Tissue and Serum miRNA Profile in Locally Advanced Breast Cancer (LABC) in Response to Neo-Adjuvant Chemotherapy (NAC) Treatment

被引:52
作者
Al-Khanbashi, Manal [1 ]
Caramuta, Stefano [2 ]
Alajmi, Adil M. [3 ]
Al-Haddabi, Ibrahim [4 ]
Al-Riyami, Marwa [4 ]
Lui, Weng-Onn [2 ]
Al-Moundhri, Mansour S. [1 ]
机构
[1] Sultan Qaboos Univ, Dept Med, Coll Med & Hlth Sci, Med Oncol Unit, Muscat, Oman
[2] Karolinska Inst, Karolinska Univ Hosp Solna, Dept Oncol Pathol, Canc Ctr Karolinska, Stockholm, Sweden
[3] Sultan Qaboos Univ, Dept Surg, Coll Med & Hlth Sci, Muscat, Oman
[4] Sultan Qaboos Univ, Dept Pathol, Coll Med, Muscat, Oman
来源
PLOS ONE | 2016年 / 11卷 / 04期
关键词
LYMPH-NODE METASTASIS; GENE-EXPRESSION; DOWN-REGULATION; POTENTIAL ROLE; TUMOR RELAPSE; MICRORNA; SURVIVAL; MIR-21; IDENTIFICATION; BIOMARKERS;
D O I
10.1371/journal.pone.0152032
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction MicroRNAs (miRNAs) are small non-coding RNA that plays a vital role in cancer progression. Neo-adjuvant chemotherapy (NAC) has become the standard of care for locally advanced breast cancer. The aim of this study was to evaluate miRNA alterations during NAC using multiple samples of tissue and serum to correlate miRNA expression with clinico-pathological features and patient outcomes. Methods Tissue and serum samples were collected from patients with locally advanced breast cancer undergoing NAC at four time points: time of diagnosis, after the first and fourth cycle of doxorubicin/cyclophosphamide treatment, and after the fourth cycle of docetaxel administration. First, we evaluated the miRNA expression profiles in tissue and correlated expression with clinico-pathological features. Then, a panel of four miRNAs (miR-451, miR-3200, miR-21, and miR-205) in serum samples was further validated using quantitative reverse-transcription polymerase chain reaction (RT-qPCR). The alterations in serum levels of miRNA, associations with clinical and pathological responses, correlation with clinico-pathological features, and survival outcomes were studied using Friedman, Mann-Whitney U, and Spearman, Wilcoxon signed-ranks tests. P <= 0.05 was considered statistically significant. Results We analyzed 72 tissue samples and 108 serum samples from 9 patients and 27 patients, respectively. MicroRNA expression profiling of tumor versus normal tissue revealed more than 100 differentially expressed miRNAs. Serum miR-451 levels were significantly decreased during treatment, and higher serum levels were associated with improved clinical and pathological responses and disease-free survival. This is one of the early reports on miR-3200 in response to treatment in breast cancer, as serum levels of miR-3200 found to decline during NAC, and higher serum levels were associated with lower residual breast cancer burden and relapse rates at time of diagnosis. Conclusion Variations in serum miRNA levels during NAC treatment may be therapeutically significant for predicting response and survival outcomes.
引用
收藏
页数:22
相关论文
共 46 条
[1]   Direct Serum Assay for MicroRNA-21 Concentrations in Early and Advanced Breast Cancer [J].
Asaga, Sota ;
Kuo, Christine ;
Nguyen, Tung ;
Terpenning, Marilou ;
Giuliano, Armando E. ;
Hoon, Dave S. B. .
CLINICAL CHEMISTRY, 2011, 57 (01) :84-91
[2]  
Ashish B A, 2005, J CANCER RES THER, V1, P21
[3]   Oncogenic miR-181a/b afect the DNA damage response in aggressive breast cancer [J].
Bisso, Andrea ;
Faleschini, Michela ;
Zampa, Federico ;
Capaci, Valeria ;
De Santa, Jacopo ;
Santarpia, Libero ;
Piazza, Silvano ;
Cappelletti, Vera ;
Daidone, Mariagrazia ;
Agami, Reuven ;
Del Sal, Giannino .
CELL CYCLE, 2013, 12 (11) :1679-1687
[4]   Identification of extracellular miRNA in human cerebrospinal fluid by next-generation sequencing [J].
Burgos, Kasandra Lovette ;
Javaherian, Ashkan ;
Bomprezzi, Roberto ;
Ghaffari, Layla ;
Rhodes, Susan ;
Courtright, Amanda ;
Tembe, Waibhav ;
Kim, Seungchan ;
Metpally, Raghu ;
Van Keuren-Jensen, Kendall .
RNA, 2013, 19 (05) :712-722
[5]   Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia [J].
Calin, GA ;
Dumitru, CD ;
Shimizu, M ;
Bichi, R ;
Zupo, S ;
Noch, E ;
Aldler, H ;
Rattan, S ;
Keating, M ;
Rai, K ;
Rassenti, L ;
Kipps, T ;
Negrini, M ;
Bullrich, F ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) :15524-15529
[6]   Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers [J].
Calin, GA ;
Sevignani, C ;
Dan Dumitru, C ;
Hyslop, T ;
Noch, E ;
Yendamuri, S ;
Shimizu, M ;
Rattan, S ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :2999-3004
[7]   Long-term outcome of neoadjuvant therapy for locally advanced breast carcinoma - Effective clinical downstaging allows breast preservation and predicts outstanding local control and survival [J].
Cance, WG ;
Carey, LA ;
Calvo, BF ;
Sartor, C ;
Sawyer, L ;
Moore, DT ;
Rosenman, J ;
Ollila, DW ;
Graham, M .
ANNALS OF SURGERY, 2002, 236 (03) :295-303
[8]   MicroRNAs and Triple Negative Breast Cancer [J].
D'Ippolito, Elvira ;
Iorio, Marilena V. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (11) :22202-22220
[9]   Detection methods for microRNAs in clinic practice [J].
de Planell-Saguer, Mariangels ;
Celina Rodicio, Maria .
CLINICAL BIOCHEMISTRY, 2013, 46 (10-11) :869-878
[10]  
Edge S.B., 2010, AJCC cancer staging manual, V649