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本文引用的文献

1
Therapeutic Cell-Cycle-Decoy Efficacy of a Telomerase-Dependent Adenovirus in an Orthotopic Model of Chemotherapy-Resistant Human Stomach Carcinomatosis Peritonitis Visualized With FUCCI Imaging.利用FUCCI成像在化疗耐药性人胃癌腹膜转移原位模型中评估端粒酶依赖性腺病毒的治疗性细胞周期诱饵疗效。
J Cell Biochem. 2017 Nov;118(11):3635-3642. doi: 10.1002/jcb.25593. Epub 2017 Jul 31.
2
Tumor-specific cell-cycle decoy by Salmonella typhimurium A1-R combined with tumor-selective cell-cycle trap by methioninase overcome tumor intrinsic chemoresistance as visualized by FUCCI imaging.鼠伤寒沙门氏菌A1-R的肿瘤特异性细胞周期诱饵与甲硫氨酸酶的肿瘤选择性细胞周期陷阱相结合,克服了肿瘤内在的化学抗性,这在FUCCI成像中得以显现。
Cell Cycle. 2016 Jul 2;15(13):1715-23. doi: 10.1080/15384101.2016.1181240. Epub 2016 May 6.
3
Salmonella typhimurium A1-R and Cell-Cycle Decoy Therapy of Cancer.鼠伤寒沙门氏菌A1-R与癌症的细胞周期诱饵疗法
Methods Mol Biol. 2016;1409:165-75. doi: 10.1007/978-1-4939-3515-4_14.
4
Cancer cells mimic in vivo spatial-temporal cell-cycle phase distribution and chemosensitivity in 3-dimensional Gelfoam® histoculture but not 2-dimensional culture as visualized with real-time FUCCI imaging.通过实时FUCCI成像观察发现,癌细胞在三维明胶海绵组织培养中模拟体内时空细胞周期阶段分布和化学敏感性,但在二维培养中则不然。
Cell Cycle. 2015;14(6):808-19. doi: 10.1080/15384101.2014.1000685.
5
Tumor-targeting Salmonella typhimurium A1-R decoys quiescent cancer cells to cycle as visualized by FUCCI imaging and become sensitive to chemotherapy.肿瘤靶向性鼠伤寒沙门氏菌A1-R诱使静止癌细胞进入细胞周期,这可通过FUCCI成像观察到,并且使癌细胞对化疗敏感。
Cell Cycle. 2014;13(24):3958-63. doi: 10.4161/15384101.2014.964115.
6
Selective methioninase-induced trap of cancer cells in S/G2 phase visualized by FUCCI imaging confers chemosensitivity.通过FUCCI成像观察到,甲硫氨酸酶选择性诱导癌细胞滞留在S/G2期可赋予化疗敏感性。
Oncotarget. 2014 Sep 30;5(18):8729-36. doi: 10.18632/oncotarget.2369.
7
Spatial-temporal FUCCI imaging of each cell in a tumor demonstrates locational dependence of cell cycle dynamics and chemoresponsiveness.肿瘤中每个细胞的时空FUCCI成像显示了细胞周期动力学和化学敏感性的位置依赖性。
Cell Cycle. 2014;13(13):2110-9. doi: 10.4161/cc.29156. Epub 2014 May 8.
8
Invading cancer cells are predominantly in G0/G1 resulting in chemoresistance demonstrated by real-time FUCCI imaging.实时 FUCCI 成像显示,侵袭性癌细胞主要处于 G0/G1 期,从而导致化疗耐药。
Cell Cycle. 2014;13(6):953-60. doi: 10.4161/cc.27818. Epub 2014 Jan 20.
9
A genetically engineered oncolytic adenovirus decoys and lethally traps quiescent cancer stem-like cells in S/G2/M phases.一种基因工程的溶瘤腺病毒可以诱骗并在 S/G2/M 期使静止的癌症干细胞样细胞致死性地陷入陷阱。
Clin Cancer Res. 2013 Dec 1;19(23):6495-505. doi: 10.1158/1078-0432.CCR-13-0742. Epub 2013 Sep 30.
10
The bulge area is the origin of nestin-expressing pluripotent stem cells of the hair follicle.隆突区域是毛囊中巢蛋白表达的多能干细胞的起源地。
J Cell Biochem. 2011 Aug;112(8):2046-50. doi: 10.1002/jcb.23122.

通过实时FUCCI成像观察到,细胞周期依赖性耐药静止癌细胞在化疗后诱导肿瘤血管生成。

Cell-cycle-dependent drug-resistant quiescent cancer cells induce tumor angiogenesis after chemotherapy as visualized by real-time FUCCI imaging.

作者信息

Yano Shuya, Takehara Kiyoto, Tazawa Hiroshi, Kishimoto Hiroyuki, Urata Yasuo, Kagawa Shunsuke, Fujiwara Toshiyoshi, Hoffman Robert M

机构信息

a AntiCancer, Inc. , San Diego , CA , USA.

b Department of Surgery , University of California San Diego , CA , USA.

出版信息

Cell Cycle. 2017 Mar 4;16(5):406-414. doi: 10.1080/15384101.2016.1220461. Epub 2016 Aug 11.

DOI:10.1080/15384101.2016.1220461
PMID:27715464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5351920/
Abstract

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.

摘要

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。