Nakayama T, Taback B, Turner R, Morton D L, Hoon D S
Department of Molecular Oncology, John Wayne Cancer Institute, 2200 Santa Monica Blvd., Santa Monica, CA 904304, USA.
Am J Pathol. 2001 Apr;158(4):1371-8. doi: 10.1016/S0002-9440(10)64088-6.
In-transit melanoma is characterized by an aggressive pattern of recurrence that is associated with a poorer prognosis. Because in-transit melanoma is considered to result from the intralymphatic trapping of melanoma cells between the primary tumor and regional lymph nodes, it provides an excellent model to assess genetic events associated with early metastasis. The hypothesis of this study was to determine whether in-transit metastases are clonal in origin and therefore, may have specific genetic alterations uniquely associated with this disease and the development of early metastasis. This was assessed using loss of heterozygosity (LOH) analysis for specific DNA microsatellite loci. Seventy-nine paraffin-embedded in-transit melanoma lesions from 25 patients (range, 2 to 9 lesions per patient; average, 3.4 lesions per patient) were assessed for LOH using eight microsatellite DNA markers on six chromosomes. In 19 of 25 patients (76%) LOH was demonstrated for at least one marker. The most frequent microsatellite marker demonstrating LOH was D9S157 (56%). Using LOH microsatellite markers to assess intertumor heterogeneity, six of 79 tumors (7.6%) demonstrated different profiles when compared to other lesions from the same patient. In-transit metastases from those patients demonstrating intertumor heterogeneity were further assessed using laser capture microdissection and DNA analysis, and revealed no significant intratumor heterogeneity. In conclusion, LOH was frequently observed in in-transit melanoma metastasis. Based on LOH analysis, in-transit metastases are clonal in origin. The establishment of clinically successful in-transit melanoma metastasis requires specific genetic events that seem to be unique and homogeneous for each patient.
移行转移黑色素瘤的特征是复发模式具有侵袭性,且预后较差。由于移行转移黑色素瘤被认为是黑色素瘤细胞在原发性肿瘤和区域淋巴结之间的淋巴管内滞留所致,它为评估与早期转移相关的基因事件提供了一个极佳的模型。本研究的假设是确定移行转移是否起源于克隆,因此可能具有与该疾病及早期转移发展独特相关的特定基因改变。这通过对特定DNA微卫星位点进行杂合性缺失(LOH)分析来评估。对来自25例患者的79个石蜡包埋的移行转移黑色素瘤病灶(范围为每位患者2至9个病灶;平均每位患者3.4个病灶),使用六条染色体上的八个微卫星DNA标记评估LOH。在25例患者中的19例(76%),至少有一个标记显示出LOH。显示LOH最频繁的微卫星标记是D9S157(56%)。使用LOH微卫星标记评估肿瘤间异质性时,79个肿瘤中有6个(7.6%)与同一患者的其他病灶相比显示出不同的图谱。对那些显示肿瘤间异质性的患者的移行转移灶,进一步使用激光捕获显微切割和DNA分析进行评估,结果显示肿瘤内无显著异质性。总之,在移行转移黑色素瘤中经常观察到LOH。基于LOH分析,移行转移起源于克隆。临床上成功建立移行转移黑色素瘤需要特定的基因事件,这些事件似乎对每位患者都是独特且同质的。