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      Novel combination of serum microRNA for detecting breast cancer in the early stage

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          Abstract

          MicroRNA (miRNA), which are stably present in serum, have been reported to be potentially useful for detecting cancer. In the present study, we examined the expression profiles of serum miRNA in several large cohorts to identify novel miRNA that can be used to detect early stage breast cancer. We comprehensively evaluated the serum miRNA expression profiles using highly sensitive microarray analysis. A total of 1280 serum samples of breast cancer patients stored in the National Cancer Center Biobank were used. In addition, 2836 serum samples were obtained from non‐cancer controls, 451 from patients with other types of cancers, and 63 from patients with non‐breast benign diseases. The samples were divided into a training cohort including non‐cancer controls, other cancers and breast cancer, and a test cohort including non‐cancer controls and breast cancer. The training cohort was used to identify a combination of miRNA that could detect breast cancer, and the test cohort was used to validate that combination. miRNA expressions were compared between patients with breast cancer and non‐breast cancer, and a combination of five miRNA (miR‐1246, miR‐1307‐3p, miR‐4634, miR‐6861‐5p and miR‐6875‐5p) was found to be able to detect breast cancer. This combination had a sensitivity of 97.3%, specificity of 82.9% and accuracy of 89.7% for breast cancer in the test cohort. In addition, this combination could detect early stage breast cancer (sensitivity of 98.0% for Tis).

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          DIANA miRPath v.2.0: investigating the combinatorial effect of microRNAs in pathways

          MicroRNAs (miRNAs) are key regulators of diverse biological processes and their functional analysis has been deemed central in many research pipelines. The new version of DIANA-miRPath web server was redesigned from the ground-up. The user of DNA Intelligent Analysis (DIANA) DIANA-miRPath v2.0 can now utilize miRNA targets predicted with high accuracy based on DIANA-microT-CDS and/or experimentally verified targets from TarBase v6; combine results with merging and meta-analysis algorithms; perform hierarchical clustering of miRNAs and pathways based on their interaction levels; as well as elaborate sophisticated visualizations, such as dendrograms or miRNA versus pathway heat maps, from an intuitive and easy to use web interface. New modules enable DIANA-miRPath server to provide information regarding pathogenic single nucleotide polymorphisms (SNPs) in miRNA target sites (SNPs module) or to annotate all the predicted and experimentally validated miRNA targets in a selected molecular pathway (Reverse Search module). DIANA-miRPath v2.0 is an efficient and yet easy to use tool that can be incorporated successfully into miRNA-related analysis pipelines. It provides for the first time a series of highly specific tools for miRNA-targeted pathway analysis via a web interface and can be accessed at http://www.microrna.gr/miRPathv2.
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            Circulating microRNAs as blood-based markers for patients with primary and metastatic breast cancer

            Introduction MicroRNAs (miRs) are interesting new diagnostic targets that may provide important insights into the molecular pathogenesis of breast cancer. Here we evaluated, for the first time, the feasibility and clinical utility of circulating miRs as biomarkers for the detection and staging of breast cancer. Methods The relative concentrations of breast cancer-associated miR10b, miR34a, miR141 and miR155 were measured in the blood serum of 89 patients with primary breast cancer (M0, n = 59) and metastatic disease (M1, n = 30), and 29 healthy women by a TaqMan MicroRNA Assay. Results The relative concentrations of total RNA (P = 0.0001) and miR155 (P = 0.0001) in serum significantly discriminated M0-patients from healthy women, whereas miR10b (P = 0.005), miR34a (P = 0.001) and miR155 (P = 0.008) discriminated M1-patients from healthy controls. In breast cancer patients, the changes in the levels of total RNA (P = 0.0001), miR10b (P = 0.01), miR34a (P = 0.003) and miR155 (P = 0.002) correlated with the presence of overt metastases. Within the M0-cohort, patients at advanced tumor stages (pT3 to 4) had significantly more total RNA (P = 0.0001) and miR34a (P = 0.01) in their blood than patients at early tumor stages (pT1 to 2). Conclusions This pilot study provides first evidence that tumor-associated circulating miRs are elevated in the blood of breast cancer patients and associated with tumor progression.
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              Identification of circulating microRNA signatures for breast cancer detection.

              There is a quest for novel noninvasive diagnostic markers for the detection of breast cancer. The goal of this study is to identify circulating microRNA (miRNA) signatures using a cohort of Asian Chinese patients with breast cancer, and to compare miRNA profiles between tumor and serum samples. miRNA from paired breast cancer tumors, normal tissue, and serum samples derived from 32 patients were comprehensively profiled using microarrays or locked nucleic acid real-time PCR panels. Serum samples from healthy individuals (n = 22) were also used as normal controls. Significant serum miRNAs, identified by logistic regression, were validated in an independent set of serum samples from patients (n = 132) and healthy controls (n = 101). The 20 most significant miRNAs differentially expressed in breast cancer tumors included miRNA (miR)-21, miR-10b, and miR-145, previously shown to be dysregulated in breast cancer. Only 7 miRNAs were overexpressed in both tumors and serum, suggesting that miRNAs may be released into the serum selectively. Interestingly, 16 of the 20 most significant miRNAs differentially expressed in serum samples were novel. MiR-1, miR-92a, miR-133a, and miR-133b were identified as the most important diagnostic markers, and were successfully validated; receiver operating characteristic curves derived from combinations of these miRNAs exhibited areas under the curves of 0.90 to 0.91. The clinical use of miRNA signatures as a noninvasive diagnostic strategy is promising, but should be further validated for different subtypes of breast cancers. ©2013 AACR.
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                Author and article information

                Journal
                Cancer Sci
                Cancer Sci
                10.1111/(ISSN)1349-7006
                CAS
                Cancer Science
                John Wiley and Sons Inc. (Hoboken )
                1347-9032
                1349-7006
                04 March 2016
                March 2016
                : 107
                : 3 ( doiID: 10.1111/cas.2016.107.issue-3 )
                : 326-334
                Affiliations
                [ 1 ] Department of Breast and Medical OncologyNational Cancer Center Hospital TokyoJapan
                [ 2 ] Department of Medical Oncology and Translational ResearchGraduate School of Medical Sciences Kumamoto University KumamotoJapan
                [ 3 ] Department of Breast SurgeryNational Cancer Center Hospital TokyoJapan
                [ 4 ]New Frontiers Research Institute, Toray Industries KanagawaJapan
                [ 5 ] Division of GeneticsFundamental Innovative Oncology Core Center National Cancer Center Research Institute TokyoJapan
                [ 6 ] Division of Molecular and Cellular MedicineFundamental Innovative Oncology Core Center National Cancer Center Research Institute TokyoJapan
                [ 7 ] Department of Functional AnalysisFundamental Innovative Oncology Core Center National Cancer Center Research Institute TokyoJapan
                [ 8 ] Medical Genome CenterNational Center for Geriatrics and Gerontology AichiJapan
                Author notes
                [*] [* ] Correspondence

                Takahiro Ochiya, Division of Molecular and Cellular Medicine, National Cancer Center Research Institute, 5‐1‐1, Tsukiji, Chuo‐ku, Tokyo 104‐0045, Japan.

                Tel: +81‐3‐3542‐2511; Fax: +81‐3‐5565‐0727;

                E‐mail: tochiya@ 123456ncc.go.jp

                Article
                CAS12880
                10.1111/cas.12880
                4814263
                26749252
                6cea4928-3b0b-4d1e-88c4-19165e597d9b
                © 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 02 September 2015
                : 23 December 2015
                : 03 January 2016
                Page count
                Pages: 9
                Funding
                Funded by: New Energy and Industrial Technology Development Organization
                Funded by: National Cancer Center Research and Development Fund
                Award ID: 23‐A‐16
                Award ID: 23‐A‐21
                Award ID: 26‐A‐4
                Funded by: Ministry of Health, Labour and Welfare of Japan
                Award ID: 14S‐3
                Award ID: 14S‐4
                Award ID: 17S‐3
                Award ID: 17S‐5
                Award ID: 20S‐3
                Award ID: 20S‐6
                Funded by: Japan Agency for Medical Research and Development
                Categories
                Original Article
                Original Articles
                Clinical Research
                Custom metadata
                2.0
                cas12880
                March 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.8.5 mode:remove_FC converted:30.03.2016

                Oncology & Radiotherapy
                biomarker,breast cancer,cancer screening,liquid biopsy,microrna
                Oncology & Radiotherapy
                biomarker, breast cancer, cancer screening, liquid biopsy, microrna

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