Soufir N, Lacapere J J, Bertrand G, Matichard E, Meziani R, Mirebeau D, Descamps V, Gérard B, Archimbaud A, Ollivaud L, Bouscarat F, Baccard M, Lanternier G, Saïag P, Lebbé C, Basset-Seguin N, Crickx B, Cave H, Grandchamp B
Laboratoire de Biochimie Hormonale et Génétique, Hôpital Bichat-Claude Bernard, 46 rue henri Huchard, Paris 75018, France.
Br J Cancer. 2004 Jan 26;90(2):503-9. doi: 10.1038/sj.bjc.6601503.
Germline anomalies of the INK4a-ARF and Cdk4 genes were sought in a series of 89 patients suspected of having a genetic predisposition to melanoma. Patients were selected based on the following criteria: (a) familial melanoma (23 cases), (b) multiple primary melanoma (MPM; 18 cases), (c) melanoma and additional unrelated cancers (13 cases), (d) age at diagnosis less than 25 years (21 cases), and (e) nonphoto-induced melanoma (NPIM; 14 cases). Mutations of INK4a-ARF and Cdk4 were characterised by automated sequencing, and germline deletions of INK4a-ARF were also examined by real-time quantitative PCR. Seven germline changes of INK4a-ARF, five of which were novel, were found in seven patients (8%). Four were very likely to be pathogenic mutations and were found in three high-risk melanoma families and in a patient who had a pancreatic carcinoma in addition to melanoma. Three variants of uncertain significance were detected in one MPM patient, one patient <25 years, and one NPIM patient. No germline deletion of INK4a-ARF was found in 71 patients, and no Cdk4 mutation was observed in the 89 patients. This study confirms that INK4a-ARF mutations are infrequent outside stringent familial criteria, and that germline INK4a-ARF deletions are rarely involved in genetic predisposition to melanoma.
在一系列89例疑似有黑色素瘤遗传易感性的患者中,研究了INK4a - ARF和Cdk4基因的种系异常。患者根据以下标准选择:(a)家族性黑色素瘤(23例),(b)多发性原发性黑色素瘤(MPM;18例),(c)黑色素瘤合并其他不相关癌症(13例),(d)诊断时年龄小于25岁(21例),以及(e)非光诱导性黑色素瘤(NPIM;14例)。通过自动测序对INK4a - ARF和Cdk4的突变进行了表征,并且还通过实时定量PCR检测了INK4a - ARF的种系缺失。在7例患者(8%)中发现了7种INK4a - ARF的种系变化,其中5种是新发现的。4种很可能是致病突变,在3个高危黑色素瘤家族以及1例除黑色素瘤外还患有胰腺癌的患者中发现。在1例MPM患者、1例年龄小于25岁的患者和1例NPIM患者中检测到3种意义未明的变异。71例患者中未发现INK4a - ARF的种系缺失,89例患者中未观察到Cdk4突变。本研究证实,在严格的家族标准之外,INK4a - ARF突变并不常见,并且种系INK4a - ARF缺失很少参与黑色素瘤的遗传易感性。