SISTER CHROMATID EXCHANGE ANALYSIS IN FAMILIAL GROUPS OF MALIGNANT-MELANOMA PATIENTS

被引:8
作者
ILLENI, MT [1 ]
ROVINI, D [1 ]
GRASSI, C [1 ]
LOMBARDO, C [1 ]
PLACUCCI, M [1 ]
SQUICCIARINI, P [1 ]
CASCINELLI, N [1 ]
GHIDONI, A [1 ]
机构
[1] UNIV MILAN,DIPARTIMENTO GENET BIOL MICRORGANISMI,I-20122 MILAN,ITALY
关键词
D O I
10.1016/0165-4608(91)90100-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Sister chromatid exchange (SCE) analysis was carried out on peripheral blood lymphocytes of 20 familial malignant melanoma (FMM) and 39 sporadic malignant melanoma (SMM) untreated patients, belonging to 10 and 39 families, respectively. The study was extended to 39 unaffected close relatives of FMM patients, to 187 unaffected close relatives of SMM patients, and to 20 unaffected unrelated individuals (control group), all examined under the same conditions. The mean SCE rates/cell were significantly higher in MM families than in the control group, and in melanoma patients than in their close relatives. The mean SCE levels of FMM and SMM patients, (8.4 +/- 0.8 and 8.0 +/- 0.3, respectively) were similar, and so were the distributions of individuals in classes of increasing SCE values (with a modal value at 7-8 SCEs/cell). The mean SCE levels of close relatives of FMM and SMM patients were also similar (5.4 +/- 0.2 and 5.4 +/- 0.1, respectively, with a modal value at 4-5 SCEs/cell), and slightly higher than in the control group (4.7 +/- 0.2 SCEs/cell). More than 7 SCEs/cell were observed in the majority (41 of 59) of FMM or SMM patients, in a smaller fraction (25 of 227) unaffected relatives, and in none of 20 unrelated unaffected individuals. These observations favor the hypothesis that higher SCE levels may be an expression of constitutional lesions predisposing to this neoplastic disease.
引用
收藏
页码:237 / 246
页数:10
相关论文
共 27 条
[1]
BERGMAN W, 1989, 2ND INT C MEL VEN, P90
[2]
CYTOGENETICS IN HEREDITARY MALIGNANT-MELANOMA AND DYSPLASTIC NEVUS SYNDROME - IS DYSPLASTIC NEVUS SYNDROME A CHROMOSOME INSTABILITY DISORDER [J].
CAPORASO, N ;
GREENE, MH ;
TSAI, S ;
PICKLE, LW ;
MULVIHILL, JJ .
CANCER GENETICS AND CYTOGENETICS, 1987, 24 (02) :299-314
[3]
DRACOPOLI NC, 1989, 2ND INT C MEL VEN, P119
[4]
MALIGNANT-MELANOMA - SISTER CHROMATID EXCHANGE ANALYSIS IN 3 FAMILIES [J].
GHIDONI, A ;
PRIVITERA, E ;
RAIMONDI, E ;
ROVINI, D ;
ILLENI, MT ;
CASCINELLI, N .
CANCER GENETICS AND CYTOGENETICS, 1983, 9 (04) :347-354
[5]
GHIDONI A, 1984, SISTER CHROMATID EXC, P855
[6]
HIGH-RISK OF MALIGNANT-MELANOMA IN MELANOMA-PRONE FAMILIES WITH DYSPLASTIC NEVI [J].
GREENE, MH ;
CLARK, WH ;
TUCKER, MA ;
KRAEMER, KH ;
ELDER, DE ;
FRASER, MC .
ANNALS OF INTERNAL MEDICINE, 1985, 102 (04) :458-465
[7]
CHROMOSOME REARRANGEMENTS IN DYSPLASTIC NEVUS SYNDROME PREDISPOSING TO MALIGNANT-MELANOMA [J].
HECHT, F ;
HECHT, BK .
CANCER GENETICS AND CYTOGENETICS, 1988, 35 (01) :73-78
[8]
FIBROBLASTS FROM PATIENTS WITH HEREDITARY CUTANEOUS MALIGNANT-MELANOMA ARE ABNORMALLY SENSITIVE TO THE MUTAGENIC EFFECT OF SIMULATED SUNLIGHT AND 4-NITROQUINOLINE 1-OXIDE [J].
HOWELL, JN ;
GREENE, MH ;
CORNER, RC ;
MAHER, VM ;
MCCORMICK, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (04) :1179-1183
[9]
ILLENI MT, 1989, 2ND INT C MEL VEN, P122
[10]
SISTER CHROMATID EXCHANGES, HYPERDIPLOIDY AND CHROMOSOMAL REARRANGEMENTS STUDIES IN CELLS FROM MELANOMA-PRONE INDIVIDUALS BELONGING TO FAMILIES WITH THE DYSPLASTIC NEVUS SYNDROME [J].
JASPERS, NGJ ;
ROZADEJONGH, EJM ;
DONSELAAR, IG ;
VANVELZENTILLEMANS, JTM ;
VANHEMEL, JO ;
RUMKE, P ;
VANDERKAMP, AWM .
CANCER GENETICS AND CYTOGENETICS, 1987, 24 (01) :33-43