首页> 美国卫生研究院文献>World Journal of Gastroenterology >Predictive value of Ki67 and p53 in locally advanced rectal cancer: Correlation with thymidylate synthase and histopathological tumor regression after neoadjuvant 5-FU-based chemoradiotherapy
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Predictive value of Ki67 and p53 in locally advanced rectal cancer: Correlation with thymidylate synthase and histopathological tumor regression after neoadjuvant 5-FU-based chemoradiotherapy

机译:Ki67和p53在局部晚期直肠癌中的预测价值:新辅助基于5FU的放化疗后与胸苷酸合酶和组织病理学肿瘤消退的相关性

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摘要

AIM: To investigate the predictive value of Ki67 and p53 and their correlation with thymidylate synthase (TS) gene expression in a rectal cancer patient cohort treated according to a standardized recommended neoadjuvant treatment regimen.METHODS: Formalin fixed, paraffin embedded pre-therapeutical tumor biopsies (n = 22) and post-therapeutical resection specimens (n = 40) from patients with rectal adenocarcinoma (clinical UICC stage II/III) receiving standardized neoadjuvant 5-fluorouracil (5-FU) based chemoradiotherapy were studied for Ki67 and p53 expression by immunohistochemistry and correlated with TS mRNA expression by quantitative TaqMan real-time PCR after laser microdissection. The results were compared with histopathological tumor regression according to a standardized semiquantitative score grading system.RESULTS: Responders (patients with high tumor regression) showed a significantly lower Ki67 expression than non-responders in the pre-therapeutical tumor biopsies (81.2% vs 16.7%; P < 0.05) as well as in the post-therapeutical resection specimens (75.8% vs 14.3%; P < 0.01). High TS mRNA expression was significantly correlated with a high Ki67 index and low TS mRNA expression was significantly correlated with a low Ki67 index in the pre-therapeutical tumor biopsies (corr. coef. = 0.46; P < 0.01) as well as in the post-therapeutical resection specimens (corr. coef. = 0.40; P < 0.05). No significant association was found between p53 and TS mRNA expression or tumor regression.CONCLUSION: Ki67 has, like TS, predictive value in rectal cancer patients after neoadjuvant 5-FU based chemoradiotherapy. The close correlation between Ki67 and TS indicates that TS is involved in active cell cycle processes.
机译:目的:研究Ki67和p53在根据标准推荐新辅助治疗方案治疗的直肠癌患者队列中的预测价值及其与胸苷酸合酶(TS)基因表达的相关性。方法:福尔马林固定,石蜡包埋的治疗前肿瘤活检(n = 22)和直肠癌(临床UICC II / III期)接受标准化新辅助5-氟尿嘧啶(5-FU)放化疗的直肠腺癌患者的治疗后切除标本(n = 40),通过以下方法研究Ki67和p53的表达:免疫组织化学,并通过激光显微切割后定量TaqMan实时PCR与TS mRNA表达相关。结果:根据标准化的半定量评分系统,将结果与组织病理学肿瘤消退进行了比较。结果:在治疗前的肿瘤活检中,应答者(肿瘤消退程度高的患者)的Ki67表达显着低于非应答者(81.2%比16.7%) ; P <0.05)以及治疗后切除标本(75.8%对14.3%; P <0.01)。在治疗前的肿瘤活检中,高TS mRNA表达与高Ki67指数显着相关,而低TS mRNA表达与低Ki67指数显着相关(校正系数= 0.46; P <0.01)以及在治疗后-治疗性切除标本(正确系数= 0.40; P <0.05)。结论p53与TS mRNA表达或肿瘤消退之间无显着相关性。结论:Ki67与TS一样,在新辅助5-FU放化疗后对直肠癌患者具有预测价值。 Ki67与TS之间的密切相关性表明TS参与了活跃的细胞周期过程。

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