Yano Shuya, Takehara Kiyoto, Tazawa Hiroshi, Kishimoto Hiroyuki, Urata Yasuo, Kagawa Shunsuke, Fujiwara Toshiyoshi, Hoffman Robert M
a AntiCancer, Inc. , San Diego , CA , USA.
b Department of Surgery , University of California San Diego , CA , USA.
Cell Cycle. 2017 Mar 4;16(5):406-414. doi: 10.1080/15384101.2016.1220461. Epub 2016 Aug 11.
We previously demonstrated that quiescent cancer cells in a tumor are resistant to conventional chemotherapy as visualized with a fluorescence ubiquitination cell cycle indicator (FUCCI). We also showed that proliferating cancer cells exist in a tumor only near nascent vessels or on the tumor surface as visualized with FUCCI and green fluorescent protein (GFP)-expressing tumor vessels. In the present study, we show the relationship between cell-cycle phase and chemotherapy-induced tumor angiogenesis using in vivo FUCCI real-time imaging of the cell cycle and nestin-driven GFP to detect nascent blood vessels. We observed that chemotherapy-treated tumors, consisting of mostly of quiescent cancer cells after treatment, had much more and deeper tumor vessels than untreated tumors. These newly-vascularized cancer cells regrew rapidly after chemotherapy. In contrast, formerly quiescent cancer cells decoyed to S/G phase by a telomerase-dependent adenovirus did not induce tumor angiogenesis. The present results further demonstrate the importance of the cancer-cell position in the cell cycle in order that chemotherapy be effective and not have the opposite effect of stimulating tumor angiogenesis and progression.
我们之前利用荧光泛素化细胞周期指示剂(FUCCI)证实,肿瘤中的静止癌细胞对传统化疗具有抗性。我们还表明,利用FUCCI和表达绿色荧光蛋白(GFP)的肿瘤血管可视化观察发现,增殖癌细胞仅存在于肿瘤中新生血管附近或肿瘤表面。在本研究中,我们利用细胞周期的体内FUCCI实时成像以及巢蛋白驱动的GFP来检测新生血管,展示了细胞周期阶段与化疗诱导的肿瘤血管生成之间的关系。我们观察到,化疗处理后的肿瘤在治疗后大多由静止癌细胞组成,其肿瘤血管比未处理的肿瘤更多、更深。这些新血管化的癌细胞在化疗后迅速重新生长。相比之下,通过端粒酶依赖性腺病毒诱使进入S/G期的先前静止癌细胞并未诱导肿瘤血管生成。目前的结果进一步证明了癌细胞在细胞周期中的位置对于化疗有效且不产生刺激肿瘤血管生成和进展的相反效果的重要性。