Bernués M, Casadevall C, Miró R, Caballín M R, Villavicencio H, Salvador J, Zamarrón A, Egozcue J
Institut de Biologia Fonamental, Universitat Autònoma de Barcelona, Spain.
Cancer Genet Cytogenet. 1995 Oct 15;84(2):123-7. doi: 10.1016/0165-4608(95)00044-5.
We describe the first case of a familial renal cell carcinoma cytogenetically characterized as a papillary renal cell carcinoma. Cytogenetic and molecular studies were performed on primary renal cell carcinomas and normal kidney tissue from two members of the same family. Both patients showed a normal constitutional karyotype. The two tumors analyzed from the first patient showed the numerical chromosome alterations characteristic of papillary renal cell carcinomas. From the four tumors analyzed in the second patient, three of them presented the cytogenetic pattern of papillary renal cell tumors, and the fourth showed only structural chromosome abnormalities with the presence of a del(7)t(7;7) or dup(7) in all metaphases analyzed. Chromosome 3 was cytogenetically unaffected in all tumors from both patients, and restriction fragment length polymorphism analysis performed with probe pEFD145 (3p21.1-p23) did not detect any loss of heterozygosity.
我们描述了首例经细胞遗传学鉴定为乳头状肾细胞癌的家族性肾细胞癌病例。对同一家族两名成员的原发性肾细胞癌及正常肾组织进行了细胞遗传学和分子研究。两名患者的染色体核型均正常。对首例患者的两个肿瘤进行分析,发现具有乳头状肾细胞癌特征性的染色体数目改变。对第二例患者的四个肿瘤进行分析,其中三个呈现乳头状肾细胞肿瘤的细胞遗传学模式,第四个在所有分析的中期相中仅显示结构性染色体异常,存在del(7)t(7;7)或dup(7)。两名患者所有肿瘤的染色体3在细胞遗传学上均未受影响,用探针pEFD145(3p21.1-p23)进行的限制性片段长度多态性分析未检测到任何杂合性缺失。