Endothelial Side Population Cells Contribute to Tumor Angiogenesis and Antiangiogenic Drug Resistance

被引:65
作者
Naito, Hisamichi [1 ]
Wakabayashi, Taku [1 ]
Kidoya, Hiroyasu [1 ]
Muramatsu, Fumitaka [1 ]
Takara, Kazuhiro [1 ]
Eino, Daisuke [1 ]
Yamane, Keitaro [1 ]
Iba, Tomohiro [1 ]
Takakura, Nobuyuki [1 ]
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Signal Transduct, Suita, Osaka 5650871, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
HEMATOPOIETIC STEM-CELLS; PROGENITOR CELLS; FUNCTIONAL-PROPERTIES; CANCER; IDENTIFICATION; REPAIR; VEGF; REGENERATION; MECHANISMS; EXPRESSION;
D O I
10.1158/0008-5472.CAN-15-2998
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis plays a crucial role in tumor growth, with an undisputed contribution of resident endothelial cells (EC) to new blood vessels in the tumor. Here, we report the definition of a small population of vascular-resident stem/progenitor-like EC that contributes predominantly to new blood vessel formation in the tumor. Although the surface markers of this population are similar to other ECs, those from the lung vasculature possess colony-forming ability in vitro and contribute to angiogenesis in vivo. These specific ECs actively proliferate in lung tumors, and the percentage of this population significantly increases in the tumor vasculature relative to normal lung tissue. Using genetic recombination and bone marrow trans-plant models, we show that these cells are phenotypically true ECs and do not originate from hematopoietic cells. After treatment of tumors with antiangiogenic drugs, these specific ECs selectively survived and remained in the tumor. Together, our results established that ECs in the peripheral vasculature are heterogeneous and that stem/progenitor-like ECs play an indispensable role in tumor angiogenesis as EC-supplying cells. The lack of susceptibility of these ECs to antiangiogenic drugs may account for resistance of the tumor to this drug type. Thus, inhibiting these ECs might provide a promising strategy to overcome antiangiogenic drug resistance. (C)2016 AACR.
引用
收藏
页码:3200 / 3210
页数:11
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