Refinement of breast cancer classification by molecular characterization of histological special types

被引:381
作者
Weigelt, B. [1 ]
Horlings, H. M. [1 ]
Kreike, B. [1 ]
Hayes, M. M. [2 ,3 ]
Hauptmann, M. [4 ]
Wessels, L. F. A. [4 ]
de Jong, D. [5 ]
de Vijver, M. J. Van [5 ,6 ]
Van't Veer, L. J. [1 ,5 ]
Peterse, J. L. [5 ]
机构
[1] Netherlands Canc Inst, Div Expt Therapy, NL-1066 CX Amsterdam, Netherlands
[2] British Columbia Canc Agcy, Dept Pathol, Vancouver, BC V5Z 4E6, Canada
[3] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[4] Netherlands Canc Inst, Div Mol Biol, NL-1066 CX Amsterdam, Netherlands
[5] Netherlands Canc Inst, Div Pathol, NL-1066 CX Amsterdam, Netherlands
[6] Univ Amsterdam, Acad Med Ctr, Dept Pathol, NL-1105 AZ Amsterdam, Netherlands
关键词
breast cancer; expression profiling; histological classification; molecular subtypes;
D O I
10.1002/path.2407
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Most invasive breast cancers are classified as invasive ductal carcinoma not otherwise specified (IDC NOS), whereas about 25% are defined as histological 'special types'. These special-type breast cancers are categorized into at least 17 discrete pathological entities; however, whether these also constitute discrete molecular entities remains to be determined. Current therapy decision-making is increasingly governed by the molecular classification of breast cancer (luminal, basal-like, HER2+). The molecular classification is derived from mainly IDC NOS and it is unknown whether this classification applies to all histological subtypes. We aimed to refine the breast cancer classification systems by analysing a series of 11 histological special types [invasive lobular carcinoma (ILC), tubular, mucinous A, mucinous B, neuroendocrine, apocrine, IDC with osteoclastic giant cells, micropapillary, adenoid cystic, metaplastic, and medullary carcinoma] using immunohistochemistry and genome-wide gene expression profiling. Hierarchical clustering analysis confirmed that some histological special types constitute discrete entities, such as micropapillary carcinoma, but also revealed that others, including tubular and lobular carcinoma, are very similar at the transcriptome level. When classified by expression profiling, IDC NOS and ILC contain all molecular breast cancer types (ie luminal, basal-like, HER2+), whereas histological special-type cancers, apart from apocrine carcinoma, are homogeneous and only belong to one molecular subtype. Our analysis also revealed that some special types associated with a good prognosis, such as medullary and adenoid cystic carcinomas, display a poor prognosis basal-like transcriptome, providing strong circumstantial evidence that basal-like cancers constitute a heterogeneous group. Taken together, our results imply that the correct classification of breast cancers of special histological type will allow a more accurate prognostication of breast cancer patients and facilitate the identification of optimal therapeutic strategies. Copyright (C) 2008 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:141 / 150
页数:10
相关论文
共 44 条
  • [1] High frequency of coexistence of columnar cell lesions, lobular neoplasia, and low grade ductal carcinoma in situ with invasive tubular carcinoma and invasive lobular carcinoma
    Abdel-Fatah, Tarek M. A.
    Powe, Desmond G.
    Hodi, Zsolt
    Lee, Andrew H. S.
    Reis-Filho, Jorge S.
    Ellis, Ian O.
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2007, 31 (03) : 417 - 426
  • [2] Adenoid cystic carcinoma of the breast - Molecular markers, treatment, and clinical outcome
    Arpino, G
    Clark, GM
    Mohsin, S
    Bardou, VJ
    Elledge, RM
    [J]. CANCER, 2002, 94 (08) : 2119 - 2127
  • [3] KIT is highly expressed in adenoid cystic carcinoma of the breast, a basal-like carcinoma associated with a favorable outcome
    Azoulay, S
    Laé, M
    Fréneaux, P
    Merle, S
    Al Ghuzlan, A
    Chnecker, C
    Rosty, C
    Klijanienko, J
    Sigal-Zafrani, B
    Salmon, R
    Fourquet, A
    Sastre-Garau, X
    Vincent-Salomon, A
    [J]. MODERN PATHOLOGY, 2005, 18 (12) : 1623 - 1631
  • [4] Gene expression profiling shows medullary breast cancer is a subgroup of basal breast cancers
    Bertucci, Francois
    Finetti, Pascal
    Cervera, Nathalie
    Charafe-Jauffret, Emmanuelle
    Mamessier, Emilie
    Adelaide, Jose
    Debono, Stephane
    Houvenaeghel, Gilles
    Maraninchi, Dominique
    Viens, Patrice
    Charpin, Colette
    Jacquemier, Jocelyne
    Birnbaum, Daniel
    [J]. CANCER RESEARCH, 2006, 66 (09) : 4636 - 4644
  • [5] ENDOCRINE DIFFERENTIATION IN MUCOID CARCINOMA OF THE BREAST
    CAPELLA, C
    EUSEBI, V
    MANN, B
    AZZOPARDI, JG
    [J]. HISTOPATHOLOGY, 1980, 4 (06) : 613 - 630
  • [6] The triple negative paradox: Primary tumor chemosensitivity of breast cancer subtypes
    Carey, Lisa A.
    Dees, E. Claire
    Sawyer, Lynda
    Gatti, Lisa
    Moore, Dominic T.
    Collichio, Frances
    Ollila, David W.
    Sartor, Carolyn I.
    Graham, Mark L.
    Perou, Charles M.
    [J]. CLINICAL CANCER RESEARCH, 2007, 13 (08) : 2329 - 2334
  • [7] Subcellular localization of immunohistochemical signals - Knowledge of the ultrastructural or biologic features of the antigens helps predict the signal localization and proper interpretation of immunostains
    Cheuk, W
    Chan, JKC
    [J]. INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2004, 12 (03) : 185 - 206
  • [8] Paradoxical roles of the immune system during cancer development
    de Visser, KE
    Eichten, A
    Coussens, LM
    [J]. NATURE REVIEWS CANCER, 2006, 6 (01) : 24 - 37
  • [9] Cluster analysis and display of genome-wide expression patterns
    Eisen, MB
    Spellman, PT
    Brown, PO
    Botstein, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) : 14863 - 14868
  • [10] The ductal phenotypic expression of the E-cadherin/catenin complex in tubulolobular carcinoma of the breast: an immunohistochemical and clinicopathologic study
    Esposito, Nicole N.
    Chivukula, Mamatha
    Dabbs, David J.
    [J]. MODERN PATHOLOGY, 2007, 20 (01) : 130 - 138