Abstract

Trastuzumab is established as standard care for patients with HER2-positive breast cancer both in the adjuvant and metastatic setting. However, 50% of the patients do not respond to the trastuzumab therapy, and therefore new predictive biomarkers are highly warranted. MicroRNAs (miRs) constitute a new group of biomarkers and their cellular expression can be determined in tumor samples by in situ hybridization (ISH) analysis. miR-21 is highly prevalent and up-regulated in breast cancer and has been linked to drug resistance in clinical and in vitro settings. To determine expression patterns of miR-21 in high-grade breast cancers, we examined miR-21 expression in 22 HER2-positive tumors and 15 HER2-negative high-grade tumors by ISH. The histological examination indicated that patient samples could be divided into three major expression patterns: miR-21 predominantly in tumor stroma, predominantly in cancer cells, or in both stromal and cancer cells. There was no obvious difference between the HER2-positive and HER2-negative tumors in terms of the miR-21 expression patterns and intensities. To explore the possibility that miR-21 expression levels and/or cellular localization could predict resistance to adjuvant trastuzumab in HER2-positive breast cancer patients, we analyzed additional 16 HER2-positive tumors from patients who were treated with trastuzumab in the adjuvant setting. Eight of the 16 patients showed clinical recurrence and were considered resistant. Examination of the miR-21 expression patterns and intensities revealed no association between the miR-21 scores in the cancer cell population (p = 0.69) or the stromal cells population (p = 0.13) and recurrent disease after adjuvant trastuzumab. Thus, our findings show that elevated miR-21 expression does not predict resistance to adjuvant trastuzumab.

Highlights

  • The human epidermal growth factor receptor-2 (HER2, NEU, and c-ERBB-2) is a cell surface receptor tyrosine kinase that is strongly up-regulated in more than 15% of all breast cancers [1], and breast cancer patients with HER2 overexpressing tumors have poor prognosis [2, 3]

  • MicroRNA-21 is one of the most prevalent miRs in solid tumors, and increased expression levels are associated with poor prognosis both in untreated early-stage colon cancer patients [8, 10, 15] and in breast and colon cancer patients treated with chemotherapy [8, 9, 36, 37]

  • We show that miR-21 is highly expressed in high-grade breast cancers, both in HER2positive and negative cases, and that miR-21 in situ hybridization (ISH) signal can be seen in both stromal cells and cancer cells in varying expression levels

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Summary

Introduction

The human epidermal growth factor receptor-2 (HER2, NEU, and c-ERBB-2) is a cell surface receptor tyrosine kinase that is strongly up-regulated in more than 15% of all breast cancers [1], and breast cancer patients with HER2 overexpressing tumors have poor prognosis [2, 3]. HER2-directed therapy using the humanized monoclonal antibody, trastuzumab in combination with conventional chemotherapy, improves overall survival in patients with HER2-positive breast cancers [4]. MiR-21 expression is highly increased in malignant tumors, including breast, colon, lung, and brain cancer [6, 7], and high expression levels are associated with poor prognosis [8,9,10,11]. ISH studies of tissue from breast, colon, brain, pancreas, and esophagus cancer [10,11,12,13,14] have shown that miR-21 is predominantly expressed in the stromal cells; subpopulations of miR-21 positive cancer cells are reported [10, 11, 15]

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