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本文引用的文献

1
Sorting out the functional role(s) of peroxisome proliferator-activated receptor-beta/delta (PPARbeta/delta) in cell proliferation and cancer.厘清过氧化物酶体增殖物激活受体β/δ(PPARβ/δ)在细胞增殖和癌症中的功能作用。
Biochim Biophys Acta. 2009 Dec;1796(2):230-41. doi: 10.1016/j.bbcan.2009.06.002. Epub 2009 Jun 6.
2
Regulation of peroxisome proliferator-activated receptor-beta/delta by the APC/beta-CATENIN pathway and nonsteroidal antiinflammatory drugs.APC/β-连环蛋白途径和非甾体抗炎药对过氧化物酶体增殖物激活受体-β/δ的调控
Mol Carcinog. 2009 Oct;48(10):942-52. doi: 10.1002/mc.20546.
3
Ligand activation of peroxisome proliferator-activated receptor beta/delta (PPAR beta/delta) inhibits chemically induced skin tumorigenesis.过氧化物酶体增殖物激活受体β/δ(PPARβ/δ)的配体激活可抑制化学诱导的皮肤肿瘤发生。
Carcinogenesis. 2008 Dec;29(12):2406-14. doi: 10.1093/carcin/bgn219. Epub 2008 Sep 17.
4
Ligand activation of peroxisome proliferator-activated receptor-beta/delta inhibits cell proliferation in human HaCaT keratinocytes.过氧化物酶体增殖物激活受体-β/δ的配体激活抑制人HaCaT角质形成细胞的细胞增殖。
Mol Pharmacol. 2008 Nov;74(5):1429-42. doi: 10.1124/mol.108.050609. Epub 2008 Aug 7.
5
Ligand activation of peroxisome proliferator-activated receptor beta/delta (PPARbeta/delta) attenuates carbon tetrachloride hepatotoxicity by downregulating proinflammatory gene expression.过氧化物酶体增殖物激活受体β/δ(PPARβ/δ)的配体激活通过下调促炎基因表达减轻四氯化碳肝毒性。
Toxicol Sci. 2008 Oct;105(2):418-28. doi: 10.1093/toxsci/kfn142. Epub 2008 Jul 12.
6
Role of peroxisome-proliferator-activated receptor beta/delta (PPARbeta/delta) in gastrointestinal tract function and disease.过氧化物酶体增殖物激活受体β/δ(PPARβ/δ)在胃肠道功能及疾病中的作用
Clin Sci (Lond). 2008 Aug;115(4):107-27. doi: 10.1042/CS20080022.
7
PPARbeta/delta ligands as modulators of the inflammatory response.过氧化物酶体增殖物激活受体β/δ配体作为炎症反应的调节剂
Curr Opin Investig Drugs. 2008 May;9(5):463-9.
8
Quantitative expression patterns of peroxisome proliferator-activated receptor-beta/delta (PPARbeta/delta) protein in mice.小鼠中过氧化物酶体增殖物激活受体-β/δ(PPARβ/δ)蛋白的定量表达模式
Biochem Biophys Res Commun. 2008 Jul 4;371(3):456-61. doi: 10.1016/j.bbrc.2008.04.086. Epub 2008 Apr 28.
9
Peroxisome proliferator-activated receptor-beta/delta protects against chemically induced liver toxicity in mice.过氧化物酶体增殖物激活受体-β/δ可保护小鼠免受化学诱导的肝毒性。
Hepatology. 2008 Jan;47(1):225-35. doi: 10.1002/hep.21925.
10
Ligand activation of peroxisome proliferator-activated receptor-beta/delta (PPARbeta/delta) and inhibition of cyclooxygenase 2 (COX2) attenuate colon carcinogenesis through independent signaling mechanisms.过氧化物酶体增殖物激活受体-β/δ(PPARβ/δ)的配体激活以及环氧合酶2(COX2)的抑制通过独立的信号传导机制减弱结肠癌发生。
Carcinogenesis. 2008 Jan;29(1):169-76. doi: 10.1093/carcin/bgm209. Epub 2007 Sep 24.

配体激活过氧化物酶体增殖物激活受体-β/δ 和抑制环氧化酶-2 增强抑制皮肤肿瘤发生。

Ligand activation of peroxisome proliferator-activated receptor-beta/delta and inhibition of cyclooxygenase-2 enhances inhibition of skin tumorigenesis.

机构信息

Department of Veterinary and Biomedical Sciences and The Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.

出版信息

Toxicol Sci. 2010 Jan;113(1):27-36. doi: 10.1093/toxsci/kfp212. Epub 2009 Sep 11.

DOI:10.1093/toxsci/kfp212
PMID:19748995
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2794329/
Abstract

Ligand activation of peroxisome proliferator-activated receptor (PPAR)-beta/delta and inhibition of cyclooxygenase-2 (COX-2) activity by nonsteroidal anti-inflammatory drugs can attenuate skin tumorigenesis. There is also evidence that attenuation of skin tumorigenesis by inhibition of COX-2 activity occurs through PPARbeta/delta-independent mechanisms. The present study examined the hypothesis that combining ligand activation of PPARbeta/delta with inhibition of COX-2 activity will cooperatively inhibit chemically induced skin tumor progression using both in vivo and ex vivo models. A two-stage chemical carcinogenesis bioassay was performed in wild-type and Pparbeta/delta-null mice. After 22 weeks, cohorts of both mouse lines were divided into four experimental groups: (1) control, (2) topical application of the PPARbeta/delta ligand GW0742, (3) dietary administration of the COX-2 inhibitor nimesulide, or (4) both GW0742 and nimesulide. Ligand activation of PPARbeta/delta did not influence skin tumor progression, while a modest decrease in skin tumor multiplicity was observed with dietary nimesulide. Interestingly, the combined treatment of GW0742 and nimesulide increased the efficacy of the decrease in papilloma multiplicity for 6 weeks in wild-type mice, but this effect was not found at later time points and was not found in similarly treated Pparbeta/delta-null mice. Neoplastic keratinocyte lines cultured with GW0742 and nimesulide also exhibited enhanced inhibition of cell proliferation coincident with increased expression of Keratin messenger RNAs. Results from these studies support the hypothesis that combining ligand activation of PPARbeta/delta with inhibition of COX-2 activity can inhibit chemically induced skin tumor progression by modulating differentiation.

摘要

配体激活过氧化物酶体增殖物激活受体 (PPAR)-β/δ 和非甾体抗炎药抑制环氧化酶-2 (COX-2) 活性可减轻皮肤肿瘤的发生。也有证据表明 COX-2 活性抑制通过 PPARβ/δ 非依赖性机制发生。本研究通过体内和体外模型检验了以下假设:通过激活 PPARβ/δ 配体与抑制 COX-2 活性相结合,将协同抑制化学诱导的皮肤肿瘤进展。在野生型和 Pparβ/δ 缺陷型小鼠中进行了两阶段化学致癌生物测定。22 周后,将两种小鼠系的队列分为四个实验组:(1) 对照组,(2) 局部应用 PPARβ/δ 配体 GW0742,(3) 饮食给予 COX-2 抑制剂尼美舒利,或(4) GW0742 和尼美舒利联合应用。PPARβ/δ 配体的激活并不影响皮肤肿瘤的进展,而饮食尼美舒利则观察到皮肤肿瘤多发性略有降低。有趣的是,GW0742 和尼美舒利联合治疗在 6 周内增加了野生型小鼠中多发性肿瘤减少的疗效,但在后期时间点未发现这种效果,并且在接受类似治疗的 Pparβ/δ 缺陷型小鼠中也未发现这种效果。用 GW0742 和尼美舒利培养的肿瘤角质形成细胞系也表现出细胞增殖的抑制增强,同时 Keratin 信使 RNA 的表达增加。这些研究的结果支持以下假设:通过调节分化,将 PPARβ/δ 配体的激活与 COX-2 活性的抑制相结合,可抑制化学诱导的皮肤肿瘤进展。