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合成类视黄醇对凋亡的非受体依赖性诱导

Receptor-independent induction of apoptosis by synthetic retinoids.

作者信息

Lotan R

机构信息

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas, MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

J Biol Regul Homeost Agents. 2003 Jan-Mar;17(1):13-28.

PMID:12757019
Abstract

Retinoids modulate cell proliferation, differentiation and apoptosis. Many of these effects are mediated by nuclear retinoid receptors. However, studies with certain synthetic retinoids, including some that can activate retinoid receptors, revealed that they affect cell growth and especially apoptosis by mechanisms that are independent of nuclear receptors. This chapter describes the pro-apoptotic effects of the synthetic retinoid CD437 [6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid], and structurally-related retinoids and summarizes the mechanisms by which they induce apoptosis.

摘要

维甲酸可调节细胞增殖、分化和凋亡。其中许多效应是由核维甲酸受体介导的。然而,对某些合成维甲酸(包括一些能激活维甲酸受体的化合物)的研究表明,它们通过独立于核受体的机制影响细胞生长,尤其是凋亡。本章描述了合成维甲酸CD437 [6-[3-(1-金刚烷基)-4-羟基苯基]-2-萘甲酸]以及结构相关维甲酸的促凋亡作用,并总结了它们诱导凋亡的机制。

相似文献

1
Receptor-independent induction of apoptosis by synthetic retinoids.合成类视黄醇对凋亡的非受体依赖性诱导
J Biol Regul Homeost Agents. 2003 Jan-Mar;17(1):13-28.
2
The novel retinoid 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphtalene carboxylic acid can trigger apoptosis through a mitochondrial pathway independent of the nucleus.新型维甲酸6-[3-(1-金刚烷基)-4-羟基苯基]-2-萘甲酸可通过独立于细胞核的线粒体途径触发细胞凋亡。
Cancer Res. 1999 Dec 15;59(24):6257-66.
3
Apoptosis induction in cancer cells by a novel analogue of 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalenecarboxylic acid lacking retinoid receptor transcriptional activation activity.一种缺乏视黄酸受体转录激活活性的新型6-[3-(1-金刚烷基)-4-羟基苯基]-2-萘甲酸类似物诱导癌细胞凋亡
Cancer Res. 2001 Jun 15;61(12):4723-30.
4
Evidence of a lysosomal pathway for apoptosis induced by the synthetic retinoid CD437 in human leukemia HL-60 cells.合成类视黄醇CD437诱导人白血病HL-60细胞凋亡的溶酶体途径证据。
Cell Death Differ. 2001 May;8(5):477-85. doi: 10.1038/sj.cdd.4400843.
5
Evidence supporting a role for mitochondrial respiration in apoptosis induction by the synthetic retinoid CD437.支持线粒体呼吸在合成类视黄醇CD437诱导细胞凋亡中起作用的证据。
Cancer Res. 2001 Sep 15;61(18):6698-702.
6
Antitumor activity of the retinoid-related molecules (E)-3-(4'-hydroxy-3'-adamantylbiphenyl-4-yl)acrylic acid (ST1926) and 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid (CD437) in F9 teratocarcinoma: Role of retinoic acid receptor gamma and retinoid-independent pathways.类视黄醇相关分子(E)-3-(4'-羟基-3'-金刚烷基联苯-4-基)丙烯酸(ST1926)和6-[3-(1-金刚烷基)-4-羟基苯基]-2-萘甲酸(CD437)在F9畸胎癌中的抗肿瘤活性:维甲酸受体γ和不依赖维甲酸途径的作用
Mol Pharmacol. 2006 Sep;70(3):909-24. doi: 10.1124/mol.106.023614. Epub 2006 Jun 20.
7
Induction of apoptosis in ovarian carcinoma cells by AHPN/CD437 is mediated by retinoic acid receptors.AHPN/CD437诱导卵巢癌细胞凋亡是由维甲酸受体介导的。
J Cell Physiol. 2000 Oct;185(1):61-7. doi: 10.1002/1097-4652(200010)185:1<61::AID-JCP5>3.0.CO;2-0.
8
Comparison of the mechanism of induction of apoptosis in ovarian carcinoma cells by the conformationally restricted synthetic retinoids CD437 and 4-HPR.构象受限的合成视黄酸CD437和4-HPR诱导卵巢癌细胞凋亡的机制比较
J Cell Biochem. 2003 May 15;89(2):262-78. doi: 10.1002/jcb.10505.
9
Post-transcriptional regulation of MyD118 and GADD45 in human lung carcinoma cells during 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2- naphthalene carboxylic acid-induced apoptosis.6-[3-(1-金刚烷基)-4-羟基苯基]-2-萘甲酸诱导人肺癌细胞凋亡过程中MyD118和GADD45的转录后调控
Mol Pharmacol. 1999 Apr;55(4):668-76.
10
Dual mechanisms of action of the retinoid CD437: nuclear retinoic acid receptor-mediated suppression of squamous differentiation and receptor-independent induction of apoptosis in UMSCC22B human head and neck squamous cell carcinoma cells.类视黄醇CD437的双重作用机制:核视黄酸受体介导的对UMSCC22B人头颈部鳞状细胞癌细胞鳞状分化的抑制以及非受体依赖性的细胞凋亡诱导。
Mol Pharmacol. 2000 Sep;58(3):508-14. doi: 10.1124/mol.58.3.508.

引用本文的文献

1
The antitumor toxin CD437 is a direct inhibitor of DNA polymerase α.抗肿瘤毒素CD437是DNA聚合酶α的直接抑制剂。
Nat Chem Biol. 2016 Jul;12(7):511-5. doi: 10.1038/nchembio.2082. Epub 2016 May 16.
2
Enhanced cell cycle perturbation and apoptosis mediate the synergistic effects of ST1926 and ATRA in neuroblastoma preclinical models.增强的细胞周期干扰和细胞凋亡介导 ST1926 和 ATRA 在神经母细胞瘤临床前模型中的协同作用。
Invest New Drugs. 2012 Aug;30(4):1319-30. doi: 10.1007/s10637-011-9689-2. Epub 2011 Jun 3.
3
Development of resistance to the atypical retinoid, ST1926, in the lung carcinoma cell line H460 is associated with reduced formation of DNA strand breaks and a defective DNA damage response.
肺癌细胞系H460对非典型类视黄醇ST1926产生耐药性的过程与DNA链断裂形成减少及DNA损伤反应缺陷有关。
Neoplasia. 2005 Jul;7(7):667-77. doi: 10.1593/neo.05127.