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1
Corrigendum to article "Quantitative proteomics reveals that long non-coding RNA MALAT1 interacts with DBC1 to regulate p53 acetylation''.文章《定量蛋白质组学揭示长链非编码RNA MALAT1与DBC1相互作用以调节p53乙酰化》的勘误
Nucleic Acids Res. 2021 Apr 19;49(7):4199-4202. doi: 10.1093/nar/gkab222.
2
Quantitative proteomics reveals that long non-coding RNA MALAT1 interacts with DBC1 to regulate p53 acetylation.定量蛋白质组学研究表明，长链非编码RNA MALAT1与DBC1相互作用以调控p53乙酰化。
Nucleic Acids Res. 2017 Sep 29;45(17):9947-9959. doi: 10.1093/nar/gkx600.
3
Acetylation status of P53 and the expression of DBC1, SIRT1, and androgen receptor are associated with survival in clear cell renal cell carcinoma patients.乙酰化状态的 P53 和 DBC1、SIRT1、雄激素受体的表达与透明细胞肾细胞癌患者的生存相关。
Pathology. 2013 Oct;45(6):574-80. doi: 10.1097/PAT.0b013e3283652c7a.
4
Association of lncRNA-p53 regulatory network (lincRNA-p21, lincRNA-ROR and MALAT1) and p53 with the clinicopathological features of colorectal primary lesions and tumors.长链非编码RNA-p53调控网络（lincRNA-p21、lincRNA-ROR和MALAT1）及p53与结直肠原发性病变和肿瘤临床病理特征的相关性
Oncol Lett. 2020 Jun;19(6):3937-3949. doi: 10.3892/ol.2020.11518. Epub 2020 Apr 7.
5
DBC1 phosphorylation by ATM/ATR inhibits SIRT1 deacetylase in response to DNA damage.ATM/ATR 磷酸化 DBC1 可抑制 DNA 损伤应答中的 SIRT1 去乙酰化酶。
J Mol Cell Biol. 2012 Oct;4(5):294-303. doi: 10.1093/jmcb/mjs035. Epub 2012 Jun 26.
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Quantitative Proteomics to Identify Nuclear RNA-Binding Proteins of Malat1.定量蛋白质组学鉴定 Malat1 的核 RNA 结合蛋白。
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Down-regulation of long non-coding RNA MALAT1 inhibits granulosa cell proliferation in endometriosis by up-regulating P21 via activation of the ERK/MAPK pathway.长链非编码 RNA MALAT1 的下调通过激活 ERK/MAPK 通路上调 P21 抑制子宫内膜异位症中的颗粒细胞增殖。
Mol Hum Reprod. 2019 Jan 1;25(1):17-29. doi: 10.1093/molehr/gay045.
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LncRNA MALAT1 induces the dysfunction of β cells via reducing the histone acetylation of the PDX-1 promoter in type 1 diabetes.长链非编码 RNA MALAT1 通过降低 1 型糖尿病中 PDX-1 启动子的组蛋白乙酰化来诱导 β 细胞功能障碍。
Exp Mol Pathol. 2020 Jun;114:104432. doi: 10.1016/j.yexmp.2020.104432. Epub 2020 Mar 31.
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Breast cancer metastasis suppressor 1 modulates SIRT1-dependent p53 deacetylation through interacting with DBC1.乳腺癌转移抑制因子1通过与DBC1相互作用来调节SIRT1依赖的p53去乙酰化。
Am J Cancer Res. 2016 Jun 1;6(6):1441-9. eCollection 2016.
10
The long non-coding RNA MALAT1 promotes the migration and invasion of hepatocellular carcinoma by sponging miR-204 and releasing SIRT1.长链非编码RNA MALAT1通过吸附miR-204并释放SIRT1促进肝细胞癌的迁移和侵袭。
Tumour Biol. 2017 Jul;39(7):1010428317718135. doi: 10.1177/1010428317718135.

引用本文的文献

1
Targeting the p53 signaling pathway in cancers: Molecular mechanisms and clinical studies.癌症中靶向p53信号通路：分子机制与临床研究
MedComm (2020). 2023 May 28;4(3):e288. doi: 10.1002/mco2.288. eCollection 2023 Jun.
2
Deciphering the acetylation code of p53 in transcription regulation and tumor suppression.解析 p53 在转录调控和肿瘤抑制中的乙酰化密码。
Oncogene. 2022 May;41(22):3039-3050. doi: 10.1038/s41388-022-02331-9. Epub 2022 Apr 29.

Corrigendum to article "Quantitative proteomics reveals that long non-coding RNA MALAT1 interacts with DBC1 to regulate p53 acetylation''.

作者信息

Chen Ruibing, Liu Yun, Zhuang Hao, Yang Baicai, Hei Kaiwen, Xiao Mingming, Hou Chunyu, Gao Huajun, Zhang Xinran, Jia Chenxi, Li Lingjun, Li Yongmei, Zhang Ning

机构信息

Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy; Department of Genetics & Department of Medical Microbiology, School of Basic Medical Sciences; Research Center of Basic Medical Sciences; Tianjin Medical University, Tianjin 300070, China.

Department of Hepatic Biliary Pancreatic Surgery, Cancer Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan Province 450000, China.

出版信息

Nucleic Acids Res. 2021 Apr 19;49(7):4199-4202. doi: 10.1093/nar/gkab222.

DOI:10.1093/nar/gkab222
PMID:33751109
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8053087/
Abstract
摘要