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E-GEOD-40954 GSE40954 transcription profiling by array Homo sapiens

TP53 mutation status and gene expression profiles are powerful prognostic markers of breast cancer

·发布 Sept. 18, 2012 ·更新 May 3, 2014
162
样本数
81
实验数
5
芯片平台
1
相关文献
实验描述

Background: Gene expression profiling of breast carcinomas has increased our understanding of the heterogeneous biology of this disease and promises to impact clinical care. The aim of this study was to evaluate the prognostic value of gene expression-based classification along with established prognostic markers and mutation status of the TP53 gene, in a group of breast cancer patients with long-term (12-16 years) follow-up. Methods: The clinical and histopathological parameters of 200 breast cancer patients were studied for their effects on clinical outcome using univariate/multivariate Cox regression. The prognostic impact of mutations in the TP53 gene, identified using TTGE and sequencing, was also evaluated. Eighty of the samples were analyzed for gene expression using 42K cDNA microarrays and the patients were assigned to five previously defined molecular expression groups. The strength of the gene expression based classification versus standard markers was evaluated by adding this variable to the Cox regression model used to analyze all samples. Results: Both univariate and multivariate analysis showed that TP53 mutation status, tumor size and lymph node status were the strongest predictors of breast cancer survival for the whole group of patients. Analyses of the patients with gene expression data showed that TP53 mutation status, gene expression based classification, tumor size and lymph node status were significant predictors of survival. The TP53 mutation status showed strong association with the ?basal-like? and ?ERBB2+? gene expression subgroups, and tumors with mutation had a characteristic gene expression pattern. Conclusions: TP53 mutation status and gene-expression based groups are important survival markers of breast cancer, and these molecular markers may provide prognostic information that complements clinical variables. The study adds experience and knowledge to an ongoing characterization and classification of the disease. Experiment set consisting of 80 primary breast carcinomas collected at Ulleval University Hospital (ULL-samples), Oslo, Norway from 1990-94, and one normal sample from breast reduction surgery.

参考文献
TP53 mutation status and gene expression profiles are powerful prognostic markers of breast cancer.
Langer�d A, Zhao H, Borgan �, Nesland JM, Bukholm IR, Ikdahl T, K�resen R, B�rresen-Dale AL, Jeffrey SS
PMID: 17504517
芯片平台
A-GEOD-8650
SMD Print_621 Homo sapiens(7 例)
A-GEOD-3341
SHDP(23 例)
A-GEOD-3114
SHCB(8 例)
A-GEOD-3314
SHDM(13 例)
A-GEOD-2790
SHCP(30 例)
样本属性
cell type
normal breast tissue, primary breast carcinoma
ID
DNR-N-AO100 (Ambion), ULL-D-013, ULL-D-016, ULL-D-023, ULL-D-037, ULL-D-038, ULL-D-044, ULL-D-048, ULL-D-053, ULL-D-056, ULL-D-057, ULL-D-065, ULL-D-066, ULL-D-067, ULL-D-071, ULL-D-074, ULL-D-075, ULL-D-080, ULL-D-083, ULL-D-085, ULL-D-087, ULL-D-096, ULL-D-099, ULL-D-101, ULL-D-113, ULL-D-122, ULL-D-132, ULL-D-134, ULL-D-135, ULL-D-139, ULL-D-143, ULL-D-144, ULL-D-150, ULL-D-165, ULL-D-167, ULL-D-183, ULL-D-184, ULL-D-188, ULL-D-201, ULL-D-202, ULL-D-214, ULL-D-216, ULL-D-230, ULL-DCIS-199, ULL-L-019, ULL-L-031, ULL-L-036, ULL-L-046, ULL-L-062, ULL-L-069, ULL-L-072, ULL-L-088, ULL-L-097, ULL-L-105, ULL-L-111, ULL-L-112, ULL-L-136, ULL-L-138, ULL-L-168, ULL-L-176, ULL-L-181, ULL-L-190, ULL-L-222, ULL-MU-063, ULL-MU-079, ULL-T-002, ULL-T-007, ULL-T-011, ULL-T-014, ULL-T-020, ULL-T-022, ULL-T-024, ULL-T-026, ULL-T-027, ULL-T-028, ULL-T-060, ULL-T-123, ULL-T-169, ULL-T-177, ULL-TL-055, ULL-TL-107
Organism
Homo sapiens
reference
Stratagene Reference, amplified total RNA
实验信息
登记号
E-GEOD-40954
GEO 编号
GSE40954
实验类型
transcription profiling by array
物种
Homo sapiens
发布日期
Sept. 18, 2012
更新日期
May 3, 2014
提交者
Stanford Microarray Database、 Anita Langerod、 Hongjuan Zhao
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