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乳腺癌核苷酸切除修复功能谱分析。

Functional profiling of nucleotide Excision repair in breast cancer.

机构信息

Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, United States; Department of Radiation Oncology, Vanderbilt University Medical Center, Nashville, TN, United States.

Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, United States; Hematology and Oncology Department, Boston University School of Medicine, Boston Medical Center, Boston, MA, United States.

出版信息

DNA Repair (Amst). 2019 Oct;82:102697. doi: 10.1016/j.dnarep.2019.102697. Epub 2019 Aug 30.

DOI:10.1016/j.dnarep.2019.102697
PMID:31499327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6815104/
Abstract

Homologous recombination deficiency conferred by alterations in BRCA1 or BRCA2 are common in breast tumors and can drive sensitivity to platinum chemotherapy and PARP inhibitors. Alterations in nucleotide excision repair (NER) activity can also impact sensitivity to DNA damaging agents, but NER activity in breast cancer has been poorly characterized. Here, we apply a novel immunofluorescence-based cellular NER assay to screen a large panel of breast epithelial and cancer cell lines. Although the majority of breast cancer models are NER proficient, we identify an example of a breast cancer cell line with profound NER deficiency. We show that NER deficiency in this model is driven by epigenetic silencing of the ERCC4 gene, leading to lack of expression of the NER nuclease XPF, and that ERCC4 methylation is also strongly correlated with ERCC4 mRNA and XPF protein expression in primary breast tumors. Re-expression of XPF in the ERCC4-deficient breast cancer rescues NER deficiency and cisplatin sensitivity, but does not impact PARP inhibitor sensitivity. These findings demonstrate the potential to use functional assays to identify novel mechanisms of DNA repair deficiency and nominate NER deficiency as a platinum sensitivity biomarker in breast cancer.

摘要

BRCA1 或 BRCA2 改变导致的同源重组缺陷在乳腺癌中很常见,可导致对铂类化疗和 PARP 抑制剂的敏感性。核苷酸切除修复 (NER) 活性的改变也会影响对 DNA 损伤剂的敏感性,但乳腺癌中的 NER 活性尚未得到很好的描述。在这里,我们应用一种新的基于免疫荧光的细胞 NER 测定法来筛选大量的乳腺上皮和癌细胞系。尽管大多数乳腺癌模型的 NER 功能正常,但我们鉴定出一种具有明显 NER 缺陷的乳腺癌细胞系。我们表明,该模型中的 NER 缺陷是由 ERCC4 基因的表观遗传沉默驱动的,导致 NER 核酸内切酶 XPF 的表达缺失,并且 ERCC4 甲基化与原发性乳腺癌中的 ERCC4 mRNA 和 XPF 蛋白表达也强烈相关。在 ERCC4 缺陷型乳腺癌中重新表达 XPF 可挽救 NER 缺陷和顺铂敏感性,但不影响 PARP 抑制剂敏感性。这些发现表明可以使用功能测定来鉴定 DNA 修复缺陷的新机制,并将 NER 缺陷作为乳腺癌中的铂类敏感性生物标志物。

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本文引用的文献

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Helicase Domain Mutations Confer Nucleotide Excision Repair Deficiency and Drive Cisplatin Sensitivity in Muscle-Invasive Bladder Cancer.解旋酶结构域突变导致核苷酸切除修复缺陷并驱动肌肉浸润性膀胱癌对顺铂敏感。
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