Glucose Uptake and Intracellular pH in a Mouse Model of Ductal Carcinoma In Situ (DCIS) Suggests Metabolic Heterogeneity

Mechanisms for the progression of ductal carcinoma in situ (DCIS) to invasive breast carcinoma remain unclear. Previously we showed that the transition to invasiveness in the mammary intraepithelial neoplastic outgrowth (MINO) model of DCIS does not correlate with its serial acquisition of genetic m...

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Main Authors: Rebecca C. Lobo, Neil E. Hubbard, Patrizia Damonte, Hidetoshi Mori, Zsófia Pénzváltó, Cynthia Pham, Amanda L. Koehne, Aiza C. Go, Steve E. Anderson, Peter M. Cala, Alexander D Borowsky
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-08-01
Series:Frontiers in Cell and Developmental Biology
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Online Access:http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00093/full
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author Rebecca C. Lobo
Neil E. Hubbard
Patrizia Damonte
Hidetoshi Mori
Zsófia Pénzváltó
Cynthia Pham
Amanda L. Koehne
Aiza C. Go
Steve E. Anderson
Peter M. Cala
Alexander D Borowsky
author_facet Rebecca C. Lobo
Neil E. Hubbard
Patrizia Damonte
Hidetoshi Mori
Zsófia Pénzváltó
Cynthia Pham
Amanda L. Koehne
Aiza C. Go
Steve E. Anderson
Peter M. Cala
Alexander D Borowsky
author_sort Rebecca C. Lobo
collection DOAJ
description Mechanisms for the progression of ductal carcinoma in situ (DCIS) to invasive breast carcinoma remain unclear. Previously we showed that the transition to invasiveness in the mammary intraepithelial neoplastic outgrowth (MINO) model of DCIS does not correlate with its serial acquisition of genetic mutations. We hypothesized instead that progression to invasiveness depends on a change in the microenvironment and that precancer cells might create a more tumor-permissive microenvironment secondary to changes in glucose uptake and metabolism. Immunostaining for glucose transporter 1 (GLUT1) and the hypoxia marker carbonic anhydrase 9 (CAIX) in tumor, normal mammary gland and MINO (precancer) tissue showed differences in expression. The uptake of the fluorescent glucose analog dye, 2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) amino]-2-deoxy-D-glucose (2-NBDG), reflected differences in the cellular distributions of glucose uptake in normal mammary epithelial cells (nMEC), MINO and Met1 cancer cells, with a broad distribution in the MINO population. The intracellular pH (pHi) measured using the fluorescent ratio dye 2’,7’-bis(2-carboxyethyl)-5(6)-155 carboxyfluorescein-AM (BCECF-AM) revealed expected differences between normal and cancer cells (low and high, respectively), and a mixed distribution in the MINO cells, with a subset of cells in the MINO having an increased rate of acidification when proton efflux was inhibited. Invasive tumor cells had a more alkaline baseline pHi with high rates of proton production coupled with higher rates of proton export, compared with nMEC. MINO cells displayed considerable variation in baseline pHi that separated into two distinct populations: MINO high and MINO low. MINO high had a noticeably higher mean acidification rate compared with nMEC, but relatively high baseline pHi similar to tumor cells. MINO low cells also had an increased acidification rate compared with nMEC, but with a more acidic pHi similar to nMEC. These findings demonstrate that MINO is heterogeneous with respect to intracellular pH regulation which may be associated with an acidified regional microenvironment. A change in the pH of the microenvironment might contribute to a tumor-permissive or tumor-promoting progression. We are not aware of any previous work showing that a sub-population of cells in in situ precancer exhibits a higher than normal proton production and export rate.
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spelling doaj.art-9e7d49b7397a4306af756ad0fcf9327e2022-12-22T03:46:20ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2016-08-01410.3389/fcell.2016.00093205898Glucose Uptake and Intracellular pH in a Mouse Model of Ductal Carcinoma In Situ (DCIS) Suggests Metabolic HeterogeneityRebecca C. Lobo0Neil E. Hubbard1Patrizia Damonte2Hidetoshi Mori3Zsófia Pénzváltó4Cynthia Pham5Amanda L. Koehne6Aiza C. Go7Steve E. Anderson8Peter M. Cala9Alexander D Borowsky10University of California at DavisUniversity of California at DavisUniversity of California at DavisUniversity of California at DavisUniversity of California at DavisUniversity of California at DavisUniversity of California at DavisUniversity of California at DavisUniversity of California at DavisUniversity of California at DavisUniversity of California at DavisMechanisms for the progression of ductal carcinoma in situ (DCIS) to invasive breast carcinoma remain unclear. Previously we showed that the transition to invasiveness in the mammary intraepithelial neoplastic outgrowth (MINO) model of DCIS does not correlate with its serial acquisition of genetic mutations. We hypothesized instead that progression to invasiveness depends on a change in the microenvironment and that precancer cells might create a more tumor-permissive microenvironment secondary to changes in glucose uptake and metabolism. Immunostaining for glucose transporter 1 (GLUT1) and the hypoxia marker carbonic anhydrase 9 (CAIX) in tumor, normal mammary gland and MINO (precancer) tissue showed differences in expression. The uptake of the fluorescent glucose analog dye, 2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) amino]-2-deoxy-D-glucose (2-NBDG), reflected differences in the cellular distributions of glucose uptake in normal mammary epithelial cells (nMEC), MINO and Met1 cancer cells, with a broad distribution in the MINO population. The intracellular pH (pHi) measured using the fluorescent ratio dye 2’,7’-bis(2-carboxyethyl)-5(6)-155 carboxyfluorescein-AM (BCECF-AM) revealed expected differences between normal and cancer cells (low and high, respectively), and a mixed distribution in the MINO cells, with a subset of cells in the MINO having an increased rate of acidification when proton efflux was inhibited. Invasive tumor cells had a more alkaline baseline pHi with high rates of proton production coupled with higher rates of proton export, compared with nMEC. MINO cells displayed considerable variation in baseline pHi that separated into two distinct populations: MINO high and MINO low. MINO high had a noticeably higher mean acidification rate compared with nMEC, but relatively high baseline pHi similar to tumor cells. MINO low cells also had an increased acidification rate compared with nMEC, but with a more acidic pHi similar to nMEC. These findings demonstrate that MINO is heterogeneous with respect to intracellular pH regulation which may be associated with an acidified regional microenvironment. A change in the pH of the microenvironment might contribute to a tumor-permissive or tumor-promoting progression. We are not aware of any previous work showing that a sub-population of cells in in situ precancer exhibits a higher than normal proton production and export rate.http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00093/fullTumor Microenvironmentintracellular pHductal carcinoma in situglucose uptaketumor heterogeneitymouse mammary carcinoma model
spellingShingle Rebecca C. Lobo
Neil E. Hubbard
Patrizia Damonte
Hidetoshi Mori
Zsófia Pénzváltó
Cynthia Pham
Amanda L. Koehne
Aiza C. Go
Steve E. Anderson
Peter M. Cala
Alexander D Borowsky
Glucose Uptake and Intracellular pH in a Mouse Model of Ductal Carcinoma In Situ (DCIS) Suggests Metabolic Heterogeneity
Frontiers in Cell and Developmental Biology
Tumor Microenvironment
intracellular pH
ductal carcinoma in situ
glucose uptake
tumor heterogeneity
mouse mammary carcinoma model
title Glucose Uptake and Intracellular pH in a Mouse Model of Ductal Carcinoma In Situ (DCIS) Suggests Metabolic Heterogeneity
title_full Glucose Uptake and Intracellular pH in a Mouse Model of Ductal Carcinoma In Situ (DCIS) Suggests Metabolic Heterogeneity
title_fullStr Glucose Uptake and Intracellular pH in a Mouse Model of Ductal Carcinoma In Situ (DCIS) Suggests Metabolic Heterogeneity
title_full_unstemmed Glucose Uptake and Intracellular pH in a Mouse Model of Ductal Carcinoma In Situ (DCIS) Suggests Metabolic Heterogeneity
title_short Glucose Uptake and Intracellular pH in a Mouse Model of Ductal Carcinoma In Situ (DCIS) Suggests Metabolic Heterogeneity
title_sort glucose uptake and intracellular ph in a mouse model of ductal carcinoma in situ dcis suggests metabolic heterogeneity
topic Tumor Microenvironment
intracellular pH
ductal carcinoma in situ
glucose uptake
tumor heterogeneity
mouse mammary carcinoma model
url http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00093/full
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