| Literature DB >> 28454317 |
Hideyuki Ohzawa1, Atsushi Miki2, Takumi Teratani3, Satomi Shiba1, Yasunaru Sakuma2, Wataru Nishimura4, Yasuko Noda4, Noriyoshi Fukushima5, Hirofumi Fujii6, Yasuo Hozumi1, Hirofumi Mukai7, Yoshikazu Yasuda2.
Abstract
Pathological complete response (pCR) is considered to be a useful prognostic marker for neoadjuvant chemotherapy to improve the survival rate of patients with operable breast cancer. In the present study, we identified differentially expressed microRNAs (miRNAs) between pCR and non-pCR groups of patients with human epidermal growth factor receptor 2 (HER2)-positive breast cancer who received neoadjuvant chemotherapy with trastuzumab. Expression profiles were examined by miRNA microarrays using total RNA extracted from formalin-fixed, paraffin-embedded tissues from pretreatment biopsy specimens. Significant differences were observed in miRNAs associated with pCR between the luminal B-like (HER2-positive) and HER2-positive (nonluminal) subtypes, which were further classified according to their estrogen receptor (ER) status. Prediction models constructed with differentially expressed miRNAs performed well. In conclusion, the combination of miRNA profiles and ER status may improve the accuracy of pCR prediction in patients with HER2-positive breast cancer and enable the development of personalized treatment regimens.Entities:
Keywords: breast cancer; human epidermal growth factor receptor 2; microRNA; neoadjuvant chemotherapy; pathological complete response
Year: 2017 PMID: 28454317 PMCID: PMC5403717 DOI: 10.3892/ol.2017.5628
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967