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人乳腺癌中的二氢嘧啶脱氢酶(DPD)活性及免疫组化DPD表达

DPD activity and immunohistochemical DPD expression in human breast cancer.

作者信息

Horiguchi Jun, Yoshida Takashi, Koibuchi Yukio, Iijima Kotaro, Ninomiya Jun, Takei Hiroyuki, Yokoe Takao, Iino Yuichi, Morishita Yasuo

机构信息

Second Department of Surgery, Gunma University Faculty of Medicine, Gunma 371-8511, Japan.

出版信息

Oncol Rep. 2004 Jan;11(1):65-72.

Abstract

We investigated dihydropyrimidine dehydrogenase (DPD) activity and its expression in breast cancer cases, and evaluated the prognostic significance of DPD expression in invasive breast cancer. A total of 49 paired of breast cancer tissues and the adjacent normal breast tissues were evaluated in this study. DPD expression of 191 patients with invasive breast cancer was also evaluated immunohistochemically. DPD activity in breast cancer ranged from 13.4-360.0 pmol/mg/min (mean, 162.9 pmol/mg/min). DPD activity in breast cancer tissues was significantly (p<0.001) higher than in adjacent normal breast tissue. DPD activity was significantly higher in DPD expression-positive tumors than DPD expression-negative tumors. The level of DPD activity was correlated with DPD expression. Patients with DPD expression-positive tumors had a significantly (p<0.05) poorer prognosis in disease-free survival compared to those with DPD-negative tumors. When evaluated in patients treated with 5-FU or 5-FU derivatives, DPD expression was a significantly (p<0.05) poorer prognostic factor in disease-free and overall survival. Using a Cox proportional hazards model, nodal status, ER status, and DPD expression were independent prognostic factors for both disease-free and overall survival. In conclusion, DPD expression may function as a marker of DPD activity and may be a prognostic indicator for patients with breast cancer.

摘要

我们研究了二氢嘧啶脱氢酶(DPD)在乳腺癌病例中的活性及其表达情况,并评估了DPD表达在浸润性乳腺癌中的预后意义。本研究共评估了49对乳腺癌组织及相邻的正常乳腺组织。还采用免疫组织化学方法评估了191例浸润性乳腺癌患者的DPD表达情况。乳腺癌中的DPD活性范围为13.4 - 360.0 pmol/mg/min(均值为162.9 pmol/mg/min)。乳腺癌组织中的DPD活性显著高于相邻正常乳腺组织(p<0.001)。DPD表达阳性肿瘤中的DPD活性显著高于DPD表达阴性肿瘤。DPD活性水平与DPD表达相关。与DPD阴性肿瘤患者相比,DPD表达阳性肿瘤患者的无病生存期预后显著较差(p<0.05)。在接受5-氟尿嘧啶(5-FU)或5-FU衍生物治疗的患者中进行评估时,DPD表达在无病生存期和总生存期方面均是显著较差的预后因素(p<0.05)。使用Cox比例风险模型,淋巴结状态、雌激素受体(ER)状态和DPD表达是无病生存期和总生存期的独立预后因素。总之,DPD表达可能作为DPD活性的标志物,并且可能是乳腺癌患者的预后指标。

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