Karagiannis George S, Pastoriza Jessica M, Borriello Lucia, Jafari Rojin, Coste Anouchka, Condeelis John S, Oktay Maja H, Entenberg David
Department of Anatomy and Structural Biology, Albert Einstein College of Medicine; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine; Integrated Imaging Program, Albert Einstein College of Medicine;
Department of Anatomy and Structural Biology, Albert Einstein College of Medicine; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine; Department of Surgery, Montefiore Medical Center.
J Vis Exp. 2019 Jun 26(148). doi: 10.3791/59633.
The most common cause of cancer related mortality is metastasis, a process that requires dissemination of cancer cells from the primary tumor to secondary sites. Recently, we established that cancer cell dissemination in primary breast cancer and at metastatic sites in the lung occurs only at doorways called Tumor MicroEnvironment of Metastasis (TMEM). TMEM doorway number is prognostic for distant recurrence of metastatic disease in breast cancer patients. TMEM doorways are composed of a cancer cell which over-expresses the actin regulatory protein Mena in direct contact with a perivascular, proangiogenic macrophage which expresses high levels of TIE2 and VEGF, where both of these cells are tightly bound to a blood vessel endothelial cell. Cancer cells can intravasate through TMEM doorways due to transient vascular permeability orchestrated by the joint activity of the TMEM-associated macrophage and the TMEM-associated Mena-expressing cancer cell. In this manuscript, we describe two methods for assessment of TMEM-mediated transient vascular permeability: intravital imaging and fixed tissue immunofluorescence. Although both methods have their advantages and disadvantages, combining the two may provide the most complete analyses of TMEM-mediated vascular permeability as well as microenvironmental prerequisites for TMEM function. Since the metastatic process in breast cancer, and possibly other types of cancer, involves cancer cell dissemination via TMEM doorways, it is essential to employ well established methods for the analysis of the TMEM doorway activity. The two methods described here provide a comprehensive approach to the analysis of TMEM doorway activity, either in naïve or pharmacologically treated animals, which is of paramount importance for pre-clinical trials of agents that prevent cancer cell dissemination via TMEM.
癌症相关死亡的最常见原因是转移,这一过程需要癌细胞从原发性肿瘤扩散到继发性位点。最近,我们证实原发性乳腺癌和肺转移位点处的癌细胞扩散仅发生在称为转移瘤微环境(TMEM)的通道处。TMEM通道数量可预测乳腺癌患者转移性疾病的远处复发。TMEM通道由一个过度表达肌动蛋白调节蛋白Mena的癌细胞组成,该癌细胞与表达高水平TIE2和VEGF的血管周围促血管生成巨噬细胞直接接触,这两种细胞都紧密结合在血管内皮细胞上。由于TMEM相关巨噬细胞和TMEM相关表达Mena的癌细胞的联合活动协调了短暂的血管通透性,癌细胞可以通过TMEM通道进入血管。在本论文中,我们描述了两种评估TMEM介导的短暂血管通透性的方法:活体成像和固定组织免疫荧光。虽然这两种方法都有其优缺点,但将两者结合可能会提供对TMEM介导的血管通透性以及TMEM功能的微环境前提条件的最完整分析。由于乳腺癌以及可能其他类型癌症的转移过程涉及癌细胞通过TMEM通道的扩散,因此采用成熟的方法来分析TMEM通道活性至关重要。这里描述的两种方法为分析TMEM通道活性提供了一种全面的方法,无论是在未经处理的还是经过药物处理的动物中,这对于预防癌细胞通过TMEM扩散的药物的临床前试验至关重要。