He Yulong, Rajantie Iiro, Ilmonen Maritta, Makinen Taija, Karkkainen Marika J, Haiko Paula, Salven Petri, Alitalo Kari
Molecular/Cancer Biology Laboratory and Ludwig Institute for Cancer Research, Biomedicum Helsinki, Helsinki University Central Hospital, and Institute of Biomedicine, Biomedicum Helsinki, University of Helsinki, Helsinki, Finland.
Cancer Res. 2004 Jun 1;64(11):3737-40. doi: 10.1158/0008-5472.CAN-04-0088.
Endothelial progenitor cells have been shown to contribute to angiogenesis in various tumor models. Here, we have studied the relative contributions of bone marrow (BM)-derived endothelial progenitors and pre-existing lymphatic vessels to tumor lymphangiogenesis. We did not find significant incorporation of genetically marked BM-derived cells in lymphatic vessels during tumor- or vascular endothelial growth factor C-induced lymphangiogenesis. The degree of tumor lymphangiogenesis correlated with lymphatic vessel density in the peritumoral area, and despite tumor lymphangiogenesis, lymphatic metastasis failed to occur in gene-targeted vascular endothelial growth factor C(+/-) mice that have hypoplasia of the lymphatic network. Our data demonstrate that during tumor lymphangiogenesis and cancer cell dissemination via the lymphatics, the newly formed lymphatic vessels sprout from the pre-existing local lymphatic network with little if any incorporation of BM-derived endothelial progenitor cells.
内皮祖细胞已被证明在各种肿瘤模型中有助于血管生成。在此,我们研究了骨髓(BM)来源的内皮祖细胞和已有的淋巴管对肿瘤淋巴管生成的相对贡献。在肿瘤或血管内皮生长因子C诱导的淋巴管生成过程中,我们未发现基因标记的BM来源细胞显著掺入淋巴管。肿瘤淋巴管生成的程度与瘤周区域的淋巴管密度相关,并且尽管存在肿瘤淋巴管生成,但在淋巴管网络发育不全的基因靶向血管内皮生长因子C(+/-)小鼠中未发生淋巴转移。我们的数据表明,在肿瘤淋巴管生成和癌细胞通过淋巴管扩散过程中,新形成的淋巴管从已有的局部淋巴管网络中芽生,很少有BM来源的内皮祖细胞掺入,即使有也很少。