Skip to main content
Erschienen in: Breast Cancer Research and Treatment 2/2014

01.06.2014 | Preclinical study

Epithelial mesenchymal transition in early invasive breast cancer: an immunohistochemical and reverse phase protein array study

verfasst von: Mohammed A. Aleskandarany, Ola H. Negm, Andrew R. Green, Mohamed A. H. Ahmed, Christopher C. Nolan, Patrick J. Tighe, Ian O. Ellis, Emad A. Rakha

Erschienen in: Breast Cancer Research and Treatment | Ausgabe 2/2014

Einloggen, um Zugang zu erhalten

Abstract

Epithelial mesenchymal transition (EMT), as defined by loss of epithelial characteristics and gain of a mesenchymal phenotype, has been reported in vivo although the occurrence of events remains unclear. This study aims at exploration of EMT portraits of breast cancer (BC) with relevance to different molecular pathways, especially potential EMT triggers and BC molecular subtypes. Immunohistochemical (IHC) expression of markers/triggers of EMT was studied on a well-defined cohort of invasive non-lobular BC (n = 1,035), prepared as tissue microarrays. IHC panel of biomarkers included cadherins (cad; E-cad and N-cad), TGFβ1, PIK3CA, pAkt, and others. Reverse phase protein array (RPPA) was performed for quantitative analysis of proteins extracted from formalin fixed paraffin embedded tissues of a subset of cases from this cohort. Four combinatorial phenotypic groups representing cadherin switch were defined, including E-cad+/N-cad, E-cad/N-cad, E-cad+/N-cad+, and E-cad/N-cad+. Statistically significant association was noticed between these phenotypes and histological tumour grade, tumour type and size and NPI staging classes. The E-cad/N-cad switch occurred more frequently in the triple negative molecular class, both basal and non-basal, and in the HER2+ subtype than in luminal BC. Significant outcome differences were observed between cadherin switch combinatorial groups regarding BCSS and DMFS (p < 0.001). Results of RPPA confirm those observed using IHC regarding differential expressions of EMT markers/triggers. EMT/cadherin switch programs in BC appear to occur in synergy with TGFβ1 and PIK3/Akt pathways activation. These data explain, at translational proteomic level, the molecular heterogeneity and in turn the varied clinical behaviour of BC molecular subtypes. RPPA is a promising high-throughput technique in monitoring subtle quantitative changes in protein expression in archival material.
Literatur
1.
Zurück zum Zitat Thiery JP, Sleeman JP (2006) Complex networks orchestrate epithelial-mesenchymal transitions. Nat Rev Mol Cell Biol 7(2):131–142PubMedCrossRef Thiery JP, Sleeman JP (2006) Complex networks orchestrate epithelial-mesenchymal transitions. Nat Rev Mol Cell Biol 7(2):131–142PubMedCrossRef
2.
Zurück zum Zitat Moustakas A, Heldin CH (2007) Signaling networks guiding epithelial-mesenchymal transitions during embryogenesis and cancer progression. Cancer Sci 98(10):1512–1520PubMedCrossRef Moustakas A, Heldin CH (2007) Signaling networks guiding epithelial-mesenchymal transitions during embryogenesis and cancer progression. Cancer Sci 98(10):1512–1520PubMedCrossRef
3.
Zurück zum Zitat Thiery JP (2002) Epithelial-mesenchymal transitions in tumour progression. Nat Rev Cancer 2(6):442–454PubMedCrossRef Thiery JP (2002) Epithelial-mesenchymal transitions in tumour progression. Nat Rev Cancer 2(6):442–454PubMedCrossRef
4.
Zurück zum Zitat Iwatsuki M et al (2010) Epithelial-mesenchymal transition in cancer development and its clinical significance. Cancer Sci 101(2):293–299PubMedCrossRef Iwatsuki M et al (2010) Epithelial-mesenchymal transition in cancer development and its clinical significance. Cancer Sci 101(2):293–299PubMedCrossRef
7.
Zurück zum Zitat Polyak K, Weinberg RA (2009) Transitions between epithelial and mesenchymal states: acquisition of malignant and stem cell traits. Nat Rev Cancer 9(4):265–273PubMedCrossRef Polyak K, Weinberg RA (2009) Transitions between epithelial and mesenchymal states: acquisition of malignant and stem cell traits. Nat Rev Cancer 9(4):265–273PubMedCrossRef
8.
Zurück zum Zitat Wu Y, Zhou BP (2008) New insights of epithelial-mesenchymal transition in cancer metastasis. Acta Biochim Biophys Sin (Shanghai) 40(7):643–650CrossRef Wu Y, Zhou BP (2008) New insights of epithelial-mesenchymal transition in cancer metastasis. Acta Biochim Biophys Sin (Shanghai) 40(7):643–650CrossRef
9.
Zurück zum Zitat Xue C et al (2003) The gatekeeper effect of epithelial-mesenchymal transition regulates the frequency of breast cancer metastasis. Cancer Res 63(12):3386–3394PubMed Xue C et al (2003) The gatekeeper effect of epithelial-mesenchymal transition regulates the frequency of breast cancer metastasis. Cancer Res 63(12):3386–3394PubMed
10.
Zurück zum Zitat Giampieri S et al (2009) Localized and reversible TGF[beta] signalling switches breast cancer cells from cohesive to single cell motility. Nat Cell Biol 11(11):1287–1296PubMedCentralPubMedCrossRef Giampieri S et al (2009) Localized and reversible TGF[beta] signalling switches breast cancer cells from cohesive to single cell motility. Nat Cell Biol 11(11):1287–1296PubMedCentralPubMedCrossRef
11.
Zurück zum Zitat Tarin D (2005) The fallacy of epithelial mesenchymal transition in neoplasia. Cancer Res 65(14):5996–6001PubMedCrossRef Tarin D (2005) The fallacy of epithelial mesenchymal transition in neoplasia. Cancer Res 65(14):5996–6001PubMedCrossRef
12.
Zurück zum Zitat Wicki A et al (2006) Tumor invasion in the absence of epithelial-mesenchymal transition: podoplanin-mediated remodeling of the actin cytoskeleton. Cancer Cell 9(4):261–272PubMedCrossRef Wicki A et al (2006) Tumor invasion in the absence of epithelial-mesenchymal transition: podoplanin-mediated remodeling of the actin cytoskeleton. Cancer Cell 9(4):261–272PubMedCrossRef
13.
Zurück zum Zitat Tse JC, Kalluri R (2007) Mechanisms of metastasis: epithelial-to-mesenchymal transition and contribution of tumor microenvironment. J Cell Biochem 101(4):816–829PubMedCrossRef Tse JC, Kalluri R (2007) Mechanisms of metastasis: epithelial-to-mesenchymal transition and contribution of tumor microenvironment. J Cell Biochem 101(4):816–829PubMedCrossRef
14.
Zurück zum Zitat Wendt MK, Smith JA, Schiemann WP (2010) Transforming growth factor-beta-induced epithelial-mesenchymal transition facilitates epidermal growth factor-dependent breast cancer progression. Oncogene 29(49):6485–6498PubMedCentralPubMedCrossRef Wendt MK, Smith JA, Schiemann WP (2010) Transforming growth factor-beta-induced epithelial-mesenchymal transition facilitates epidermal growth factor-dependent breast cancer progression. Oncogene 29(49):6485–6498PubMedCentralPubMedCrossRef
15.
Zurück zum Zitat Yang J et al (2004) Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis. Cell 117(7):927–939PubMedCrossRef Yang J et al (2004) Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis. Cell 117(7):927–939PubMedCrossRef
16.
Zurück zum Zitat Lamouille S, Derynck R (2011) Emergence of the phosphoinositide 3-kinase-Akt-mammalian target of rapamycin axis in transforming growth factor-beta-induced epithelial-mesenchymal transition. Cells Tissues Organs 193(1–2):8–22PubMedCrossRef Lamouille S, Derynck R (2011) Emergence of the phosphoinositide 3-kinase-Akt-mammalian target of rapamycin axis in transforming growth factor-beta-induced epithelial-mesenchymal transition. Cells Tissues Organs 193(1–2):8–22PubMedCrossRef
17.
Zurück zum Zitat Albasri A et al (2009) C-terminal Tensin-like (CTEN) is an oncogene which alters cell motility possibly through repression of E-cadherin in colorectal cancer. J Pathol 218(1):57–65PubMedCrossRef Albasri A et al (2009) C-terminal Tensin-like (CTEN) is an oncogene which alters cell motility possibly through repression of E-cadherin in colorectal cancer. J Pathol 218(1):57–65PubMedCrossRef
18.
Zurück zum Zitat Peinado H, Portillo F, Cano A (2004) Transcriptional regulation of cadherins during development and carcinogenesis. Int J Dev Biol 48(5–6):365–375PubMedCrossRef Peinado H, Portillo F, Cano A (2004) Transcriptional regulation of cadherins during development and carcinogenesis. Int J Dev Biol 48(5–6):365–375PubMedCrossRef
19.
20.
Zurück zum Zitat Ahmed N, Thompson EW, Quinn MA (2007) Epithelial-mesenchymal interconversions in normal ovarian surface epithelium and ovarian carcinomas: an exception to the norm. J Cell Physiol 213(3):581–588PubMedCrossRef Ahmed N, Thompson EW, Quinn MA (2007) Epithelial-mesenchymal interconversions in normal ovarian surface epithelium and ovarian carcinomas: an exception to the norm. J Cell Physiol 213(3):581–588PubMedCrossRef
22.
Zurück zum Zitat Lin K et al (2010) The role of B-RAF mutations in melanoma and the induction of EMT via dysregulation of the NF-kappaB/Snail/RKIP/PTEN circuit. Genes Cancer 1(5):409–420PubMedCentralPubMedCrossRef Lin K et al (2010) The role of B-RAF mutations in melanoma and the induction of EMT via dysregulation of the NF-kappaB/Snail/RKIP/PTEN circuit. Genes Cancer 1(5):409–420PubMedCentralPubMedCrossRef
23.
Zurück zum Zitat Sarrio D et al (2008) Epithelial-mesenchymal transition in breast cancer relates to the basal-like phenotype. Cancer Res 68(4):989–997PubMedCrossRef Sarrio D et al (2008) Epithelial-mesenchymal transition in breast cancer relates to the basal-like phenotype. Cancer Res 68(4):989–997PubMedCrossRef
24.
Zurück zum Zitat Spurrier B, Ramalingam S, Nishizuka S (2008) Reverse-phase protein lysate microarrays for cell signaling analysis. Nat Protoc 3(11):1796–1808PubMedCrossRef Spurrier B, Ramalingam S, Nishizuka S (2008) Reverse-phase protein lysate microarrays for cell signaling analysis. Nat Protoc 3(11):1796–1808PubMedCrossRef
25.
Zurück zum Zitat Speer R et al (2007) Development of reverse phase protein microarrays for clinical applications and patient-tailored therapy. Cancer Genomics Proteomics 4(3):157–164PubMed Speer R et al (2007) Development of reverse phase protein microarrays for clinical applications and patient-tailored therapy. Cancer Genomics Proteomics 4(3):157–164PubMed
26.
27.
Zurück zum Zitat Abd El-Rehim DM et al (2005) High-throughput protein expression analysis using tissue microarray technology of a large well-characterised series identifies biologically distinct classes of breast cancer confirming recent cDNA expression analyses. Int J Cancer 116(3):340–350PubMedCrossRef Abd El-Rehim DM et al (2005) High-throughput protein expression analysis using tissue microarray technology of a large well-characterised series identifies biologically distinct classes of breast cancer confirming recent cDNA expression analyses. Int J Cancer 116(3):340–350PubMedCrossRef
28.
Zurück zum Zitat Rakha EA et al (2009) Triple-negative breast cancer: distinguishing between basal and nonbasal subtypes. Clin Cancer Res 15(7):2302–2310PubMedCrossRef Rakha EA et al (2009) Triple-negative breast cancer: distinguishing between basal and nonbasal subtypes. Clin Cancer Res 15(7):2302–2310PubMedCrossRef
29.
Zurück zum Zitat Aleskandarany MA et al (2010) Growth fraction as a predictor of response to chemotherapy in node-negative breast cancer. Int J Cancer 126(7):1761–1769PubMed Aleskandarany MA et al (2010) Growth fraction as a predictor of response to chemotherapy in node-negative breast cancer. Int J Cancer 126(7):1761–1769PubMed
30.
Zurück zum Zitat Sasaki K et al (2009) Significance of twist expression and its association with E-cadherin in esophageal squamous cell carcinoma. J Exp Clin Cancer Res 28:158PubMedCentralPubMedCrossRef Sasaki K et al (2009) Significance of twist expression and its association with E-cadherin in esophageal squamous cell carcinoma. J Exp Clin Cancer Res 28:158PubMedCentralPubMedCrossRef
31.
Zurück zum Zitat Bryan RT, Tselepis C (2010) Cadherin switching and bladder cancer. J Urol 184(2):423–431 Bryan RT, Tselepis C (2010) Cadherin switching and bladder cancer. J Urol 184(2):423–431
32.
Zurück zum Zitat Yilmaz M, Christofori G (2010) Mechanisms of motility in metastasizing cells. Mol Cancer Res 8(5):629–642 Yilmaz M, Christofori G (2010) Mechanisms of motility in metastasizing cells. Mol Cancer Res 8(5):629–642
33.
Zurück zum Zitat McCarty KS Jr et al (1985) Estrogen receptor analyses. Correlation of biochemical and immunohistochemical methods using monoclonal antireceptor antibodies. Arch Pathol Lab Med 109(8):716–721PubMed McCarty KS Jr et al (1985) Estrogen receptor analyses. Correlation of biochemical and immunohistochemical methods using monoclonal antireceptor antibodies. Arch Pathol Lab Med 109(8):716–721PubMed
34.
Zurück zum Zitat Nirmalan NJ et al (2009) Development and validation of a novel protein extraction methodology for quantitation of protein expression in formalin-fixed paraffin-embedded tissues using western blotting. J Pathol 217(4):497–506PubMedCrossRef Nirmalan NJ et al (2009) Development and validation of a novel protein extraction methodology for quantitation of protein expression in formalin-fixed paraffin-embedded tissues using western blotting. J Pathol 217(4):497–506PubMedCrossRef
35.
Zurück zum Zitat Cheang MC et al (2008) Basal-like breast cancer defined by five biomarkers has superior prognostic value than triple-negative phenotype. Clin Cancer Res 14(5):1368–1376PubMedCrossRef Cheang MC et al (2008) Basal-like breast cancer defined by five biomarkers has superior prognostic value than triple-negative phenotype. Clin Cancer Res 14(5):1368–1376PubMedCrossRef
36.
Zurück zum Zitat Nguyen DX, Massague J (2007) Genetic determinants of cancer metastasis. Nat Rev Genet 8(5):341–352PubMedCrossRef Nguyen DX, Massague J (2007) Genetic determinants of cancer metastasis. Nat Rev Genet 8(5):341–352PubMedCrossRef
37.
Zurück zum Zitat Yoder BJ, Wilkinson EJ, Massoll NA (2007) Molecular and morphologic distinctions between infiltrating ductal and lobular carcinoma of the breast. Breast J 13(2):172–179PubMedCrossRef Yoder BJ, Wilkinson EJ, Massoll NA (2007) Molecular and morphologic distinctions between infiltrating ductal and lobular carcinoma of the breast. Breast J 13(2):172–179PubMedCrossRef
38.
Zurück zum Zitat Ellis IO et al (2005) Pathology reporting of breast disease : a joint document incorporating the third edition of the NHS Breast Screening Programme’s Guidelines for pathology reporting in breast cancer screening and the second edition of the Royal College of Pathologists’ minimum dataset for breast cancer histopathology. In: NHS Cancer Screening Programmes, Royal College of Pathologists, London Ellis IO et al (2005) Pathology reporting of breast disease : a joint document incorporating the third edition of the NHS Breast Screening Programme’s Guidelines for pathology reporting in breast cancer screening and the second edition of the Royal College of Pathologists’ minimum dataset for breast cancer histopathology. In: NHS Cancer Screening Programmes, Royal College of Pathologists, London
39.
Zurück zum Zitat Marginean F et al (2010) Histological features of medullary carcinoma and prognosis in triple-negative basal-like carcinomas of the breast. Mod Pathol 23(10):1357–1363PubMedCrossRef Marginean F et al (2010) Histological features of medullary carcinoma and prognosis in triple-negative basal-like carcinomas of the breast. Mod Pathol 23(10):1357–1363PubMedCrossRef
40.
Zurück zum Zitat Aleskandarany M et al (2010) Epithelial mesenchymal transition in invasive breast carcinoma: molecular pathways and relation to molecular subtypes. J Pathol 222(S1):S1–S51CrossRef Aleskandarany M et al (2010) Epithelial mesenchymal transition in invasive breast carcinoma: molecular pathways and relation to molecular subtypes. J Pathol 222(S1):S1–S51CrossRef
41.
Zurück zum Zitat Mahler-Araujo B et al (2008) Reduction of E-cadherin expression is associated with non-lobular breast carcinomas of basal-like and triple negative phenotype. J Clin Pathol 61(5):615–620PubMedCrossRef Mahler-Araujo B et al (2008) Reduction of E-cadherin expression is associated with non-lobular breast carcinomas of basal-like and triple negative phenotype. J Clin Pathol 61(5):615–620PubMedCrossRef
Metadaten
Titel
Epithelial mesenchymal transition in early invasive breast cancer: an immunohistochemical and reverse phase protein array study
verfasst von
Mohammed A. Aleskandarany
Ola H. Negm
Andrew R. Green
Mohamed A. H. Ahmed
Christopher C. Nolan
Patrick J. Tighe
Ian O. Ellis
Emad A. Rakha
Publikationsdatum
01.06.2014
Verlag
Springer US
Erschienen in
Breast Cancer Research and Treatment / Ausgabe 2/2014
Print ISSN: 0167-6806
Elektronische ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-014-2927-5

Weitere Artikel der Ausgabe 2/2014

Breast Cancer Research and Treatment 2/2014 Zur Ausgabe

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.