Serum miR-125b is a non-invasive predictive biomarker of the pre-operative chemoradiotherapy responsiveness in patients with rectal adenocarcinoma

被引:56
作者
D'Angelo, Edoardo [1 ,2 ]
Fassan, Matteo [3 ]
Maretto, Isacco [1 ]
Pucciarelli, Salvatore [1 ]
Zanon, Carlo [4 ]
Digito, Maura [1 ]
Rugge, Massimo [3 ]
Nitti, Donato [1 ]
Agostini, Marco [1 ,2 ,5 ]
机构
[1] Univ Padua, Dept Surg Oncol & Gastroenterol Sci, Padua, Italy
[2] Fdn Citta Speranza, Pediat Res Inst, Nanoinspired Biomed Lab, Padua, Italy
[3] Univ Padua, Surg Pathol & Cytopathol Unit, Dept Med DIMED, Padua, Italy
[4] Citta Speranza, Pediat Res Inst, Neuroblastoma Lab, Padua, Italy
[5] Methodist Hosp, Res Inst, Dept Nanomed, 6535 Fannin, Houston, TX 77030 USA
关键词
rectal cancer; microRNA; miR-125b; circulating; pre-operative chemoradiotherapy; MICRORNA EXPRESSION; NEOADJUVANT CHEMORADIOTHERAPY; COLORECTAL-CANCER; RESISTANCE; STATISTICS; APOPTOSIS; GROWTH; GENES;
D O I
10.18632/oncotarget.8725
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Therapeutic management of Locally Advanced Rectal Cancer (LARC) involves pre-operative chemoradiotherapy (pCRT) followed by surgery. However, after pCRT the complete pathological response is approximately 20%, whereas in 20 to 40% of patients the response is poor or absent. Methods: Cancer biopsy specimens (n=38) and serum samples (n=34) obtained before pCRT from 38 LARC patients were included in the study. Patients were classified in responders (R, tumor regression grade [TRG] 1-2; n=16) and non-responders (NR, TRG 3-5; n=22) according to the pathological response observed upon surgery. We performed miRNA microarrays analysis on biopsy specimens, and validated the selected candidates both by qRT-PCR (tissue and serum) and by in situ hybridization (tissue, miR-125b) analyses. Results: Eleven miRNAs were significantly different between R and NR (miR-154, miR-409-3p, miR-127-3p, miR-214*, miR-299-5p and miR-125b overexpressed in NR; miR-33a, miR-30e, miR-338-3p, miR-200a and miR-378 decreased). In particular, miR-125b resulted to be the best candidate to discriminate the two groups (AUC of 0.9026; 95% CI, 0.7618-1.043). Additionally, miR-125b serum levels were significantly overexpressed in NR patients compared to R (p-value=0.0087), with an excellent discriminating power (AUC of 0.782; 95% CI, 0.6123-0.9518). Conclusions: The obtained results further support the clinical impact of miRNA analysis. High miR-125b expression in tissue and serum were associated with a poor treatment response in LARC patients, therefore miR-125b could be considered as a possible novel non-invasive biomarker of response in LARC treatment.
引用
收藏
页码:28647 / 28657
页数:11
相关论文
共 47 条
[1]   A functional biological network centered on XRCC3: a new possible marker of chemoradiotherapy resistance in rectal cancer patients [J].
Agostini, Marco ;
Zangrando, Andrea ;
Pastrello, Chiara ;
D'Angelo, Edoardo ;
Romano, Gabriele ;
Giovannoni, Roberto ;
Giordan, Marco ;
Maretto, Isacco ;
Bedin, Chiara ;
Zanon, Carlo ;
Digito, Maura ;
Esposito, Giovanni ;
Mescoli, Claudia ;
Lavitrano, Marialuisa ;
Rizzolio, Flavio ;
Jurisica, Igor ;
Giordano, Antonio ;
Pucciarelli, Salvatore ;
Nitti, Donato .
CANCER BIOLOGY & THERAPY, 2015, 16 (08) :1160-1171
[2]  
Agostini Marco, 2014, Front Biosci (Schol Ed), V6, P110
[3]   Dysregulation of microRNA-34a expression causes drug-resistance to 5-FU in human colon cancer DLD-1 cells [J].
Akao, Yukihiro ;
Noguchi, Shunsuke ;
Iio, Akio ;
Kojima, Keitaro ;
Takagi, Takeshi ;
Naoe, Tomoki .
CANCER LETTERS, 2011, 300 (02) :197-204
[4]   Regulation of placenta growth factor by microRNA-125b in hepatocellular cancer [J].
Alpini, Gianfranco ;
Glaser, Shannon S. ;
Zhang, Jing-Ping ;
Francis, Heather ;
Han, Yuyan ;
Gong, Jiao ;
Stokes, Allison ;
Francis, Taylor ;
Hughart, Nathan ;
Hubble, Levi ;
Zhuang, Shi-Mei ;
Meng, Fanyin .
JOURNAL OF HEPATOLOGY, 2011, 55 (06) :1339-1345
[5]   Good guy or bad guy: the opposing roles of microRNA 125b in cancer [J].
Banzhaf-Strathmann, Julia ;
Edbauer, Dieter .
CELL COMMUNICATION AND SIGNALING, 2014, 12
[6]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[7]   Locally advanced rectal cancer: The importance of a multidisciplinary approach [J].
Berardi, Rossana ;
Maccaroni, Elena ;
Onofri, Azzurra ;
Morgese, Francesca ;
Torniai, Mariangela ;
Tiberi, Michela ;
Ferrini, Consuelo ;
Cascinu, Stefano .
WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (46) :17279-17287
[8]   MicroRNA expression patterns to differentiate pancreatic adenocarcinoma from normal pancreas and chronic pancreatitis [J].
Bloomston, Mark ;
Frankel, Wendy L. ;
Petrocca, Fabio ;
Volinia, Stefano ;
Alder, Hansjuerg ;
Hagan, John P. ;
Liu, Chang-Gong ;
Bhatt, Darshna ;
Taccioli, Cristian ;
Croce, Carlo M. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 297 (17) :1901-1908
[9]   miR-192/miR-215 Influence 5-Fluorouracil Resistance through Cell Cycle-Mediated Mechanisms Complementary to Its Post-transcriptional Thymidilate Synthase Regulation [J].
Boni, Valentina ;
Bitarte, Nerea ;
Cristobal, Ion ;
Zarate, Ruth ;
Rodriguez, Javier ;
Maiello, Evaristo ;
Garcia-Foncillas, Jesus ;
Bandres, Eva .
MOLECULAR CANCER THERAPEUTICS, 2010, 9 (08) :2265-2275
[10]   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