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甲状腺癌中的p53基因突变

p53 gene mutation in thyroid carcinoma.

作者信息

Ho Y S, Tseng S C, Chin T Y, Hsieh L L, Lin J D

机构信息

Department of Pathology, Chang-Gung Memorial Hospital, Taipei, Taiwan, ROC.

出版信息

Cancer Lett. 1996 May 15;103(1):57-63. doi: 10.1016/0304-3835(96)04196-1.

Abstract

The pattern of p53 protein expression was examined in 92 cases of thyroid carcinoma. When the cases were divided into two groups with regard to their cytoplasmic staining only or nucleus staining only, the frequency of the nucleus staining group was significantly higher in the poorly differentiated carcinoma (PDC) and undifferentiated carcinoma (UDC) groups (10.5% and 25%) compared with the other groups of histologic subtype (0%). The results suggest positivity in nucleus staining for p53 may be a marker for the biologically worse carcinomas, PDC and UDC, however, tumors showing only cytoplasmic staining of p53 favor a fair prognosis. In this paper, we also elucidate the spectrum of genotypic aberrations of p53 in each histological subtype. Of 92 thyroid tumor samples analyzed, the overall frequency of p53 mutation was 8.5%. The mutations occurred in 4.35% (2/46) ot WDC, 17.2% (5/29) of PDC, and 16.7% (1/6) of oncocytic carcinoma. Two of five PDC cases and one papillary carcinoma revealed point mutations in exon 8 as follows; GTG (val) to CTG (leu) at codon 272 in case 23T, CGA (arg) to CCA (pro) at codon 306 in case of 30T, and CGG (arg) to AGG (arg) at codon 282 in case 28T. All of the p53 mutations detected were represented by single nucleotide changes including two missense and one silent mutation. In contrast to the missense mutations found in PDC, it is interesting to note that the silent mutation was checked in 28T of well differentiated papillary carcinoma. These results represents molecular evidence that p53 gene aberration associated with overexpression of the mutant form of p53 protein plays a crucial role in the biologically aggressive subtypes of thyroid carcinoma, and point mutation only was not sufficient to be a prognostic marker for the biologically aggressive malignancy of thyroid tumors. There was no p53 gene aberration found in four cases of undifferentiated carcinoma (UDC) studied. The results suggest that other unknown factors should be responsible for the aggressiveness in some UDC of thyroid carcinoma except overexpression of p53.

摘要

对92例甲状腺癌病例进行了p53蛋白表达模式的检测。当仅根据细胞质染色或仅细胞核染色将病例分为两组时,与其他组织学亚型组(0%)相比,在低分化癌(PDC)和未分化癌(UDC)组中,细胞核染色组的频率显著更高(分别为10.5%和25%)。结果表明,p53细胞核染色阳性可能是生物学行为较差的癌(PDC和UDC)的一个标志物,然而,仅显示p53细胞质染色的肿瘤预后较好。在本文中,我们还阐明了各组织学亚型中p53基因畸变的范围。在分析的92个甲状腺肿瘤样本中,p53突变的总体频率为8.5%。突变发生在4.35%(2/46)的WDC、17.2%(5/29)的PDC和16.7%(1/6)的嗜酸细胞癌中。5例PDC病例中的2例和1例乳头状癌在外显子8中发现了点突变,如下所示:病例23T中密码子272处的GTG(缬氨酸)突变为CTG(亮氨酸),病例30T中密码子306处的CGA(精氨酸)突变为CCA(脯氨酸),病例28T中密码子282处的CGG(精氨酸)突变为AGG(精氨酸)。检测到的所有p53突变均由单核苷酸变化代表,包括两个错义突变和一个沉默突变。与在PDC中发现的错义突变不同,有趣的是,在高分化乳头状癌的28T中检测到了沉默突变。这些结果代表了分子证据,即与p53蛋白突变形式的过表达相关的p53基因畸变在甲状腺癌的生物学侵袭性亚型中起关键作用,并且仅点突变不足以作为甲状腺肿瘤生物学侵袭性恶性肿瘤的预后标志物。在所研究的4例未分化癌(UDC)中未发现p53基因畸变。结果表明,除了p53过表达外,其他未知因素应负责某些甲状腺癌UDC的侵袭性。

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