Sinicrope F A, Hart J, Michelassi F, Lee J J
Departments of Gastrointestinal Medical Oncology and Digestive Diseases and Biomathematics, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Clin Cancer Res. 1995 Oct;1(10):1103-10.
The bcl-2 proto-oncogene encodes a Mr 25,000 protein that has been shown to prevent apoptosis or programmed cell death. The bcl-2 protein is detectable in basal cells of normal colonic epithelium, and an altered topographic distribution of this protein is found in colonic neoplasms. However, the clinical significance of abnormal bcl-2 expression in colon carcinomas remains unknown. We examined the prognostic value of the bcl-2 protein in TNM stage II colon carcinomas and its relationship to DNA ploidy, cell proliferation indices, p53 expression, and clinicopathological features. We analyzed 119 resected and otherwise untreated, paraffin-embedded stage II colon carcinomas for bcl-2 and p53 protein expression using immunohistochemistry. DNA ploidy and proliferative index (% S-phase + % G2-M) were determined by flow cytometry, and tumor grade and vascular microinvasion were assessed on histological sections. Cytoplasmic expression of the bcl-2 protein was detected in 72 (66%) of 110 carcinomas, and a high level of expression was significantly correlated with diploid DNA content (P = 0.02) and low proliferative activity (P = 0.005). bcl-2 was not associated with nuclear p53 expression. In a univariate analysis, a higher fraction of bcl-2-positive tumor cells was associated with better relapse-free survival (P = 0.02) and overall survival (P = 0.05) rates. Moreover, a high level of bcl-2 expression was an independent predictor of better relapse-free survival (P = 0.04), but not overall survival (P = 0.14), after adjustment for other variables, including proliferative index, DNA ploidy, and race. In conclusion, bcl-2 overexpression is associated with favorable prognostic features and may predict clinical outcome in stage II colon carcinomas.
bcl-2原癌基因编码一种分子量为25000的蛋白质,该蛋白质已被证明可防止细胞凋亡或程序性细胞死亡。在正常结肠上皮的基底细胞中可检测到bcl-2蛋白,并且在结肠肿瘤中发现该蛋白的拓扑分布发生改变。然而,bcl-2在结肠癌中异常表达的临床意义仍不清楚。我们研究了bcl-2蛋白在TNM II期结肠癌中的预后价值及其与DNA倍体、细胞增殖指数、p53表达和临床病理特征的关系。我们使用免疫组织化学分析了119例切除后未经其他治疗的石蜡包埋II期结肠癌的bcl-2和p53蛋白表达。通过流式细胞术测定DNA倍体和增殖指数(%S期+%G2-M期),并在组织切片上评估肿瘤分级和血管微浸润。在110例癌组织中有72例(66%)检测到bcl-2蛋白的细胞质表达,高水平表达与二倍体DNA含量(P = 0.02)和低增殖活性(P = 0.005)显著相关。bcl-2与核p53表达无关。在单因素分析中,较高比例的bcl-2阳性肿瘤细胞与更好的无复发生存率(P = 0.02)和总生存率(P = 0.05)相关。此外,在对包括增殖指数、DNA倍体和种族等其他变量进行校正后,高水平的bcl-2表达是更好的无复发生存率(P = 0.04)的独立预测因子,但不是总生存率(P = 0.14)的独立预测因子。总之,bcl-2过表达与良好的预后特征相关,并且可能预测II期结肠癌的临床结局。