Yoshida R, Kiyozuka Y, Ichiyoshi H, Senzaki H, Takada H, Hioki K, Tsubura A
Department of Pathology II, Kansai Medical University, Osaka, Japan.
Anticancer Res. 1999 May-Jun;19(3B):2167-72.
Telomerase activities in endoscopically resected colorectal adenomas, surgically resected colorectal cancers and adjacent normal colonic mucosa were examined semiquantitatively by a polymerase chain reaction-based telomeric repeat amplification protocol (TRAP) assay. All normal mucosa (n = 15) presented weak telomerase activity (mean +/- SE: 0.99 +/- 0.00). When the value of 1.00 was arbitrary given to the mean activity of normal mucosa, the telomerase activity in the adenomas (n = 14) was up-regulated (2.01 +/- 0.22) relative to the normal mucosa. The telomerase activity in the high-grade atypia (severe atypia and carcinoma in situ) (2.58 +/- 0.34) was significantly higher than that in the low-grade (mild and moderate) atypia (1.59 +/- 0.18) (P < 0.05), and the adenomas 10 mm or more in diameter presented significantly higher telomerase activity (2.56 +/- 0.09) than compared to the smaller ones (1.44 +/- 0.17) (p < 0.05). Carcinomas (n = 20), showed a telomerase activity that varied from 0.97 to 16.93, which was than the greater mean telomerase activity (6.96 +/- 1.25) noted in the adenomas. The telomerase activity in the carcinomas tended to be higher in the larger (> or = 4 cm), histologically less-differentiated (moderately differentiated), late-stage (Dukes C + D), and nodal metastatic tumors, suggestive of unfavorable prognosis. These results suggests that the weak telomerase activity in normal colonic mucosa is gradually activated during the course of colorectal carcinogenesis.
采用基于聚合酶链反应的端粒重复序列扩增法(TRAP)半定量检测内镜下切除的大肠腺瘤、手术切除的大肠癌及癌旁正常结肠黏膜中的端粒酶活性。所有正常黏膜(n = 15)端粒酶活性均较弱(均值±标准误:0.99±0.00)。若将正常黏膜的平均活性值设定为1.00,则腺瘤(n = 14)中的端粒酶活性相对于正常黏膜上调(2.01±0.22)。高级别异型增生(重度异型增生和原位癌)中的端粒酶活性(2.58±0.34)显著高于低级别(轻度和中度)异型增生中的活性(1.59±0.18)(P < 0.05),直径10 mm及以上的腺瘤端粒酶活性(2.56±0.09)显著高于较小腺瘤(1.44±0.17)(P < 0.05)。20例癌组织端粒酶活性在0.97至16.93之间,高于腺瘤中的平均端粒酶活性(6.96±1.25)。癌组织中,较大(≥4 cm)、组织学分化程度较低(中度分化)、晚期(Dukes C + D期)及有淋巴结转移的肿瘤端粒酶活性往往较高,提示预后不良。这些结果表明,正常结肠黏膜中的弱端粒酶活性在大肠癌发生过程中逐渐被激活。