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本文引用的文献

1
Spatiotemporal coupling of cAMP transporter to CFTR chloride channel function in the gut epithelia.肠道上皮细胞中环磷酸腺苷(cAMP)转运体与囊性纤维化跨膜传导调节因子(CFTR)氯离子通道功能的时空耦合。
Cell. 2007 Nov 30;131(5):940-51. doi: 10.1016/j.cell.2007.09.037.
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Biotransformation and transport of the tobacco-specific carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in bile duct-cannulated wild-type and Mrp2/Abcc2-deficient (TR ) Wistar rats.胆管插管野生型和Mrp2/Abcc2基因缺陷型(TR)Wistar大鼠体内烟草特异性致癌物4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮(NNK)的生物转化与转运
Carcinogenesis. 2007 Dec;28(12):2650-6. doi: 10.1093/carcin/bgm187. Epub 2007 Aug 27.
3
Cystic fibrosis transmembrane conductance regulator function is suppressed in cigarette smokers.囊性纤维化跨膜传导调节因子的功能在吸烟者中受到抑制。
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4
Lysophosphatidic acid inhibits cholera toxin-induced secretory diarrhea through CFTR-dependent protein interactions.溶血磷脂酸通过CFTR依赖性蛋白相互作用抑制霍乱毒素诱导的分泌性腹泻。
J Exp Med. 2005 Oct 3;202(7):975-86. doi: 10.1084/jem.20050421.
5
Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners.囊性纤维化跨膜传导调节因子及其相互作用蛋白的大分子复合物
Pharmacol Ther. 2005 Nov;108(2):208-23. doi: 10.1016/j.pharmthera.2005.04.004. Epub 2005 Jun 2.
6
4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone, a component of tobacco smoke, modulates mediator release from human bronchial and alveolar epithelial cells.4-(甲基亚硝基氨基)-1-(3-吡啶基)-1-丁酮,烟草烟雾的一种成分,可调节人支气管和肺泡上皮细胞中介质的释放。
Clin Exp Immunol. 2005 Apr;140(1):46-53. doi: 10.1111/j.1365-2249.2005.02739.x.
7
Inhibition of chloride secretion in human bronchial epithelial cells by cigarette smoke extract.香烟烟雾提取物对人支气管上皮细胞氯离子分泌的抑制作用。
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Molecular assembly of cystic fibrosis transmembrane conductance regulator in plasma membrane.囊性纤维化跨膜传导调节因子在质膜中的分子组装
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9
Cytokine production by alveolar macrophages is down regulated by the alpha-methylhydroxylation pathway of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK).4-(甲基亚硝基氨基)-1-(3-吡啶基)-1-丁酮(NNK)的α-甲基羟基化途径可下调肺泡巨噬细胞的细胞因子产生。
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The MRP family of drug efflux pumps.药物外排泵的多药耐药相关蛋白(MRP)家族
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烟草致癌物 NNK 转运体 MRP2 调节肺上皮细胞中的 CFTR 功能:对肺癌的影响。

Tobacco carcinogen NNK transporter MRP2 regulates CFTR function in lung epithelia: implications for lung cancer.

机构信息

Department of Biochemistry and Molecular Biology, Wayne State University School of Medicine, 540 E. Canfield Avenue, 5312 Scott Hall, Detroit, MI 48201, USA.

出版信息

Cancer Lett. 2010 Jun 28;292(2):246-53. doi: 10.1016/j.canlet.2009.12.009. Epub 2010 Jan 20.

DOI:10.1016/j.canlet.2009.12.009
PMID:20089353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2868381/
Abstract

Lung cancer is the leading cause of cancer death in the United States. About 85% of all lung cancers are linked to tobacco smoke, in which more than 50 lung carcinogens have been identified and one of the most abundant is 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK). The human lung epithelium constitutes the first line of defense against tobacco-specific carcinogens, in which apically-localized receptors, transporters, and ion channels in the airway may play a critical role in this native defense against tobacco smoke. Here we showed that multidrug resistance protein-2 (MRP2) and cystic fibrosis transmembrane conductance regulator (CFTR), two ATP-binding cassette (ABC) transporters, are localized to the apical surfaces of plasma membrane in polarized lung epithelial cells. We observed that there is a functional coupling between CFTR and MRP2 that may be mediated by PDZ proteins. We also observed the existence of a macromolecular complex containing CFTR, MRP2, and PDZ proteins, which might form the basis for the regulatory cooperation between these two ABC transporters. Our results have important implications for cigarette smoke-associated lung diseases (such as smoke-related emphysema, chronic obstructive pulmonary disease, and lung cancer).

摘要

肺癌是美国癌症死亡的主要原因。在美国,大约 85%的肺癌与吸烟有关,其中已经鉴定出 50 多种肺癌致癌物,而含量最丰富的一种是 4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁酮(NNK)。人体肺上皮细胞构成了抵御烟草特异性致癌物的第一道防线,其中气道中位于顶端的受体、转运体和离子通道可能在这种天然的抵御烟草烟雾的过程中发挥关键作用。在这里,我们发现多药耐药蛋白 2(MRP2)和囊性纤维化跨膜电导调节因子(CFTR),两种 ABC 转运体,定位于极化肺上皮细胞的质膜顶表面。我们观察到 CFTR 和 MRP2 之间存在功能偶联,这种偶联可能是由 PDZ 蛋白介导的。我们还观察到存在一个包含 CFTR、MRP2 和 PDZ 蛋白的大分子复合物,这可能是这两种 ABC 转运体之间调节合作的基础。我们的研究结果对与吸烟有关的肺部疾病(如与吸烟有关的肺气肿、慢性阻塞性肺疾病和肺癌)具有重要意义。