Nadler Yasmine, Camp Robert L, Giltnane Jennifer M, Moeder Christopher, Rimm David L, Kluger Harriet M, Kluger Yuval
Department of Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
Breast Cancer Res. 2008;10(2):R35. doi: 10.1186/bcr1998. Epub 2008 Apr 23.
Bcl-2 antanogene-1 (Bag-1) binds the anti-apoptotic mediator Bcl-2, and enhances its activity. Bcl-2 and Bag-1 are associated with chemotherapy resistance in cancer cells. Drugs that target Bcl-2 are currently in clinical development. The purpose of the present study was to examine expression patterns of Bag-1 in a large cohort of breast tumors and to assess the association with Bcl-2, estrogen receptor, progesterone receptor and Her2/neu, and other clinical/pathological variables.
Tissue microarrays containing primary specimens from 638 patients with 10-year follow-up were employed, and the expression of Bag-1, Bcl-2, estrogen receptor, progesterone receptor and Her2/neu was assessed using our automated quantitative analysis method. We used cytokeratin to define pixels as breast cancer (tumor mask) within the array spot, and we measured biomarker expression within the mask using Cy5 conjugated antibodies.
High Bcl-2 expression was associated with improved survival in the entire cohort and in the node-positive subset (P = 0.008 and P = 0.002, respectively). High Bag-1 expression was associated with improved survival in the node-positive subset (P = 0.006). On multivariable analysis, neither Bcl-2 nor Bag-1 retained their independence as prognostic markers. Strong associations were found between Bag-1, Bcl-2, estrogen receptor and progesterone receptor.
Bag-1 and Bcl-2 expression in breast tumors is associated with improved outcome and steroid receptor positivity. Evaluation of Bcl-2 and Bag-1 expression in breast cancer may identify a subset of patients with a favorable prognosis, who might not benefit from chemotherapy or who might benefit from Bcl-2 targeting agents in addition to antihormonal therapy.
Bcl-2抗凋亡基因-1(Bag-1)与抗凋亡介质Bcl-2结合,并增强其活性。Bcl-2和Bag-1与癌细胞的化疗耐药性有关。目前,靶向Bcl-2的药物正处于临床开发阶段。本研究的目的是检测大量乳腺肿瘤队列中Bag-1的表达模式,并评估其与Bcl-2、雌激素受体、孕激素受体和Her2/neu以及其他临床/病理变量之间的关联。
采用包含638例患者原发标本且有10年随访数据的组织芯片,使用我们的自动定量分析方法评估Bag-1、Bcl-2、雌激素受体、孕激素受体和Her2/neu的表达。我们使用细胞角蛋白将芯片斑点内的像素定义为乳腺癌(肿瘤掩码),并使用Cy5偶联抗体测量掩码内的生物标志物表达。
在整个队列和淋巴结阳性亚组中,高Bcl-2表达与生存率提高相关(分别为P = 0.008和P = 0.002)。高Bag-1表达与淋巴结阳性亚组的生存率提高相关(P = 0.006)。多变量分析显示,Bcl-2和Bag-1均不再作为独立的预后标志物。Bag-1、Bcl-2、雌激素受体和孕激素受体之间存在强关联。
乳腺肿瘤中Bag-1和Bcl-2的表达与较好的预后及类固醇受体阳性相关。评估乳腺癌中Bcl-2和Bag-1的表达可能会识别出一部分预后良好的患者,这些患者可能无法从化疗中获益,或者除了抗激素治疗外还可能从靶向Bcl-2的药物中获益。