.

  1. Genotype-dependent [European journal of nuclear medicine and molecular imaging · 2026
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  4. Quantitative [EJNMMI reports · 2025
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  10. Frontiers in pharmacology · 2022
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  16. Article
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  19. Amino Acid Transporters as Potential Therapeutic Targets in Thyroid Cancer.Endocrinology and metabolism (Seoul, Korea) · 2020
    Article
  20. Article
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

15 authors at 2 institutions in 2 countries.

Susi BarolloEndocrinology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Loris BertazzaEndocrinology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Sara Watutantrige-FernandoEndocrinology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Simona CensiEndocrinology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Elisabetta CavedonEndocrinology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Francesca GaluppiniII Pathology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Gianmaria PennelliII Pathology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Ambrogio FassinaII Pathology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Marilisa CittonSurgical Pathology Unit, Department of Surgery, Oncology and Gastroenterology Sciences, University-Hospital of Padua, Padua, Italy.
Beatrice RubinEndocrinology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Raffaele PezzaniEndocrinology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
Clara BennaSurgical Pathology Unit, Department of Surgery, Oncology and Gastroenterology Sciences, University-Hospital of Padua, Padua, Italy.
Giuseppe OpocherFamilial Cancer Clinic and Oncoendocrinology, Veneto Institute of Oncology, Padova, Italy.
Maurizio IacoboneSurgical Pathology Unit, Department of Surgery, Oncology and Gastroenterology Sciences, University-Hospital of Padua, Padua, Italy.
Caterina MianEndocrinology Unit, Department of Medicine, University-Hospital of Padua, Padua, Italy.
University of Padua · ITIstituto Oncologico Veneto · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background6-18F-fluoro-L-3,4-dihydroxyphenylalanine (18F-FDOPA) PET is a useful tool in the clinical management of pheochromocytoma (PHEO) and medullary thyroid carcinoma (MTC). 18F-FDOPA is a large neutral amino acid biochemically resembling endogenous L-DOPA and taken up by the L-type amino acid transporters (LAT1 and LAT2). This study was conducted to examine the expression of the LAT system in PHEO and MTC.

methodsReal-time PCR and Western blot analyses were used to assess LAT1 and LAT2 gene and protein expression in 32 PHEO, 38 MTC, 16 normal adrenal medulla and 15 normal thyroid tissue samples. Immunohistochemistry method was applied to identify the proteins' subcellular localization.

resultsLAT1 and LAT2 were overexpressed in both PHEO and MTC by comparison with normal tissues. LAT1 presented a stronger induction than LAT2, and their greater expression was more evident in PHEO (15.1- and 4.1-fold increases, respectively) than in MTC (9.9- and 4.1-fold increases, respectively). Furthermore we found a good correlation between LAT1/2 and GLUT1 expression levels. A positive correlation was also found between urinary noradrenaline and adrenaline levels and LAT1 gene expression in PHEO. The increased expression of LAT1 is also confirmed at the protein level, in both PHEO and MTC, with a strong cytoplasmic localization.

conclusionsThe present study is the first to provide experimental evidence of the overexpression in some NET cancers (such as PHEO or MTC) of L-type amino acid transporters, and the LAT1 isoform in particular, giving the molecular basis to explain the increase of the DOPA uptake seen in such tumor cells.

Indexed as

Gene Expression Regulation, NeoplasticAdrenal Gland NeoplasmsAdultAgedAmino Acid Transport System y+Biomarkers, TumorCarcinoma, NeuroendocrineFemaleFusion Regulatory Protein 1, Light ChainsGlucose Transporter Type 1HumansLarge Neutral Amino Acid-Transporter 1MaleMiddle AgedNeoplasm ProteinsPheochromocytomaAmino Acid Transport System y+Biomarkers, TumorFusion Regulatory Protein 1, Light ChainsGlucose Transporter Type 1Large Neutral Amino Acid-Transporter 1Neoplasm ProteinsSLC2A1 protein, humanSLC7A8 protein, human

Identifiers

PMID27224648
PMCPMC4880303
OpenAlexW2395401987

What OpenQuestion holds

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LicenceCC BY
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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.