Faculty of Welfare and Health Science, Oita University, Oita, 870-1192, Japan.
Hokkaido University Research Center for Zoonosis Control, Hokkaido, 001-0020, Japan.
Clin Exp Metastasis. 2018 Dec;35(8):785-796. doi: 10.1007/s10585-018-9940-8. Epub 2018 Sep 25.
Lymphangiogenesis plays a crucial role in promoting cancer metastasis to sentinel lymph nodes (LNs) and beyond. Increasing data have shown that simvastatin, a cholesterol-lowering medication for the prevention of cardiovascular diseases, is involved in tumor growth and dissemination, and endothelial functions. This study aimed to investigate the potential effect of simvastatin on lymphatic formation and LN metastasis. Tumor models were established by subcutaneous injection of B16-F10 melanoma cells into mouse hind footpads. Simvastatin was administered (0.2 µg/g, intraperitoneal injection, IP) every other day for a total of eight times. Tissue samples were removed and examined by immunohistochemical staining and reverse transcription-polymerase chain reaction (RT-PCR) techniques. The lymphatics of LN, skin, liver, and lung exhibited morphological changes, and LN weight and metastatic area of the tumor group treated with simvastatin was lower than that of the untreated tumor group. Analysis of lymphatic size, area fraction, and lymphatic vessel density showed tissue specificity and variation to melanoma carcinogenesis in the simvastatin-treated group compared with the untreated group. In addition, LNs and cutaneous tissues showed altered expression of lymphangiogenic factors and inflammatory cytokines such as VEGF-A/-C/-D and TNF-α. These findings indicated that simvastatin may modify lymphangiogenesis and tumor progression in malignant melanoma.
淋巴管生成在促进癌症转移至前哨淋巴结 (LNs) 及更远的部位方面起着至关重要的作用。越来越多的数据表明,辛伐他汀是一种用于预防心血管疾病的降胆固醇药物,它参与肿瘤的生长和扩散以及内皮功能。本研究旨在探讨辛伐他汀对淋巴管生成和 LN 转移的潜在影响。通过将 B16-F10 黑色素瘤细胞皮下注射到小鼠后足垫来建立肿瘤模型。辛伐他汀(0.2μg/g,腹腔注射,IP)每隔一天给药一次,共给药 8 次。通过免疫组织化学染色和逆转录聚合酶链反应 (RT-PCR) 技术切除和检查组织样本。LN、皮肤、肝脏和肺部的淋巴管显示出形态学变化,并且用辛伐他汀处理的肿瘤组的 LN 重量和肿瘤转移面积低于未处理的肿瘤组。与未处理组相比,辛伐他汀处理组的淋巴管大小、面积分数和淋巴管密度分析显示出组织特异性和对黑色素瘤发生的变化。此外,LN 和皮肤组织表现出血管内皮生长因子 (VEGF)-A/-C/-D 和肿瘤坏死因子 (TNF)-α等淋巴管生成因子和炎症细胞因子的表达改变。这些发现表明,辛伐他汀可能改变恶性黑色素瘤中的淋巴管生成和肿瘤进展。