Ichimura K, Schmidt E E, Yamaguchi N, James C D, Collins V P
Department of Pathology, Sahlgrenska Hospital, Gothenburg, Sweden.
Cancer Res. 1994 Jun 15;54(12):3127-30.
Deletions of the 9p-localized type-I interferon (IFN) genes and adjacent loci often occur during the development of malignant glioma. We have applied restriction fragment length polymorphism and microsatellite analysis to 12 loci covering this region of 9p and 3 loci on 9q in 74 human glial tumor tissues to define and further localize the smallest region of hemizygous or homozygous deletion common to the tumors. Three regions of homozygous deletion were evident among the panel of tumors; only one of these, however, residing between D9S171 and the IFN alpha/omega gene cluster, was involved in multiple cases (13 glioblastomas). Hemizygous deletion of this same region was observed in an additional 27 tumors. In total these data indicate the frequent inactivation of a novel tumor suppressor gene residing adjacent to and centromeric of the type-I IFN genes in malignant gliomas.
9号染色体短臂(9p)上的I型干扰素(IFN)基因及相邻基因座的缺失在恶性胶质瘤的发生发展过程中经常出现。我们运用限制性片段长度多态性和微卫星分析方法,对74例人类神经胶质瘤组织中覆盖9p这一区域的12个基因座以及9q上的3个基因座进行检测,以确定并进一步定位这些肿瘤中共同存在的半合子或纯合子缺失的最小区域。在这组肿瘤样本中,明显存在三个纯合子缺失区域;然而,其中只有一个区域位于D9S171和IFNα/ω基因簇之间,涉及多个病例(13例胶质母细胞瘤)。在另外27个肿瘤中也观察到了同一区域的半合子缺失。总体而言,这些数据表明,在恶性胶质瘤中,一个位于I型干扰素基因附近且在着丝粒方向的新型肿瘤抑制基因经常发生失活。