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BMC Genomics. 2014 Jul 17;15(1):605. doi: 10.1186/1471-2164-15-605.
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Personalized therapy for breast cancer.乳腺癌的个性化治疗。
Clin Genet. 2014 Jul;86(1):62-7. doi: 10.1111/cge.12381. Epub 2014 Apr 9.
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Breast tumor subgroups reveal diverse clinical prognostic power.乳腺肿瘤亚组揭示了不同的临床预后能力。
Sci Rep. 2014 Feb 6;4:4002. doi: 10.1038/srep04002.
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The somatic genomic landscape of glioblastoma.胶质母细胞瘤的体细胞基因组景观。
Cell. 2013 Oct 10;155(2):462-77. doi: 10.1016/j.cell.2013.09.034.
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VisANT 4.0: Integrative network platform to connect genes, drugs, diseases and therapies.VisANT 4.0:连接基因、药物、疾病和疗法的综合网络平台。
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Integrative pathway analysis of genome-wide association studies and gene expression data in prostate cancer.前列腺癌全基因组关联研究与基因表达数据的整合通路分析
BMC Syst Biol. 2012;6 Suppl 3(Suppl 3):S13. doi: 10.1186/1752-0509-6-S3-S13. Epub 2012 Dec 17.
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Comprehensive molecular portraits of human breast tumours.人类乳腺肿瘤的全面分子特征图谱。
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MuSiC: identifying mutational significance in cancer genomes.MuSiC:识别癌症基因组中的突变意义。
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突变通路作为乳腺癌辅助治疗的指导

Mutated Pathways as a Guide to Adjuvant Therapy Treatments for Breast Cancer.

作者信息

Liu Yang, Hu Zhenjun, DeLisi Charles

机构信息

Bioinformatics Graduate Program and Department of Biomedical Engineering, Boston University, Boston, Massachusetts.

出版信息

Mol Cancer Ther. 2016 Jan;15(1):184-9. doi: 10.1158/1535-7163.MCT-15-0601. Epub 2015 Dec 1.

DOI:10.1158/1535-7163.MCT-15-0601
PMID:26625895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4707054/
Abstract

Adjuvant therapy following breast cancer surgery generally consists of either a course of chemotherapy, if the cancer lacks hormone receptors, or a course of hormonal therapy, otherwise. Here, we report a correlation between adjuvant strategy and mutated pathway patterns. In particular, we find that for breast cancer patients, pathways enriched in nonsynonymous mutations in the chemotherapy group are distinct from those of the hormonal therapy group. We apply a recently developed method that identifies collaborative pathway groups for hormone and chemotherapy patients. A collaborative group of pathways is one in which each member is altered in the same-generally large-number of samples. In particular, we find the following: (i) a chemotherapy group consisting of three pathways and a hormone therapy group consisting of 20, the members of the two groups being mutually exclusive; (ii) each group is highly enriched in breast cancer drivers; and (iii) the pathway groups are correlates of subtype-based therapeutic recommendations. These results suggest that patient profiling using these pathway groups can potentially enable the development of personalized treatment plans that may be more accurate and specific than those currently available.

摘要

乳腺癌手术后的辅助治疗通常包括

如果癌症缺乏激素受体,则进行一个疗程的化疗;否则,进行一个疗程的激素治疗。在此,我们报告辅助治疗策略与突变通路模式之间的相关性。具体而言,我们发现对于乳腺癌患者,化疗组中富含非同义突变的通路与激素治疗组的不同。我们应用一种最近开发的方法来识别激素治疗和化疗患者的协同通路组。协同通路组是指其中每个成员在相同数量(通常是大量)的样本中发生改变的组。具体而言,我们发现以下几点:(i)一个由三条通路组成的化疗组和一个由20条通路组成的激素治疗组,两组成员相互排斥;(ii)每组在乳腺癌驱动因素中高度富集;(iii)通路组与基于亚型的治疗建议相关。这些结果表明,使用这些通路组对患者进行分析有可能制定出比目前可用的治疗方案更准确、更具体的个性化治疗计划。