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新血管化与bFGF出口的转换有关,在纤维肌肉瘤多阶段发展过程中
J Kandel1, E Bossy-Wetzel, F Radvanyi
1Department of Surgery, Children's Hospital, Boston, Massachusetts 02115.
Cell
|September 20, 1991
概括
在转基因小鼠模型中,皮肤纤维沙尔科马通过增加血管化的阶段进行进展. 这与细胞外释放基本纤维细胞生长因子 (bFGF) 相关,这是一个关键的血管生成因子.
科学领域:
- 在瘤学瘤学.
- 皮肤病学 皮肤病学
- 分子生物学分子生物学
背景情况:
- 皮肤纤维肉瘤通过多阶段的途径发展.
- 新血管化是侵袭性纤维素瘤和纤维素瘤阶段的标志.
- 基本纤维细胞生长因子 (bFGF) 参与细胞生长和组织修复.
研究的目的:
- 调查bFGF在皮肤纤维瘤多阶段发展中的作用.
- 为了将bFGF局部与瘤进展和血管化相关联.
- 了解在瘤发生过程中切换到血管性表型.
主要方法:
- 利用转基因小鼠模型用于皮肤纤维素瘤的发展.
- 分析的细胞培养来自轻度纤维素瘤,侵袭性纤维素瘤和纤维素瘤病变.
- 在不同瘤阶段和正常皮肤纤维细胞中检查了bFGF合成和局部化.
主要成果:
- 基本纤维细胞生长因子 (bFGF) 在纤维瘤发育的各个阶段和正常皮肤纤维细胞中合成.
- 在侵袭性纤维素瘤和纤维素瘤阶段,bFGF局部化从细胞关联到细胞外释放的转变发生.
- 这种细胞外bFGF释放与增加的新血管化和瘤性相关.
结论:
- 皮肤纤维沙尔科马的多阶段瘤发生涉及转换到血管性表型.
- 细胞外释放的bFGF是与新血管和瘤进展相关的关键事件.
- 在这种纤维瘤模型中,bFGF出口似乎是血管性切换的关键驱动因素.
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