GLUT1 (Glucose Transporter 1) is a protein on the surface of cells that moves glucose (sugar) from the bloodstream into the cell, where it is used for energy. Cancer cells often produce much more GLUT1 than normal cells because they consume sugar at a higher rate. Pathologists can stain tissue samples for GLUT1 to help tell cancerous cells apart from benign ones.
Origin
GLUT1 stands for "GLucose Transporter 1," the first member of the SLC2A family of glucose transport proteins to be cloned and sequenced, achieved by Mueckler and colleagues in 1985. It was originally characterized in human red blood cells.
Significance in Asbestos Context
GLUT1 is used as an immunohistochemical marker to help distinguish malignant mesothelioma and other cancers from benign reactive changes in the pleura. Reactive (non-cancerous) mesothelial cells, which can look worryingly abnormal under the microscope after asbestos exposure or pleural inflammation, are typically GLUT1-negative, while mesothelioma cells are usually GLUT1-positive. This stain is rarely used alone. Pathologists combine it with other markers (such as BAP1 loss and MTAP loss) to reach a confident diagnosis. For patients, GLUT1 results in the pathology report can be an important piece of evidence supporting a malignant diagnosis, which in turn supports a legal claim.
Example Sentence
The pathology report noted that the pleural biopsy cells were strongly positive for GLUT1, supporting the diagnosis of malignant mesothelioma rather than benign reactive pleuritis.
Related Terms
Immunohistochemistry, BAP1, MTAP, Mesothelioma, Reactive Mesothelial Hyperplasia, Pleural Biopsy
Notes
- Ask your pathologist or oncologist which immunohistochemical stains were performed on your biopsy. GLUT1, BAP1, MTAP, calretinin, and others are commonly used together to confirm mesothelioma.
- Request a copy of the full pathology report (not just the summary); the specific markers tested and their results can matter for both treatment planning and a legal claim.
- If the initial biopsy was inconclusive, ask whether GLUT1 and other discriminating stains were run, or whether a second-opinion review at a mesothelioma specialty center is warranted.
- GLUT1 is not specific to mesothelioma. Many cancers express it, so its value lies in distinguishing malignant from benign cells in the right clinical context.
In the research library
11 studies in our medical research library mention GLUT1 in the title or abstract. Among the most cited:
- Comparative immunohistochemical analysis of IMP3, GLUT1, EMA, CD146, and desmin for distinguishing malignant mesothelioma from reactive mesothelial cellsH. Minato, N. Kurose, M. Fukushima, et al, 2014 · American Journal of Clinical Pathology · cited 49 times
- Malignant peritoneal mesothelioma treated by cytoreductive surgery and hyperthermic intraperitoneal chemotherapy: is GLUT1 expression a major prognostic factor? A preliminary studyJ. Hommell-Fontaine, S. Isaac, G. Passot, et al, 2013 · Annals of Surgical Oncology · cited 21 times
- Osteopontin, GLUT1 and Ki-67 expression in malignant peritoneal mesothelioma: prognostic implicationsY. Liu, G. Zheng, D. Yang, et al, 2021 · Internal Medicine Journal · cited 3 times
- BAP1 immunohistochemistry and p16 FISH to separate benign from malignant mesothelial proliferationsB.S. Sheffield, H.C. Hwang, A.F. Lee, et al, 2015 · The American Journal of Surgical Pathology · cited 139 times
- Relationship between 18F-FDG uptake on positron emission tomography and molecular biology in malignant pleural mesotheliomaK. Kaira, M. Serizawa, Y. Koh, et al, 2012 · European Journal of Cancer · cited 42 times
The journals that publish most on it: Pathology International (2), European Journal of Cancer (1), Neoplasma (1).
Category: Biological & Molecular Mechanisms · All Lexicon terms A–Z
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