Martarelli Daniele, Catalano Alfonso, Procopio Antonio, Orecchia Sara, Libener Roberta, Santoni Giorgio
Department of Experimental Medicine and Public Health, University of Camerino, 62032 Camerino, Italy.
BMC Cancer. 2006 May 17;6:130. doi: 10.1186/1471-2407-6-130.
Malignant pleural mesothelioma (MPM) is a tumor known to be resistant to conventional therapies. Thus, an in vivo model can represent an important tool for assessing the efficacy of novel approaches in the treatment of MPM.Presently, human MPM cells have been grown orthotopically in mice upon transplantation of tumor masses or tumor cell suspensions following surgery. In these models however, surgery can interfere with the tumor growth and the early stages of tumor development cannot be easily explored. Finally, results may not be so accurate due to implantation of potentially different tumor samples in different experimental groups.Our work aimed at establishing a nude mouse model xenotransplanted with human MPM cell lines in which tumor progression exhibits some features of the human disease.
Three distinct human MPM cell lines previously established from MPM patients displaying two different phenotypes, biphasic (MM-B1 and IST-Mes3) and epithelioid (IST-Mes2), were directly injected into the pleural cavity of nude mice. At different times, mice were sacrificed for autopsy, tumor nodules were counted and then removed for histology. Presence of metastases in visceral organs was also monitored.
IST-Mes2 cells were unable to grow in nude mice. MM-B1 and IST-Mes3 cells were capable of growing in nude mice and formed tumor nodules in the pleura. Post-mortem examination showed that MPM cells progressively colonized the parietal and visceral pleura, the diaphragm, the mediastinum and, lastly the lung parenchyma. No pneumo-thorax was evidenced in the mice. Pleural effusions as well as lymph node metastases were observed only at later times.
This model mimics the progression of human malignant mesothelioma and it is easy to perform and reproducible; therefore it can be useful to study human MPM biology and evaluate the efficacy of novel therapies.
恶性胸膜间皮瘤(MPM)是一种已知对传统疗法耐药的肿瘤。因此,体内模型可成为评估MPM新型治疗方法疗效的重要工具。目前,人类MPM细胞已通过在手术后移植肿瘤块或肿瘤细胞悬液在小鼠体内原位生长。然而,在这些模型中,手术会干扰肿瘤生长,且肿瘤发育的早期阶段不易探究。最后,由于在不同实验组中植入的肿瘤样本可能不同,结果可能不太准确。我们的工作旨在建立一种用人MPM细胞系异种移植的裸鼠模型,其中肿瘤进展呈现出人类疾病的一些特征。
从表现出两种不同表型(双相型(MM - B1和IST - Mes3)和上皮样型(IST - Mes2))的MPM患者中先前建立的三种不同人类MPM细胞系,直接注射到裸鼠的胸腔内。在不同时间,处死小鼠进行尸检,计数肿瘤结节,然后取出进行组织学检查。还监测内脏器官中转移灶的存在情况。
IST - Mes2细胞无法在裸鼠中生长。MM - B1和IST - Mes3细胞能够在裸鼠中生长并在胸膜中形成肿瘤结节。尸检显示,MPM细胞逐渐在壁层和脏层胸膜、膈肌、纵隔,最后在肺实质中定植。小鼠未出现气胸。仅在后期观察到胸腔积液和淋巴结转移。
该模型模拟了人类恶性胸膜间皮瘤的进展,操作简便且可重复;因此,它可用于研究人类MPM生物学并评估新型疗法的疗效。