The association of <sup>18</sup>F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (<it>SLC2A1</it>) and hypoxia-related genes (<it>HIF1A</it>, <it>VEGFA</it>, <it>APEX1</it>) in non-small cell lung cancer. <it>SLC2A1 </it>polymorphisms and FDG-PET in NSCLC patients
<p>Abstract</p> <p>Background</p> <p>Positron emission tomography imaging of lung cancers with 2-[fluorine-18]-fluoro-2-deoxy-D-glucose is a non-invasive diagnostic, and prognostic tool that measures tumor metabolism. We have analyzed the effect of solute carrier family...
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doaj-d33a98ba89274796b3b22235b109f78b2020-11-25T02:52:07ZengBMCJournal of Experimental & Clinical Cancer Research1756-99662010-06-012916910.1186/1756-9966-29-69The association of <sup>18</sup>F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (<it>SLC2A1</it>) and hypoxia-related genes (<it>HIF1A</it>, <it>VEGFA</it>, <it>APEX1</it>) in non-small cell lung cancer. <it>SLC2A1 </it>polymorphisms and FDG-PET in NSCLC patientsLee Chang HunLee Min KiKim In JooHwang Sang-HyunKim Seong-JangLee Sang-YullLee Eun Yup<p>Abstract</p> <p>Background</p> <p>Positron emission tomography imaging of lung cancers with 2-[fluorine-18]-fluoro-2-deoxy-D-glucose is a non-invasive diagnostic, and prognostic tool that measures tumor metabolism. We have analyzed the effect of solute carrier family 2 (facilitated glucose transporter), member 1 polymorphisms on 2-[fluorine-18]-fluoro-2-deoxy-D-glucose-uptake with a combination of polymorphisms of hypoxia-inducible factor 1 alpha, apurinic/apyimidinic endonuclease, and vascular endothelial growth factor A in a hypoxia-related pathway.</p> <p>Methods</p> <p>We investigated the association between solute carrier family 2 (facilitated glucose transporter), member 1 -2841A>T, hypoxia-inducible factor 1 alpha Pro582Ser, Ala588Thr, apurinic/apyimidinic endonuclease Asp148Glu, or vascular endothelial growth factor A +936C>T and 2-[fluorine-18]-fluoro-2-deoxy-D-glucose-uptake among 154 patients with non-small-cell lung cancer.</p> <p>Results</p> <p>The solute carrier family 2 (facilitated glucose transporter), member 1 -2841A>T polymorphism was significantly associated with 2-[fluorine-18]-fluoro-2-deoxy-D-glucose-uptake in combination with the apurinic/apyimidinic endonuclease Asp148Glu (T>G) polymorphism in the squamous cell type of non-small-cell lung cancer. The solute carrier family 2 (facilitated glucose transporter), member 1 TT genotype had a higher maximum standardized uptake values than the AA + AT genotype when the apurinic/apyimidinic endonuclease genotype was TT (mean maximum standardized uptake values, 12.47 ± 1.33 versus 8.46 ± 2.90, respectively; <it>P </it>= 0.028). The mean maximum standardized uptake values were not statistically different with respect to vascular endothelial growth factor A and hypoxia-inducible factor 1 alpha polymorphisms.</p> <p>Conclusion</p> <p>A glucose transporter gene polymorphism was shown to be statistically associated with glucose-uptake when the apurinic/apyimidinic endonuclease genotype is TT in patients with the squamous cell type of non-small-cell lung cancer. Our findings suggest that a newly developed tracer for positron emission tomography could be affected by genetic polymorphisms.</p> http://www.jeccr.com/content/29/1/69 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lee Chang Hun Lee Min Ki Kim In Joo Hwang Sang-Hyun Kim Seong-Jang Lee Sang-Yull Lee Eun Yup |
spellingShingle |
Lee Chang Hun Lee Min Ki Kim In Joo Hwang Sang-Hyun Kim Seong-Jang Lee Sang-Yull Lee Eun Yup The association of <sup>18</sup>F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (<it>SLC2A1</it>) and hypoxia-related genes (<it>HIF1A</it>, <it>VEGFA</it>, <it>APEX1</it>) in non-small cell lung cancer. <it>SLC2A1 </it>polymorphisms and FDG-PET in NSCLC patients Journal of Experimental & Clinical Cancer Research |
author_facet |
Lee Chang Hun Lee Min Ki Kim In Joo Hwang Sang-Hyun Kim Seong-Jang Lee Sang-Yull Lee Eun Yup |
author_sort |
Lee Chang Hun |
title |
The association of <sup>18</sup>F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (<it>SLC2A1</it>) and hypoxia-related genes (<it>HIF1A</it>, <it>VEGFA</it>, <it>APEX1</it>) in non-small cell lung cancer. <it>SLC2A1 </it>polymorphisms and FDG-PET in NSCLC patients |
title_short |
The association of <sup>18</sup>F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (<it>SLC2A1</it>) and hypoxia-related genes (<it>HIF1A</it>, <it>VEGFA</it>, <it>APEX1</it>) in non-small cell lung cancer. <it>SLC2A1 </it>polymorphisms and FDG-PET in NSCLC patients |
title_full |
The association of <sup>18</sup>F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (<it>SLC2A1</it>) and hypoxia-related genes (<it>HIF1A</it>, <it>VEGFA</it>, <it>APEX1</it>) in non-small cell lung cancer. <it>SLC2A1 </it>polymorphisms and FDG-PET in NSCLC patients |
title_fullStr |
The association of <sup>18</sup>F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (<it>SLC2A1</it>) and hypoxia-related genes (<it>HIF1A</it>, <it>VEGFA</it>, <it>APEX1</it>) in non-small cell lung cancer. <it>SLC2A1 </it>polymorphisms and FDG-PET in NSCLC patients |
title_full_unstemmed |
The association of <sup>18</sup>F-deoxyglucose (FDG) uptake of PET with polymorphisms in the glucose transporter gene (<it>SLC2A1</it>) and hypoxia-related genes (<it>HIF1A</it>, <it>VEGFA</it>, <it>APEX1</it>) in non-small cell lung cancer. <it>SLC2A1 </it>polymorphisms and FDG-PET in NSCLC patients |
title_sort |
association of <sup>18</sup>f-deoxyglucose (fdg) uptake of pet with polymorphisms in the glucose transporter gene (<it>slc2a1</it>) and hypoxia-related genes (<it>hif1a</it>, <it>vegfa</it>, <it>apex1</it>) in non-small cell lung cancer. <it>slc2a1 </it>polymorphisms and fdg-pet in nsclc patients |
publisher |
BMC |
series |
Journal of Experimental & Clinical Cancer Research |
issn |
1756-9966 |
publishDate |
2010-06-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Positron emission tomography imaging of lung cancers with 2-[fluorine-18]-fluoro-2-deoxy-D-glucose is a non-invasive diagnostic, and prognostic tool that measures tumor metabolism. We have analyzed the effect of solute carrier family 2 (facilitated glucose transporter), member 1 polymorphisms on 2-[fluorine-18]-fluoro-2-deoxy-D-glucose-uptake with a combination of polymorphisms of hypoxia-inducible factor 1 alpha, apurinic/apyimidinic endonuclease, and vascular endothelial growth factor A in a hypoxia-related pathway.</p> <p>Methods</p> <p>We investigated the association between solute carrier family 2 (facilitated glucose transporter), member 1 -2841A>T, hypoxia-inducible factor 1 alpha Pro582Ser, Ala588Thr, apurinic/apyimidinic endonuclease Asp148Glu, or vascular endothelial growth factor A +936C>T and 2-[fluorine-18]-fluoro-2-deoxy-D-glucose-uptake among 154 patients with non-small-cell lung cancer.</p> <p>Results</p> <p>The solute carrier family 2 (facilitated glucose transporter), member 1 -2841A>T polymorphism was significantly associated with 2-[fluorine-18]-fluoro-2-deoxy-D-glucose-uptake in combination with the apurinic/apyimidinic endonuclease Asp148Glu (T>G) polymorphism in the squamous cell type of non-small-cell lung cancer. The solute carrier family 2 (facilitated glucose transporter), member 1 TT genotype had a higher maximum standardized uptake values than the AA + AT genotype when the apurinic/apyimidinic endonuclease genotype was TT (mean maximum standardized uptake values, 12.47 ± 1.33 versus 8.46 ± 2.90, respectively; <it>P </it>= 0.028). The mean maximum standardized uptake values were not statistically different with respect to vascular endothelial growth factor A and hypoxia-inducible factor 1 alpha polymorphisms.</p> <p>Conclusion</p> <p>A glucose transporter gene polymorphism was shown to be statistically associated with glucose-uptake when the apurinic/apyimidinic endonuclease genotype is TT in patients with the squamous cell type of non-small-cell lung cancer. Our findings suggest that a newly developed tracer for positron emission tomography could be affected by genetic polymorphisms.</p> |
url |
http://www.jeccr.com/content/29/1/69 |
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