Steinberg J, Oyasu R, Lang S, Sintich S, Rademaker A, Lee C, Kozlowski J M, Sensibar J A
Departments of Urology, Pathology, and Preventive Medicine, Northwestern University Medical School, Chicago, Illinois 60611, USA.
Clin Cancer Res. 1997 Oct;3(10):1707-11.
Our previous observations in LNCaP cells in vitro demonstrated an association between apoptotic cell death resistance and SGP-2 (Clusterin) overexpression. Accordingly, we hypothesized that high levels of cellular SGP-2 would aid in identifying biologically aggressive prostate cancer cells with unique survival advantages. To test this hypothesis, 40 archival radical prostatectomy and/or biopsy specimens of varying grades of prostate cancer were subjected to immunohistochemical SGP-2 staining. The resulting epithelial stains were quantified subjectively on a scale of 1-3 by four independent observers. Benign prostatic epithelial cells from young donors served as controls and showed a consistently weak staining intensity. In contrast, prostate cancer specimens showed varying degrees of staining intensity that correlated with a Gleason pattern (P = 0.006). This correlation supports the hypothesis that protection from apoptotic death may account, in part, for biologically aggressive tumor behavior.
我们之前对LNCaP细胞进行的体外观察表明,凋亡细胞死亡抗性与SGP-2(簇集素)过表达之间存在关联。因此,我们推测细胞内高水平的SGP-2将有助于识别具有独特生存优势的生物学侵袭性前列腺癌细胞。为了验证这一假设,对40份不同分级的前列腺癌存档根治性前列腺切除术和/或活检标本进行了SGP-2免疫组织化学染色。由四名独立观察者对所得上皮染色进行主观评分,范围为1-3。年轻供体的良性前列腺上皮细胞作为对照,染色强度始终较弱。相比之下,前列腺癌标本显示出不同程度的染色强度,这与 Gleason 分级相关(P = 0.006)。这种相关性支持了以下假设,即免受凋亡性死亡的影响可能部分解释了生物学侵袭性肿瘤行为。