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散发性和遗传性基底细胞癌中的PTCH基因和p53基因改变

PATCHED and p53 gene alterations in sporadic and hereditary basal cell cancer.

作者信息

Ling G, Ahmadian A, Persson A, Undén A B, Afink G, Williams C, Uhlén M, Toftgård R, Lundeberg J, Pontén F

机构信息

Department of Genetics and Pathology, Rudbeck Laboratory, University Hospital, Uppsala University, S-751 85 Uppsala, Sweden.

出版信息

Oncogene. 2001 Nov 22;20(53):7770-8. doi: 10.1038/sj.onc.1204946.

Abstract

It is widely accepted that disruption of the hedgehog-patched pathway is a key event in development of basal cell cancer. In addition to patched gene alterations, p53 gene mutations are also frequent in basal cell cancer. We determined loss of heterozygosity in the patched and p53 loci as well as sequencing the p53 gene in tumors both from sporadic and hereditary cases. A total of 70 microdissected samples from tumor and adjacent skin were subjected to PCR followed by fragment analysis and DNA sequencing. We found allelic loss in the patched locus in 6/8 sporadic basal cell cancer and 17/19 hereditary tumors. All sporadic and 7/20 hereditary tumors showed p53 gene mutations. Loss of heterozygosity in the p53 locus was rare in both groups. The p53 mutations detected in hereditary tumors included rare single nucleotide deletions and unusual double-base substitutions compared to the typical ultraviolet light induced missense mutations found in sporadic tumors. Careful microdissection of individual tumors revealed genetically linked subclones with different p53 and/or patched genotype providing an insight on time sequence of genetic events. The high frequency and co-existence of genetic alterations in the patched and p53 genes suggest that both these genes are important in the development of basal cell cancer.

摘要

人们普遍认为,刺猬索尼克-帕奇通路的破坏是基底细胞癌发生发展的关键事件。除了帕奇基因改变外,p53基因突变在基底细胞癌中也很常见。我们确定了散发性和遗传性病例肿瘤中帕奇和p53基因座的杂合性缺失,并对p53基因进行了测序。总共从肿瘤和相邻皮肤中采集了70个显微切割样本,进行聚合酶链反应(PCR),随后进行片段分析和DNA测序。我们发现,在6/8例散发性基底细胞癌和17/19例遗传性肿瘤中,帕奇基因座存在等位基因缺失。所有散发性肿瘤和7/20例遗传性肿瘤均显示p53基因突变。两组中p53基因座的杂合性缺失均很少见。与散发性肿瘤中典型的紫外线诱导错义突变相比,遗传性肿瘤中检测到的p53突变包括罕见的单核苷酸缺失和不寻常的双碱基替换。对单个肿瘤进行仔细的显微切割,发现了具有不同p53和/或帕奇基因型的遗传连锁亚克隆,这为了解遗传事件的时间顺序提供了线索。帕奇基因和p53基因遗传改变的高频率和共存表明,这两个基因在基底细胞癌的发生发展中都很重要。

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