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p53 和 DR5 在结直肠癌正常和恶性组织中的表达:与晚期的相关性。

Expression of p53 and DR5 in normal and malignant tissues of colorectal cancer: correlation with advanced stages.

机构信息

Laboratoire EA 3842, Homéostasie Cellulaire et Pathologies, Faculté de Médecine et de Pharmacie, Université de Limoges, 2 rue du Dr Marcland, 87025 Limoges Cedex, France.

出版信息

Oncol Rep. 2011 Nov;26(5):1091-7. doi: 10.3892/or.2011.1404. Epub 2011 Jul 26.

Abstract

Apoptosis has to be drastically controlled in organs with important cell turnover such as the colon. Deregulation of this process is often present in tumor progression. Tissues of 82 patients treated for colorectal cancer (CRC) were analyzed using antibodies against AIF, p53, DR4, DR5, cleaved caspase-3 and the TUNEL method to detect apoptosis; whereas staining of Ki-67 was used as a proliferation marker. In situ immunohistochemical analyses were compared in non-tumor (NT) cells from normal adjacent mucous membranes with tumor (T) cells from patients with Stage I (n=6), Stage II (n=35), Stage III (n=27) and Stage IV (n=14) CRC. Results were correlated with the tumor stages and the treatment response of patients to improve the understanding of CRC development. p53 and DR5 expression decreased progressively with CRC stage, suggesting that these proteins are important markers of advanced tumor stages. Moreover, p53 appears as a prognostic factor to predict recurrence-free survival. Including the detection of p53 and DR5 for establishing the diagnosis of CRC and adapting the treatment to each patient is strongly suggested by our work.

摘要

细胞凋亡在细胞更新活跃的组织中需要被严格控制,比如结肠。该过程的失调通常存在于肿瘤进展中。我们使用针对 AIF、p53、DR4、DR5、cleaved caspase-3 和 TUNEL 方法的抗体分析了 82 位接受结直肠癌(CRC)治疗的患者的组织,以检测凋亡;而 Ki-67 的染色则被用作增殖标志物。我们对比了来自正常相邻黏膜的非肿瘤(NT)细胞和来自 I 期(n=6)、II 期(n=35)、III 期(n=27)和 IV 期(n=14)CRC 患者的肿瘤(T)细胞的原位免疫组织化学分析结果。我们将结果与肿瘤分期和患者的治疗反应相关联,以加深对 CRC 发展的理解。p53 和 DR5 的表达随着 CRC 分期逐渐降低,表明这些蛋白是晚期肿瘤的重要标志物。此外,p53 似乎是预测无复发生存的预后因素。我们的工作强烈建议将 p53 和 DR5 的检测纳入 CRC 的诊断建立,并根据每位患者的情况调整治疗方案。

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