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Contemporary management of head and neck cancers.头颈部癌症的当代管理。
Isr Med Assoc J. 2009 May;11(5):296-300.
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5-Oxo-ETE and the OXE receptor.5-氧代-二十碳四烯酸与OXE受体。
Prostaglandins Other Lipid Mediat. 2009 Sep;89(3-4):98-104. doi: 10.1016/j.prostaglandins.2009.05.002. Epub 2009 May 18.
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Redox regulation of anoikis resistance of metastatic prostate cancer cells: key role for Src and EGFR-mediated pro-survival signals.转移性前列腺癌细胞失巢凋亡抗性的氧化还原调节:Src和表皮生长因子受体介导的促生存信号的关键作用
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Levels of prostaglandin E metabolite and leukotriene E(4) are increased in the urine of smokers: evidence that celecoxib shunts arachidonic acid into the 5-lipoxygenase pathway.吸烟者尿液中前列腺素E代谢物和白三烯E4水平升高:塞来昔布将花生四烯酸分流至5-脂氧合酶途径的证据。
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Pharmacokinetics of tepoxalin and its active metabolite in broiler chickens.
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Zyflamend reduces LTB4 formation and prevents oral carcinogenesis in a 7,12-dimethylbenz[alpha]anthracene (DMBA)-induced hamster cheek pouch model.在7,12-二甲基苯并[a]蒽(DMBA)诱导的仓鼠颊囊模型中,Zyflamend可减少白三烯B4(LTB4)的形成并预防口腔癌发生。
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Activity and potential role of licofelone in the management of osteoarthritis.利考昔在骨关节炎治疗中的活性及潜在作用。
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In vitro cyclooxygenase-2 protein expression and enzymatic activity in neoplastic cells.肿瘤细胞中环氧合酶-2蛋白的体外表达及酶活性
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Cysteinyl-leukotriene receptors and cellular signals.半胱氨酰白三烯受体与细胞信号
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Lipoxygenase inhibitors induce death receptor 5/TRAIL-R2 expression and sensitize malignant tumor cells to TRAIL-induced apoptosis.脂氧合酶抑制剂可诱导死亡受体5/TRAIL-R2表达,并使恶性肿瘤细胞对TRAIL诱导的凋亡敏感。
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5-脂氧合酶在猫鳞状细胞癌中的表达及替泊沙林诱导的细胞死亡

5-lipoxygenase expression and tepoxalin-induced cell death in squamous cell carcinomas in cats.

作者信息

Wakshlag Joseph J, Peters-Kennedy Jeanine, Bushey Jennifer J, Loftus John P

机构信息

Departments of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.

出版信息

Am J Vet Res. 2011 Oct;72(10):1369-77. doi: 10.2460/ajvr.72.10.1369.

DOI:10.2460/ajvr.72.10.1369
PMID:21962280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10957241/
Abstract

OBJECTIVE

To assess expression pattern and subcellular compartmentalization of 5-lipoxygenase in cutaneous, UV radiation-induced, and oral squamous cell carcinomas (SCCs) in cats and determine the effects of cyclooxygenase or 5-lipoxygenase inhibition on proliferation or apoptosis in a feline oral squamous cell carcinoma (SCCF1) cell line.

SAMPLE

60 archived paraffin-embedded samples of SCCs from 60 cats and SCCF1 cells.

PROCEDURES

Retrospective immunohistochemical analysis of the archived samples of SCCs (20 cutaneous, 20 UV radiation-induced, and 20 oral tumors) was performed. Cell culture proliferation assays involving SCCF1 cells were performed, and tepoxalin-induced apoptosis and signaling were examined via western blotting and annexin V staining.

RESULTS

Immunohistochemically, staining for 5-lipoxygenase was most frequently of greatest intensity in oral SCCs, whereas staining of cutaneous and UV radiation-induced lesions had less consistent 5-lipoxygenase expression. Exposure of SCCF1 cells to the 5-lipoxygenase inhibitor tepoxalin resulted in apoptosis; the effect appeared to be mediated via alteration of cell signaling rather than via suppression of lipid mediators that are typically produced as a result of 5-lipoxygenase activity.

CONCLUSIONS AND CLINICAL RELEVANCE

In cats, expression of 5-lipoxygenase in SCCs appeared to differ depending on tumor location. The influence of tepoxalin-induced 5-lipoxygenase inhibition on a 5-lipoxygenase-expressing cell line coupled with the notable expression of 5-lipoxygenase in oral SCCs suggested that 5-lipoxygenase inhibition may have therapeutic benefits in affected cats. Although the safety of tepoxalin in cats has yet to be investigated, 5-lipoxygenase inhibitors should be evaluated for use as a potential treatment for SCCs in that species.

摘要

目的

评估5-脂氧合酶在猫的皮肤、紫外线辐射诱导的和口腔鳞状细胞癌(SCC)中的表达模式和亚细胞定位,并确定环氧化酶或5-脂氧合酶抑制对猫口腔鳞状细胞癌(SCCF1)细胞系增殖或凋亡的影响。

样本

来自60只猫的60份存档石蜡包埋的SCC样本和SCCF1细胞。

步骤

对存档的SCC样本(20份皮肤肿瘤、20份紫外线辐射诱导的肿瘤和20份口腔肿瘤)进行回顾性免疫组织化学分析。进行涉及SCCF1细胞的细胞培养增殖试验,并通过蛋白质印迹法和膜联蛋白V染色检测替泊沙林诱导的凋亡和信号传导。

结果

免疫组织化学显示,5-脂氧合酶染色在口腔SCC中最常呈现最强强度,而皮肤和紫外线辐射诱导病变的5-脂氧合酶表达则不太一致。SCCF1细胞暴露于5-脂氧合酶抑制剂替泊沙林会导致凋亡;这种作用似乎是通过细胞信号改变介导的,而不是通过抑制通常由5-脂氧合酶活性产生的脂质介质。

结论及临床意义

在猫中,SCC中5-脂氧合酶的表达似乎因肿瘤位置而异。替泊沙林诱导的5-脂氧合酶抑制对表达5-脂氧合酶的细胞系的影响,以及5-脂氧合酶在口腔SCC中的显著表达表明,5-脂氧合酶抑制可能对患病猫具有治疗益处。尽管替泊沙林在猫中的安全性尚未研究,但5-脂氧合酶抑制剂应用于评估作为该物种SCC的潜在治疗方法。