Murty V V, Ladanyi M, Houldsworth J, Mikraki V, Chaganti R S
Laboratory of Cancer Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.
Diagn Mol Pathol. 1992 Dec;1(4):221-8.
We have used an in situ hybridization method for analysis of expression of BCL2 and MYC on cytospun preparations of normal and malignant lymphoid cell lines and tissue sections of normal and malignant lymph nodes. The probes comprised 50-mer antisense oligonucleotides starting at the ATG codons of exon 3 of BCL2 and exon 2 of MYC. We studied the expression of these two genes in frozen tissue sections of biopsy specimens derived from normal and hyperplastic lymph nodes, B-cell lymphomas carrying the t(14;18)(q32;q21) and t(8;14)(q24;q32) translocations, and T-cell lymphomas with clonal chromosome abnormalities. While all proliferating cells expressed both genes, BCL2 expression was increased two- to threefold in follicular lymphomas with t(14;18) and MYC expression was increased two- to four-fold in high-grade lymphomas with t(8;14). These results are consistent with previous data on deregulated expression of these genes obtained from study of lymphoma cell lines carrying the relevant translocations.
我们采用原位杂交方法,对正常和恶性淋巴样细胞系的细胞涂片制剂以及正常和恶性淋巴结的组织切片中BCL2和MYC的表达进行分析。探针由起始于BCL2第3外显子的ATG密码子和MYC第2外显子的50聚体反义寡核苷酸组成。我们研究了这两个基因在取自正常和增生性淋巴结、携带t(14;18)(q32;q21)和t(8;14)(q24;q32)易位的B细胞淋巴瘤以及具有克隆性染色体异常的T细胞淋巴瘤的活检标本冷冻组织切片中的表达。虽然所有增殖细胞均表达这两个基因,但在携带t(14;18)的滤泡性淋巴瘤中BCL2表达增加了2至3倍,在携带t(8;14)的高级别淋巴瘤中MYC表达增加了2至4倍。这些结果与先前通过对携带相关易位的淋巴瘤细胞系研究获得的这些基因表达失调的数据一致。