Padera Timothy P, Kadambi Ananth, di Tomaso Emmanuelle, Carreira Carla Mouta, Brown Edward B, Boucher Yves, Choi Noah C, Mathisen Douglas, Wain John, Mark Eugene J, Munn Lance L, Jain Rakesh K
E. L. Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, 100 Blossom Street, Boston, MA 02114, USA.
Science. 2002 Jun 7;296(5574):1883-6. doi: 10.1126/science.1071420. Epub 2002 Apr 25.
Lymphatic metastasis contributes to mortality from solid tumors. Whether metastasizing cancer cells reach lymph nodes via intratumor lymphatic vessels is unknown. Here, we examine functional lymphatics associated with mouse tumors expressing normal or elevated levels of vascular endothelial growth factor-C (VEGF-C), a molecule that stimulates lymphangiogenesis. Although VEGF-C overexpression increased lymphatic surface area in the tumor margin and lymphatic metastasis, these tumors contained no functional lymphatics, as assessed by four independent functional assays and immunohistochemical staining. These findings suggest that the functional lymphatics in the tumor margin alone are sufficient for lymphatic metastasis and should be targeted therapeutically.
淋巴转移是实体瘤致死的原因之一。转移的癌细胞是否通过肿瘤内淋巴管到达淋巴结尚不清楚。在此,我们研究了与表达正常或升高水平血管内皮生长因子C(VEGF-C,一种刺激淋巴管生成的分子)的小鼠肿瘤相关的功能性淋巴管。尽管VEGF-C过表达增加了肿瘤边缘的淋巴表面积和淋巴转移,但通过四项独立的功能测定和免疫组织化学染色评估,这些肿瘤中不存在功能性淋巴管。这些发现表明,仅肿瘤边缘的功能性淋巴管就足以发生淋巴转移,应作为治疗靶点。