Liebelt A G, Sass B, Lombard L S
Registry of Experimental Cancers, NIH, Bethesda, MD 20892.
J Exp Pathol. 1987 Spring;3(2):115-45.
The purpose of this study is to review the pertinent literature on the incidence, methods of induction and pathogenesis of ovarian tumors of mice. Strains of mice with a high incidence of spontaneously occurring granulosa cell tumors (gct) and tubular adenomas (ta) are the C3HeB/Fe and C3HeB/De; strain HAN:NMRI developed Sertoli cell tumors and (DBA x Ce)F1 hybrids had a high incidence gct. Ninety-five percent of hybrid (C57BL/6J x C3H/HeJ)F1 WxWv mice which lack germ cells develop complex tubular adenomas. Strain LT, in which a high percentage of ovarian ova develop parthenogenetically, develops has a high incidence of teratomas. The use of hormones, castration and transplantation of the ovaries in a number of inbred strains results in a high incidence of ovarian tumors; in strain Maf/Sp gct and luteomas were induced in 82%. Irradiation with gamma rays produced a similar incidence of ovarian tumors in (C57L x A)F1 hybrids. The chemical inducing the highest incidence (92%) of ovarian tumors of mice is 9,10 Dimethyl 1,2 benzanthracene (DMBA). Recently, 4-Vinylcyclohexene was shown to induce a high incidence of ovarian tumors. A number of rare ovarian tumors were reported. Described are five androblastomas composed of either Leydig or Sertoli cells or a combination of the two cell types and a single undifferentiated androblastoma. Seven teratomas were described, three of which contained large amounts of neural tissue; another was classified as a teratoma with a parieto-visceral yolk-sac carcinoma component.
本研究的目的是回顾有关小鼠卵巢肿瘤的发病率、诱导方法和发病机制的相关文献。自发发生颗粒细胞瘤(gct)和管状腺瘤(ta)发病率高的小鼠品系是C3HeB/Fe和C3HeB/De;HAN:NMRI品系发生了支持细胞瘤,而(DBA×Ce)F1杂交种gct的发病率很高。缺乏生殖细胞的95%的杂交(C57BL/6J×C3H/HeJ)F1 WxWv小鼠会发展为复杂的管状腺瘤。LT品系中,高比例的卵巢卵进行孤雌生殖,畸胎瘤的发病率很高。在一些近交系中使用激素、阉割和卵巢移植会导致卵巢肿瘤的高发病率;在Maf/Sp品系中,82%诱导产生了gct和黄体瘤。用γ射线照射(C57L×A)F1杂交种产生了类似的卵巢肿瘤发病率。诱发小鼠卵巢肿瘤发病率最高(92%)的化学物质是9,10-二甲基-1,2-苯并蒽(DMBA)。最近,4-乙烯基环己烯被证明可诱发高发病率的卵巢肿瘤。报告了一些罕见的卵巢肿瘤。描述了5例由莱迪希细胞或支持细胞或两种细胞类型组合构成的成雄细胞瘤以及1例未分化成雄细胞瘤。描述了7例畸胎瘤,其中3例含有大量神经组织;另一例被归类为具有体壁-内脏卵黄囊癌成分的畸胎瘤。