共 61 条
ΔNp63 activates the Fanconi anemia DNA repair pathway and limits the efficacy of cisplatin treatment in squamous cell carcinoma
被引:21
作者:

Bretz, Anne Catherine
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Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany

Gittler, Miriam P.
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Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany

Charles, Joel P.
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Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany

Gremke, Niklas
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Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany

Eckhardt, Ines
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Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany

Mernberger, Marco
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Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany

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Nist, Andrea
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机构:
Univ Marburg, Genom Core Facil, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany

Wanzel, Michael
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany
Univ Giessen, D-35043 Marburg, Germany
Marburg Lung Ctr, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany

Stiewe, Thorsten
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany
Univ Marburg, Genom Core Facil, D-35043 Marburg, Germany
Univ Giessen, D-35043 Marburg, Germany
Marburg Lung Ctr, D-35043 Marburg, Germany Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany
机构:
[1] Univ Marburg, Inst Mol Oncol, D-35043 Marburg, Germany
[2] Univ Marburg, Univ Hosp Giessen & Marburg, Dept Otorhinolaryngol Head & Neck Surg, D-35033 Marburg, Germany
[3] Univ Duisburg Essen, Inst Cell Biol, D-45122 Essen, Germany
[4] Univ Marburg, Genom Core Facil, D-35043 Marburg, Germany
[5] Univ Giessen, D-35043 Marburg, Germany
[6] Marburg Lung Ctr, D-35043 Marburg, Germany
基金:
欧洲研究理事会;
关键词:
CROSS-LINK REPAIR;
TRANSCRIPTIONAL REGULATION;
MTOR PATHWAY;
P63;
CANCER;
FANCD2;
P53;
PROLIFERATION;
HEAD;
REPRESSION;
D O I:
10.1093/nar/gkw036
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
TP63, a member of the p53 gene family gene, encodes the Delta Np63 protein and is one of the most frequently amplified genes in squamous cell carcinomas (SCC) of the head and neck (HNSCC) and lungs (LUSC). Using an epiallelic series of siRNAs with intrinsically different knockdown abilities, we show that the complete loss of Delta Np63 strongly impaired cell proliferation, whereas partial Delta Np63 depletion rendered cells hypersensitive to cisplatin accompanied by an accumulation of DNA damage. Expression profiling revealed wide-spread transcriptional regulation of DNA repair genes and in particular Fanconi anemia (FA) pathway components such as FANCD2 and RAD18 known to be crucial for the repair of cisplatin-induced interstrand crosslinks. In SCC patients Delta Np63 levels significantly correlate with FANCD2 and RAD18 - expression confirming Delta Np63 as a key activator of the FA pathway in vivo. Mechanistically, Delta Np63 bound an upstream enhancer of FANCD2 inactive in primary keratinocytes but aberrantly activated by Delta Np63 in SCC. Consistently, depletion of FANCD2 sensitized to cisplatin similar to depletion of Delta Np63. Together, our results demonstrate that Delta Np63 directly activates the FA pathway in SCC and limits the efficacy of cisplatin treatment. Targeting Delta Np63 therefore would not only inhibit SCC proliferation but also sensitize tumors to chemotherapy.
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收藏
页码:3204 / 3218
页数:15
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