1号染色体等位基因缺失在结肠癌中的预后价值。
Prognostic value of chromosome 1p allelic loss in colon cancer.
作者信息
Ogunbiyi O A, Goodfellow P J, Gagliardi G, Swanson P E, Birnbaum E H, Fleshman J W, Kodner I J, Moley J F
机构信息
Department of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
出版信息
Gastroenterology. 1997 Sep;113(3):761-6. doi: 10.1016/s0016-5085(97)70169-0.
BACKGROUND & AIMS: Current evidence suggests that there may be a tumor-suppressor gene on chromosome 1p associated with colorectal cancer. The aim of the present study was to determine whether allelic loss on chromosome 1p is of prognostic value in colorectal cancer.
METHODS
Polymerase chain reaction was used to assess allelic loss of five chromosome 1p microsatellite markers in tumor specimens. Genomic DNA was prepared from archival tumor and corresponding normal tissue specimens from 116 patients who had undergone curative treatment for adenocarcinoma of the colon. Allelic loss was correlated with disease-free interval and survival.
RESULTS
Deletion of 1p sequence was detected in 22 of 82 tumors. Deletions of the microsatellite markers D1S228 (1p36) and HY-TM1 (1p32) were significantly associated with poor survival (P < 0.05): relative risk, 4.1; 95% confidence interval, 1.25-9.23 for D1S228; and relative risk, 6.6; 95% confidence interval, 1.4-19 for HY-TM1. Loss of heterozygosity at D1S228 was also associated with shorter disease-free interval: relative risk, 4.5; 95% confidence interval, 1.3-11.
CONCLUSIONS
Allelic loss in the 1p36 and 1p32 regions of chromosome 1 appears to be an independent predictor of poor prognosis in patients with adenocarcinoma of the colon.
背景与目的
目前的证据表明,1号染色体短臂上可能存在与结直肠癌相关的肿瘤抑制基因。本研究的目的是确定1号染色体短臂上等位基因缺失在结直肠癌中是否具有预后价值。
方法
采用聚合酶链反应评估肿瘤标本中5个1号染色体短臂微卫星标记的等位基因缺失情况。从116例接受结肠癌腺癌根治性治疗的患者的存档肿瘤及相应正常组织标本中提取基因组DNA。将等位基因缺失与无病生存期和生存率进行相关性分析。
结果
在82个肿瘤中的22个检测到1号染色体短臂序列缺失。微卫星标记D1S228(1p36)和HY-TM1(1p32)的缺失与较差的生存率显著相关(P < 0.05):D1S228的相对风险为4.1;95%置信区间为1.25 - 9.23;HY-TM1的相对风险为6.6;95%置信区间为1.4 - 19。D1S228杂合性缺失也与较短的无病生存期相关:相对风险为4.5;95%置信区间为1.3 - 11。
结论
1号染色体1p36和1p32区域的等位基因缺失似乎是结肠癌患者预后不良的独立预测因素。