Reedijk Michael, Pinnaduwage Dushanthi, Dickson Brendan C, Mulligan Anna Marie, Zhang Hui, Bull Shelley B, O'Malley Frances P, Egan Sean E, Andrulis Irene L
Department of Surgical Oncology, University of Toronto, Toronto, ON, Canada, M5G 2M9.
Breast Cancer Res Treat. 2008 Oct;111(3):439-48. doi: 10.1007/s10549-007-9805-3. Epub 2007 Nov 8.
Expression of the JAG1 Notch ligand has previously been shown to correlate with poor overall survival in women with advanced breast cancer. We undertook to test whether expression of JAG1 is associated with reduced disease free survival (DFS) in 887 samples from a prospectively accrued LNN cohort with a median follow-up greater than 8 years. Moderate to high JAG1 mRNA expression was associated with reduced DFS in univariate analysis (hazard ratio of 1.58; 95% confidence interval, 1.03-2.40; P = 0.034) and correlated with large tumor size, ER and PgR negativity, high tumor grade, and p53 antibody reactivity. Although elevated risk of reduced DFS in patients with high JAG1 mRNA did not persist with adjustment for other prognostic factors, it did in combination with HER2. JAG1 mRNA was positively associated with expression of basal breast cancer markers, however, in contrast to the finding that basal gene expression is most strongly associated with reduced DFS in the first 36 months of follow-up, JAG1 mRNA expression was associated with reduced DFS through the full follow-up period. Also, tumors expressing high levels of both mRNA and protein showed reduced DFS as compared to all other groups in univariate analysis (hazard ratio of 1.73; 95% confidence interval, 1.09-2.74; P = 0.020). Thus, JAG1 expression is associated with poor DFS in LNN breast cancer. As JAG1 is a target of several oncogenic signaling pathways, and is a ligand for Notch, these data provide novel insights into signaling that may contribute to progression of early stage breast cancer.
先前的研究表明,JAG1 Notch配体的表达与晚期乳腺癌女性的总生存期较差相关。我们对来自前瞻性积累的LNN队列的887个样本进行检测,以检验JAG1的表达是否与无病生存期(DFS)缩短相关,该队列的中位随访时间超过8年。在单变量分析中,JAG1 mRNA的中度至高度表达与DFS缩短相关(风险比为1.58;95%置信区间为1.03 - 2.40;P = 0.034),并且与肿瘤体积大、雌激素受体(ER)和孕激素受体(PgR)阴性、肿瘤分级高以及p53抗体反应性相关。尽管在对其他预后因素进行调整后,JAG1 mRNA水平高的患者DFS缩短的风险不再持续存在,但与人类表皮生长因子受体2(HER2)联合时仍存在。JAG1 mRNA与基底样乳腺癌标志物的表达呈正相关,然而,与基底样基因表达在随访的前36个月与DFS缩短最密切相关的发现相反,JAG1 mRNA表达在整个随访期间都与DFS缩短相关。此外,在单变量分析中,与所有其他组相比,同时表达高水平mRNA和蛋白的肿瘤显示DFS缩短(风险比为1.73;95%置信区间为1.09 - 2.74;P = 0.020)。因此,JAG1表达与LNN乳腺癌患者的DFS较差相关。由于JAG1是几种致癌信号通路的靶点,并且是Notch的配体,这些数据为可能导致早期乳腺癌进展的信号传导提供了新的见解。