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类视黄醇可上调连接蛋白43,但非维生素A类胡萝卜素则不能,这一过程需要视黄酸受体(RARs)参与。

Upregulation of connexin 43 by retinoids but not by non-provitamin A carotenoids requires RARs.

作者信息

Vine Alex L, Bertram John S

机构信息

Cancer Research Center of Hawaii, University of Hawaii at Manoa, Honolulu 96813, USA.

出版信息

Nutr Cancer. 2005;52(1):105-13. doi: 10.1207/s15327914nc5201_13.

Abstract

Expression of connexin 43 (Cx43) is correlated with reduced indexes of neoplasia and is upregulated by cancer-preventive retinoids and carotenoids in nontransformed human and murine fibroblasts and keratinocytes. The molecular mechanism of upregulation, however, is poorly understood. Three retinoic acid receptor (RAR) antagonists (Ro 41-5253, BMS453, and BMS493) were capable of suppressing retinoid-induced Cx43 protein expression in 10T1/2 cells. However, Ro 41-5253 did not suppress protein expression by the non-provitamin A carotenoids astaxanthin or lycopene. In contrast, Cx43 induction by astaxanthin but not by a RAR-specific retinoid was inhibited by GW9662, an antagonist of peroxisome proliferator activated receptor-gamma activation. Simultaneous treatment with the maximally effective concentration of a retinoid and with beta-carotene or the non-provitamin A carotenoid astaxanthin resulted in supraadditive upregulation of Cx43 expression, again indicating separate mechanisms of gene regulation by these two cancer preventive agents.

摘要

连接蛋白43(Cx43)的表达与肿瘤形成指标的降低相关,并且在未转化的人和小鼠成纤维细胞及角质形成细胞中,癌症预防类视黄醇和类胡萝卜素可使其表达上调。然而,上调的分子机制却知之甚少。三种视黄酸受体(RAR)拮抗剂(Ro 41-5253、BMS453和BMS493)能够抑制10T1/2细胞中类视黄醇诱导的Cx43蛋白表达。然而,Ro 41-5253并未抑制非维生素A类胡萝卜素虾青素或番茄红素的蛋白表达。相反,过氧化物酶体增殖物激活受体γ激活拮抗剂GW9662抑制了虾青素而非RAR特异性类视黄醇诱导的Cx43表达。用最大有效浓度的类视黄醇与β-胡萝卜素或非维生素A类胡萝卜素虾青素同时处理,导致Cx43表达超加性上调,这再次表明这两种癌症预防剂的基因调控机制不同。

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