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布洛芬通过诱导p75NTR肿瘤抑制蛋白的表达来抑制膀胱癌细胞的存活。

Ibuprofen inhibits survival of bladder cancer cells by induced expression of the p75NTR tumor suppressor protein.

作者信息

Khwaja Fatima, Allen Jeff, Lynch John, Andrews Peter, Djakiew Daniel

机构信息

Department of Cell Biology, Georgetown University Medical Center, Washington, DC 20057-1436, USA.

出版信息

Cancer Res. 2004 Sep 1;64(17):6207-13. doi: 10.1158/0008-5472.CAN-03-3814.

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) are used to reduce inflammation and as analgesics by inhibition of cyclooxygenase-2. At higher concentrations, some NSAIDs inhibit proliferation and induce apoptosis of cancer cells. Although several molecular mechanisms have been postulated to explain the anticancer effects of NSAIDs, they do not involve merely the inhibition of cyclooxygenase-2, and a more proximate initiator molecule may be regulated by NSAIDs to inhibit growth. The p75 neurotrophin receptor (p75NTR) is a proximate cell membrane receptor glycoprotein that has been identified as a tumor and metastasis suppressor. We observed that NSAID treatment of cell lines from bladder and other organs induced expression of the p75NTR protein. Of the different types of NSAIDs examined, ibuprofen was more efficacious than aspirin and acetaminophen and comparable with (R)-flurbiprofen and indomethacin in induction of p75NTR protein expression. This rank order NSAID induction of the p75NTR protein correlated with the ability of these NSAIDs to reduce cancer cell survival. To examine a mechanistic relationship between ibuprofen induction of p75NTR protein and inhibition of survival, bladder cancer cells were transfected with ponasterone A-inducible vectors that expressed a death domain-deleted (DeltaDD) or intracellular domain-deleted (DeltaICD) p75NTR product that acts as a dominant negative antagonist of the intact p75NTR protein. Expression of DeltaDD and DeltaICD rescued cells from ibuprofen inhibition of growth. These observations suggest that p75NTR is an important upstream modulator of the anticancer effects of NSAIDs and that ibuprofen induction of the p75NTR protein establishes an alternate mechanism by which ibuprofen may exert an anticancer effect.

摘要

非甾体抗炎药(NSAIDs)通过抑制环氧化酶-2来减轻炎症并用作镇痛药。在较高浓度下,一些NSAIDs会抑制癌细胞的增殖并诱导其凋亡。尽管已经提出了几种分子机制来解释NSAIDs的抗癌作用,但它们不仅仅涉及环氧化酶-2的抑制,而且NSAIDs可能会调节一个更直接的起始分子来抑制生长。p75神经营养因子受体(p75NTR)是一种直接的细胞膜受体糖蛋白,已被确定为肿瘤和转移抑制因子。我们观察到,用NSAIDs处理膀胱和其他器官的细胞系会诱导p75NTR蛋白的表达。在所检测的不同类型的NSAIDs中,布洛芬比阿司匹林和对乙酰氨基酚更有效,在诱导p75NTR蛋白表达方面与(R)-氟比洛芬和吲哚美辛相当。这种NSAIDs诱导p75NTR蛋白的排序与这些NSAIDs降低癌细胞存活率的能力相关。为了研究布洛芬诱导p75NTR蛋白与抑制存活之间的机制关系,用孕诺酮A诱导型载体转染膀胱癌细胞,该载体表达作为完整p75NTR蛋白的显性负性拮抗剂的死亡结构域缺失(DeltaDD)或细胞内结构域缺失(DeltaICD)的p75NTR产物。DeltaDD和DeltaICD的表达使细胞免受布洛芬对生长的抑制。这些观察结果表明,p75NTR是NSAIDs抗癌作用的重要上游调节因子,并且布洛芬诱导p75NTR蛋白建立了一种布洛芬可能发挥抗癌作用的替代机制。

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