Karenko L, Hyytinen E, Sarna S, Ranki A
Department of Dermatology and Venereal Diseases, Helsinki University Central Hospital, Finland.
J Invest Dermatol. 1997 Jan;108(1):22-9. doi: 10.1111/1523-1747.ep12285617.
The etiology of cutaneous T-cell lymphomas (CTCL) is unknown. We studied the pattern of chromosomal abnormalities with G-banding and interphase in situ hybridization methods in blood mononuclear cells in 17 patients representing the different phases of CTCL or the premalignant condition, parapsoriasis en plaque, and in 10 control persons. We used biotinylated centromere-specific probes with fluorescent detection (FISH) for chromosomes 1, 11, 8, and 17 and similar, enzymatically detectable, digoxigenin-labeled probes for chromosomes 1, 6, 12, 17, and 18. In G-banding, all patients showed numerical and structural chromosome aberrations. Numerical aberrations of chromosomes 6, 13, 15, and 17, marker chromosomes, and structural aberrations of chromosomes 3, 9, and 13 were increased in mycosis fungoides (MF) compared with healthy controls. In four of five patients the detection of a chromosomal clone preceded relapse or progression of the disease. In FISH of interphase cells, the cells abnormal for chromosomes 8 or 11, and for all four chromosomes collectively, were increased in MF and in Sezary Syndrome (SS). FISH and G-banding methods agreed statistically significantly for the detection of monosomy. Also, digoxigenin-labeled probes hybridized to interphases or mitoses detected aberrations corresponding to those observed with G-banding. Thus, chromosomally abnormal cells can be found in the peripheral blood of both parapsoriasis en plaque and CTCL patients. They can be detected with interphase cytogenetical methods, which obviates the need for dividing cells, often difficult to accomplish in CTCL.
皮肤T细胞淋巴瘤(CTCL)的病因尚不清楚。我们采用G显带和间期原位杂交方法,研究了17例代表CTCL不同阶段或癌前状态——斑块状副银屑病的患者以及10例对照者血液单核细胞中的染色体异常模式。我们使用生物素化的着丝粒特异性探针结合荧光检测(FISH)技术检测1号、11号、8号和17号染色体,并用类似的、酶促检测的地高辛配体标记探针检测1号、6号、12号、17号和18号染色体。在G显带分析中,所有患者均显示出染色体数目和结构异常。与健康对照相比,蕈样肉芽肿(MF)患者中6号、13号、15号和十七号染色体的数目异常、标记染色体以及3号、9号和13号染色体的结构异常有所增加。在五例患者中有四例,染色体克隆的检测先于疾病的复发或进展。在间期细胞的FISH检测中,8号或11号染色体以及所有四条染色体均异常的细胞在MF和Sezary综合征(SS)中有所增加。FISH和G显带方法在检测单体性方面具有显著的统计学一致性。此外,与间期或有丝分裂杂交的地高辛配体标记探针检测到的畸变与G显带观察到的畸变一致。因此,在斑块状副银屑病和CTCL患者的外周血中均可发现染色体异常细胞。可以通过间期细胞遗传学方法检测到这些细胞,这避免了对分裂细胞的需求,而在CTCL中获得分裂细胞往往很困难。