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p53肿瘤抑制基因在涎腺腺样囊性癌和黏液表皮样癌中的表达。

Expression of p53 tumor suppressor gene in adenoid cystic and mucoepidermoid carcinomas of the salivary glands.

作者信息

Kiyoshima T, Shima K, Kobayashi I, Matsuo K, Okamura K, Komatsu S, Rasul A M, Sakai H

机构信息

Department of Oral Pathology, Faculty of Dentistry, Kyushu University, 3-1-1 Maidashi, Higashi-ku, 812-8582, Fukuoka, Japan.

出版信息

Oral Oncol. 2001 Apr;37(3):315-22. doi: 10.1016/s1368-8375(00)00083-x.

DOI:10.1016/s1368-8375(00)00083-x
PMID:11287288
Abstract

Seventeen adenoid cystic carcinomas (ACCs) and 27 mucoepidermoid carcinomas (MECs) occurring in the salivary glands were analyzed for p53 tumor suppressor gene alteration (exons 5-8) and protein expression. The cell proliferation activity was also examined by Ki-67 immunohistochemistry. The p53 alterations were detected in three samples (17.6%) of ACC and in four samples (14.8%) of MEC, and were only found in carcinomas arising in the minor salivary glands. The occurrence of the p53 gene alteration is less frequent in ACC and MEC than that in other kinds of tumors, and therefore does not seem to play a critical role in the course of the tumorigenesis in ACC and MEC. All ACC samples arising from the minor salivary glands exhibiting p53 gene alterations showed recurrence/metastasis, thus suggesting a poor outcome of these patients. All ACCs and three out of four MECs samples with p53 gene alterations showed the lowest degree of p53 immunostaining ratio, thus suggesting that no correlation exists between the p53 gene alterations and the p53 immunostaining in these salivary gland carcinomas. No significant relationship was demonstrated between the immunostaining ratio of either p53 or Ki-67 and the morphological growth pattern or patient clinical course in the ACC samples. The p53 immunopositivity in MEC correlated to the histological grade. The Ki-67 immunostaining ratio was also significantly related to the histological grade and the clinical course in MEC.

摘要

对发生于唾液腺的17例腺样囊性癌(ACC)和27例黏液表皮样癌(MEC)进行p53肿瘤抑制基因改变(第5 - 8外显子)及蛋白表达分析。同时通过Ki-67免疫组化检测细胞增殖活性。在3例(17.6%)ACC样本和4例(14.8%)MEC样本中检测到p53改变,且仅见于小唾液腺发生的癌。p53基因改变在ACC和MEC中的发生率低于其他类型肿瘤,因此似乎在ACC和MEC的肿瘤发生过程中不发挥关键作用。所有来自小唾液腺且表现出p53基因改变的ACC样本均出现复发/转移,提示这些患者预后不良。所有发生p53基因改变的ACC样本以及4例MEC样本中的3例均显示出最低程度的p53免疫染色率,表明在这些唾液腺癌中p53基因改变与p53免疫染色之间不存在相关性。在ACC样本中,p53或Ki-67的免疫染色率与形态学生长模式或患者临床病程之间未显示出显著关系。MEC中的p53免疫阳性与组织学分级相关。Ki-67免疫染色率在MEC中也与组织学分级及临床病程显著相关。

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