Shao Lenan, Ouchi Tomoki, Sakamoto Maya, Mori Shiro, Kodama Tetsuya
Laboratory of Biomedical Engineering for Cancer, Department of Biomedical Engineering, Graduate School of Biomedical Engineering, Tohoku University, 4-1 Seiryo, Aoba, Sendai, Miyagi 980-8575, Japan; Department of Oral and Maxillofacial Surgery, Tongji Hospital, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan 430030, China.
Laboratory of Biomedical Engineering for Cancer, Department of Biomedical Engineering, Graduate School of Biomedical Engineering, Tohoku University, 4-1 Seiryo, Aoba, Sendai, Miyagi 980-8575, Japan.
Biochem Biophys Res Commun. 2015 May 8;460(3):543-8. doi: 10.1016/j.bbrc.2015.03.066. Epub 2015 Mar 27.
Iatrogenic induction of regional and distant cancer metastases is a risk associated with clinical resection of tumor-positive sentinel lymph nodes. However, there have been no studies of this risk in a mouse model of cancer metastasis. Here, we report that resection of a tumor-bearing subiliac lymph node (SiLN) enhanced lung metastasis in a mouse model of lymph node metastasis. Bioluminescence imaging revealed that metastatic tumor cells in the secondary lymph node continued to grow after resection of the SiLN, and that the probability of metastasis to the lungs was increased when the interval between SiLN inoculation and resection was reduced. Futhermore, histological analysis demonstrated that latents in the lung were stimulated to grow after resection of the SiLN. Fluorescence imaging indicated that the route of tumor cell dissemination from SiLN to the lung was the venous system located over the SiLN. We speculate that our mouse model will be useful for studying the mechanisms of tumor cell latency, with a view to improving the detection and treatment of latent metastases.
医源性诱导局部和远处癌症转移是肿瘤阳性前哨淋巴结临床切除相关的一种风险。然而,在癌症转移的小鼠模型中尚未有关于这种风险的研究。在此,我们报告在淋巴结转移的小鼠模型中,切除荷瘤的髂下淋巴结(SiLN)会增强肺转移。生物发光成像显示,在切除SiLN后,次级淋巴结中的转移性肿瘤细胞继续生长,并且当SiLN接种与切除之间的间隔缩短时,转移至肺部的概率增加。此外,组织学分析表明,切除SiLN后肺中的潜伏灶被刺激生长。荧光成像表明,肿瘤细胞从SiLN扩散至肺部的途径是位于SiLN上方的静脉系统。我们推测,我们的小鼠模型将有助于研究肿瘤细胞潜伏的机制,以期改善潜伏转移的检测和治疗。