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晚期人类胸膜癌的“患者样”裸鼠转移模型

"Patient-like" nude mouse metastatic model of advanced human pleural cancer.

作者信息

Astoul P, Colt H G, Wang X, Boutin C, Hoffman R M

机构信息

Department of Pulmonary and Critical Care Medicine, UCSD Medical Center 92093.

出版信息

J Cell Biochem. 1994 Sep;56(1):9-15. doi: 10.1002/jcb.240560104.

Abstract

Pleural cancer in humans is a frequently occurring tumor. Recently, clinical trials have suggested that chemotherapy and immunotherapy administered intrapleurally may elicit responses in early-stage diseases. However, at radiological and pleural endoscopic evaluation, most of the patients are found to have a visceral pleural involvement that is generally refractory to therapy and leads to a poor prognosis. The goal of this study was to construct a nude mouse model of human parietal- and visceral-pleural cancer that could reflect the clinical picture for this disease. The model could then be useful for drug discovery for pleural cancer. A well-differentiated human lung adenocarcinoma was used as intact tissue for implantation. Ten mice underwent parietal-pleural implantation and ten mice visceral-pleural implantation via a novel thoracotomy procedure we have developed. Symptoms of tumor growth were determined from weight loss, respiratory distress, or debilitation. Actual tumor growth and spread were measured at autopsy. The mouse survival curves of each group were estimated by the Kaplan-Meier method and the difference of the median survival times was assessed by the Log-rank test. The slopes of mean-mouse weight curves were compared using a standard two-sample t-test. A 100% take rate was achieved in constructing the pleural cancer models. Tumor growth was initially assessed by symptomatology and survival: the median survival time was, respectively, 27.9 days and 31 days for visceral-pleural and parietal-pleural implanted groups (P < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

人类胸膜癌是一种常见肿瘤。最近,临床试验表明,经胸膜内给予化疗和免疫疗法可能会在早期疾病中引发反应。然而,在放射学和胸膜内镜评估中,大多数患者被发现存在脏层胸膜受累,这通常对治疗难治,并导致预后不良。本研究的目的是构建一种能反映该疾病临床情况的人壁层和脏层胸膜癌裸鼠模型。然后该模型可用于胸膜癌的药物研发。一种高分化人肺腺癌被用作植入的完整组织。通过我们开发的一种新型开胸手术,十只小鼠接受壁层胸膜植入,十只小鼠接受脏层胸膜植入。通过体重减轻、呼吸窘迫或衰弱来确定肿瘤生长的症状。在尸检时测量实际肿瘤生长和扩散情况。每组小鼠的生存曲线采用Kaplan-Meier法估计,中位生存时间的差异采用Log-rank检验评估。使用标准双样本t检验比较平均小鼠体重曲线的斜率。构建胸膜癌模型的成功率为100%。最初通过症状学和生存率评估肿瘤生长:脏层胸膜和壁层胸膜植入组的中位生存时间分别为27.9天和31天(P<0.05)。(摘要截断于250字)

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