Biologic markers in axillary node-negative breast cancer: Differential expression in invasive ductal carcinoma versus invasive lobular carcinoma

Ana Maria Gonzalez-Angulo*, Aysegul Sahin, Savitry Krishnamurthy, Ying Yang, Shu Wan Kau, Gabriel N. Hortobagyi, Massimo Cristofanilli

*Corresponding author for this work

Research output: Contribution to journalArticle

21 Scopus citations

Abstract

Purpose: The objective of this study was to compare the differential expression of established histopathologic and biologic markers of proliferation, apoptosis, and angiogenesis in invasive lobular carcinoma (ILC) and invasive ductal carcinoma (IDC) in a group of axillary node-negative breast cancers. Patients and Methods: Two hundred twenty patients with axillary node-negative ILC and IDC who underwent surgery at the University of Texas M. D. Anderson Cancer Center between 1978 and 1995 had tissue available for analysis. Of these, 206 (94%) had IDC and 14 (6%) had ILC. Estrogen receptors, progesterone receptors, tumor and stromal expression of vascular endothelial growth factor receptor 2, CD44, laminin-5, E-cadherin, and topoisomerase-2 were evaluated by immunohistochemical analysis. HER2/neu and α6β4 integrin were evaluated by in situ hybridization. The Fisher exact test was used to calculate significant differences between ILC and IDC. Median age was 59 years. Results: Invasive lobular carcinoma was more likely to occur in patients aged > 50 years. Invasive lobular carcinoma tended to be > 2 cm (50% vs. 39%), have a nuclear grade of 1/2 (100% vs. 72%), be estrogen receptor positive (93% vs. 70%), HER2/neu negative (92% vs. 68%), have high CD44 expression (31% vs. 16%), low stromal vascular endothelial growth factor receptor 2 expression (36% vs. 47%), no E-cadherin expression (0 vs. 90%), and low laminin-5 expression (15% vs. 25%), compared with IDC. Conclusion: Invasive lobular carcinoma and IDC might be distinct histologic types of breast cancer with different expression of biologic markers. These differences, not all being statistically significant in this small study, might generate hypotheses to develop tailored options for future systemic therapy.

Original languageEnglish (US)
Pages (from-to)396-400
Number of pages5
JournalClinical breast cancer
Volume7
Issue number5
DOIs
StatePublished - Dec 2006

Keywords

  • CD44
  • E-cadherin

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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