Drewa G, Powierska-Czarny J
Katedra i Zakład Biologii, Akademii Medycznej im. Ludwika Rydygiera w Bydgoszczy.
Postepy Hig Med Dosw. 1998;52(4):367-80.
Cytogenetic analysis has contributed significantly to defining genomic region frequently altered in malignant melanoma. In the case of 1p, 6q i 9p consistent losses or partial deletions have predicted the location of tumor suppressor genes. Recent evidence suggests that the p16 CDKN2 gene located at 9p21 is important in sporadic and familial melanoma pathogenesis.
细胞遗传学分析对确定恶性黑色素瘤中经常发生改变的基因组区域做出了重大贡献。在1p、6q和9p的情况下,一致的缺失或部分缺失预示了肿瘤抑制基因的位置。最近的证据表明,位于9p21的p16 CDKN2基因在散发性和家族性黑色素瘤发病机制中很重要。