Ravdin P M, Tandon A K, Allred D C, Clark G M, Fuqua S A, Hilsenbeck S H, Chamness G C, Osborne C K
Department of Medicine, University of Texas Health Science Center, San Antonio 78284.
J Clin Oncol. 1994 Mar;12(3):467-74. doi: 10.1200/JCO.1994.12.3.467.
We attempted to replicate and improve on our previous study (N Engl J Med 322:297-302, 1990) that showed that 34-kd cathepsin D levels as determined by Western blotting strongly correlated with disease-free survival (DFS) and overall survival (OS) of axillary node-negative (N-) breast cancer patients. We also examined the prognostic significance of cathepsin D measured by immunohistochemistry (IHC) in these patients.
Western blotting was performed on cytosols from frozen tumor specimens of 927 N- breast cancer patients in the San Antonio Breast Tumor Bank. The monoclonal antibody M1G8 was used to detect cathepsin D (in previous study, a polyclonal antiserum had been used). The same monoclonal antibody was also used for frozen-section IHC staining of tumor specimens from 562 N- patients from the same tumor bank. Levels of cathepsin D expression were then correlated with DFS and OS.
Although the levels of cathepsin D expression as measured by Western blotting and IHC correlated with each other and with levels of cathepsin D measured in previous work using Western blotting with the polyclonal antiserum, in this present study, using the monoclonal antibody M1G8, we were unable to demonstrate that cathepsin D expression (measured by either Western blotting or by IHC) correlates with DFS or OS.
In this study, cathepsin D expression as determined by either Western blotting or IHC using the monoclonal antibody M1G8 failed to improve the prognostic evaluation of N- breast cancer patients. The role of cathepsin D expression as a prognostic factor is still not precisely defined, raising questions about its use in the routine evaluation of N- breast cancer patients.
我们试图重复并改进我们之前的研究(《新英格兰医学杂志》322:297 - 302, 1990),该研究表明通过蛋白质印迹法测定的34-kd组织蛋白酶D水平与腋窝淋巴结阴性(N-)乳腺癌患者的无病生存期(DFS)和总生存期(OS)密切相关。我们还研究了通过免疫组织化学(IHC)测定的组织蛋白酶D在这些患者中的预后意义。
对圣安东尼奥乳腺肿瘤库中927例N-乳腺癌患者的冷冻肿瘤标本的细胞溶质进行蛋白质印迹分析。使用单克隆抗体M1G8检测组织蛋白酶D(在之前的研究中使用的是多克隆抗血清)。同一单克隆抗体也用于对来自同一肿瘤库的562例N-患者的肿瘤标本进行冷冻切片IHC染色。然后将组织蛋白酶D表达水平与DFS和OS进行关联分析。
尽管通过蛋白质印迹法和IHC测定的组织蛋白酶D表达水平相互关联,并且与之前使用多克隆抗血清进行蛋白质印迹分析测得的组织蛋白酶D水平相关,但在本研究中,使用单克隆抗体M1G8,我们无法证明组织蛋白酶D表达(通过蛋白质印迹法或IHC测定)与DFS或OS相关。
在本研究中,使用单克隆抗体M1G8通过蛋白质印迹法或IHC测定的组织蛋白酶D表达未能改善对N-乳腺癌患者的预后评估。组织蛋白酶D表达作为预后因素的作用仍未明确界定,这引发了关于其在N-乳腺癌患者常规评估中应用的疑问。