Takayama K, Ogata K, Nakanishi Y, Yatsunami J, Kawasaki M, Hara N
Research Institute for Diseases of the Chest, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Cancer J Sci Am. 1996 Jul-Aug;2(4):212-6.
The bcl-2 gene belongs to a new category of oncogene that inhibits programmed cell death (apoptosis). No data are available on the frequency or clinical importance of its expression in patients with small cell lung cancer (SCLC), although its expression is reported in SCLC cell lines. We investigated the correlation between bcl-2 expression and prognosis, including response to chemotherapy, in SCLC patients and report our findings here.
Tumor specimens biopsied bronchoscopically in 38 SCLC patients were used for immunohistochemical study. Bcl-2 oncoprotein was detected by obtaining an immunostain using a specific monoclonal antibody, DAKO-bcl-2, 124. All patients received more than two courses of chemotherapy with 3- to 4-week intervals.
We detected bcl-2 expression in 21 of the 38 SCLC patients (55%). In 17 patients with bcl-2-negative tumors, the objective response to chemotherapy was 76% with 12% complete response and in 21 patients with bcl-2-positive tumors it was 62% with 8% complete response. The difference in response rate was not significant. In patients with bcl-2-positive tumors, survival time tended to be shorter than in those with bcl-2-negative tumors. There was no significant correlation between bcl-2 expression and clinical factors (gender, age, smoking, performance score, staging).
In 21 of the 38 SCLC patients bcl-2 oncoprotein was abnormally expressed and its expression may be associated with shorter survival times and poor response to chemotherapy.
bcl-2基因属于一类新的癌基因,可抑制程序性细胞死亡(凋亡)。虽然有报道称其在小细胞肺癌(SCLC)细胞系中有表达,但关于其在SCLC患者中的表达频率或临床重要性尚无相关数据。我们研究了SCLC患者中bcl-2表达与预后(包括化疗反应)之间的相关性,并在此报告我们的研究结果。
对38例SCLC患者经支气管镜活检获取的肿瘤标本进行免疫组织化学研究。使用特异性单克隆抗体DAKO-bcl-2 124进行免疫染色以检测bcl-2癌蛋白。所有患者均接受了超过两个疗程的化疗,化疗间隔为3至4周。
我们在38例SCLC患者中的21例(55%)检测到bcl-2表达。在17例bcl-2阴性肿瘤患者中,化疗的客观缓解率为76%,完全缓解率为12%;在21例bcl-2阳性肿瘤患者中,缓解率为62%,完全缓解率为8%。缓解率差异无统计学意义。bcl-2阳性肿瘤患者的生存时间往往比bcl-2阴性肿瘤患者短。bcl-2表达与临床因素(性别、年龄、吸烟、体能状态评分、分期)之间无显著相关性。
38例SCLC患者中有21例bcl-2癌蛋白异常表达,其表达可能与较短的生存时间和化疗反应不佳有关。