Quantum dots-based molecular classification of breast cancer by quantitative spectroanalysis of hormone receptors and HER2

被引:81
作者
Chen, Chuang [1 ,2 ,3 ]
Sun, Sheng-Rong [4 ]
Gong, Yi-Ping [5 ]
Qi, Chu-Bo [6 ]
Peng, Chun-Wei [1 ,2 ,3 ]
Yang, Xue-Qin [1 ,2 ,3 ]
Liu, Shao-Ping [1 ,2 ,3 ]
Peng, Jun [7 ,8 ]
Zhu, Shan [4 ]
Hu, Ming-Bai [1 ,2 ,3 ]
Pang, Dai-Wen [9 ,10 ]
Li, Yan [1 ,2 ,3 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Dept Oncol, Wuhan 430071, Peoples R China
[2] Hubei Key Lab Tumor Biol Behav, Wuhan 430071, Peoples R China
[3] Hubei Canc Clin Study Ctr, Wuhan 430071, Peoples R China
[4] Wuhan Univ, Renmin Hosp, Dept Breast & Thyroid Surg, Wuhan 430060, Hubei, Peoples R China
[5] Hubei Canc Hosp, Dept Breast Surg, Wuhan 430079, Hubei, Peoples R China
[6] Hubei Canc Hosp, Dept Pathol, Wuhan 430079, Hubei, Peoples R China
[7] Wuhan Jiayuan Quantum Dots Co Ltd, Wuhan 430074, Peoples R China
[8] Wuhan Tumor Nanometer Diag Engn Res Ctr, Wuhan 430074, Peoples R China
[9] Wuhan Univ, Key Lab Analyt Chem Biol & Med, Minist Educ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[10] Wuhan Univ, State Key Lab Virol, Wuhan 430072, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Quantum dots; Breast carcinoma; Molecular classification; Hormone receptor; HER2; Quantitative analysis; ESTROGEN-RECEPTOR; GENE-EXPRESSION; PROGESTERONE-RECEPTORS; ADJUVANT CHEMOTHERAPY; ENDOCRINE RESISTANCE; TAMOXIFEN; SUBTYPES; THERAPY; IMMUNOHISTOCHEMISTRY; IDENTIFICATION;
D O I
10.1016/j.biomaterials.2011.06.029
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The emerging molecular breast cancer (BC) classification based on key molecules, including hormone receptors (HRs), and human epidermal growth factor receptor 2 (HER2) has been playing an important part of clinical practice guideline. The current molecular classification mainly based on their fingerprints, however, could not provide enough essential information for treatment decision making. The molecular information on both patterns and quantities could be more helpful to heterogeneities understanding for BC personalized medicine. Here we conduct quantitative determination of HRs and HER2 by quantum dots (QDs)-based quantitative spectral analysis, which had excellent consistence with traditional method. Moreover, we establish a new molecular classification system of BC by integrating the quantitative information of HER2 and HRs, which could better reveal BC heterogeneity and identify 5 molecular subtypes with different 5-year prognosis. Furthermore, the emerging 5 molecular subtypes based on simple quantitative molecules information could be as informative as multi-genes analysis in routine practice, and might help formulate a more personalized comprehensive therapy strategy and prognosis prediction. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7592 / 7599
页数:8
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