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p63(TA和ΔN亚型)在人原发性高分化颊癌中的表达

Expression of p63 (TA and deltaN isoforms) in human primary well differentiated buccal carcinomas.

作者信息

Chen Y-K, Hsue S-S, Lin L-M

机构信息

Oral Pathology Department, School of Dentistry, Kaohsiung Medical University, Kaohsiung, Taiwan, ROC.

出版信息

Int J Oral Maxillofac Surg. 2004 Jul;33(5):493-7. doi: 10.1016/j.ijom.2003.10.023.

Abstract

Abnormalities in the p53 gene have been regarded as the most consistent genetic abnormalities detected in head and neck squamous cell carcinogenesis. Two new members of the p53 gene family, p73 and p63, have recently been identified. We investigated the expression of the two N-terminal p63 isoforms (TA and deltaN isoforms) in human primary well-differentiated buccal squamous cell carcinoma. Both TAp63 and deltaNp63 isoforms were detected in the basal/suprabasal layers of all of the five specimens of normal buccal mucosa. The deltaNp63 isoform was found in all of the 23 specimens of human primary well-differentiated buccal carcinoma whereas TAp63 isoform was absent in 18 (78.3%) of the 23 specimens. The immunostaining patterns of both TAp63 and deltaNp63 isoforms were similar in that the p63 positivity was noted mainly in the peripheral cells of tumor nests whereas negative staining was observed in the areas with keratin pearl formation. A higher number of T3-T4 patients and patients with recurrence showed negative staining of TAp63 than T1-T2 patients and patients without recurrence but the difference was not statistically significant. These results suggested that specific p63 isoforms were associated with human oral squamous cell carcinogenesis. The deltaNp63 isoforms might be involved in epithelial differentiation and proliferation in human oral carcinogenesis whereas there was evidence for a possible role of TAp63 under-expression in human oral tumorigenesis.

摘要

p53基因异常被认为是在头颈部鳞状细胞癌发生过程中检测到的最一致的基因异常。最近发现了p53基因家族的两个新成员,即p73和p63。我们研究了两种N端p63异构体(TA和deltaN异构体)在人原发性高分化颊部鳞状细胞癌中的表达。在所有5例正常颊黏膜标本的基底/基底上层均检测到TAp63和deltaNp63异构体。在23例人原发性高分化颊癌标本中均发现了deltaNp63异构体,而在23例标本中的18例(78.3%)中未检测到TAp63异构体。TAp63和deltaNp63异构体的免疫染色模式相似,即p63阳性主要见于肿瘤巢的周边细胞,而在有角化珠形成的区域观察到阴性染色。与T1-T2期患者和无复发患者相比,T3-T4期患者和复发患者中TAp63阴性染色的比例更高,但差异无统计学意义。这些结果表明,特定的p63异构体与人类口腔鳞状细胞癌的发生有关。deltaNp63异构体可能参与人类口腔癌发生过程中的上皮分化和增殖,而有证据表明TAp63表达不足在人类口腔肿瘤发生中可能起作用。

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