Regulation of Nutrient Transport in Quiescent, Lactating, and Neoplastic Mammary Epithelia

The specific aims of this proposal are to characterize the role of GLUT1 and other potential glucose transporters in lactating and neoplastic mammary epithelia, to identify novel transporters or sorters, to describe their developmental regulation, and to test possible associations between glucose tr...

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description The specific aims of this proposal are to characterize the role of GLUT1 and other potential glucose transporters in lactating and neoplastic mammary epithelia, to identify novel transporters or sorters, to describe their developmental regulation, and to test possible associations between glucose transport and the neoplastic phenotype. Double-label immunofluorescence and subcellular fractionation by density gradient centrifugation independently demonstrate that GLUT1 is localized in the Golgi in response to the hormonal milieu of lactation, both in vitro and in vivo; corresponding with this, lactose biosynthesis is increased several-fold. Northern and Western blots for GLUT1 and GLUT5 indicate that the developmental regulation of glucose transporters is isoform-specific, and a precipitous decline in GLUT1 levels at weaning appears not to be due to transcriptional effects, but to changes in translational efficiency or GLUT1 protein degradation. Differential display analysis has shown six genes differentially expressed in mammary epithelial cells treated with prolactin and dexamethasone. One of these is lactate dehydrogenase A, and five are novel, and represent potential candidates to explain the Golgi sequestration of GLUT1 observed in secretion medium. The ability to understand and alter the amount of subcellular targeting of GLUT1 may have therapeutic implications in breast cancer. Original contains color plates: All DTIC reproductions will be in black and white.
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Double-label immunofluorescence and subcellular fractionation by density gradient centrifugation independently demonstrate that GLUT1 is localized in the Golgi in response to the hormonal milieu of lactation, both in vitro and in vivo; corresponding with this, lactose biosynthesis is increased several-fold. Northern and Western blots for GLUT1 and GLUT5 indicate that the developmental regulation of glucose transporters is isoform-specific, and a precipitous decline in GLUT1 levels at weaning appears not to be due to transcriptional effects, but to changes in translational efficiency or GLUT1 protein degradation. Differential display analysis has shown six genes differentially expressed in mammary epithelial cells treated with prolactin and dexamethasone. One of these is lactate dehydrogenase A, and five are novel, and represent potential candidates to explain the Golgi sequestration of GLUT1 observed in secretion medium. The ability to understand and alter the amount of subcellular targeting of GLUT1 may have therapeutic implications in breast cancer. Original contains color plates: All DTIC reproductions will be in black and white.</description><language>eng</language><subject>Anatomy and Physiology ; ANTIGENS ; Biochemistry ; BIOSYNTHESIS ; BREAST CANCER ; CARBOHYDRATES ; CELLS(BIOLOGY) ; CENTRIFUGE SEPARATION ; DENSITY ; DENSITY GRADIENT CENTRIFUGATION ; DEXAMETHASONE ; DIFFERENTIAL DISPLAY ANALYSIS ; DISACCHARIDES ; ENZYMES ; EPITHELIUM ; FRACTIONATION ; GENES ; Genetic Engineering and Molecular Biology ; GLUCOSE ; GLUCOSE TRANSPORTER ISOFORMS ; GLUT1 ; GLUT5 ; GLYCOPROTEINS ; GOLGI APPARATUS ; GRADIENTS ; HYDROCARBONS ; IMMUNOCHEMISTRY ; IMMUNOFLUORESCENCE ; IN VITRO ANALYSIS ; IN VIVO ANALYSIS ; LACTATES ; LACTATING ; LACTIC DEHYDROGENASE ; LACTOSE ; MAMMARY GLANDS ; Medicine and Medical Research ; NEOPLASMS ; NEOPLASTIC MAMMARY EPITHELIA ; NORTHERN BLOTS ; NUTRIENTS ; Organic Chemistry ; PHENOTYPES(BIOLOGY) ; PROLACTIN ; PROTEIN DEGRADATION ; PROTEINS(CONJUGATED) ; QUIESCENT ; SECRETION ; SORTING ; SUBCELLULAR FRACTIONATION ; TRANSCRIPTIONAL ; TRANSPORT ; WESTERN BLOTS</subject><creationdate>1996</creationdate><rights>APPROVED FOR PUBLIC RELEASE</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,780,885,27567,27568</link.rule.ids><linktorsrc>$$Uhttps://apps.dtic.mil/sti/citations/ADB220593$$EView_record_in_DTIC$$FView_record_in_$$GDTIC$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Haney, Peter M</creatorcontrib><creatorcontrib>WASHINGTON UNIV ST LOUIS MO</creatorcontrib><title>Regulation of Nutrient Transport in Quiescent, Lactating, and Neoplastic Mammary Epithelia</title><description>The specific aims of this proposal are to characterize the role of GLUT1 and other potential glucose transporters in lactating and neoplastic mammary epithelia, to identify novel transporters or sorters, to describe their developmental regulation, and to test possible associations between glucose transport and the neoplastic phenotype. Double-label immunofluorescence and subcellular fractionation by density gradient centrifugation independently demonstrate that GLUT1 is localized in the Golgi in response to the hormonal milieu of lactation, both in vitro and in vivo; corresponding with this, lactose biosynthesis is increased several-fold. Northern and Western blots for GLUT1 and GLUT5 indicate that the developmental regulation of glucose transporters is isoform-specific, and a precipitous decline in GLUT1 levels at weaning appears not to be due to transcriptional effects, but to changes in translational efficiency or GLUT1 protein degradation. Differential display analysis has shown six genes differentially expressed in mammary epithelial cells treated with prolactin and dexamethasone. One of these is lactate dehydrogenase A, and five are novel, and represent potential candidates to explain the Golgi sequestration of GLUT1 observed in secretion medium. The ability to understand and alter the amount of subcellular targeting of GLUT1 may have therapeutic implications in breast cancer. 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Double-label immunofluorescence and subcellular fractionation by density gradient centrifugation independently demonstrate that GLUT1 is localized in the Golgi in response to the hormonal milieu of lactation, both in vitro and in vivo; corresponding with this, lactose biosynthesis is increased several-fold. Northern and Western blots for GLUT1 and GLUT5 indicate that the developmental regulation of glucose transporters is isoform-specific, and a precipitous decline in GLUT1 levels at weaning appears not to be due to transcriptional effects, but to changes in translational efficiency or GLUT1 protein degradation. Differential display analysis has shown six genes differentially expressed in mammary epithelial cells treated with prolactin and dexamethasone. One of these is lactate dehydrogenase A, and five are novel, and represent potential candidates to explain the Golgi sequestration of GLUT1 observed in secretion medium. The ability to understand and alter the amount of subcellular targeting of GLUT1 may have therapeutic implications in breast cancer. Original contains color plates: All DTIC reproductions will be in black and white.</abstract><oa>free_for_read</oa></addata></record>
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source DTIC Technical Reports
subjects Anatomy and Physiology
ANTIGENS
Biochemistry
BIOSYNTHESIS
BREAST CANCER
CARBOHYDRATES
CELLS(BIOLOGY)
CENTRIFUGE SEPARATION
DENSITY
DENSITY GRADIENT CENTRIFUGATION
DEXAMETHASONE
DIFFERENTIAL DISPLAY ANALYSIS
DISACCHARIDES
ENZYMES
EPITHELIUM
FRACTIONATION
GENES
Genetic Engineering and Molecular Biology
GLUCOSE
GLUCOSE TRANSPORTER ISOFORMS
GLUT1
GLUT5
GLYCOPROTEINS
GOLGI APPARATUS
GRADIENTS
HYDROCARBONS
IMMUNOCHEMISTRY
IMMUNOFLUORESCENCE
IN VITRO ANALYSIS
IN VIVO ANALYSIS
LACTATES
LACTATING
LACTIC DEHYDROGENASE
LACTOSE
MAMMARY GLANDS
Medicine and Medical Research
NEOPLASMS
NEOPLASTIC MAMMARY EPITHELIA
NORTHERN BLOTS
NUTRIENTS
Organic Chemistry
PHENOTYPES(BIOLOGY)
PROLACTIN
PROTEIN DEGRADATION
PROTEINS(CONJUGATED)
QUIESCENT
SECRETION
SORTING
SUBCELLULAR FRACTIONATION
TRANSCRIPTIONAL
TRANSPORT
WESTERN BLOTS
title Regulation of Nutrient Transport in Quiescent, Lactating, and Neoplastic Mammary Epithelia
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