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Facilitated glucose transporter (GLUT family) (GLUT (for individual family members, e.g., GLUT1, GLUT4))

Target
GLUT (for individual family members, e.g., GLUT1, GLUT4)
Molecular classification
Transporter, Major facilitator superfamily (MFS)
01

Overview

Facilitated glucose transport is mediated by a family of intrinsic membrane proteins called facilitative glucose transporters or GLUTs, which efficiently catalyze the bidirectional movement of glucose across the plasma membrane according to its concentration gradient without energy expenditure[1][2][3][5]. Multiple isoforms (GLUT1 to GLUT14 in humans) show tissue specificity, substrate selectivity, and regulation by hormones such as insulin (notably GLUT4 in adipose and muscle)[1][2][5]. These proteins are characterized by 12 transmembrane segments and belong to the major facilitator superfamily of transporters[1][5].\n\nIn summary, \"Facilitated glucose transport\" describes a physiological process, and the proper canonical target entry should be one of the GLUT proteins (e.g., **Facilitated glucose transporter type 1 (GLUT1)** or **Facilitated glucose transporter type 4 (GLUT4)**, etc.), depending on biological context[1][2][5]. The current name is not sufficiently specific and should be corrected for structured data extraction.

Other names
Glucose transporterGLUT familySolute carrier family 2 (SLC2A)Monosaccharide transporter
02

Mechanism of action

Insulin promotes translocation of GLUT4 to plasma membrane, increasing glucose uptake in muscle/adipose tissue[1][2][3]\nInhibition or modulation of GLUT expression or function can alter glucose homeostasis

03

Biological functions

Glucose transport across plasma membraneRegulation of cellular glucose uptakeHomeostasis of blood glucoseInsulin-mediated glucose uptake (esp. GLUT4)
04

Disease associations

Diabetes mellitus (defects or regulation in GLUT4 and others)[1][2][3]Cancer (altered glucose metabolism via upregulation of GLUTs)Neurodegenerative diseases (GLUT1 deficiency syndrome)Obesity (GLUT4 regulation and insulin resistance)
05

Safety considerations

Hypoglycemia with interventions increasing glucose uptakeOff-target effects due to ubiquitous expression of some GLUTsImpaired glucose uptake in essential tissues (e.g., brain in GLUT1 deficiency)
06

Interacting drugs

Insulin (regulates activity and cellular localization, particularly GLUT4)[1][3]

3 more in the full profile.

07

Biomarkers

GLUT1 or GLUT4 expression levels (used in diagnosis/monitoring in certain cancers, GLUT1 deficiency syndrome, and in research for metabolic status)[2]

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