Clifford S L, Kaminetsky C P, Cirisano F D, Dodge R, Soper J T, Clarke-Pearson D L, Berchuck A
Department of Obstetrics and Gynecology/Division of Gynecologic Oncology, Duke University Comprehensive Cancer Center, Duke University Medical Center, Durham, NC 27710, USA.
Am J Obstet Gynecol. 1997 Jun;176(6):S229-32. doi: 10.1016/s0002-9378(97)70380-6.
This study was conducted to determine whether overexpression of the p53 tumor suppressor gene is associated with poor outcome in early-stage endometrial cancers and whether a racial difference in the frequency of p53 overexpression contributes to the observed racial disparity in survival rates.
Immunostaining for the p53 gene was performed in 164 women with stage I endometrial adenocarcinomas.
Overexpression of mutant p53 protein was seen in 28 out of 164 (17%) cases and was associated with a poor histologic grade (p = 0.003) and a nonendometrioid histologic appearance (p = 0.06). Overexpression also was three times more frequent in blacks (15 out of 44, 34%) than in whites (13 out of 117, 11%) (p = 0.003). Recurrent disease developed in 15 out of 164 (9%) cases and was more than twice as frequent in cases when the p53 gene was overexpressed (5 out of 28, 18%) than in cases with normal expression (10 out of 136, 7%). Recurrent disease was seen in 6 out of 44 (14%) blacks compared to 9 out of 117 (8%) whites.
These data support the hypothesis that differences in the frequency of alteration of the p53 tumor suppressor gene contribute to the racial disparity in endometrial cancer survival.
本研究旨在确定p53肿瘤抑制基因的过表达是否与早期子宫内膜癌的不良预后相关,以及p53过表达频率的种族差异是否导致了观察到的生存率种族差异。
对164例I期子宫内膜腺癌女性患者进行p53基因免疫染色。
164例患者中有28例(17%)出现突变型p53蛋白过表达,且与组织学分级差(p = 0.003)和非子宫内膜样组织学表现相关(p = 0.06)。黑人中过表达的频率(44例中有15例,34%)是白人(117例中有13例,11%)的三倍多(p = 0.003)。164例患者中有15例(9%)出现复发性疾病,p53基因过表达的病例中复发性疾病的频率(28例中有5例,18%)是正常表达病例(136例中有10例,7%)的两倍多。黑人中44例中有6例(14%)出现复发性疾病,而白人中117例中有9例(8%)出现复发性疾病。
这些数据支持以下假设,即p53肿瘤抑制基因改变频率的差异导致了子宫内膜癌生存率的种族差异。