Department of Genetics and Laboratory Animal Breeding, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland.
J Radiat Res. 2011;52(2):147-58. doi: 10.1269/jrr.10035. Epub 2011 Feb 19.
Genetics of susceptibility to radiation-induced hematopoietic neoplasms and somatic chromosomal aberrations were analyzed in 305 backcross (CcS-17xCcS-2)xCcS-2 mice of two CcS/Dem recombinant congenic strains. Irradiated CcS-2 mice were previously shown to exhibit high frequency of myeloid neoplasms whereas irradiated CcS-17 mice were susceptible to T-cell lymphomas. Mice were exposed to four whole-body irradiation doses of 1.7 Gy at one week intervals, which resulted in 139 hematopoietic neoplasms. The hematopoietic neoplasms were classified according to the Bethesda proposals for classification of lymphoid and nonlymphoid hematopoietic neoplasms in mice. Genotyping of mice with 24 microsatellite markers and subsequent statistical analysis indicated linkage of the radiation induced T-lymphomas to two loci on chromosome 10 (D10Mit134) and chromosome 12 (D12Mit52). T-lymphoma susceptibility appeared to be linked to D10Mit134 in a sex dependent way. In contrast, the myeloid-granulocytic leukemias susceptibility is linked to combined effects of chromosome 5 (D5Mit179) and 16 (D16Mit34). Cytogenetic analysis was performed according to the standard G-bands procedure and confirmed using FISH method. We found non-random numerical and structural chromosomal changes in lymphoid neoplasms. Cytogenetic analysis indicated chromosomal aberrations presumably associated with lymphomagenesis, no specific cancer-related rearrangements were observed.
在两个 CcS/Dem 重组近交系的 305 只回交(CcS-17xCcS-2)xCcS-2 小鼠中,分析了辐射诱导的造血肿瘤和体细胞染色体畸变易感性的遗传基础。先前的研究表明,辐射后的 CcS-2 小鼠易发生髓系肿瘤,而辐射后的 CcS-17 小鼠易发生 T 细胞淋巴瘤。将小鼠暴露于四个全身体照射剂量为 1.7 Gy 的剂量,间隔一周,导致 139 例造血肿瘤。根据用于小鼠淋巴样和非淋巴样造血肿瘤分类的贝塞斯达建议对造血肿瘤进行分类。用 24 个微卫星标记对小鼠进行基因分型,并进行随后的统计分析表明,辐射诱导的 T 细胞淋巴瘤与染色体 10(D10Mit134)和染色体 12(D12Mit52)上的两个位点有关。T 细胞淋巴瘤易感性似乎与 D10Mit134 呈性别依赖性相关。相比之下,髓系-粒细胞性白血病的易感性与染色体 5(D5Mit179)和 16(D16Mit34)的联合效应有关。根据标准 G 带程序进行细胞遗传学分析,并使用 FISH 方法进行验证。我们发现了淋巴肿瘤中非随机的数值和结构染色体变化。细胞遗传学分析表明存在与淋巴瘤发生相关的染色体畸变,但未观察到特定的与癌症相关的重排。