The role of nuclear receptor co-activator 4 in erythropoiesis (Reply to Nai .).
作者信息
Santana-Codina Naiara, Gableske Sebastian, Fleming Mark D., Harper J. Wade, Kimmelman Alec C., Mancias Joseph D.
机构信息
Division of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA.
Department of Pathology, Boston Children's Hospital and Harvard Medical School, 320 Longwood Avenue, Boston, MA.
出版信息
Haematologica. 2019 Dec;104(12):e585-e586. doi: 10.3324/haematol.2019.235226.
Abstract
摘要
相似文献
1
The role of nuclear receptor co-activator 4 in erythropoiesis (Reply to Nai .).核受体共激活因子4在红细胞生成中的作用（对奈伊的回复）。
Haematologica. 2019 Dec;104(12):e585-e586. doi: 10.3324/haematol.2019.235226.
2
Tamoxifen erythroid toxicity revealed by studying the role of nuclear receptor co-activator 4 in erythropoiesis.通过研究核受体共激活因子4在红细胞生成中的作用揭示他莫昔芬的红细胞毒性。
Haematologica. 2019 Aug;104(8):e383-e384. doi: 10.3324/haematol.2019.224857.
3
A regulatory role for RIP140 in nuclear receptor activation.RIP140在核受体激活中的调控作用。
Mol Endocrinol. 1998 Jun;12(6):864-81. doi: 10.1210/mend.12.6.0123.
4
Peroxisome proliferator-activated receptor (PPAR)-binding protein (PBP) but not PPAR-interacting protein (PRIP) is required for nuclear translocation of constitutive androstane receptor in mouse liver.过氧化物酶体增殖物激活受体（PPAR）结合蛋白（PBP）而非PPAR相互作用蛋白（PRIP）是小鼠肝脏中组成型雄烷受体核转位所必需的。
Biochem Biophys Res Commun. 2006 Aug 25;347(2):485-95. doi: 10.1016/j.bbrc.2006.06.129. Epub 2006 Jun 30.
5
Dissecting the molecular mechanism of nuclear receptor action: transcription coactivators and corepressors.剖析核受体作用的分子机制：转录共激活因子与共抑制因子。
Exp Mol Med. 2000 Jun 30;32(2):53-60. doi: 10.1038/emm.2000.10.
6
The expanding cosmos of nuclear receptor coactivators.核受体共激活因子的扩展领域
Cell. 2006 May 5;125(3):411-4. doi: 10.1016/j.cell.2006.04.021.
7
Transcription coactivator PRIP, the peroxisome proliferator-activated receptor (PPAR)-interacting protein, is redundant for the function of nuclear receptors PParalpha and CAR, the constitutive androstane receptor, in mouse liver.转录共激活因子PRIP，即过氧化物酶体增殖物激活受体（PPAR）相互作用蛋白，对小鼠肝脏中核受体过氧化物酶体增殖物激活受体α（PParalpha）和组成型雄甾烷受体（CAR）的功能来说是多余的。
Gene Expr. 2007;13(4-5):255-69. doi: 10.3727/000000006780666948.
8
PGC-1 and PERC, coactivators of the estrogen receptor-related receptor gamma.PGC-1和PERC，雌激素受体相关受体γ的共激活因子。
Biochem Biophys Res Commun. 2002 Dec 20;299(5):872-9. doi: 10.1016/s0006-291x(02)02753-5.
9
Negative cross-talk between Nur77 and small heterodimer partner and its role in apoptotic cell death of hepatoma cells.Nur77与小分子异源二聚体伴侣之间的负性相互作用及其在肝癌细胞凋亡性细胞死亡中的作用。
Mol Endocrinol. 2005 Apr;19(4):950-63. doi: 10.1210/me.2004-0209. Epub 2004 Dec 29.
10
NCOA4 maintains murine erythropoiesis via cell autonomous and non-autonomous mechanisms.NCOA4 通过细胞自主和非自主机制维持小鼠的红细胞生成。
Haematologica. 2019 Jul;104(7):1342-1354. doi: 10.3324/haematol.2018.204123. Epub 2019 Jan 10.
引用本文的文献
1
Role of Nuclear Receptors in Controlling Erythropoiesis.核受体在控制红细胞生成中的作用。
Int J Mol Sci. 2022 Mar 3;23(5):2800. doi: 10.3390/ijms23052800.
本文引用的文献
1
Tamoxifen erythroid toxicity revealed by studying the role of nuclear receptor co-activator 4 in erythropoiesis.通过研究核受体共激活因子4在红细胞生成中的作用揭示他莫昔芬的红细胞毒性。
Haematologica. 2019 Aug;104(8):e383-e384. doi: 10.3324/haematol.2019.224857.
2
NCOA4 maintains murine erythropoiesis via cell autonomous and non-autonomous mechanisms.NCOA4 通过细胞自主和非自主机制维持小鼠的红细胞生成。
Haematologica. 2019 Jul;104(7):1342-1354. doi: 10.3324/haematol.2018.204123. Epub 2019 Jan 10.
3
Thyroid hormone receptor beta and NCOA4 regulate terminal erythrocyte differentiation.甲状腺激素受体β和 NCOA4 调节终末红细胞分化。
Proc Natl Acad Sci U S A. 2017 Sep 19;114(38):10107-10112. doi: 10.1073/pnas.1711058114. Epub 2017 Sep 1.
4
Ferroptosis is an autophagic cell death process.铁死亡是一种自噬性细胞死亡过程。
Cell Res. 2016 Sep;26(9):1021-32. doi: 10.1038/cr.2016.95. Epub 2016 Aug 12.
5
Autophagy promotes ferroptosis by degradation of ferritin.自噬通过降解铁蛋白促进铁死亡。
Autophagy. 2016 Aug 2;12(8):1425-8. doi: 10.1080/15548627.2016.1187366. Epub 2016 May 31.
6
Oxidative stress contributes to the tamoxifen-induced killing of breast cancer cells: implications for tamoxifen therapy and resistance.氧化应激促进他莫昔芬诱导的乳腺癌细胞杀伤：对他莫昔芬治疗及耐药性的影响
Sci Rep. 2016 Feb 17;6:21164. doi: 10.1038/srep21164.
7
NCOA4 Deficiency Impairs Systemic Iron Homeostasis.NCOA4 缺乏会损害全身铁稳态。
Cell Rep. 2016 Jan 26;14(3):411-421. doi: 10.1016/j.celrep.2015.12.065. Epub 2016 Jan 14.
8
Ferritinophagy via NCOA4 is required for erythropoiesis and is regulated by iron dependent HERC2-mediated proteolysis.通过NCOA4的铁蛋白自噬是红细胞生成所必需的，并受铁依赖性HERC2介导的蛋白水解调节。
Elife. 2015 Oct 5;4:e10308. doi: 10.7554/eLife.10308.
9
Quantitative proteomics identifies NCOA4 as the cargo receptor mediating ferritinophagy.定量蛋白质组学鉴定 NCOA4 为介导铁蛋白自噬的货物受体。
Nature. 2014 May 1;509(7498):105-9. doi: 10.1038/nature13148. Epub 2014 Mar 30.
Zotero 插件