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在非小细胞肺癌中,BRCA1相关蛋白1(BAP1)表达缺失的情况较为罕见。

Loss of BRCA1-associated protein 1 (BAP1) expression is rare in non-small cell lung cancer.

作者信息

Owen Daniel, Sheffield Brandon S, Ionescu Diana, Churg Andrew

机构信息

Department of Pathology, Vancouver General Hospital, Vancouver, British Columbia, Canada V5Z 1M9.

Department of Pathology, Abbotsford Regional Hospital and Cancer Center, Abbotsford, British Columbia, Canada V2S 0C2.

出版信息

Hum Pathol. 2017 Feb;60:82-85. doi: 10.1016/j.humpath.2016.10.005. Epub 2016 Oct 28.

Abstract

BRCA1-associated protein 1 (BAP1) is a tumor suppressor gene involved in regulation of the cell cycle, cellular differentiation, repair of DNA damage, and apoptosis. In the distinction of malignant mesothelioma from benign mesothelial proliferations, immunohistochemical loss of BAP1, the protein expressed by the BAP1 gene, has proven highly specific for malignant mesothelioma. However, few studies have investigated the rate of BAP1 loss in tumors that commonly metastasize to the pleura. Our objective is to determine the rate of BAP1 loss in non-small cell lung cancer (NSCLC). Immunohistochemistry for BAP1 was performed using tissue microarrays containing 133 confirmed cases of NSCLC (80 of lung adenocarcinoma and 53 of squamous cell carcinoma). Cases were interpreted as showing BAP1 loss if nuclear staining was completely absent in all tumor cells and present in stromal and inflammatory cells that served as internal controls. Cases showing no BAP1 staining in the internal controls were excluded. After exclusion of 32 cases for technical reasons, only 1 case of pulmonary adenocarcinoma of 101 cases of NSCLC (69 adenocarcinoma and 32 squamous cell carcinoma; 1.0% of cases) showed BAP1 loss. We conclude that loss of BAP1 expression is a rare event in NSCLC. Therefore, BAP1 is a potentially useful addition to the immunohistochemical markers used to distinguish mesothelioma from pleural metastasis of NSCLC.

摘要

BRCA1相关蛋白1(BAP1)是一种肿瘤抑制基因,参与细胞周期调控、细胞分化、DNA损伤修复和细胞凋亡。在鉴别恶性间皮瘤与良性间皮增生时,BAP1基因所表达的蛋白BAP1免疫组化缺失已被证明对恶性间皮瘤具有高度特异性。然而,很少有研究调查通常转移至胸膜的肿瘤中BAP1缺失的发生率。我们的目的是确定非小细胞肺癌(NSCLC)中BAP1缺失的发生率。使用包含133例确诊NSCLC病例(80例肺腺癌和53例鳞状细胞癌)的组织芯片进行BAP1免疫组化检测。如果所有肿瘤细胞中完全没有核染色,而作为内部对照的基质和炎症细胞中有核染色,则病例被解释为显示BAP1缺失。内部对照中无BAP1染色的病例被排除。因技术原因排除32例后,101例NSCLC病例(69例腺癌和32例鳞状细胞癌)中仅1例肺腺癌(占病例的1.0%)显示BAP1缺失。我们得出结论,BAP1表达缺失在NSCLC中是罕见事件。因此,BAP1是用于鉴别间皮瘤与NSCLC胸膜转移的免疫组化标志物中一种潜在有用的补充。

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