首页> 外文期刊>Urology >Deleted-in-colon-cancer protein expression in patients with adenocarcinoma of the urinary tract and a history of colorectal cancer.
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Deleted-in-colon-cancer protein expression in patients with adenocarcinoma of the urinary tract and a history of colorectal cancer.

机译:尿路腺癌和大肠癌病史患者的结肠癌蛋白表达缺失。

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OBJECTIVES: To assess whether immunostaining for deleted-in-colon-cancer (DCC) protein, a previously established prognostic marker in colon and bladder cancer, may assist in resolving the uncommon differential diagnostic dilemma of distinguishing primary from secondary urothelial adenocarcinoma. METHODS: The study group consisted of 12 patients with adenocarcinoma involving the bladder or ureter and previously resected colorectal carcinoma between 1988 and 2002. All patients were initially considered to have primary urothelial transitional cell carcinoma, and the management strategy was conducted accordingly. The clinical data were recorded from the charts, and immunohistochemical staining for DCC was performed on formalin-fixed paraffin-embedded tissues containing the primary colorectal cancer and ensuing urinary tract tumor. Staining was defined as positive when at least 25% of the tumor cells were immunoreactive for DCC. RESULTS: Of the 12 patients, 10 presented with bladder and 2 with ureteral adenocarcinoma. All secondary tumors originated from a primary carcinoma invariably located along the left colon or rectum. The overall 5-year disease-specific survival rate from the time of colectomy was 31% at a median follow-up of 50 +/- 8 months. Of the 12 patients, 5 (41%) had positive DCC immunoreactivity. In all cases, concordant expression of DCC was found in the primary colorectal cancer and the ensuing tumor in the urinary tract. The survival time from colectomy was significantly longer for the DCC-positive subgroup (median 59 months, 95% confidence interval 41 to 77) than in the DCC-negative subgroup (median 23 months, 95% confidence interval 13 to 37). Likewise, the time lag between colectomy and tumor recurrence in the urinary tract was significantly longer in the patients with DCC-positive tumors (median 35 months) than in those with DCC-negative tumors (median 10 months). CONCLUSIONS: DCC immunoreactivity was consistently observed in secondary bladder or ureteral adenocarcinoma when the primary colorectal lesion expresses DCC, and thus may serve to establish the origin of the tumor. Positive DCC protein expression in secondary urinary tract adenocarcinoma of colorectal origin may identify a subset of patients with a relatively favorable prognosis. Additional studies are required to confirm our results.
机译:目的:为了评估结肠癌和膀胱癌中先前建立的预后标志物结肠癌缺失(DCC)蛋白的免疫染色是否有助于解决区分原发性尿路上皮腺癌与继发性尿路上皮腺癌的罕见鉴别诊断难题。方法:该研究组由1988年至2002年之间的12例腺癌累及膀胱或输尿管癌的患者和先前切除的结直肠癌患者组成。所有患者最初被认为是原发性尿路上皮移行细胞癌,并据此采取了治疗策略。从图表记录临床数据,并在包含原发性大肠癌和随后的尿路肿瘤的福尔马林固定石蜡包埋的组织上进行DCC的免疫组织化学染色。当至少25%的肿瘤细胞对DCC具有免疫反应性时,染色被定义为阳性。结果:在12例患者中,有10例表现为膀胱,2例表现为输尿管腺癌。所有继发性肿瘤均起源于原发癌,始终位于左结肠或直肠。从结肠切除术开始,总体5年疾病特异性存活率为31%,中位随访时间为50 +/- 8个月。在12名患者中,有5名(41%)的DCC免疫反应阳性。在所有情况下,DCC在原发性结直肠癌和随后的尿路肿瘤中均表达一致。 DCC阳性亚组(中位数59个月,95%置信区间41至77)从结肠切除术的存活时间明显长于DCC阴性亚组(中位数23个月,95%置信区间13至37)。同样,DCC阳性肿瘤患者(中位35个月)的结肠切除术与尿道肿瘤复发之间的时间间隔明显长于DCC阴性肿瘤患者(中位10个月)。结论:当原发性结直肠病变表达DCC时,在继发性膀胱或输尿管腺癌中始终观察到DCC免疫反应性,因此可能有助于确定肿瘤的起源。 DCC蛋白在大肠源性继发性尿路腺癌中的阳性表达可能会鉴定出预后相对较好的患者。需要进行其他研究以确认我们的结果。

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