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      Progress in the clinical detection of heterogeneity in breast cancer

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          Abstract

          Breast cancer is currently the most common form of cancer and the second‐leading cause of death from cancer in women. Though considerable progress has been made in the treatment of breast cancer, the heterogeneity of tumors (both inter‐ and intratumor) remains a considerable diagnostic and prognostic challenge. From clinical observation to genetic mutations, the history of understanding the heterogeneity of breast cancer is lengthy and detailed. Effectively detecting heterogeneity in breast cancer is important during treatment. Various methods of depicting this heterogeneity are now available and include genetic, pathologic, and imaging analysis. These methods allow characterization of the heterogeneity of breast cancer on a genetic level, providing greater insight during the process of establishing an effective therapeutic plan. This study reviews how the understanding of tumor heterogeneity in breast cancer evolved, and further summarizes recent advances in the detection and monitoring of this heterogeneity in patients with breast cancer.

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          Semiconductor nanocrystals as fluorescent biological labels.

          Semiconductor nanocrystals were prepared for use as fluorescent probes in biological staining and diagnostics. Compared with conventional fluorophores, the nanocrystals have a narrow, tunable, symmetric emission spectrum and are photochemically stable. The advantages of the broad, continuous excitation spectrum were demonstrated in a dual-emission, single-excitation labeling experiment on mouse fibroblasts. These nanocrystal probes are thus complementary and in some cases may be superior to existing fluorophores.
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            Gene expression and benefit of chemotherapy in women with node-negative, estrogen receptor-positive breast cancer.

            The 21-gene recurrence score (RS) assay quantifies the likelihood of distant recurrence in women with estrogen receptor-positive, lymph node-negative breast cancer treated with adjuvant tamoxifen. The relationship between the RS and chemotherapy benefit is not known. The RS was measured in tumors from the tamoxifen-treated and tamoxifen plus chemotherapy-treated patients in the National Surgical Adjuvant Breast and Bowel Project (NSABP) B20 trial. Cox proportional hazards models were utilized to test for interaction between chemotherapy treatment and the RS. A total of 651 patients were assessable (227 randomly assigned to tamoxifen and 424 randomly assigned to tamoxifen plus chemotherapy). The test for interaction between chemotherapy treatment and RS was statistically significant (P = .038). Patients with high-RS (> or = 31) tumors (ie, high risk of recurrence) had a large benefit from chemotherapy (relative risk, 0.26; 95% CI, 0.13 to 0.53; absolute decrease in 10-year distant recurrence rate: mean, 27.6%; SE, 8.0%). Patients with low-RS (< 18) tumors derived minimal, if any, benefit from chemotherapy treatment (relative risk, 1.31; 95% CI, 0.46 to 3.78; absolute decrease in distant recurrence rate at 10 years: mean, -1.1%; SE, 2.2%). Patients with intermediate-RS tumors did not appear to have a large benefit, but the uncertainty in the estimate can not exclude a clinically important benefit. The RS assay not only quantifies the likelihood of breast cancer recurrence in women with node-negative, estrogen receptor-positive breast cancer, but also predicts the magnitude of chemotherapy benefit.
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              Quantitative monitoring of gene expression patterns with a complementary DNA microarray.

              A high-capacity system was developed to monitor the expression of many genes in parallel. Microarrays prepared by high-speed robotic printing of complementary DNAs on glass were used for quantitative expression measurements of the corresponding genes. Because of the small format and high density of the arrays, hybridization volumes of 2 microliters could be used that enabled detection of rare transcripts in probe mixtures derived from 2 micrograms of total cellular messenger RNA. Differential expression measurements of 45 Arabidopsis genes were made by means of simultaneous, two-color fluorescence hybridization.
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                Author and article information

                Contributors
                sun137@sina.com
                Journal
                Cancer Med
                Cancer Med
                10.1002/(ISSN)2045-7634
                CAM4
                Cancer Medicine
                John Wiley and Sons Inc. (Hoboken )
                2045-7634
                24 October 2016
                December 2016
                : 5
                : 12 ( doiID: 10.1002/cam4.2016.5.issue-12 )
                : 3475-3488
                Affiliations
                [ 1 ] Department of Breast and Thyroid SurgeryRenmin Hospital of Wuhan University Wuhan Hubei 430060China
                [ 2 ] Department of PathologyRenmin Hospital of Wuhan University Wuhan Hubei 430060China
                Author notes
                [*] [* ] Correspondence

                Sheng‐Rong Sun, Department of Breast and Thyroid Surgery, Renmin Hospital of Wuhan University, No 238 Jiefang Road, Wuchang District, Wuhan, Hubei 430060, China. Tel: +8613707198696; E‐mail: sun137@ 123456sina.com

                [†]

                These authors contributed equally to this work and should be considered co‐first authors.

                Article
                CAM4943
                10.1002/cam4.943
                5224851
                27774765
                7d8d3752-920d-42fe-8e63-ce93f02ce6d7
                © 2016 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 03 June 2016
                : 22 September 2016
                : 23 September 2016
                Page count
                Figures: 4, Tables: 0, Pages: 14, Words: 9541
                Funding
                Funded by: National Key Scientific Instrument and Equipment Development Project
                Award ID: 20133655893
                Funded by: Natural Science Foundation of Hubei Province
                Award ID: 2013CFB374
                Award ID: 2014CKB509
                Funded by: National Science Foundation of China
                Award ID: 81230031
                Award ID: 81471781
                Categories
                Review
                Clinical Cancer Research
                Reviews
                Custom metadata
                2.0
                cam4943
                December 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.0.0 mode:remove_FC converted:09.01.2017

                Oncology & Radiotherapy
                breast cancer,genomic analysis,heterogeneity,imaging analysis,pathologic analysis

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