AntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA; Department of Gastroenterological Surgery; Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences; Okayama, Japan.
AntiCancer, Inc; San Diego, CA USA; Department of Surgery; University of California, San Diego; San Diego, CA USA.
Cell Cycle. 2014;13(6):953-60. doi: 10.4161/cc.27818. Epub 2014 Jan 20.
Invasive cancer cells are a critical target in order to prevent metastasis. In the present report, we demonstrate real-time visualization of cell cycle kinetics of invading cancer cells in 3-dimensional (3D) Gelfoam® histoculture, which is in vivo-like. A fluorescence ubiquitination cell cycle indicator (FUCCI) whereby G0/G1 cells express a red fluorescent protein and S/G2/M cells express a green fluorescent protein was used to determine the cell cycle position of invading and non-invading cells. With FUCCI 3D confocal imaging, we observed that cancer cells in G0/G1 phase in Gelfoam® histoculture migrated more rapidly and further than cancer cells in S/G2/M phases. Cancer cells ceased migrating when they entered S/G2/M phases and restarted migrating after cell division when the cells re-entered G0/G1. Migrating cancer cells also were resistant to cytotoxic chemotherapy, since they were preponderantly in G0/G1, where cytotoxic chemotherapy is not effective. The results of the present report suggest that novel therapy targeting G0/G1 cancer cells should be developed to prevent metastasis.
为了防止转移,侵袭性癌细胞是一个关键的靶点。在本报告中,我们展示了在类似于体内环境的 3D Gelfoam®组织培养中实时观察侵袭性癌细胞细胞周期动力学的情况。荧光泛素细胞周期指示剂(FUCCI),其中 G0/G1 细胞表达红色荧光蛋白,S/G2/M 细胞表达绿色荧光蛋白,用于确定侵袭性和非侵袭性细胞的细胞周期位置。通过 FUCCI 3D 共聚焦成像,我们观察到 Gelfoam®组织培养中的 G0/G1 期癌细胞比 S/G2/M 期癌细胞迁移得更快、更远。当癌细胞进入 S/G2/M 期时,它们停止迁移,在细胞分裂后重新进入 G0/G1 期时重新开始迁移。迁移的癌细胞也对细胞毒性化疗有抗性,因为它们主要处于 G0/G1 期,而细胞毒性化疗在这个阶段无效。本报告的结果表明,应该开发针对 G0/G1 癌细胞的新型治疗方法来预防转移。