There is limited expression by normal tissues: erythrocytes8, testicular germinal cells, renal tubules, perineurium8, endothelial cells of the blood-brain barrier vessels and placenta (trophoblast and capillaries).
It is expressed by a range of carcinomas, including breast, head and neck, bladder, renal cell and lung.
GLUT1 is strongly expressed in colorectal carcinomas:
Normal colonic epithelium |
0/388, 0/>807, 0/119 |
||
Acute inflammation/regeneration without dysplasia |
4/59 |
||
Inflammatory bowel disease without dysplasia |
5/79 |
||
DALM |
9/99 |
||
Hyperplastic polyp |
0/468 |
||
Serrated adenoma |
3/148 |
||
Tubular adenoma |
0/77, 1/448 |
||
Tubulovillous adenoma |
8/107, 0/128 |
||
Villous adenoma |
4/128 |
||
Adenoma NOS |
|||
Adenoma in long standing colitis |
4/59 |
||
Adenoma not contiguous with a carcinoma |
0/1710 |
||
Adenoma contiguous with a carcinoma |
4/1410 |
||
Colorectal carcinoma |
|||
Diffuse GLUT1 staining (>50% of cells) is associated with metastases and a higher mortality7,8.
Malignant cells blocks prepared from body cavity effusions show positivity for GLUT-1:
Benign effusions |
|||
Malignant effusions |
|||
Based on studies of cell blocks, cystic squamous cell carcinoma of the head and neck stains, whereas benign cystic squamous cell lesions are negative:
Benign cystic squamous lesions |
|||
Metastatic squamous cell carcinomas with cystic / liquifactive degeneration |
16/165 , 14/156 |
||
Mesotheliomas show distinct linear membrane staining, with or without cytoplasmic staining.
|
||||||||
Reactive mesothelium |
40/401 |
|
|
|
||||
epithelioid |
0/481 |
9/481 |
12/481 |
15/481 |
||||
biphasic |
epithelioid areas |
1/111 |
6/111 |
3/111 |
1/111 |
|||
sarcomatoid areas |
4/111 |
3/111 |
2/111 |
2/111 |
||||
sarcomatoid |
0/11 |
1/11 |
0/11 |
0/11 |
||||
Lung |
0/281 |
1/281 |
3/281 |
24/281 |
||||
2/301 |
11/301 |
6/301 |
11/301 |
|||||
Identification of malignant cells in cystic squamous cell lesion of the head and neck.
Identification of invasive malignancy in colorectal epithelial neoplasms.
A promising marker for the differentiation of benign from malignant mesothelium.
References
3 Zimmerman RL, Goonewardene S,Fogt F Glucose transporter Glut-1 is of limited value for detecting breast carcinoma in serous effusions. Mod Pathol 2001; 14:748-51 FULL TEXT
6 Chandan VS, Faquin WC, Wilbur DC, et al. The utility of GLUT-1 immunolocalization in cell blocks: An adjunct to the fine needle aspiration diagnosis of cystic squamous lesions of the head and neck. Cancer 2006; 108:124-8 FULL TEXT
7 Haber RS, Rathan A, Weiser KR, et al. GLUT1 glucose transporter expression in colorectal carcinoma: a marker for poor prognosis. Cancer 1998; 83:34-40 FULL TEXT
8 Younes M, Lechago LV,Lechago J. Overexpression of the human erythrocyte glucose transporter occurs as a late event in human colorectal carcinogenesis and is associated with an increased incidence of lymph node metastases. Clin Cancer Res 1996; 2:1151-4 FULL TEXT
10 Bakiet S, O'Sullivan J, Izzuan M et al. Glut1 staining pattern in contiguous and non-contiguous colorectal adenomas and their corresponding cancers. Abstract P32, Pathological Society July 2006.
This page last revised 20.6.2007.
©SMUHT/PW Bishop