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基底细胞癌不同组织学变体中p53、增殖细胞核抗原(PCNA)、Ki-67和bcl-2的免疫组织化学细胞核染色

Immunohistochemical nuclear staining for p53, PCNA, Ki-67 and bcl-2 in different histologic variants of basal cell carcinoma.

作者信息

Mateoiu Claudia, Pirici A, Bogdan Fl

机构信息

Faculty of Medicine, University of Medicine and Pharmacy of Craiova, Romania.

出版信息

Rom J Morphol Embryol. 2011;52(1 Suppl):315-9.

Abstract

BACKGROUND

Basal cell carcinoma is the most common form of human cancer. Increased expression of p53 has been found in the majority of basal cell carcinomas (BCCs); however, UV-light-induced signature mutations are present in only about 50% of cases. Increased nuclear staining with an immunohistochemical marker of proliferation and apoptosis has been correlated with aggressive behavior in BCC.

OBJECTIVE

Our purpose was to correlate markers expression of apoptosis (p53 and bcl-2) and cell proliferation (Ki-67 and PCNA) with histological indicators of tumor severity.

METHODS

We used immunohistochemical stains for p53, PCNA, and Ki-67, in superficial, nodular and sclerosing BCC, to determine whether the staining patterns differ in these different histologic variants of BCC.

RESULTS

Bcl-2 expression was significant in basal cell carcinomas said to be aggressive (morpheaform and nodular types). Of the studied tumors, 66.7% (n=14) strongly expressed p53. Our results show a greater expression of Ki-67 in nodular and superficial basal cell carcinoma. PCNA showed a strong expression in all types of tumors.

CONCLUSION

Studies employing molecular and genetic biology techniques, associated with histomorphology, lead to the identification of risk factors in the development of more recurring and aggressive lesions.

摘要

背景

基底细胞癌是人类最常见的癌症形式。在大多数基底细胞癌(BCC)中发现p53表达增加;然而,紫外线诱导的特征性突变仅在约50%的病例中出现。增殖和凋亡免疫组化标志物的核染色增加与基底细胞癌的侵袭性相关。

目的

我们的目的是将凋亡标志物(p53和bcl-2)和细胞增殖标志物(Ki-67和PCNA)的表达与肿瘤严重程度的组织学指标相关联。

方法

我们对浅表性、结节性和硬化性基底细胞癌进行p53、PCNA和Ki-67免疫组化染色,以确定这些不同组织学类型的基底细胞癌的染色模式是否不同。

结果

bcl-2表达在所谓侵袭性基底细胞癌(硬斑病样和结节型)中显著。在研究的肿瘤中,66.7%(n = 14)强烈表达p53。我们的结果显示结节性和浅表性基底细胞癌中Ki-67表达更高。PCNA在所有类型的肿瘤中均呈强表达。

结论

采用分子和遗传生物学技术并结合组织形态学的研究,有助于识别更易复发和侵袭性病变发生发展中的危险因素。

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