[1]高丽云,黄 娟,李 潇,等.2,3,7,8-四氯二苯并对二噁英在不同组织器官中的作用机制[J].新乡医学院学报,2018,35(9):751-754.[doi:10.7683/xxyxyxb.2018.09.001]
 N/A.N/A[J].Journal of Xinxiang Medical University,2018,35(9):751-754.[doi:10.7683/xxyxyxb.2018.09.001]
点击复制

2,3,7,8-四氯二苯并对二噁英在不同组织器官中的作用机制
分享到:

《新乡医学院学报》[ISSN:1004-7239/CN:41-1186/R]

卷:
35
期数:
2018年9
页码:
751-754
栏目:
专家论坛
出版日期:
2018-09-05

文章信息/Info

Title:
N/A
作者:
高丽云1黄 娟1李 潇2谷莉莉1李 娜1王 晓1曹 佳1吴卫东1
(1.新乡医学院公共卫生学院毒理学教研室,河南 新乡 453003;2.郑州人民医院口腔科,河南 郑州 451000)
Author(s):
N/A
N/A
关键词:
2378-四氯二苯并对二噁英芳香烃受体作用机制
Keywords:
N/A
分类号:
B845.6
DOI:
10.7683/xxyxyxb.2018.09.001
文献标志码:
A
摘要:
二噁英是一类氯代含氧三环芳烃类化合物,其中2,3,7,8-四氯二苯并对二噁英(TCDD)是二噁英中毒性最强的一种,常作为研究二噁英毒性效应的代表性受试物。芳香烃受体(AHR)是一种配体依赖的转录因子,TCDD是AHR的配体。TCDD与AHR具有极强的亲和力,可介导动物组织结构和生理因素等方面相关化合物的毒理学效应,并参与一些重要的生理学过程,如信号传递、细胞分化等。目前,TCDD长期低剂量暴露对人类健康的危害越来越受到关注,然而,TCDD通过AHR信号通路在不同组织器官中的作用机制很少系统地报道,因此,本文对TCDD在人体不同组织器官中的作用机制进行综述。
Abstract:
N/A

参考文献/References:

[1] BAK S M,IIDA M,SOSHILOV A A,et al.Auto-induction mechanism of aryl hydrocarbon receptor 2(AHR2) gene by TCDD-activated AHR1 and AHR2 in the redseabream (Pagrus major)[J].Arch Toxicol,2017,91(1):301-312.
[2] SORG O.AHR signalling and dioxin toxicity[J].Toxicol Lett,2014,230(2):225-233.
[3] GHOTBADDINI M,POWELL J B.The AHR ligand,TCDD,regulates androgen receptor activity differently in androgen-sensitive versus castration-resistant human prostate cancer cells[J].Int J Environ Res Public Health,2015,12(7):7506-7518.
[4] 杨永滨,郑明辉,刘征涛.二恶英类毒理学研究新进展[J].生态毒理学报,2006,1(2):105-115.
[5] 鞠强,余茜,宋宁静,等.芳香烃受体在人表皮、毛囊和皮脂腺上的表达及其意义[J].中华皮肤科杂志,2011,44(11):761-764.
[6] 余茜,胡婷婷,莫晓辉,等.二噁英对人皮脂腺芳香烃受体及芳香烃受体核转运蛋白表达的影响[J].环境与健康杂志,2014,31(1):23-26.
[7] HU T,PAN Z,YU Q,et al.Benzo (a) pyrene induces interleukin (IL)-6 production and reduces lipid synthesis in human sz95 sebocytes via the aryl hydrocarbon receptor signaling pathway[J].Environ Toxicol Pharmacol,2016,43:54-60.
[8] HU T,WANG D,YU Q,et al.Aryl hydrocarbon receptor negatively regulates lipid synthesis and involves in cell differentiation of sz95 sebocytes in vitro[J].Chem Biol Interact,2016,258:52-58.
[9] FORRESTER A R.Aryl hydrocarbon receptor activation in primary human keratinocytes and epidermal equivalents:the relevance to chlorance[D].Newcastle:Newcastle University,2012.
[10] 鞠强,项蕾红,ZOUBOULIS C C,等.氯痤疮的研究进展[J].中华皮肤科杂志,2008,41(6):413-415.
[11] FURUE M,TAKAHARA M,NAKAHARA T,et al.Role of AHR/arnt system in skin homeostasis[J].Arch Dermatol Res,2014,306(9):769-779.
[12] 汤乃军,董丽,刘静,等.2,3,7,8-四氯二苯并二噁英对人芳香烃受体和转化生长因子α mRNA表达的影响[J].中华预防医学杂志,2008,42(1):21-24.
[13] GOTOVDORJ T,LEE E,LIM Y,et al.2,3,7,8-tetrachlorodibenzo-p-dioxin induced cell-specific drug transporters with acquired cisplatin resistance in cisplatin sensitive cancer cells[J].J Korean Med Sci,2014,29(9):1188-1198.
[14] BRANDSTATTER O,SCHANZ O,VORAC J,et al.Balancing intestinal and systemic inflammation through cell type-specific expression of the aryl hydrocarbon receptor repressor[J].Sci Rep,2016,6:26091.
[15] FRACCHIOLLA N S,ANNALORO C,GUIDOTTI F,et al.2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) role in hematopoiesis and in hematologic diseases:a critical review[J].Toxicology,2016,374:60-68.
[16] PENG T L,CHEN J,MAO W,et al.Aryl hydrocarbon receptor pathway activation enhances gastric cancer cell invasiveness likely through a c-Jun-dependent induction of matrix metalloproteinase-9[J].BMC Cell Biology,2009,10(1):1-7.
[17] JAEGER C,TISCHKAU S A.Role of aryl hydrocarbon receptor in circadian clock disruption and metabolic dysfunction[J].Envir Health Insights,2016,10:133-141.
[18] HUMPHREY-JOHNSON A,ABUKALAM R,ELTOM S E.Stability of the aryl hydrocarbon receptor and its regulated genes in the low activity variant of hepa-1 cell line[J].Toxicol Lett,2015,233(2):59-67.
[19] ALEKSUNES L M,KLAASSEN C D.Coordinated regulation of hepatic phase Ⅰ and Ⅱ drug-metabolizing genes and transporters using AhR-,CAR-,PXR-,PPARα-,and Nrf2-null mice[J].Drug Metab Dispos,2012,40(7):1366-1379.
[20] WALKIN L,HERRICK S E,SUMMERS A,et al.The role of mouse strain differences in the susceptibility to fibrosis:a systematic review[J].Fibrogenesis Tissue Repair,2013,6(1):1-12.
[21] KRAUS P,XING X,LIM S L,et al.Mouse strain specific gene expression differences for illumina microarray expression profiling in embryos[J].BMC Res Notes,2012,5(1):1-17.
[22] DOERING J A,TANG S,PENG H,et al.High conservation in transcriptomic and proteomic response of white sturgeon to equipotent concentrations of 2,3,7,8-TCDD,PCB 77,and benzo(a) pyrene[J].Environ Sci Technol,2016,50(9):4826-4835.
[23] MADEEN E P,LOHR C V,YOU H,et al.Dibenzo[def,p]chrysene transplacental carcinogenesis in wild-type,CYP1B1 knockout,and CYP1B1 humanized mice[J].Mol Carcinog,2017,56(1):163-171.
[24] BABAN B,LIU J Y,MOZAFFARI M S.Aryl hydrocarbon receptor agonist,leflunomide,protects the ischemic-reperfused kidney:role of tregs and stem cells[J].Am J Physiol Regul Integr Comp Physiol,2012,303(11):R1136-R1146.
[25] PARK B V,PAN F.The role of nuclear receptors in regulation of Th17/Treg biology and its implications for diseases[J].Cell Mol Immunol,2015,12(5):533-542.
[26] ALUNNO A,BARTOLONI E,BISTONI O,et al.Balance between regulatory T and Th17 cells in systemic lupus erythematosus:the old and the new[J].Clin Dev Immunol,2012,2012(4):823085.
[27] REYES-REYES E M,RAMOS I N,TAVERA-GARCIA M A,et al.The aryl hydrocarbon receptor agonist benzo(a)pyrene reactivates LINE-1 in HepG2 cells through canonical TGF-β1 signaling:implications in hepatocellular carcinogenesis[J].Am J Cancer Res,2016,6(5):1066-1077.
[28] LUO L J,WANG D D,WANG J,et al.Diverse roles of mir-335 in development and progression of cancers[J].Tumour Biol,2016,37(12):15399-15410.
[29] CHEN Y Y,CHAN K M.Regulation of vitellogenin (vtg1) and estrogen receptor(er) gene expression in zebrafish (danio rerio) following the administration of Cd2+ and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)[J].Chemosphere,2016,147:467-476.
[30] HELLE J,BADER M I,KEILER A M,et al.Cross-talk in the female rat mammary gland:influence of aryl hydrocarbon receptor on estrogen receptor signaling[J].Environ Health Perspect,2016,124(5):601-610.
[31] LICZNERSKA B,BAER-DUBOWSKA W.Indole-3-carbinol and its role in chronic diseases[J].Adv Exp Med Biol,2016,928:131-154.
[32] CASALS-CASAS C,DESVERGNE B.Endocrine disruptors:from endocrine to metabolic disruption[J].Annu Rev Physiol,2011,73:135-162.
[33] LICZNERSKA B,SZAEFER H,WIERZCHOWSKI M,et al.Resveratrol and its methoxy derivatives modulate the expression of estrogen metabolism enzymes in breast epithelial cells by ahr down-regulation[J].Mol Cell Biochem,2017,425(1/2):169-179.
[34] HUANG Q,CHEN Y,CHEN Q,et al.Dioxin-like rather than non-dioxin-like pcbs promote the development of endometriosis through stimulation of endocrine-inflammation interactions[J].Arch Toxicol,2017,91(4):1915-1924.
[35] BAKER B B,YEE J S,MEYER D N,et al.Histological and transcriptomic changes in male zebrafish testes due to early life exposure to low level 2,3,7,8-tetrachlorodibenzo-p-dioxin[J].Zebrafish,2016,13(5):413-423.
[36] CAVALLINI A,LIPPOLIS C,VACCA M,et al.The effects of chronic lifelong activation of the ahr pathway by industrial chemical pollutants on female human reproduction[J].PLoS One,2016,11(3):e0152181.
[37] SOAVE I,CASERTA D,WENGER J,et al.Environment and endometriosis:a toxic relationship[J].Eur Rev Med Pharmacol Sci,2015,19(11):1964-1972.
[38] CIOFFI M,VIETRI M T.Current insights and future advances in endometriosis diagnostics[J].Interferon,2012,51:8.

相似文献/References:

[1]高丽云,郭肖利,李 潇,等.2,3,7,8-四氯二苯并二噁英诱导腭裂发生中相关信号通路的作用研究进展[J].新乡医学院学报,2020,37(1):001.[doi:10.7683/xxyxyxb.2020.01.001]

更新日期/Last Update: 2018-09-05