CtBP1/2 differentially regulate genomic stability and DNA repair pathway in high-grade serous ovarian cancer cell
文献类型：期刊论文
| 作者 | He,YingYing; He,Zhicheng; Lin,Jian; Chen,Cheng; Chen,Yuanzhi; Liu,Shubai |
| 刊名 | ONCOGENESIS
 |
| 出版日期 | 2021 |
| 卷号 | 10期号:7页码:49 |
| 关键词 | BINDING-PROTEIN CTBP TRANSCRIPTIONAL COREPRESSOR NEGATIVE MODULATION PROMOTES APOPTOSIS GENE-EXPRESSION DAMAGE RESPONSE PK OVEREXPRESSION PHOSPHOPROTEIN TRANSFORMATION |
| ISSN号 | 2157-9024 |
| DOI | 10.1038/s41389-021-00344-9 |
| 英文摘要 | The C-terminal binding proteins (CtBPs), CtBP1 and CtBP2, are transcriptional co-repressor that interacts with multiple transcriptional factors to modulate the stability of chromatin. CtBP proteins were identified with overexpression in the high-grade serous ovarian carcinoma (HGSOC). However, little is known about CtBP proteins' regulatory roles in genomic stability and DNA repair in HGSOC. In this study, we combined whole-transcriptome analysis with multiple research methods to investigate the role of CtBP1/2 in genomic stability. Several key functional pathways were significantly enriched through whole transcription profile analysis of CtBP1/2 knockdown SKOV3 cells, including DNA damage repair, apoptosis, and cell cycle. CtBP1/2 knockdown induced cancer cell apoptosis, increased genetic instability, and enhanced the sensitivity to DNA damage agents, such as gamma-irradiation and chemotherapy drug (Carboplatin and etoposide). The results of DNA fiber assay revealed that CtBP1/2 contribute differentially to the integrity of DNA replication track and stability of DNA replication recovery. CtBP1 protects the integrity of stalled forks under metabolic stress condition during prolonged periods of replication, whereas CtBP2 acts a dominant role in stability of DNA replication recovery. Furthermore, CtBP1/2 knockdown shifted the DSBs repair pathway from homologous recombination (HR) to non-homologous end joining (NHEJ) and activated DNA-PK in SKOV3 cells. Interesting, blast through TCGA tumor cases, patients with CtBP2 genetic alternation had a significantly longer overall survival time than unaltered patients. Together, these results revealed that CtBP1/2 play a different regulatory role in genomic stability and DSBs repair pathway bias in serous ovarian cancer cells. It is possible to generate novel potential targeted therapy strategy and translational application for serous ovarian carcinoma patients with a predictable better clinical outcome. |
| WOS记录号 | WOS:000672427700001 |
| 源URL | [http://ir.kib.ac.cn/handle/151853/73459]  |
| 专题 | 中国科学院昆明植物研究所 |
| 作者单位 | 1.Yunnan Univ, Sch Chem Sci & Technol, Kunming 650091, Yunnan, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China 3.Chinese Acad Sci, Kunming Inst Bot, Key Lab Phytochem & Plant Resources West China, Kunming 650201, Yunnan, Peoples R China |
| 推荐引用方式 GB/T 7714 | He,YingYing,He,Zhicheng,Lin,Jian,et al. CtBP1/2 differentially regulate genomic stability and DNA repair pathway in high-grade serous ovarian cancer cell[J]. ONCOGENESIS,2021,10(7):49. |
| APA | He,YingYing,He,Zhicheng,Lin,Jian,Chen,Cheng,Chen,Yuanzhi,&Liu,Shubai.(2021).CtBP1/2 differentially regulate genomic stability and DNA repair pathway in high-grade serous ovarian cancer cell.ONCOGENESIS,10(7),49. |
| MLA | He,YingYing,et al."CtBP1/2 differentially regulate genomic stability and DNA repair pathway in high-grade serous ovarian cancer cell".ONCOGENESIS 10.7(2021):49. |
入库方式： OAI收割
来源：昆明植物研究所
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