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乳腺癌组织中Ku70/86表达的免疫组织化学分析。

Immunohistochemical analysis of Ku70/86 expression of breast cancer tissues.

作者信息

Someya Masanori, Sakata Koh-ichi, Matsumoto Yoshihisa, Satoh Masaaki, Narimatsu Hideaki, Hareyama Masato

机构信息

Department of Radiology, Sapporo Medical University, School of Medicine, Hokkaido, Japan.

出版信息

Oncol Rep. 2007 Dec;18(6):1483-7.

Abstract

DNA-dependent protein kinase (DNA-PK) has an important role in DNA double-strand break repair. We previously demonstrated the association of DNA-PK activity in peripheral blood lymphocytes (PBL) with incidence of chromosomal aberrations and risk of cancer. In this study, we examined the expression of Ku70 and Ku86 in breast cancer tissue and normal breast tissue with immunohistochemistry. We also measured the DNA-PK activity in PBL of the same patient. One hundred and ten breast cancer patients were included in this study. The expression of Ku70, and Ku86 in normal mammary epithelial cells and breast cancer cells obtained from surgical specimens was immunohistochemically examined. DNA-PK activity of PBL was measured by DNA-pull-down assay. The expression of Ku70 and that of Ku86 tended to parallel each other in normal and cancer tissues. There was also a relationship in the expression of Ku70 and Ku86 between cancer tissues and normal tissues in the same samples. Lower expression of Ku70 or Ku86 tended to be associated with higher malignant nuclear grade of cancer cells and higher frequency of axillary lymph node metastasis. The staining score of Ku70 or Ku86 of normal mammary epithelial cells or breast cancer cells had no significant relationship with DNA-PK activity of PBL. In conclusion, breast cancer cells inherited the characteristics of expression of Ku proteins from original mammary epithelial cells. The staining score of Ku70 or Ku86 of normal or cancer cells had no significant relationship with DNA-PK activity of PBL. This may be due to limitations in the assay sensitivity of immunohistochemistry.

摘要

DNA依赖蛋白激酶(DNA-PK)在DNA双链断裂修复中起重要作用。我们之前证明了外周血淋巴细胞(PBL)中的DNA-PK活性与染色体畸变发生率及癌症风险相关。在本研究中,我们采用免疫组织化学方法检测了乳腺癌组织和正常乳腺组织中Ku70和Ku86的表达。我们还测定了同一患者PBL中的DNA-PK活性。本研究纳入了110例乳腺癌患者。通过免疫组织化学方法检测了手术标本中获得的正常乳腺上皮细胞和乳腺癌细胞中Ku70和Ku86的表达。通过DNA下拉试验测定PBL的DNA-PK活性。在正常组织和癌组织中,Ku70和Ku86的表达倾向于相互平行。在同一样本的癌组织中,Ku70和Ku86的表达之间也存在关联。Ku70或Ku86表达较低往往与癌细胞较高的恶性核分级及腋窝淋巴结转移的较高频率相关。正常乳腺上皮细胞或乳腺癌细胞中Ku70或Ku86的染色评分与PBL的DNA-PK活性无显著关系。总之,乳腺癌细胞继承了原始乳腺上皮细胞Ku蛋白的表达特征。正常或癌细胞中Ku70或Ku86的染色评分与PBL的DNA-PK活性无显著关系。这可能是由于免疫组织化学检测灵敏度的局限性所致。

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