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Published in: BMC Cancer 1/2016

Open Access 01-12-2016 | Research article

Local iron homeostasis in the breast ductal carcinoma microenvironment

Authors: Oriana Marques, Graça Porto, Alexandra Rêma, Fátima Faria, Arnaud Cruz Paula, Maria Gomez-Lazaro, Paula Silva, Berta Martins da Silva, Carlos Lopes

Published in: BMC Cancer | Issue 1/2016

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Abstract

Background

While the deregulation of iron homeostasis in breast epithelial cells is acknowledged, iron-related alterations in stromal inflammatory cells from the tumor microenvironment have not been explored.

Methods

Immunohistochemistry for hepcidin, ferroportin 1 (FPN1), transferrin receptor 1 (TFR1) and ferritin (FT) was performed in primary breast tissues and axillary lymph nodes in order to dissect the iron-profiles of epithelial cells, lymphocytes and macrophages. Furthermore, breast carcinoma core biopsies frozen in optimum cutting temperature (OCT) compound were subjected to imaging flow cytometry to confirm FPN1 expression in the cell types previously evaluated and determine its cellular localization.

Results

We confirm previous results by showing that breast cancer epithelial cells present an ‘iron-utilization phenotype’ with an increased expression of hepcidin and TFR1, and decreased expression of FT. On the other hand, lymphocytes and macrophages infiltrating primary tumors and from metastized lymph nodes display an ‘iron-donor’ phenotype, with increased expression of FPN1 and FT, concomitant with an activation profile reflected by a higher expression of TFR1 and hepcidin. A higher percentage of breast carcinomas, compared to control mastectomy samples, present iron accumulation in stromal inflammatory cells, suggesting that these cells may constitute an effective tissue iron reservoir. Additionally, not only the deregulated expression of iron-related proteins in epithelial cells, but also on lymphocytes and macrophages, are associated with clinicopathological markers of breast cancer poor prognosis, such as negative hormone receptor status and tumor size.

Conclusions

The present results reinforce the importance of analyzing the tumor microenvironment in breast cancer, extending the contribution of immune cells to local iron homeostasis in the tumor microenvironment context.
Literature
1.
go back to reference Ferlay J SI, Ervik M, Dkshit R, Eser S, Mathers C, Rebelo M, Parkin DM, Forman D, Bray F. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide. In: IARC CancerBase. International Agency for Research on Cancer, Lyon, France. 2013. http://globocan.iarc.fr. Accessed 20-09-2014 2014. Ferlay J SI, Ervik M, Dkshit R, Eser S, Mathers C, Rebelo M, Parkin DM, Forman D, Bray F. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide. In: IARC CancerBase. International Agency for Research on Cancer, Lyon, France. 2013. http://​globocan.​iarc.​fr. Accessed 20-09-2014 2014.
2.
go back to reference Richardson DR, Kalinowski DS, Lau S, Jansson PJ, Lovejoy DB. Cancer cell iron metabolism and the development of potent iron chelators as anti-tumour agents. Biochim Biophys Acta. 2009;1790:702–17.CrossRefPubMed Richardson DR, Kalinowski DS, Lau S, Jansson PJ, Lovejoy DB. Cancer cell iron metabolism and the development of potent iron chelators as anti-tumour agents. Biochim Biophys Acta. 2009;1790:702–17.CrossRefPubMed
3.
go back to reference Thompson HJ, Kennedy K, Witt M, Juzefyk J. Effect of dietary iron deficiency or excess on the induction of mammary carcinogenesis by 1-methyl-1-nitrosourea. Carcinogenesis. 1991;12:111–4.CrossRefPubMed Thompson HJ, Kennedy K, Witt M, Juzefyk J. Effect of dietary iron deficiency or excess on the induction of mammary carcinogenesis by 1-methyl-1-nitrosourea. Carcinogenesis. 1991;12:111–4.CrossRefPubMed
4.
go back to reference Singh M, Lu J, Briggs SP, McGinley JN, Haegele AD, Thompson HJ. Effect of excess dietary iron on the promotion stage of 1-methyl-1-nitrosourea-induced mammary carcinogenesis: pathogenetic characteristics and distribution of iron. Carcinogenesis. 1994;15:1567–70.CrossRefPubMed Singh M, Lu J, Briggs SP, McGinley JN, Haegele AD, Thompson HJ. Effect of excess dietary iron on the promotion stage of 1-methyl-1-nitrosourea-induced mammary carcinogenesis: pathogenetic characteristics and distribution of iron. Carcinogenesis. 1994;15:1567–70.CrossRefPubMed
5.
go back to reference Hrabinski D, Hertz JL, Tantillo C, Berger V, Sherman AR. Iron repletion attenuates the protective effects of iron deficiency in DMBA-induced mammary tumors in rats. Nutr Cancer. 1995;24:133–42.CrossRefPubMed Hrabinski D, Hertz JL, Tantillo C, Berger V, Sherman AR. Iron repletion attenuates the protective effects of iron deficiency in DMBA-induced mammary tumors in rats. Nutr Cancer. 1995;24:133–42.CrossRefPubMed
6.
go back to reference Diwan BA, Kasprzak KS, Anderson LM. Promotion of dimethylbenz[a]anthracene-initiated mammary carcinogenesis by iron in female Sprague–Dawley rats. Carcinogenesis. 1997;18:1757–62.CrossRefPubMed Diwan BA, Kasprzak KS, Anderson LM. Promotion of dimethylbenz[a]anthracene-initiated mammary carcinogenesis by iron in female Sprague–Dawley rats. Carcinogenesis. 1997;18:1757–62.CrossRefPubMed
8.
go back to reference Cui Y, Vogt S, Olson N, Glass AG, Rohan TE. Levels of zinc, selenium, calcium, and iron in benign breast tissue and risk of subsequent breast cancer. Cancer Epidemiol Biomarkers Prev. 2007;16:1682–5.CrossRefPubMed Cui Y, Vogt S, Olson N, Glass AG, Rohan TE. Levels of zinc, selenium, calcium, and iron in benign breast tissue and risk of subsequent breast cancer. Cancer Epidemiol Biomarkers Prev. 2007;16:1682–5.CrossRefPubMed
9.
go back to reference Elliott RL, Elliott MC, Wang F, Head JF. Breast carcinoma and the role of iron metabolism. A cytochemical, tissue culture, and ultrastructural study. Ann N Y Acad Sci. 1993;698:159–66.CrossRefPubMed Elliott RL, Elliott MC, Wang F, Head JF. Breast carcinoma and the role of iron metabolism. A cytochemical, tissue culture, and ultrastructural study. Ann N Y Acad Sci. 1993;698:159–66.CrossRefPubMed
10.
go back to reference Miller LD, Coffman LG, Chou JW, Black MA, Bergh J, D'Agostino Jr R, et al. An iron regulatory gene signature predicts outcome in breast cancer. Cancer Res. 2011;71:6728–37.CrossRefPubMedPubMedCentral Miller LD, Coffman LG, Chou JW, Black MA, Bergh J, D'Agostino Jr R, et al. An iron regulatory gene signature predicts outcome in breast cancer. Cancer Res. 2011;71:6728–37.CrossRefPubMedPubMedCentral
11.
go back to reference Shpyleva SI, Tryndyak VP, Kovalchuk O, Starlard-Davenport A, Chekhun VF, Beland FA, et al. Role of ferritin alterations in human breast cancer cells. Breast Cancer Res Treat. 2011;126:63–71.CrossRefPubMed Shpyleva SI, Tryndyak VP, Kovalchuk O, Starlard-Davenport A, Chekhun VF, Beland FA, et al. Role of ferritin alterations in human breast cancer cells. Breast Cancer Res Treat. 2011;126:63–71.CrossRefPubMed
12.
go back to reference Zhang S, Chen Y, Guo W, Yuan L, Zhang D, Xu Y, et al. Disordered hepcidin-ferroportin signaling promotes breast cancer growth. Cell Signal. 2014;26:2539–50.CrossRefPubMed Zhang S, Chen Y, Guo W, Yuan L, Zhang D, Xu Y, et al. Disordered hepcidin-ferroportin signaling promotes breast cancer growth. Cell Signal. 2014;26:2539–50.CrossRefPubMed
13.
go back to reference Pinnix ZK, Miller LD, Wang W, D'Agostino Jr R, Kute T, Willingham MC, et al. Ferroportin and iron regulation in breast cancer progression and prognosis. Sci Transl Med. 2010;2:43ra56.CrossRefPubMedPubMedCentral Pinnix ZK, Miller LD, Wang W, D'Agostino Jr R, Kute T, Willingham MC, et al. Ferroportin and iron regulation in breast cancer progression and prognosis. Sci Transl Med. 2010;2:43ra56.CrossRefPubMedPubMedCentral
15.
go back to reference DeNardo DG, Coussens LM. Inflammation and breast cancer. Balancing immune response: crosstalk between adaptive and innate immune cells during breast cancer progression. Breast Cancer Res. 2007;9:212.CrossRefPubMedPubMedCentral DeNardo DG, Coussens LM. Inflammation and breast cancer. Balancing immune response: crosstalk between adaptive and innate immune cells during breast cancer progression. Breast Cancer Res. 2007;9:212.CrossRefPubMedPubMedCentral
16.
go back to reference Ruffell B, Au A, Rugo HS, Esserman LJ, Hwang ES, Coussens LM. Leukocyte composition of human breast cancer. Proc Natl Acad Sci U S A. 2012;109:2796–801.CrossRefPubMedPubMedCentral Ruffell B, Au A, Rugo HS, Esserman LJ, Hwang ES, Coussens LM. Leukocyte composition of human breast cancer. Proc Natl Acad Sci U S A. 2012;109:2796–801.CrossRefPubMedPubMedCentral
17.
go back to reference Bissell MJ, Hines WC. Why don't we get more cancer? A proposed role of the microenvironment in restraining cancer progression. Nat Med. 2011;17:320–9.CrossRefPubMedPubMedCentral Bissell MJ, Hines WC. Why don't we get more cancer? A proposed role of the microenvironment in restraining cancer progression. Nat Med. 2011;17:320–9.CrossRefPubMedPubMedCentral
18.
go back to reference Mantovani A, Allavena P, Sica A, Balkwill F. Cancer-related inflammation. Nature. 2008;454:436–44.CrossRefPubMed Mantovani A, Allavena P, Sica A, Balkwill F. Cancer-related inflammation. Nature. 2008;454:436–44.CrossRefPubMed
19.
go back to reference Pollack MS, da Silva BM, Moshief RD, Groshen S, Bognacki J, Dupont B, et al. Ferritin secretion by human mononuclear cells: association with HLA phenotype. Clin Immunol Immunopathol. 1983;27:124–34.CrossRefPubMed Pollack MS, da Silva BM, Moshief RD, Groshen S, Bognacki J, Dupont B, et al. Ferritin secretion by human mononuclear cells: association with HLA phenotype. Clin Immunol Immunopathol. 1983;27:124–34.CrossRefPubMed
20.
go back to reference Dorner MH, Silverstone A, Nishiya K, de Sostoa A, Munn G, de Sousa M. Ferritin synthesis by human T lymphocytes. Science. 1980;209:1019–21.CrossRefPubMed Dorner MH, Silverstone A, Nishiya K, de Sostoa A, Munn G, de Sousa M. Ferritin synthesis by human T lymphocytes. Science. 1980;209:1019–21.CrossRefPubMed
21.
go back to reference Alkhateeb AA, Han B, Connor JR. Ferritin stimulates breast cancer cells through an iron-independent mechanism and is localized within tumor-associated macrophages. Breast Cancer Res Treat. 2013;137:733–44.CrossRefPubMed Alkhateeb AA, Han B, Connor JR. Ferritin stimulates breast cancer cells through an iron-independent mechanism and is localized within tumor-associated macrophages. Breast Cancer Res Treat. 2013;137:733–44.CrossRefPubMed
22.
go back to reference Jezequel P, Campion L, Spyratos F, Loussouarn D, Campone M, Guerin-Charbonnel C, et al. Validation of tumor-associated macrophage ferritin light chain as a prognostic biomarker in node-negative breast cancer tumors: A multicentric 2004 national PHRC study. Int J Cancer. 2012;131:426–37.CrossRefPubMed Jezequel P, Campion L, Spyratos F, Loussouarn D, Campone M, Guerin-Charbonnel C, et al. Validation of tumor-associated macrophage ferritin light chain as a prognostic biomarker in node-negative breast cancer tumors: A multicentric 2004 national PHRC study. Int J Cancer. 2012;131:426–37.CrossRefPubMed
23.
go back to reference Corna G, Campana L, Pignatti E, Castiglioni A, Tagliafico E, Bosurgi L, et al. Polarization dictates iron handling by inflammatory and alternatively activated macrophages. Haematologica. 2010;95:1814–22.CrossRefPubMedPubMedCentral Corna G, Campana L, Pignatti E, Castiglioni A, Tagliafico E, Bosurgi L, et al. Polarization dictates iron handling by inflammatory and alternatively activated macrophages. Haematologica. 2010;95:1814–22.CrossRefPubMedPubMedCentral
24.
go back to reference Recalcati S, Locati M, Marini A, Santambrogio P, Zaninotto F, De Pizzol M, et al. Differential regulation of iron homeostasis during human macrophage polarized activation. Eur J Immunol. 2010;40:824–35.CrossRefPubMed Recalcati S, Locati M, Marini A, Santambrogio P, Zaninotto F, De Pizzol M, et al. Differential regulation of iron homeostasis during human macrophage polarized activation. Eur J Immunol. 2010;40:824–35.CrossRefPubMed
25.
go back to reference Shin DY, Chung J, Joe Y, Pae HO, Chang KC, Cho GJ, et al. Pretreatment with CO-releasing molecules suppresses hepcidin expression during inflammation and endoplasmic reticulum stress through inhibition of the STAT3 and CREBH pathways. Blood. 2012;119:2523–32.CrossRefPubMed Shin DY, Chung J, Joe Y, Pae HO, Chang KC, Cho GJ, et al. Pretreatment with CO-releasing molecules suppresses hepcidin expression during inflammation and endoplasmic reticulum stress through inhibition of the STAT3 and CREBH pathways. Blood. 2012;119:2523–32.CrossRefPubMed
26.
go back to reference Tesfay L, Clausen KA, Kim JW, Hegde P, Wang X, Miller LD, et al. Hepcidin Regulation in Prostate and Its Disruption in Prostate Cancer. Cancer Res. 2015;75:2254–63.CrossRefPubMed Tesfay L, Clausen KA, Kim JW, Hegde P, Wang X, Miller LD, et al. Hepcidin Regulation in Prostate and Its Disruption in Prostate Cancer. Cancer Res. 2015;75:2254–63.CrossRefPubMed
27.
go back to reference Wallander ML, Zumbrennen KB, Rodansky ES, Romney SJ, Leibold EA. Iron-independent phosphorylation of iron regulatory protein 2 regulates ferritin during the cell cycle. J Biol Chem. 2008;283:23589–98.CrossRefPubMedPubMedCentral Wallander ML, Zumbrennen KB, Rodansky ES, Romney SJ, Leibold EA. Iron-independent phosphorylation of iron regulatory protein 2 regulates ferritin during the cell cycle. J Biol Chem. 2008;283:23589–98.CrossRefPubMedPubMedCentral
28.
go back to reference Dong HY, Wilkes S, Yang HS. CD71 is Selectively and Ubiquitously Expressed at High Levels in Erythroid Precursors of All Maturation Stages: A Comparative Immunochemical Study With Glycophorin A and Hemoglobin A. Am J Surg Pathol. 2011;35:723–32.CrossRefPubMed Dong HY, Wilkes S, Yang HS. CD71 is Selectively and Ubiquitously Expressed at High Levels in Erythroid Precursors of All Maturation Stages: A Comparative Immunochemical Study With Glycophorin A and Hemoglobin A. Am J Surg Pathol. 2011;35:723–32.CrossRefPubMed
29.
go back to reference Pietras K, Ostman A. Hallmarks of cancer: interactions with the tumor stroma. Exp Cell Res. 2010;316:1324–31.CrossRefPubMed Pietras K, Ostman A. Hallmarks of cancer: interactions with the tumor stroma. Exp Cell Res. 2010;316:1324–31.CrossRefPubMed
30.
go back to reference Vargas AC, McCart Reed AE, Waddell N, Lane A, Reid LE, Smart CE, et al. Gene expression profiling of tumour epithelial and stromal compartments during breast cancer progression. Breast Cancer Res Treat. 2012;135:153–65.CrossRefPubMed Vargas AC, McCart Reed AE, Waddell N, Lane A, Reid LE, Smart CE, et al. Gene expression profiling of tumour epithelial and stromal compartments during breast cancer progression. Breast Cancer Res Treat. 2012;135:153–65.CrossRefPubMed
32.
34.
go back to reference Coffelt SB, Kersten K, Doornebal CW, Weiden J, Vrijland K, Hau C-S, et al. IL-17-producing γδ T cells and neutrophils conspire to promote breast cancer metastasis. Nature. 2015;522:345–8.CrossRefPubMedPubMedCentral Coffelt SB, Kersten K, Doornebal CW, Weiden J, Vrijland K, Hau C-S, et al. IL-17-producing γδ T cells and neutrophils conspire to promote breast cancer metastasis. Nature. 2015;522:345–8.CrossRefPubMedPubMedCentral
35.
36.
go back to reference Macedo MF, de Sousa M. Transferrin and the transferrin receptor: of magic bullets and other concerns. Inflamm Allergy Drug Targets. 2008;7:41–52.CrossRefPubMed Macedo MF, de Sousa M. Transferrin and the transferrin receptor: of magic bullets and other concerns. Inflamm Allergy Drug Targets. 2008;7:41–52.CrossRefPubMed
37.
go back to reference Chen Y, Zhang S, Wang X, Guo W, Wang L, Zhang D, et al. Disordered signaling governing ferroportin transcription favors breast cancer growth. Cell Signal. 2015;27:168–76.CrossRefPubMed Chen Y, Zhang S, Wang X, Guo W, Wang L, Zhang D, et al. Disordered signaling governing ferroportin transcription favors breast cancer growth. Cell Signal. 2015;27:168–76.CrossRefPubMed
39.
go back to reference Taylor M, Qu A, Anderson ER, Matsubara T, Martin A, Gonzalez FJ, et al. Hypoxia-inducible factor-2alpha mediates the adaptive increase of intestinal ferroportin during iron deficiency in mice. Gastroenterology. 2011;140:2044–55.CrossRefPubMedPubMedCentral Taylor M, Qu A, Anderson ER, Matsubara T, Martin A, Gonzalez FJ, et al. Hypoxia-inducible factor-2alpha mediates the adaptive increase of intestinal ferroportin during iron deficiency in mice. Gastroenterology. 2011;140:2044–55.CrossRefPubMedPubMedCentral
40.
go back to reference Manger B, Weiss A, Hardy KJ, Stobo JD. A transferrin receptor antibody represents one signal for the induction of IL 2 production by a human T cell line. J Immunol. 1986;136:532–8.PubMed Manger B, Weiss A, Hardy KJ, Stobo JD. A transferrin receptor antibody represents one signal for the induction of IL 2 production by a human T cell line. J Immunol. 1986;136:532–8.PubMed
41.
go back to reference Paulnock DM, Lambert LE. Identification and Characterization of Monoclonal-Antibodies Specific for Macrophages at Intermediate Stages in the Tumoricidal Activation Pathway. J Immunol. 1990;144:765–73.PubMed Paulnock DM, Lambert LE. Identification and Characterization of Monoclonal-Antibodies Specific for Macrophages at Intermediate Stages in the Tumoricidal Activation Pathway. J Immunol. 1990;144:765–73.PubMed
42.
go back to reference Knutson MD, Oukka M, Koss LM, Aydemir F, Wessling-Resnick M. Iron release from macrophages after erythrophagocytosis is up-regulated by ferroportin 1 overexpression and down-regulated by hepcidin. Proc Natl Acad Sci U S A. 2005;102:1324–8.CrossRefPubMedPubMedCentral Knutson MD, Oukka M, Koss LM, Aydemir F, Wessling-Resnick M. Iron release from macrophages after erythrophagocytosis is up-regulated by ferroportin 1 overexpression and down-regulated by hepcidin. Proc Natl Acad Sci U S A. 2005;102:1324–8.CrossRefPubMedPubMedCentral
43.
go back to reference Delaby C, Pilard N, Puy H, Canonne-Hergaux F. Sequential regulation of ferroportin expression after erythrophagocytosis in murine macrophages: early mRNA induction by haem, followed by iron-dependent protein expression. Biochem J. 2008;411:123–31.CrossRefPubMed Delaby C, Pilard N, Puy H, Canonne-Hergaux F. Sequential regulation of ferroportin expression after erythrophagocytosis in murine macrophages: early mRNA induction by haem, followed by iron-dependent protein expression. Biochem J. 2008;411:123–31.CrossRefPubMed
44.
go back to reference Zhang Y, Cheng SQ, Zhang MY, Zhen LN, Pang D, Zhang QY, et al. High-Infiltration of Tumor-Associated Macrophages Predicts Unfavorable Clinical Outcome for Node-Negative Breast Cancer. PLoS ONE. 2013;8:e76147.CrossRefPubMedPubMedCentral Zhang Y, Cheng SQ, Zhang MY, Zhen LN, Pang D, Zhang QY, et al. High-Infiltration of Tumor-Associated Macrophages Predicts Unfavorable Clinical Outcome for Node-Negative Breast Cancer. PLoS ONE. 2013;8:e76147.CrossRefPubMedPubMedCentral
45.
go back to reference Mahmoud SMA, Paish EC, Powe DG, Macmillan RD, Grainge MJ, Lee AHS, et al. Tumor-Infiltrating CD8(+) Lymphocytes Predict Clinical Outcome in Breast Cancer. J Clin Oncol. 2011;29:1949–55.CrossRefPubMed Mahmoud SMA, Paish EC, Powe DG, Macmillan RD, Grainge MJ, Lee AHS, et al. Tumor-Infiltrating CD8(+) Lymphocytes Predict Clinical Outcome in Breast Cancer. J Clin Oncol. 2011;29:1949–55.CrossRefPubMed
46.
go back to reference Liu SZ, Lachapelle J, Leung S, Gao DX, Foulkes WD, Nielsen TO. CD8(+) lymphocyte infiltration is an independent favorable prognostic indicator in basal-like breast cancer. Breast Cancer Res. 2012;14:R48.CrossRefPubMedPubMedCentral Liu SZ, Lachapelle J, Leung S, Gao DX, Foulkes WD, Nielsen TO. CD8(+) lymphocyte infiltration is an independent favorable prognostic indicator in basal-like breast cancer. Breast Cancer Res. 2012;14:R48.CrossRefPubMedPubMedCentral
47.
go back to reference Britten KJ, Jones DB, De Sousa M, Wright DH. The distribution of iron and iron binding proteins in spleen with reference to Hodgkin's disease. Br J Cancer. 1986;54:277–86.CrossRefPubMedPubMedCentral Britten KJ, Jones DB, De Sousa M, Wright DH. The distribution of iron and iron binding proteins in spleen with reference to Hodgkin's disease. Br J Cancer. 1986;54:277–86.CrossRefPubMedPubMedCentral
48.
go back to reference Arezes J, Costa M, Vieira I, Dias V, Kong XL, Fernandes R, et al. Non-Transferrin-Bound Iron (NTBI) Uptake by T Lymphocytes: Evidence for the Selective Acquisition of Oligomeric Ferric Citrate Species. PLoS ONE. 2013;8:e79870.CrossRefPubMedPubMedCentral Arezes J, Costa M, Vieira I, Dias V, Kong XL, Fernandes R, et al. Non-Transferrin-Bound Iron (NTBI) Uptake by T Lymphocytes: Evidence for the Selective Acquisition of Oligomeric Ferric Citrate Species. PLoS ONE. 2013;8:e79870.CrossRefPubMedPubMedCentral
49.
go back to reference Pinto JP, Arezes J, Dias V, Oliveira S, Vieira I, Costa M, et al. Physiological implications of NTBI uptake by T lymphocytes. Front Pharmacol. 2014;5:24.CrossRefPubMedPubMedCentral Pinto JP, Arezes J, Dias V, Oliveira S, Vieira I, Costa M, et al. Physiological implications of NTBI uptake by T lymphocytes. Front Pharmacol. 2014;5:24.CrossRefPubMedPubMedCentral
51.
go back to reference de Sousa M. Lymphocyte circulation: experimental and clinical aspects. New York: John Wiley and Sons; 1981. de Sousa M. Lymphocyte circulation: experimental and clinical aspects. New York: John Wiley and Sons; 1981.
52.
go back to reference de Sousa M. An outsider's perspective--ecotaxis revisited: an integrative review of cancer environment, iron and immune system cells. Integr Biol. 2011;3:343–9.CrossRef de Sousa M. An outsider's perspective--ecotaxis revisited: an integrative review of cancer environment, iron and immune system cells. Integr Biol. 2011;3:343–9.CrossRef
53.
go back to reference Sharma M, Beck AH, Webster JA, Espinosa I, Montgomery K, Varma S, et al. Analysis of stromal signatures in the tumor microenvironment of ductal carcinoma in situ. Breast Cancer Res Treat. 2010;123:397–404.CrossRefPubMedPubMedCentral Sharma M, Beck AH, Webster JA, Espinosa I, Montgomery K, Varma S, et al. Analysis of stromal signatures in the tumor microenvironment of ductal carcinoma in situ. Breast Cancer Res Treat. 2010;123:397–404.CrossRefPubMedPubMedCentral
54.
go back to reference Ma XJ, Dahiya S, Richardson E, Erlander M, Sgroi DC. Gene expression profiling of the tumor microenvironment during breast cancer progression. Breast Cancer Res. 2009;11:R7.CrossRefPubMedPubMedCentral Ma XJ, Dahiya S, Richardson E, Erlander M, Sgroi DC. Gene expression profiling of the tumor microenvironment during breast cancer progression. Breast Cancer Res. 2009;11:R7.CrossRefPubMedPubMedCentral
Metadata
Title
Local iron homeostasis in the breast ductal carcinoma microenvironment
Authors
Oriana Marques
Graça Porto
Alexandra Rêma
Fátima Faria
Arnaud Cruz Paula
Maria Gomez-Lazaro
Paula Silva
Berta Martins da Silva
Carlos Lopes
Publication date
01-12-2016
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2016
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-016-2228-y

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