Nathanson S D, Nelson L T, Lee M
Department of Surgery, Henry Ford Hospital, Detroit, MI 48202.
Clin Exp Metastasis. 1993 Jan;11(1):45-54. doi: 10.1007/BF00880065.
A malignant tumor that arose spontaneously in the subcutaneous tissue of the back of a C57BL/6 female mouse was found to metastasize spontaneously to the liver. The primary and metastatic tumors, SML (spontaneous metastasis to the liver) 1 and SML 2, were established in vitro in long-term cell suspension culture and were passaged 10 times in vivo for 18 months. When 100,000 cells were injected subcutaneously in the orthotopic position, tumor growth appeared in 60% of the SML 1 mice and 100% of the SML 2 mice. SML 1 did not grow when injected in the footpad, while SML 2 did. The median survival was 47 days for SML 1 and 48.5 days for SML 2 (P = 0.013). The pattern of metastasis was similar for both tumor cell lines, irrespective of intravenous or subcutaneous injection routes. Spontaneous metastasis of the SML 2 line occurred from both the orthotopic and heterotopic sites, while the SML 1 metastasized spontaneously from the orthotopic site only. Liver metastasis appeared in > 90% of the mice for both SML 1 and SML 2. Metastasis to the spleen occurred in about half the mice. Other sites of metastasis were the ovaries (36% and 52%, respectively, for SML 1 and SML 2), the kidneys (approximately 15%) and the small bowel (very rarely). Metastasis to the lungs did not occur except very rarely in the later passages of the SML 2 line. Histologic, immunohistochemical and electron microscopic studies showed a histiocytic tumor with macrophage characteristics. The cells exhibited chemotaxis toward liver extracellular matrix and reduced motility toward collagen IV, laminin and fibronectin compared to the B16-F10 melanoma line. This spontaneously occurring tumor should prove useful for the study of organ-specific metastasis to the liver.
在一只C57BL/6雌性小鼠背部皮下组织中自发产生的恶性肿瘤被发现可自发转移至肝脏。原发性肿瘤和转移性肿瘤,即SML(自发转移至肝脏)1和SML 2,在长期细胞悬液培养中建立了体外培养体系,并在体内传代10次,历时18个月。当将100,000个细胞原位皮下注射时,60%的SML 1小鼠和100%的SML 2小鼠出现肿瘤生长。SML 1注射到足垫时不生长,而SML 2则生长。SML 1的中位生存期为47天,SML 2为48.5天(P = 0.013)。两种肿瘤细胞系的转移模式相似,与静脉注射或皮下注射途径无关。SML 2系的自发转移发生于原位和异位部位,而SML 1仅从原位自发转移。SML 1和SML 2的小鼠中均有> 90%出现肝转移。约一半的小鼠发生脾转移。其他转移部位为卵巢(SML 1和SML 2分别为36%和52%)、肾脏(约15%)和小肠(非常罕见)。除了在SML 2系后期传代中非常罕见的情况外,未发生肺转移。组织学、免疫组织化学和电子显微镜研究显示为具有巨噬细胞特征的组织细胞肿瘤。与B16-F10黑色素瘤细胞系相比,这些细胞对肝细胞外基质表现出趋化性,对IV型胶原、层粘连蛋白和纤连蛋白的运动性降低。这种自发产生的肿瘤应被证明对研究肝脏的器官特异性转移有用。