Langerød Anita, Zhao Hongjuan, Borgan Ørnulf, Nesland Jahn M, Bukholm Ida R K, Ikdahl Tone, Kåresen Rolf, Børresen-Dale Anne-Lise, Jeffrey Stefanie S
Department of Genetics, Institute for Cancer Research, Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway N-0310.
Breast Cancer Res. 2007;9(3):R30. doi: 10.1186/bcr1675.
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 (tumour protein p53) in a group of breast cancer patients with long-term (12 to 16 years) follow-up.
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 temporal temperature gradient gel electrophoresis and sequencing, was also evaluated. Eighty of the samples were analyzed for gene expression using 42 K 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.
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. Breast cancer cases in the 'basal-like' and 'ERBB2+' gene expression subgroups had a very high mortality the first two years, while the 'highly proliferating luminal' cases developed the disease more slowly, showing highest mortality after 5 to 8 years. The TP53 mutation status showed strong association with the 'basal-like' and 'ERBB2+' subgroups, and tumors with mutation had a characteristic gene expression pattern.
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.
乳腺癌的基因表达谱分析增进了我们对这种疾病异质性生物学的理解,并有望影响临床治疗。本研究的目的是评估基于基因表达的分类以及既定预后标志物和TP53基因(肿瘤蛋白p53)突变状态在一组接受长期(12至16年)随访的乳腺癌患者中的预后价值。
使用单变量/多变量Cox回归研究200例乳腺癌患者的临床和组织病理学参数对临床结局的影响。还评估了使用时间温度梯度凝胶电泳和测序鉴定的TP53基因突变的预后影响。使用42K cDNA微阵列对80个样本进行基因表达分析,并将患者分为五个先前定义的分子表达组。通过将该变量添加到用于分析所有样本的Cox回归模型中,评估基于基因表达的分类与标准标志物相比的强度。
单变量和多变量分析均显示,TP53突变状态、肿瘤大小和淋巴结状态是整个患者组乳腺癌生存的最强预测因子。对有基因表达数据的患者进行的分析表明,TP53突变状态、基于基因表达的分类、肿瘤大小和淋巴结状态是生存的重要预测因子。“基底样”和“ERBB2+”基因表达亚组中的乳腺癌病例在头两年死亡率非常高,而“高增殖性管腔型”病例疾病发展较慢,在5至8年后显示出最高死亡率。TP53突变状态与“基底样”和“ERBB2+”亚组密切相关,具有突变的肿瘤具有特征性的基因表达模式。
TP53突变状态和基于基因表达的分组是乳腺癌重要的生存标志物,这些分子标志物可能提供补充临床变量的预后信息。该研究为正在进行的疾病特征描述和分类增添了经验和知识。