Exploring molecular links between lymph node invasion and cancer prognosis in human breast cancer

被引:8
作者
Kim, Sangwoo [1 ]
Nam, Hojung [2 ]
Lee, Doheon [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
[2] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
基金
新加坡国家研究基金会;
关键词
GENE-EXPRESSION SIGNATURE; CLINICAL-IMPLICATIONS; METASTASIS; MACROPHAGES; CARCINOMAS; ANGIOGENESIS; PROGRESSION; PROFILES; SURVIVAL; MARKERS;
D O I
10.1186/1752-0509-5-S2-S4
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Background: Lymph node invasion is one of the most powerful clinical factors in cancer prognosis. However, molecular level signatures of their correlation are remaining poorly understood. Here, we propose a new approach, monotonically expressed gene analysis (MEGA), to correlate transcriptional patterns of lymph node invasion related genes with clinical outcome of breast cancer patients. Results: Using MEGA, we scored all genes with their transcriptional patterns over progression levels of lymph node invasion from 278 non-metastatic breast cancer samples. Applied on 65 independent test data, our gene sets of top 20 scores (positive and negative correlations) showed significant associations with prognostic measures such as cancer metastasis, relapse and survival. Our method showed better accuracy than conventional two class comparison methods. We could also find that expression patterns of some genes are strongly associated with stage transition of pathological T and N at specific time. Additionally, some pathways including T-cell immune response and wound healing serum response are expected to be related with cancer progression from pathway enrichment and common motif binding site analyses of the inferred gene sets. Conclusions: By applying MEGA, we can find possible molecular links between lymph node invasion and cancer prognosis in human breast cancer, supported by evidences of feasible gene expression patterns and significant results of meta-analysis tests.
引用
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页数:14
相关论文
共 52 条
[1]
Breast cancer molecular signatures as determined by SAGE: correlation with lymph node status [J].
Abba, Martin C. ;
Sun, Hongxia ;
Hawkins, Kathleen A. ;
Drake, Jeffrey A. ;
Hu, Yuhui ;
Nunez, Maria I. ;
Gaddis, Sally ;
Shi, Tao ;
Horvath, Steve ;
Sahin, Aysegul ;
Aldaz, C. Marcelo .
MOLECULAR CANCER RESEARCH, 2007, 5 (09) :881-890
[2]
Byrne KJO, 2000, EUROPEAN J CANC OXFO, V36, P151
[3]
CARTER CL, 1989, CANCER-AM CANCER SOC, V63, P181, DOI 10.1002/1097-0142(19890101)63:1<181::AID-CNCR2820630129>3.0.CO
[4]
2-H
[5]
Gene expression signature of fibroblast serum response predicts human cancer progression: Similarities between tumors and wounds [J].
Chang, HY ;
Sneddon, JB ;
Alizadeh, AA ;
Sood, R ;
West, RB ;
Montgomery, K ;
Chi, JT ;
van de Rijn, M ;
Botstein, D ;
Brown, PO .
PLOS BIOLOGY, 2004, 2 (02) :206-214
[6]
CHARACTERIZATION OF SAP-1, A PROTEIN RECRUITED BY SERUM RESPONSE FACTOR TO THE C-FOS SERUM RESPONSE ELEMENT [J].
DALTON, S ;
TREISMAN, R .
CELL, 1992, 68 (03) :597-612
[7]
Paradoxical roles of the immune system during cancer development [J].
de Visser, KE ;
Eichten, A ;
Coussens, LM .
NATURE REVIEWS CANCER, 2006, 6 (01) :24-37
[8]
CD4+ T Cells Regulate Pulmonary Metastasis of Mammary Carcinomas by Enhancing Protumor Properties of Macrophages [J].
DeNardo, David G. ;
Barreto, Jairo B. ;
Andreu, Pauline ;
Vasquez, Lesley ;
Tawfik, David ;
Kolhatkar, Nikita ;
Coussens, Lisa M. .
CANCER CELL, 2009, 16 (02) :91-102
[9]
DAVID: Database for annotation, visualization, and integrated discovery [J].
Dennis, G ;
Sherman, BT ;
Hosack, DA ;
Yang, J ;
Gao, W ;
Lane, HC ;
Lempicki, RA .
GENOME BIOLOGY, 2003, 4 (09)
[10]
DISTRIBUTION OF THE ESTIMATORS FOR AUTOREGRESSIVE TIME-SERIES WITH A UNIT ROOT [J].
DICKEY, DA ;
FULLER, WA .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1979, 74 (366) :427-431