Skip to main content
Erschienen in: Breast Cancer Research and Treatment 1/2012

01.07.2012 | Review

Molecular insights on basal-like breast cancer

verfasst von: Mev Dominguez Valentin, Sabrina Daniela da Silva, Maud Privat, Moulay Alaoui-Jamali, Yves-Jean Bignon

Erschienen in: Breast Cancer Research and Treatment | Ausgabe 1/2012

Einloggen, um Zugang zu erhalten

Abstract

Molecular classification of breast cancer (BC) identified diverse subgroups that encompass distinct biological behavior and clinical implications, in particular in relation to prognosis, spread, and incidence of recurrence. Basal-like breast cancers (BLBC) compose up to 15% of BC and are characterized by lack of estrogen receptor (ER), progesterone receptor (PR), and HER-2 amplification with expression of basal cytokeratins 5/6, 14, 17, epidermal growth factor receptor (EGFR), and/or c-KIT. There is an overlap in definition between triple-negative BC and BLBC due to the triple-negative profile of BLBC. Also, most BRCA1-associated BCs are BLBC, triple negative, and express basal cytokeratins (5/6, 14, 17) and EGFR. There is a link between sporadic BLBC (occurring in women without germline BRCA1 mutations) with dysfunction of the BRCA1 pathway. Despite the molecular and clinical similarities, these subtypes respond differently to neoadjuvant therapy. BLBCs are associated with an aggressive phenotype, high histological grade, poor clinical behavior, and high rates of recurrences and/or metastasis. Their molecular features render these tumors especially refractory to anti-hormonal-based therapies and the overall prognosis of this subset remains poor. In this article, the molecular profile, genomic, and epigenetic characteristics as well as BRCA1 pathway dysfunction, clinicopathological behavior, and therapeutic options in BLBC are presented, with emphasis on the discordant findings in current literature.
Literatur
1.
Zurück zum Zitat Haupt B, Ro JY, Schwartz MR (2010) Basal-like breast carcinoma: a phenotypically distinct entity. Arch Pathol Lab Med 134:130–133PubMed Haupt B, Ro JY, Schwartz MR (2010) Basal-like breast carcinoma: a phenotypically distinct entity. Arch Pathol Lab Med 134:130–133PubMed
2.
Zurück zum Zitat Rakha EA, El-Sayed ME, Green AR et al (2007) Prognostic markers in triple-negative breast cancer. Cancer 109:25–32PubMedCrossRef Rakha EA, El-Sayed ME, Green AR et al (2007) Prognostic markers in triple-negative breast cancer. Cancer 109:25–32PubMedCrossRef
4.
Zurück zum Zitat Weigelt B, Reis-Filho JS (2010) Molecular profiling currently offers no more than tumour morphology and basic immunohistochemistry. Breast Cancer Res. doi:10.1186/BCR2734 Weigelt B, Reis-Filho JS (2010) Molecular profiling currently offers no more than tumour morphology and basic immunohistochemistry. Breast Cancer Res. doi:10.​1186/​BCR2734
5.
Zurück zum Zitat Perou CM, Sørlie T, Eisen MB et al (2000) Molecular portraits of human breast tumour. Nature 406:747–752PubMedCrossRef Perou CM, Sørlie T, Eisen MB et al (2000) Molecular portraits of human breast tumour. Nature 406:747–752PubMedCrossRef
6.
Zurück zum Zitat Yehiely F, Moyano JV, Evans JR et al (2006) Deconstructing the molecular portrait of basal-like breast cancer. Trends Mol Med 12(11):537–544PubMedCrossRef Yehiely F, Moyano JV, Evans JR et al (2006) Deconstructing the molecular portrait of basal-like breast cancer. Trends Mol Med 12(11):537–544PubMedCrossRef
7.
Zurück zum Zitat Sørlie T, Perou CM, Tibshirani R et al (2001) Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications. Proc Natl Acad Sci USA 98:10869–10874PubMedCrossRef Sørlie T, Perou CM, Tibshirani R et al (2001) Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications. Proc Natl Acad Sci USA 98:10869–10874PubMedCrossRef
8.
Zurück zum Zitat Niemeier LA, Dabbs DJ, Beriwal S et al (2010) Androgen receptor in breast cancer: expression in estrogen receptor-positive tumors and in estrogen receptor-negative tumors with apocrine differentiation. Mod Pathol 23:205–212PubMedCrossRef Niemeier LA, Dabbs DJ, Beriwal S et al (2010) Androgen receptor in breast cancer: expression in estrogen receptor-positive tumors and in estrogen receptor-negative tumors with apocrine differentiation. Mod Pathol 23:205–212PubMedCrossRef
9.
Zurück zum Zitat Irvin WJ Jr, Carey LA (2008) What is triple-negative breast cancer? Eur J Cancer 44:2799–2805PubMedCrossRef Irvin WJ Jr, Carey LA (2008) What is triple-negative breast cancer? Eur J Cancer 44:2799–2805PubMedCrossRef
10.
Zurück zum Zitat Rakha EA, Elsheikh SE, Aleskandarany MA et al (2009) Triple-negative breast cancer: distinguishing between basal and nonbasal subtypes. Clin Cancer Res 15:2302–2310PubMedCrossRef Rakha EA, Elsheikh SE, Aleskandarany MA et al (2009) Triple-negative breast cancer: distinguishing between basal and nonbasal subtypes. Clin Cancer Res 15:2302–2310PubMedCrossRef
11.
Zurück zum Zitat Schneider BP, Winer EP, Foulkes WD et al (2008) Triple-negative breast cancer: risk factors to potential targets. Clin Cancer Res 14:8010–8018 ReviewPubMedCrossRef Schneider BP, Winer EP, Foulkes WD et al (2008) Triple-negative breast cancer: risk factors to potential targets. Clin Cancer Res 14:8010–8018 ReviewPubMedCrossRef
12.
Zurück zum Zitat Gastaldi S, Comoglio PM, Trusolino L (2010) The Met oncogene and basal-like breast cancer: another culprit to watch out for? Breast Cancer Res. doi:10.1186/BCR2617 Gastaldi S, Comoglio PM, Trusolino L (2010) The Met oncogene and basal-like breast cancer: another culprit to watch out for? Breast Cancer Res. doi:10.​1186/​BCR2617
13.
Zurück zum Zitat Herschkowitz JI, Simin K, Weigman VJ et al (2007) Identification of conserved gene expression features between murine mammary carcinoma models and human breast tumors. Genome Biol. doi: 10.1186/gb-2007-8-5-r76 Herschkowitz JI, Simin K, Weigman VJ et al (2007) Identification of conserved gene expression features between murine mammary carcinoma models and human breast tumors. Genome Biol. doi: 10.​1186/​gb-2007-8-5-r76
14.
Zurück zum Zitat Hennessy BT, Gonzalez-Angulo AM, Stemke-Hale K et al (2009) Characterization of a naturally occurring breast cancer subset enriched in epithelial-to-mesenchymal transition and stem cell characteristics. Cancer Res 69:4116–4124PubMedCrossRef Hennessy BT, Gonzalez-Angulo AM, Stemke-Hale K et al (2009) Characterization of a naturally occurring breast cancer subset enriched in epithelial-to-mesenchymal transition and stem cell characteristics. Cancer Res 69:4116–4124PubMedCrossRef
15.
Zurück zum Zitat Prat A, Parker JS, Karginova O et al (2010) Phenotypic and molecular characterization of the claudin-low intrinsic subtype of breast cancer. Breast Cancer Res. doi:10.1186/BCR2635 Prat A, Parker JS, Karginova O et al (2010) Phenotypic and molecular characterization of the claudin-low intrinsic subtype of breast cancer. Breast Cancer Res. doi:10.​1186/​BCR2635
16.
Zurück zum Zitat Herschkowitz JI, Zhao W, Zhang M et al (2011) Breast cancer special feature: comparative oncogenomics identifies breast tumors enriched in functional tumor-initiating cells. Proc Natl Acad Sci USA. doi:10.1073/pnas.1018862108 Herschkowitz JI, Zhao W, Zhang M et al (2011) Breast cancer special feature: comparative oncogenomics identifies breast tumors enriched in functional tumor-initiating cells. Proc Natl Acad Sci USA. doi:10.​1073/​pnas.​1018862108
17.
Zurück zum Zitat Farmer P, Bonnefoi H, Becette V et al (2005) Identification of molecular apocrine breast tumours by microarray analysis. Oncogene 24:4660–4671PubMedCrossRef Farmer P, Bonnefoi H, Becette V et al (2005) Identification of molecular apocrine breast tumours by microarray analysis. Oncogene 24:4660–4671PubMedCrossRef
18.
Zurück zum Zitat Lopez-Garcia MA, Geyer FC, Lacroix-Triki M et al (2010) Breast cancer precursors revisited: molecular features and progression pathways. Histopathology 57:171–192PubMedCrossRef Lopez-Garcia MA, Geyer FC, Lacroix-Triki M et al (2010) Breast cancer precursors revisited: molecular features and progression pathways. Histopathology 57:171–192PubMedCrossRef
19.
Zurück zum Zitat Nielsen TO, Hsu FD, Jensen K et al (2004) Immunohistochemical and clinical characterization of the basal-like subtype of invasive breast carcinoma. Clin Cancer Res 10:5367–5374PubMedCrossRef Nielsen TO, Hsu FD, Jensen K et al (2004) Immunohistochemical and clinical characterization of the basal-like subtype of invasive breast carcinoma. Clin Cancer Res 10:5367–5374PubMedCrossRef
20.
Zurück zum Zitat Sorlie T, Tibshirani R, Parker J et al (2003) Repeated observation of breast tumor subtypes in independent gene expression data sets. Proc Natl Acad Sci USA 100:8418–8423PubMedCrossRef Sorlie T, Tibshirani R, Parker J et al (2003) Repeated observation of breast tumor subtypes in independent gene expression data sets. Proc Natl Acad Sci USA 100:8418–8423PubMedCrossRef
21.
Zurück zum Zitat Böcker W, Bier B, Freytag G et al (1992) An immunohistochemical study of the breast using antibodies to basal and luminal keratins, alpha-smooth muscle actin, vimentin, collagen IV and laminin. Part I: normal breast and benign proliferative lesions. Virchows Arch A Pathol Anat Histopathol 421:315–322PubMedCrossRef Böcker W, Bier B, Freytag G et al (1992) An immunohistochemical study of the breast using antibodies to basal and luminal keratins, alpha-smooth muscle actin, vimentin, collagen IV and laminin. Part I: normal breast and benign proliferative lesions. Virchows Arch A Pathol Anat Histopathol 421:315–322PubMedCrossRef
22.
Zurück zum Zitat Korsching E, Packeisen J, Agelopoulos K et al (2002) Cytogenetic alterations and cytokeratin expression patterns in breast cancer: integrating a new model of breast differentiation into cytogenetic pathways of breast carcinogenesis. Lab Investig 82:1525–1533PubMed Korsching E, Packeisen J, Agelopoulos K et al (2002) Cytogenetic alterations and cytokeratin expression patterns in breast cancer: integrating a new model of breast differentiation into cytogenetic pathways of breast carcinogenesis. Lab Investig 82:1525–1533PubMed
23.
Zurück zum Zitat Choo JR, Nielsen TO (2010) Biomarkers for basal-like breast cancer. Cancers 2:1040–1065CrossRef Choo JR, Nielsen TO (2010) Biomarkers for basal-like breast cancer. Cancers 2:1040–1065CrossRef
24.
Zurück zum Zitat Khramtsov AI, Khramtsova GF, Tretiakova M et al (2010) Wnt/beta-catenin pathway activation is enriched in basal-like breast cancers and predicts poor outcome. Am J Pathol 176:2911–2920PubMedCrossRef Khramtsov AI, Khramtsova GF, Tretiakova M et al (2010) Wnt/beta-catenin pathway activation is enriched in basal-like breast cancers and predicts poor outcome. Am J Pathol 176:2911–2920PubMedCrossRef
25.
Zurück zum Zitat Turashvili G, Bouchal J, Burkadze G et al (2006) Wnt signaling pathway in mammary gland development and carcinogenesis. Pathobiology 73:213–223PubMedCrossRef Turashvili G, Bouchal J, Burkadze G et al (2006) Wnt signaling pathway in mammary gland development and carcinogenesis. Pathobiology 73:213–223PubMedCrossRef
26.
Zurück zum Zitat Rubovszky G, Udvarhelyi N, Horváth Z et al (2010) Triple-negative breast carcinoma—review of current literature. Magy Onkol 54:325–335 ReviewPubMedCrossRef Rubovszky G, Udvarhelyi N, Horváth Z et al (2010) Triple-negative breast carcinoma—review of current literature. Magy Onkol 54:325–335 ReviewPubMedCrossRef
27.
Zurück zum Zitat Honeth G, Bendahl PO, Ringnér M et al (2008) The CD44+/CD24− phenotype is enriched in basal-like breast tumors. Breast Cancer Res. doi:10.1186/BCR2108 Honeth G, Bendahl PO, Ringnér M et al (2008) The CD44+/CD24− phenotype is enriched in basal-like breast tumors. Breast Cancer Res. doi:10.​1186/​BCR2108
28.
Zurück zum Zitat Rakha EA, Reis-Filho JS, Ellis IO (2008) Basal-like breast cancer: a critical review. J Clin Oncol 26:2568–2581 ReviewPubMedCrossRef Rakha EA, Reis-Filho JS, Ellis IO (2008) Basal-like breast cancer: a critical review. J Clin Oncol 26:2568–2581 ReviewPubMedCrossRef
29.
Zurück zum Zitat Kwei KA, Kung Y, Salari K et al (2010) Genomic instability in breast cancer: pathogenesis and clinical implications. Mol Oncol 4:255–256PubMedCrossRef Kwei KA, Kung Y, Salari K et al (2010) Genomic instability in breast cancer: pathogenesis and clinical implications. Mol Oncol 4:255–256PubMedCrossRef
30.
Zurück zum Zitat Bergamaschi A, Kim YH, Wang P et al (2006) Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer. Genes Chromosomes Cancer 45:1033–1040PubMedCrossRef Bergamaschi A, Kim YH, Wang P et al (2006) Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer. Genes Chromosomes Cancer 45:1033–1040PubMedCrossRef
31.
Zurück zum Zitat Toft DJ, Cryns VL (2011) Minireview: basal-like breast cancer: from molecular profiles to targeted therapies. Mol Endocrinol 25:199–211 ReviewPubMedCrossRef Toft DJ, Cryns VL (2011) Minireview: basal-like breast cancer: from molecular profiles to targeted therapies. Mol Endocrinol 25:199–211 ReviewPubMedCrossRef
32.
Zurück zum Zitat Letessier A, Sircoulomb F, Ginestier C et al (2006) Frequency, prognostic impact, and subtype association of 8p12, 8q24, 11q13, 12p13, 17q12, and 20q13 amplifications in breast cancers. BMC Cancer. doi:10.1186/1471-2407-6-245 Letessier A, Sircoulomb F, Ginestier C et al (2006) Frequency, prognostic impact, and subtype association of 8p12, 8q24, 11q13, 12p13, 17q12, and 20q13 amplifications in breast cancers. BMC Cancer. doi:10.​1186/​1471-2407-6-245
33.
Zurück zum Zitat Adélaïde J, Finetti P, Bekhouche I et al (2007) Integrated profiling of basal and luminal breast cancers. Cancer Res 67:11565–11575PubMedCrossRef Adélaïde J, Finetti P, Bekhouche I et al (2007) Integrated profiling of basal and luminal breast cancers. Cancer Res 67:11565–11575PubMedCrossRef
34.
Zurück zum Zitat Wang ZC, Lin M, Wei LJ et al (2004) Loss of heterozygosity and its correlation with expression profiles in subclasses of invasive breast cancers. Cancer Res 64:64–71PubMedCrossRef Wang ZC, Lin M, Wei LJ et al (2004) Loss of heterozygosity and its correlation with expression profiles in subclasses of invasive breast cancers. Cancer Res 64:64–71PubMedCrossRef
35.
Zurück zum Zitat Liu F, Chen X, Allali-Hassan A et al (2009) Discovery of a 2, 4-diamino-7-aminoalkoxyquinazoline as a potent and selective inhibitor of histone lysine methyltransferase G9a. J Med Chem 52:7950–7953PubMedCrossRef Liu F, Chen X, Allali-Hassan A et al (2009) Discovery of a 2, 4-diamino-7-aminoalkoxyquinazoline as a potent and selective inhibitor of histone lysine methyltransferase G9a. J Med Chem 52:7950–7953PubMedCrossRef
36.
Zurück zum Zitat Roll JD, Rivenbark AG, Jones WD et al (2008) DNMT3b overexpression contributes to a hypermethylator phenotype in human breast cancer cell lines. Mol Cancer. doi:10.1186/1476-4598-7-15 Roll JD, Rivenbark AG, Jones WD et al (2008) DNMT3b overexpression contributes to a hypermethylator phenotype in human breast cancer cell lines. Mol Cancer. doi:10.​1186/​1476-4598-7-15
37.
Zurück zum Zitat Parrella P, Poeta ML, Gallo AP et al (2004) Nonrandom distribution of aberrant promoter methylation of cancer-related genes in sporadic breast tumors. Clin Cancer Res 10:5349–5354PubMedCrossRef Parrella P, Poeta ML, Gallo AP et al (2004) Nonrandom distribution of aberrant promoter methylation of cancer-related genes in sporadic breast tumors. Clin Cancer Res 10:5349–5354PubMedCrossRef
38.
Zurück zum Zitat Li S, Rong M, Iacopetta B (2006) DNA hypermethylation in breast cancer and its association with clinicopathological features. Cancer Lett 237:272–280PubMedCrossRef Li S, Rong M, Iacopetta B (2006) DNA hypermethylation in breast cancer and its association with clinicopathological features. Cancer Lett 237:272–280PubMedCrossRef
39.
Zurück zum Zitat Holm K, Hegardt C, Staaf J et al (2010) Molecular subtypes of breast cancer are associated with characteristic DNA methylation patterns. Breast Cancer Res. doi:10.1186/BCR2590 Holm K, Hegardt C, Staaf J et al (2010) Molecular subtypes of breast cancer are associated with characteristic DNA methylation patterns. Breast Cancer Res. doi:10.​1186/​BCR2590
40.
Zurück zum Zitat Bae YK, Brown A, Garrett E et al (2004) Hypermethylation in histologically distinct classes of breast cancer. Clin Cancer Res 10:5998–6005PubMedCrossRef Bae YK, Brown A, Garrett E et al (2004) Hypermethylation in histologically distinct classes of breast cancer. Clin Cancer Res 10:5998–6005PubMedCrossRef
41.
Zurück zum Zitat Dumont N, Wilson MB, Crawford YG et al (2008) Sustained induction of epithelial to mesenchymal transition activates DNA methylation of genes silenced in basal-like breast cancers. Proc Natl Acad Sci USA 105:14867–14872PubMedCrossRef Dumont N, Wilson MB, Crawford YG et al (2008) Sustained induction of epithelial to mesenchymal transition activates DNA methylation of genes silenced in basal-like breast cancers. Proc Natl Acad Sci USA 105:14867–14872PubMedCrossRef
42.
Zurück zum Zitat Elsheikh SE, Green AR, Rakha EA et al (2009) Global histone modifications in breast cancer correlate with tumor phenotypes, prognostic factors, and patient outcome. Cancer Res 69:3802–3809PubMedCrossRef Elsheikh SE, Green AR, Rakha EA et al (2009) Global histone modifications in breast cancer correlate with tumor phenotypes, prognostic factors, and patient outcome. Cancer Res 69:3802–3809PubMedCrossRef
43.
Zurück zum Zitat Van’t Veer LJ, Dai H, van de Vijver MJ et al (2002) Gene expression profiling predicts clinical outcome of breast cancer. Nature 415:530–536CrossRef Van’t Veer LJ, Dai H, van de Vijver MJ et al (2002) Gene expression profiling predicts clinical outcome of breast cancer. Nature 415:530–536CrossRef
44.
Zurück zum Zitat Waddell N, Arnold J, Cocciardi S et al (2010) Subtypes of familial breast tumours revealed by expression and copy number profiling. Breast Cancer Res Treat 123:661–677PubMedCrossRef Waddell N, Arnold J, Cocciardi S et al (2010) Subtypes of familial breast tumours revealed by expression and copy number profiling. Breast Cancer Res Treat 123:661–677PubMedCrossRef
45.
Zurück zum Zitat Hedenfalk I, Ringner M, Ben-Dor A et al (2003) Molecular classification of familial non-BRCA1/BRCA2 breast cancer. Proc Natl Acad Sci USA 100:2532–2537PubMedCrossRef Hedenfalk I, Ringner M, Ben-Dor A et al (2003) Molecular classification of familial non-BRCA1/BRCA2 breast cancer. Proc Natl Acad Sci USA 100:2532–2537PubMedCrossRef
46.
Zurück zum Zitat Sørlie T (2004) Molecular portraits of breast cancer: tumour subtypes as distinct disease entities. Eur J Cancer 40:2667–2675 ReviewPubMedCrossRef Sørlie T (2004) Molecular portraits of breast cancer: tumour subtypes as distinct disease entities. Eur J Cancer 40:2667–2675 ReviewPubMedCrossRef
47.
Zurück zum Zitat Rakha EA, Reis-Filho JS, Ellis IO (2008) Impact of basal-like breast carcinoma determination for a more specific therapy. Pathobiology 75:95–103PubMedCrossRef Rakha EA, Reis-Filho JS, Ellis IO (2008) Impact of basal-like breast carcinoma determination for a more specific therapy. Pathobiology 75:95–103PubMedCrossRef
48.
Zurück zum Zitat Gorski JJ, Kennedy RD, Hosey AM et al (2009) The complex relationship between BRCA1 and ERalpha in hereditary breast cancer. Clin Cancer Res 15:1514–1518PubMedCrossRef Gorski JJ, Kennedy RD, Hosey AM et al (2009) The complex relationship between BRCA1 and ERalpha in hereditary breast cancer. Clin Cancer Res 15:1514–1518PubMedCrossRef
49.
Zurück zum Zitat Ray PS, Wang J, Qu Y et al (2010) FOXC1 is a potential prognostic biomarker with functional significance in basal-like breast cancer. Cancer Res 70:3870–3876PubMedCrossRef Ray PS, Wang J, Qu Y et al (2010) FOXC1 is a potential prognostic biomarker with functional significance in basal-like breast cancer. Cancer Res 70:3870–3876PubMedCrossRef
50.
Zurück zum Zitat Yamamoto Y, Iwase H (2010) Clinicopathological features and treatment strategy for triple-negative breast cancer. Int J Clin Oncol 15(4):341–351PubMedCrossRef Yamamoto Y, Iwase H (2010) Clinicopathological features and treatment strategy for triple-negative breast cancer. Int J Clin Oncol 15(4):341–351PubMedCrossRef
51.
Zurück zum Zitat Kobayashi S (2008) Basal-like subtype of breast cancer: a review of its unique characteristics and their clinical significance. Breast Cancer 15:153–158PubMedCrossRef Kobayashi S (2008) Basal-like subtype of breast cancer: a review of its unique characteristics and their clinical significance. Breast Cancer 15:153–158PubMedCrossRef
52.
Zurück zum Zitat Millikan RC, Newman B, Tse CK, Moorman PG et al (2008) Epidemiology of basal-like breast cancer. Breast Cancer Res Treat 109:123–139PubMedCrossRef Millikan RC, Newman B, Tse CK, Moorman PG et al (2008) Epidemiology of basal-like breast cancer. Breast Cancer Res Treat 109:123–139PubMedCrossRef
53.
Zurück zum Zitat Fong PC, Boss DS, Yap TA et al (2009) Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med 361:123–134PubMedCrossRef Fong PC, Boss DS, Yap TA et al (2009) Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med 361:123–134PubMedCrossRef
54.
Zurück zum Zitat Ismail-Khan R, Bui MM (2010) A review of triple-negative breast cancer. Cancer Control 17:173–176PubMed Ismail-Khan R, Bui MM (2010) A review of triple-negative breast cancer. Cancer Control 17:173–176PubMed
55.
Zurück zum Zitat Dong Y, Li A, Wang J et al (2010) Synthetic lethality through combined Notch-epidermal growth factor receptor pathway inhibition in basal-like breast cancer. Cancer Res 70:5465–5474PubMedCrossRef Dong Y, Li A, Wang J et al (2010) Synthetic lethality through combined Notch-epidermal growth factor receptor pathway inhibition in basal-like breast cancer. Cancer Res 70:5465–5474PubMedCrossRef
56.
Zurück zum Zitat Rodríguez-Pinilla SM, Sarrió D, Honrado E et al (2007) Vimentin and laminin expression is associated with basal-like phenotype in both sporadic and BRCA1-associated breast carcinomas. J Clin Pathol 60:1006–1012PubMedCrossRef Rodríguez-Pinilla SM, Sarrió D, Honrado E et al (2007) Vimentin and laminin expression is associated with basal-like phenotype in both sporadic and BRCA1-associated breast carcinomas. J Clin Pathol 60:1006–1012PubMedCrossRef
57.
Zurück zum Zitat Rodríguez-Pinilla SM, Sarrió D, Honrado E et al (2006) Prognostic significance of basal-like phenotype and fascin expression in node-negative invasive breast carcinomas. Clin Cancer Res 12:1533–1539PubMedCrossRef Rodríguez-Pinilla SM, Sarrió D, Honrado E et al (2006) Prognostic significance of basal-like phenotype and fascin expression in node-negative invasive breast carcinomas. Clin Cancer Res 12:1533–1539PubMedCrossRef
58.
Zurück zum Zitat Li H, Cherukuri P, Li N et al (2007) Nestin is expressed in the basal/myoepithelial layer of the mammary gland and is a selective marker of basal epithelial breast tumors. Cancer Res 67:501–510PubMedCrossRef Li H, Cherukuri P, Li N et al (2007) Nestin is expressed in the basal/myoepithelial layer of the mammary gland and is a selective marker of basal epithelial breast tumors. Cancer Res 67:501–510PubMedCrossRef
59.
Zurück zum Zitat Parry S, Savage K, Marchiò C et al (2008) Nestin is expressed in basal-like and triple negative breast cancers. J Clin Pathol 61:1045–1050PubMedCrossRef Parry S, Savage K, Marchiò C et al (2008) Nestin is expressed in basal-like and triple negative breast cancers. J Clin Pathol 61:1045–1050PubMedCrossRef
60.
Zurück zum Zitat Charafe-Jauffret E, Monville F, Bertucci F et al (2007) Moesin expression is a marker of basal breast carcinomas. Int J Cancer 121:1779–1785PubMedCrossRef Charafe-Jauffret E, Monville F, Bertucci F et al (2007) Moesin expression is a marker of basal breast carcinomas. Int J Cancer 121:1779–1785PubMedCrossRef
61.
Zurück zum Zitat Elsheikh SE, Green AR, Rakha EA et al (2008) Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype. Br J Cancer 99:327–334PubMedCrossRef Elsheikh SE, Green AR, Rakha EA et al (2008) Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype. Br J Cancer 99:327–334PubMedCrossRef
62.
Zurück zum Zitat Pinilla SM, Honrado E, Hardisson D et al (2006) Caveolin-1 expression is associated with a basal-like phenotype in sporadic and hereditary breast cancer. Breast Cancer Res Treat 99:85–90PubMedCrossRef Pinilla SM, Honrado E, Hardisson D et al (2006) Caveolin-1 expression is associated with a basal-like phenotype in sporadic and hereditary breast cancer. Breast Cancer Res Treat 99:85–90PubMedCrossRef
63.
Zurück zum Zitat Savage K, Lambros MB, Robertson D et al (2007) Caveolin 1 is overexpressed and basal-like and metaplastic breast carcinomas: a morphologic, ultrastructural, amplified in a subset of immunohistochemical, and in situ hybridization analysis. Clin Cancer Res 13:90–101PubMedCrossRef Savage K, Lambros MB, Robertson D et al (2007) Caveolin 1 is overexpressed and basal-like and metaplastic breast carcinomas: a morphologic, ultrastructural, amplified in a subset of immunohistochemical, and in situ hybridization analysis. Clin Cancer Res 13:90–101PubMedCrossRef
64.
Zurück zum Zitat Savage K, Leung S, Todd SK et al (2008) Distribution and significance of caveolin 2 expression in normal breast and invasive breast cancer: an immunofluorescence and immunohistochemical analysis. Breast Cancer Res Treat 110:245–256PubMedCrossRef Savage K, Leung S, Todd SK et al (2008) Distribution and significance of caveolin 2 expression in normal breast and invasive breast cancer: an immunofluorescence and immunohistochemical analysis. Breast Cancer Res Treat 110:245–256PubMedCrossRef
65.
Zurück zum Zitat Lu S, Simin K, Khan A et al (2008) Analysis of integrin beta4 expression in human breast cancer: association with basal-like tumors and prognostic significance. Clin Cancer Res 14:1050–1058PubMedCrossRef Lu S, Simin K, Khan A et al (2008) Analysis of integrin beta4 expression in human breast cancer: association with basal-like tumors and prognostic significance. Clin Cancer Res 14:1050–1058PubMedCrossRef
66.
Zurück zum Zitat Reis-Filho JS, Steele D, Di Palma S et al (2006) Distribution and significance of nerve growth factor receptor (NGFR/p75NTR) in normal, benign and malignant breast tissue. Mod Pathol 19:307–319PubMedCrossRef Reis-Filho JS, Steele D, Di Palma S et al (2006) Distribution and significance of nerve growth factor receptor (NGFR/p75NTR) in normal, benign and malignant breast tissue. Mod Pathol 19:307–319PubMedCrossRef
67.
Zurück zum Zitat Hasegawa M, Moritani S, Murakumo Y et al (2008) CD109 expression in basal-like breast carcinoma. Pathol Int 58:288–294PubMedCrossRef Hasegawa M, Moritani S, Murakumo Y et al (2008) CD109 expression in basal-like breast carcinoma. Pathol Int 58:288–294PubMedCrossRef
68.
Zurück zum Zitat Matos I, Dufloth R, Alvarenga M et al (2005) p63, cytokeratin 5, and P-cadherin: three molecular markers to distinguish basal phenotype in breast carcinomas. Virchows Arch 447:688–694PubMedCrossRef Matos I, Dufloth R, Alvarenga M et al (2005) p63, cytokeratin 5, and P-cadherin: three molecular markers to distinguish basal phenotype in breast carcinomas. Virchows Arch 447:688–694PubMedCrossRef
69.
Zurück zum Zitat Paredes J, Lopes N, Milanezi F et al (2007) P-cadherin and cytokeratin 5: useful adjunct markers to distinguish basal-like ductal carcinomas in situ. Virchows Arch 450:73–80PubMedCrossRef Paredes J, Lopes N, Milanezi F et al (2007) P-cadherin and cytokeratin 5: useful adjunct markers to distinguish basal-like ductal carcinomas in situ. Virchows Arch 450:73–80PubMedCrossRef
70.
Zurück zum Zitat Zabouo G, Imbert AM, Jacquemier J et al (2009) CD146 expression is associated with a poor prognosis in human breast tumors and with enhanced motility in breast cancer cell lines. Breast Cancer Res 11:R1PubMedCrossRef Zabouo G, Imbert AM, Jacquemier J et al (2009) CD146 expression is associated with a poor prognosis in human breast tumors and with enhanced motility in breast cancer cell lines. Breast Cancer Res 11:R1PubMedCrossRef
71.
Zurück zum Zitat Klingbeil P, Natrajan R, Everitt G et al (2010) CD44 is overexpressed in basal-like breast cancers but is not a driver of 11p13 amplification. Breast Cancer Res Treat 120:95–109PubMedCrossRef Klingbeil P, Natrajan R, Everitt G et al (2010) CD44 is overexpressed in basal-like breast cancers but is not a driver of 11p13 amplification. Breast Cancer Res Treat 120:95–109PubMedCrossRef
72.
Zurück zum Zitat Viale G, Rotmensz N, Maisonneuve P et al (2009) Invasive ductal carcinoma of the breast with the “triple-negative” phenotype: prognostic implications of EGFR immunoreactivity. Breast Cancer Res Treat 116:317–328PubMedCrossRef Viale G, Rotmensz N, Maisonneuve P et al (2009) Invasive ductal carcinoma of the breast with the “triple-negative” phenotype: prognostic implications of EGFR immunoreactivity. Breast Cancer Res Treat 116:317–328PubMedCrossRef
73.
Zurück zum Zitat Mani SA, Yang J, Brooks M et al (2007) Mesenchyme Forkhead 1 (FOXC2) plays a key role in metastasis and is associated with aggressive basal-like breast cancers. Proc Natl Acad Sci USA 104:10069–10074PubMedCrossRef Mani SA, Yang J, Brooks M et al (2007) Mesenchyme Forkhead 1 (FOXC2) plays a key role in metastasis and is associated with aggressive basal-like breast cancers. Proc Natl Acad Sci USA 104:10069–10074PubMedCrossRef
74.
Zurück zum Zitat Umemura S, Shirane M, Takekoshi S et al (2009) Overexpression of E2F-5 correlates with a pathological basal phenotype and a worse clinical outcome. Br J Cancer 100:764–771PubMedCrossRef Umemura S, Shirane M, Takekoshi S et al (2009) Overexpression of E2F-5 correlates with a pathological basal phenotype and a worse clinical outcome. Br J Cancer 100:764–771PubMedCrossRef
75.
Zurück zum Zitat Ribeiro-Silva A, Ramalho LN, Garcia SB et al (2005) p63 correlates with both BRCA1 and cytokeratin 5 in invasive breast carcinomas: further evidence for the pathogenesis of the basal phenotype of breast cancer. Histopathology 47:458–466PubMedCrossRef Ribeiro-Silva A, Ramalho LN, Garcia SB et al (2005) p63 correlates with both BRCA1 and cytokeratin 5 in invasive breast carcinomas: further evidence for the pathogenesis of the basal phenotype of breast cancer. Histopathology 47:458–466PubMedCrossRef
76.
Zurück zum Zitat Rakha EA, Putti TC, Abd El-Rehim DM et al (2006) Morphological and immunophenotypic analysis of breast carcinomas with basal and myoepithelial differentiation. J Pathol 208:495–506PubMedCrossRef Rakha EA, Putti TC, Abd El-Rehim DM et al (2006) Morphological and immunophenotypic analysis of breast carcinomas with basal and myoepithelial differentiation. J Pathol 208:495–506PubMedCrossRef
77.
Zurück zum Zitat Herschkowitz JI, He X, Fan C et al (2008) The functional loss of the retinoblastoma tumour suppressor is a common event in basal-like and luminal B breast carcinomas. Breast Cancer Res 10(5):R75PubMedCrossRef Herschkowitz JI, He X, Fan C et al (2008) The functional loss of the retinoblastoma tumour suppressor is a common event in basal-like and luminal B breast carcinomas. Breast Cancer Res 10(5):R75PubMedCrossRef
78.
Zurück zum Zitat Kuroda H, Ishida F, Nakai M et al (2008) Basal cytokeratin expression in relation to biological factors in breast cancer. Hum Pathol 39:1744–1750PubMedCrossRef Kuroda H, Ishida F, Nakai M et al (2008) Basal cytokeratin expression in relation to biological factors in breast cancer. Hum Pathol 39:1744–1750PubMedCrossRef
79.
Zurück zum Zitat Walter O, Prasad M, Lu S et al (2009) IMP3 is a novel biomarker for triple negative invasive mammary carcinoma associated with a more aggressive phenotype. Hum Pathol 40:1528–1533PubMedCrossRef Walter O, Prasad M, Lu S et al (2009) IMP3 is a novel biomarker for triple negative invasive mammary carcinoma associated with a more aggressive phenotype. Hum Pathol 40:1528–1533PubMedCrossRef
80.
Zurück zum Zitat Skaland I, Janssen EA, Gudlaugsson E et al (2009) The prognostic value of the proliferation marker phosphohistone H3 (PPH3) in luminal, basal-like and triple negative phenotype invasive lymph node-negative breast cancer. Cell Oncol 31:261–271PubMed Skaland I, Janssen EA, Gudlaugsson E et al (2009) The prognostic value of the proliferation marker phosphohistone H3 (PPH3) in luminal, basal-like and triple negative phenotype invasive lymph node-negative breast cancer. Cell Oncol 31:261–271PubMed
81.
Zurück zum Zitat Zhang H, Rakha EA, Ball GR et al (2010) The proteins FABP7 and OATP2 are associated with the basal phenotype and patient outcome in human breast cancer. Breast Cancer Res Treat 121:41–51PubMedCrossRef Zhang H, Rakha EA, Ball GR et al (2010) The proteins FABP7 and OATP2 are associated with the basal phenotype and patient outcome in human breast cancer. Breast Cancer Res Treat 121:41–51PubMedCrossRef
82.
Zurück zum Zitat Tang XY, Umemura S, Tsukamoto H et al (2010) Overexpression of fatty acid binding protein-7 correlates with basal-like subtype of breast cancer. Pathol Res Pract 206:98–101PubMedCrossRef Tang XY, Umemura S, Tsukamoto H et al (2010) Overexpression of fatty acid binding protein-7 correlates with basal-like subtype of breast cancer. Pathol Res Pract 206:98–101PubMedCrossRef
83.
Zurück zum Zitat Moyano JV, Evans JR, Chen F et al (2006) AlphaB-crystallin is a novel oncoprotein that predicts poor clinical outcome in breast cancer. J Clin Invest 116:261–270PubMedCrossRef Moyano JV, Evans JR, Chen F et al (2006) AlphaB-crystallin is a novel oncoprotein that predicts poor clinical outcome in breast cancer. J Clin Invest 116:261–270PubMedCrossRef
84.
Zurück zum Zitat Sitterding SM, Wiseman WR, Schiller CL et al (2008) AlphaB-crystallin: a novel marker of invasive basal-like and metaplastic breast carcinomas. Ann Diagn Pathol 12:33–40PubMedCrossRef Sitterding SM, Wiseman WR, Schiller CL et al (2008) AlphaB-crystallin: a novel marker of invasive basal-like and metaplastic breast carcinomas. Ann Diagn Pathol 12:33–40PubMedCrossRef
Metadaten
Titel
Molecular insights on basal-like breast cancer
verfasst von
Mev Dominguez Valentin
Sabrina Daniela da Silva
Maud Privat
Moulay Alaoui-Jamali
Yves-Jean Bignon
Publikationsdatum
01.07.2012
Verlag
Springer US
Erschienen in
Breast Cancer Research and Treatment / Ausgabe 1/2012
Print ISSN: 0167-6806
Elektronische ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-011-1934-z

Weitere Artikel der Ausgabe 1/2012

Breast Cancer Research and Treatment 1/2012 Zur Ausgabe

Update Onkologie

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