Predictive and Prognostic Value of Selected MicroRNAs in Luminal Breast Cancer

被引:40
作者
Amorim, Maria [1 ,2 ]
Lobo, Joao [1 ,3 ,4 ]
Fontes-Sousa, Mario [1 ,5 ]
Estevao-Pereira, Helena [1 ,2 ]
Salta, Sofia [1 ]
Lopes, Paula [1 ,3 ]
Coimbra, Nuno [1 ,3 ,4 ]
Antunes, Luis [6 ]
de Souse, Susana Palma [5 ]
Henrique, Rui [1 ,3 ,4 ]
Jeronimo, Carmen [1 ,4 ]
机构
[1] Portuguese Oncol Inst Porto IPO Porto, IPO Porto Res Ctr CI IPOP, Canc Biol & Epigenet Grp, Porto, Portugal
[2] Univ Porto, ICBAS, Inst Biomed Sci Abel Salazar, Oncol, Porto, Portugal
[3] Portuguese Oncol Inst Porto, Dept Pathol, Porto, Portugal
[4] Univ Porto, ICBAS, Inst Biomed Sci Abel Salazar, Dept Pathol & Mol Immunol, Porto, Portugal
[5] Portuguese Oncol Inst Porto, Dept Med Oncol, Porto, Portugal
[6] Portuguese Oncol Inst Porto, Dept Epidemiol, Porto, Portugal
关键词
Breast cancer; luminal subtype; endocrine therapy; endocrine resistance; biomarkers; microRNAs; ENDOCRINE RESISTANCE; TAMOXIFEN RESISTANCE; MOLECULAR PORTRAITS; DIFFERENTIAL EXPRESSION; BETA-CATENIN; PROMOTES EMT; SURVIVAL; MECHANISMS; SUBTYPES; FAMILY;
D O I
10.3389/fgene.2019.00815
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Breast cancer (BrC) is the most frequent malignancy and the leading cause of cancer death among women worldwide. Approximately 70% of BrC are classified as luminal-like subtype, expressing the estrogen receptor. One of the most common and effective adjuvant therapies for this BrC subtype is endocrine therapy. However, its effectiveness is limited, with relapse occurring in up to 40% of patients. Because microRNAs have been associated with several mechanisms underlying endocrine resistance and sensitivity, they may serve as predictive and/or prognostic biomarkers in this setting. Hence, the main goal of this study was to investigate whether miRNAs deregulated in endocrine-resistant BrC may be clinically relevant as prognostic and predictive biomarkers in patients treated with adjuvant endocrine therapy. A global expression assay allowed for the identification of microRNAs differentially expressed between luminal BrC patients with or without recurrence after endocrine adjuvant therapy. Then, six microRNAs were chosen for validation using quantitative reverse transcription polymerase chain reaction in a larger set of tissue samples. Thus, miR-30c-5p, miR-30b-5p, miR-182-5p, and miR-200b-3p were found to be independent predictors of clinical benefit from endocrine therapy. Moreover, miR-182-5p and miR-200b-3p displayed independent prognostic value for disease recurrence in luminal BrC patients after endocrine therapy. Our results indicate that selected miRNAs' panels may constitute clinically useful ancillary tools for management of luminal BrC patients. Nevertheless, additional validation, ideally in a multicentric setting, is required to confirm our findings.
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页数:16
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共 68 条
[1]   Overcoming endocrine resistance in hormone receptor-positive breast cancer [J].
AlFakeeh, A. ;
Brezden-Masley, C. .
CURRENT ONCOLOGY, 2018, 25 :S18-S27
[2]   Decoding the usefulness of non-coding RNAs as breast cancer markers [J].
Amorim, Maria ;
Salta, Sofia ;
Henrique, Rui ;
Jeronimo, Carmen .
JOURNAL OF TRANSLATIONAL MEDICINE, 2016, 14
[3]   Stepwise analysis of MIR9 loci identifies miR-9-5p to be involved in Oestrogen regulated pathways in breast cancer patients [J].
Barbano, Raffaela ;
Pasculli, Barbara ;
Rendina, Michelina ;
Fontana, Andrea ;
Fusilli, Caterina ;
Copetti, Massimiliano ;
Castellana, Stefano ;
Valori, Vanna Maria ;
Morritti, Maria ;
Graziano, Paolo ;
Luigi, Ciuffreda ;
Coco, Michelina ;
Picardo, Francesco ;
Mazza, Tommaso ;
Evron, Ella ;
Murgo, Roberto ;
Maiello, Evaristo ;
Esteller, Manel ;
Fazio, Vito Michele ;
Parrella, Paola .
SCIENTIFIC REPORTS, 2017, 7
[4]   MicroRNA-30c inhibits human breast tumour chemotherapy resistance by regulating TWF1 and IL-11 [J].
Bockhorn, Jessica ;
Dalton, Rachel ;
Nwachukwu, Chika ;
Huang, Simo ;
Prat, Aleix ;
Yee, Kathy ;
Chang, Ya-Fang ;
Huo, Dezheng ;
Wen, Yujia ;
Swanson, Kaitlin E. ;
Qiu, Tyler ;
Lu, Jun ;
Park, Seo Young ;
Dolan, M. Eileen ;
Perou, Charles M. ;
Olopade, Olufunmilayo I. ;
Clarke, Michael F. ;
Greene, Geoffrey L. ;
Liu, Huiping .
NATURE COMMUNICATIONS, 2013, 4
[5]   MicroRNA-519a-3p mediates apoptosis resistance in breast cancer cells and their escape from recognition by natural killer cells [J].
Breunig, Christian ;
Pahl, Jens ;
Kueblbeck, Moritz ;
Miller, Matthias ;
Antonelli, Daniela ;
Erdem, Nese ;
Wirth, Cornelia ;
Will, Rainer ;
Bott, Alexander ;
Cerwenka, Adelheid ;
Wiemann, Stefan .
CELL DEATH & DISEASE, 2017, 8 :e2973-e2973
[6]   A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells [J].
Burk, Ulrike ;
Schubert, Joerg ;
Wellner, Ulrich ;
Schmalhofer, Otto ;
Vincan, Elizabeth ;
Spaderna, Simone ;
Brabletz, Thomas .
EMBO REPORTS, 2008, 9 (06) :582-589
[7]   3rd ESO-ESMO international consensus guidelines for Advanced Breast Cancer (ABC 3) [J].
Cardoso, F. ;
Costa, A. ;
Senkus, E. ;
Aapro, M. ;
Andre, F. ;
Barrios, C. H. ;
Bergh, J. ;
Bhattacharyya, G. ;
Biganzoli, L. ;
Cardoso, M. J. ;
Carey, L. ;
Corneliussen-James, D. ;
Curigliano, G. ;
Dieras, V. ;
El Saghir, N. ;
Eniu, A. ;
Fallowfield, L. ;
Fenech, D. ;
Francis, P. ;
Gelmon, K. ;
Gennari, A. ;
Harbeck, N. ;
Hudis, C. ;
Kaufman, B. ;
Krop, I. ;
Mayer, M. ;
Meijer, H. ;
Mertz, S. ;
Ohno, S. ;
Pagani, O. ;
Papadopoulos, E. ;
Peccatori, F. ;
Pernault-Llorca, F. ;
Piccart, M. J. ;
Pierga, J. Y. ;
Rugo, H. ;
Shockney, L. ;
Sledge, G. ;
Swain, S. ;
Thomssen, C. ;
Tutt, A. ;
Vorobiof, D. ;
Xu, B. ;
Norton, L. ;
Winer, E. .
BREAST, 2017, 31 :244-259
[8]   Using microRNAs as Novel Predictors of Urologic Cancer Survival: An Integrated Analysis [J].
Chen, Zhicong ;
Zhan, Yonghao ;
Chi, Jieshan ;
Guo, Shuyuan ;
Zhong, Xinliang ;
He, Anbang ;
Zheng, Jianrong ;
Gong, Yanqing ;
Li, Xuesong ;
Zhou, Liqun .
EBIOMEDICINE, 2018, 34 :94-107
[9]   MicroRNA-30a inhibits cell migration and invasion by downregulating vimentin expression and is a potential prognostic marker in breast cancer [J].
Cheng, Chun-Wen ;
Wang, Hsiao-Wei ;
Chang, Chia-Wei ;
Chu, Hou-Wei ;
Chen, Cheng-You ;
Yu, Jyh-Cherng ;
Chao, Jui-I ;
Liu, Huei-Fang ;
Ding, Shian-ling ;
Shen, Chen-Yang .
BREAST CANCER RESEARCH AND TREATMENT, 2012, 134 (03) :1081-1093
[10]   Up-regulation of miR-182 by β-catenin in breast cancer increases tumorigenicity and invasiveness by targeting the matrix metalloproteinase inhibitor RECK [J].
Chiang, Chi-Hsiang ;
Hou, Ming-Feng ;
Hung, Wen-Chun .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2013, 1830 (04) :3067-3076