Evidence map›Paper›PMID 41034261›Full record

ArticleScientific reports2025

Clinicopathological analysis of GLUT-1, GLS1, and GLS2 expression in breast cancer tissues from Jordanian patients.

Haneen A Basheer, Ahlam Zaid Alkilani, Samir Al Bashir, Maram A Alhusban, Lina Elsalem, Sura Bilal AlOmari, Qosay Mahmoud Sharqiah, Kamyar Afarinkia

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

8 authors.

Haneen A BasheerDepartment of Pharmacy, Faculty of Pharmacy, Zarqa University, Zarqa, 13110, Jordan. hbasheer@zu.edu.jo.
Ahlam Zaid AlkilaniDepartment of Pharmacy, Faculty of Pharmacy, Zarqa University, Zarqa, 13110, Jordan.
Samir Al BashirDepartment of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan.
Maram A AlhusbanDepartment of Pharmacy, Faculty of Pharmacy, Zarqa University, Zarqa, 13110, Jordan.
Lina ElsalemFaculty of Medicine, Department of Pharmacology, Jordan University of Science and Technology, Irbid, Jordan.
Sura Bilal AlOmariDepartment of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan.
Qosay Mahmoud SharqiahDepartment of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan.
Kamyar AfarinkiaSchool of Biomedical Sciences, University of West London, London, W5 5RF, UK.

Funding

the Scientific Research Support Fund (SRSF) at Ministry of Higher Education and Scientific Research, Amman, Jordan (Grant no. MPH/1/33/2021).
6 · The paper itself

Abstract

Breast cancer remains the most common malignancy among women, with significant heterogeneity in molecular subtypes and clinical outcomes. This study examines the clinicopathological significance of GLUT-1, GLS1, and GLS2 expression in breast cancer tissues from Jordanian patients, focusing on their role in metabolic reprogramming and potential as therapeutic targets. Using tissue microarray analysis and immunohistochemistry, we evaluated 306 invasive breast cancer cases and 52 normal tissue samples. Overexpression of all three markers was observed in tumor tissues compared to normal samples (p ≤ .01). GLUT-1 and GLS2 showed significant associations with higher tumor grades and triple-negative breast cancer (TNBC) subtypes, highlighting their potential role in aggressive tumor biology. Conversely, GLS1 expression was consistently elevated in cancer tissues but did not vary significantly across grades or subtypes. Strong correlations between high GLUT-1/GLS2 expression and Ki-67 proliferative index underscore their contributions to tumor proliferation and metabolic adaptation. Population-specific patterns, such as the higher GLS2 expression in HER2-negative cases, reflect potential genetic or environmental influences unique to Jordanian patients. These findings emphasize the critical role of metabolic reprogramming in breast cancer progression and underscore the translational potential of targeting GLUT-1 and GLS2, particularly in aggressive subtypes like TNBC. Further research is warranted to explore functional mechanisms and validate these markers in diverse populations. This study provides novel insights into the metabolic dynamics of breast cancer, offering a foundation for regionally tailored therapeutic strategies.

Indexed as

Breast NeoplasmsExcitatory Amino Acid Transporter 2Glucose Transporter Type 1AdultAgedBiomarkers, TumorFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryJordanMiddle AgedTriple Negative Breast NeoplasmsBiomarkers, TumorExcitatory Amino Acid Transporter 2Glucose Transporter Type 1SLC2A1 protein, humanBreast cancerGLUT-1GlutaminasesMetabolic reprogrammingTriple-negative breast cancer

Identifiers

PMID41034261
PMCPMC12489116

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