Suppr超能文献

膳食苯乙基异硫氰酸酯和萝卜硫素的癌症化学预防的分子靶点。

Molecular targets of dietary phenethyl isothiocyanate and sulforaphane for cancer chemoprevention.

机构信息

Graduate Program in Pharmaceutical Science, Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.

出版信息

AAPS J. 2010 Mar;12(1):87-97. doi: 10.1208/s12248-009-9162-8. Epub 2009 Dec 15.

Abstract

Development of cancer is a long-term and multistep process which comprises initiation, progression, and promotion stages of carcinogenesis. Conceivably, it can be targeted and interrupted along these different stages. In this context, many naturally occurring dietary compounds from our daily consumption of fruits and vegetables have been shown to possess cancer preventive effects. Phenethyl isothiocyanate (PEITC) and sulforaphane (SFN) are two of the most widely investigated isothiocyanates from the crucifers. Both have been found to be very potent chemopreventive agents in numerous animal carcinogenesis models as well as cell culture models. They exert their chemopreventive effects through regulation of diverse molecular mechanisms. In this review, we will discuss the molecular targets of PEITC and SFN potentially involved in cancer chemoprevention. These include the regulation of drug-metabolizing enzymes phase I cytochrome P450s and phase II metabolizing enzymes. In addition, the signaling pathways including Nrf2-Keap 1, anti-inflammatory NFkappaB, apoptosis, and cell cycle arrest as well as some receptors will also be discussed. Furthermore, we will also discuss the similarities and their potential differences in the regulation of these molecular targets by PEITC and SFN.

摘要

癌症的发生是一个长期的、多步骤的过程,包括致癌作用的起始、促进和进展阶段。可以想象,它可以在这些不同阶段被靶向和中断。在这种情况下,许多天然存在的饮食化合物,来自于我们日常食用的水果和蔬菜,已被证明具有预防癌症的作用。苯乙基异硫氰酸酯(PEITC)和萝卜硫素(SFN)是两种研究最广泛的来自十字花科的异硫氰酸酯。在许多动物致癌模型和细胞培养模型中,它们都被发现是非常有效的化学预防剂。它们通过调节多种分子机制发挥其化学预防作用。在这篇综述中,我们将讨论 PEITC 和 SFN 潜在参与癌症化学预防的分子靶点。这些包括对药物代谢酶 I 相细胞色素 P450 和 II 相代谢酶的调节。此外,还将讨论包括 Nrf2-Keap1、抗炎 NFκB、细胞凋亡和细胞周期停滞以及一些受体在内的信号通路。此外,我们还将讨论 PEITC 和 SFN 对这些分子靶点的调节的相似性及其潜在差异。

相似文献

1
Molecular targets of dietary phenethyl isothiocyanate and sulforaphane for cancer chemoprevention.
AAPS J. 2010 Mar;12(1):87-97. doi: 10.1208/s12248-009-9162-8. Epub 2009 Dec 15.
3
Advances in molecular signaling mechanisms of β-phenethyl isothiocyanate antitumor effects.
J Agric Food Chem. 2015 Apr 8;63(13):3311-22. doi: 10.1021/jf504627e. Epub 2015 Mar 30.
4
Chemopreventive activity of sulforaphane.
Drug Des Devel Ther. 2018 Sep 11;12:2905-2913. doi: 10.2147/DDDT.S100534. eCollection 2018.
6
Multi-targeted prevention of cancer by sulforaphane.
Cancer Lett. 2008 Oct 8;269(2):291-304. doi: 10.1016/j.canlet.2008.04.018. Epub 2008 May 27.
7

引用本文的文献

1
Cancer-specific Regulation of Metabolic and Epigenetic Pathways by Dietary Phytochemicals.
Pharm Res. 2025 Aug;42(8):1443-1457. doi: 10.1007/s11095-025-03898-0. Epub 2025 Aug 4.
2
Sulforaphane Wrapped in Self-Assembled Nanomicelle Enhances the Effect of Sonodynamic Therapy on Glioma.
Pharmaceutics. 2024 Dec 30;17(1):34. doi: 10.3390/pharmaceutics17010034.
3
Epigenetic Properties of Compounds Contained in Functional Foods Against Cancer.
Biomolecules. 2024 Dec 26;15(1):15. doi: 10.3390/biom15010015.
4
The Anti-AGEing and RAGEing Potential of Isothiocyanates.
Molecules. 2024 Dec 19;29(24):5986. doi: 10.3390/molecules29245986.
5
Synergistic Inhibition of Breast Carcinoma Cell Proliferation by Quercetin and Sulforaphane via Activation of the ERK/MAPK Pathway.
Cell Biochem Biophys. 2025 Jun;83(2):2533-2546. doi: 10.1007/s12013-024-01662-6. Epub 2025 Jan 6.
7
The Potential of Glucosinolates and Their Hydrolysis Products as Inhibitors of Cytokine Storms.
Molecules. 2024 Oct 11;29(20):4826. doi: 10.3390/molecules29204826.
10
Making watercress () cropping sustainable: genomic insights into enhanced phosphorus use efficiency in an aquatic crop.
Front Plant Sci. 2023 Nov 7;14:1279823. doi: 10.3389/fpls.2023.1279823. eCollection 2023.

本文引用的文献

2
The Nrf2-antioxidant response element signaling pathway and its activation by oxidative stress.
J Biol Chem. 2009 May 15;284(20):13291-5. doi: 10.1074/jbc.R900010200. Epub 2009 Jan 30.
4
Tissue differences in the modulation of rat cytochromes P450 and phase II conjugation systems by dietary doses of phenethyl isothiocyanate.
Food Chem Toxicol. 2008 Dec;46(12):3677-83. doi: 10.1016/j.fct.2008.09.046. Epub 2008 Sep 26.
6
Sulforaphane suppressed LPS-induced inflammation in mouse peritoneal macrophages through Nrf2 dependent pathway.
Biochem Pharmacol. 2008 Oct 15;76(8):967-73. doi: 10.1016/j.bcp.2008.07.036. Epub 2008 Aug 7.
8
Regulation of estrogen receptor alpha expression in human breast cancer cells by sulforaphane.
J Nutr Biochem. 2009 Mar;20(3):195-201. doi: 10.1016/j.jnutbio.2008.02.002. Epub 2008 Jul 7.
9
Serotonin receptors, novel targets of sulforaphane identified by proteomic analysis in Caco-2 cells.
Cancer Res. 2008 Jul 1;68(13):5487-91. doi: 10.1158/0008-5472.CAN-07-6171.
10
Covalent binding to tubulin by isothiocyanates. A mechanism of cell growth arrest and apoptosis.
J Biol Chem. 2008 Aug 8;283(32):22136-46. doi: 10.1074/jbc.M802330200. Epub 2008 Jun 3.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验