PMID- 26406406 OWN - NLM STAT- MEDLINE DCOM- 20161018 LR - 20220318 IS - 1875-8592 (Electronic) IS - 1574-0153 (Linking) VI - 15 IP - 6 DP - 2015 TI - MiR-4728-3p could act as a marker of HER2 status. PG - 807-14 LID - 10.3233/CBM-150524 [doi] AB - BACKGROUND: MiR-4728 was recently identified to be related with HER2 in several cell lines and limited tissue samples. OBJECTIVE: To investigate whether miR-4728 could predict HER2 status in a larger cohort. METHODS: The expression of miR-4728-3p and miR-4728-5p was identified in breast cancer (BC) and gastric cancer (GC) tissues with different HER2 status using quantitative reverse transcription polymerase chain reaction (qRT-PCR) and fluorescence in situ hybridization (FISH). An additional 22 plasma samples was investigated to explore the potential application of miR-4728 as a non-invasive biomarker in predicting HER2 status. RESULTS: MiR-4728-3p and miR-4728-5p were significantly up-regulated in HER2-positive patients compared with HER2-negative patients. Compared with the expression in adjacent normal tissues, miR-4728-3p and miR-4728-5p were both elevated in HER2-negative and HER2-positive GC tissues but only miR-4728-3p in HER2-positive BC tissues. Further analyses revealed that miR-4728-3p had greater ability than miR-4728-5p in discriminating subgroups with different intensity of HER2 staining in both BC and GC patients. In addition, miR-4728-3p but not miR-4728-5p was significantly up-regulated in plasma of BC patients with positive HER2. CONCLUSIONS: MiR-4728-3p had better ability in distinguishing patients with different status of HER2 than miR-4728-5p. And plasma miR-4728-3p might act as a non-invasive biomarker in predicting HER2 status. FAU - Li, Hai AU - Li H AD - Department of Pathology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Zhou, Xin AU - Zhou X AD - Department of Oncology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Zhu, Jun AU - Zhu J AD - Department of Radiation Oncology, Jiangsu Cancer Hospital, Nanjing, Jiangsu, China. FAU - Cheng, Wenfang AU - Cheng W AD - Department of Gastroenterology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Zhu, Wei AU - Zhu W AD - Department of Oncology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Shu, Yongqian AU - Shu Y AD - Department of Oncology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Liu, Ping AU - Liu P AD - Department of Oncology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China. LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Netherlands TA - Cancer Biomark JT - Cancer biomarkers : section A of Disease markers JID - 101256509 RN - 0 (Biomarkers, Tumor) RN - 0 (MIRN4728 microRNA, human) RN - 0 (MicroRNAs) RN - 0 (RNA, Messenger) RN - 0 (Receptors, Estrogen) RN - 0 (Receptors, Progesterone) RN - EC 2.7.10.1 (ERBB2 protein, human) RN - EC 2.7.10.1 (Receptor, ErbB-2) SB - IM MH - Biomarkers, Tumor/*genetics MH - Breast Neoplasms/*genetics/metabolism/pathology MH - Carcinoma, Ductal, Breast/*genetics/metabolism/pathology MH - Carcinoma, Lobular/*genetics/metabolism/pathology MH - Case-Control Studies MH - Female MH - Follow-Up Studies MH - Gene Expression Regulation, Neoplastic MH - Humans MH - Immunoenzyme Techniques MH - In Situ Hybridization, Fluorescence MH - Male MH - MicroRNAs/*genetics MH - Middle Aged MH - Neoplasm Grading MH - Neoplasm Staging MH - Prognosis MH - RNA, Messenger/genetics MH - Real-Time Polymerase Chain Reaction MH - Receptor, ErbB-2/*genetics/metabolism MH - Receptors, Estrogen/metabolism MH - Receptors, Progesterone/metabolism MH - Reverse Transcriptase Polymerase Chain Reaction MH - Stomach Neoplasms/*genetics/metabolism/pathology OTO - NOTNLM OT - HER2 OT - marker OT - miR-4728 EDAT- 2015/09/26 06:00 MHDA- 2016/10/19 06:00 CRDT- 2015/09/26 06:00 PHST- 2015/09/26 06:00 [entrez] PHST- 2015/09/26 06:00 [pubmed] PHST- 2016/10/19 06:00 [medline] AID - CBM--1-CBM524 [pii] AID - 10.3233/CBM-150524 [doi] PST - ppublish SO - Cancer Biomark. 2015;15(6):807-14. doi: 10.3233/CBM-150524.