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前列腺素E2通过EP3增强肺腺癌细胞中Ras信号通路的激活。

Prostaglandin E2 reinforces the activation of Ras signal pathway in lung adenocarcinoma cells via EP3.

作者信息

Yano Tomohiro, Zissel Gernot, Muller-Qernheim Joachim, Jae Shin Sung, Satoh Haruna, Ichikawa Tomio

机构信息

Department of Food Science Research for Health, National Institute of Health and Nutrition, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8636, Japan.

出版信息

FEBS Lett. 2002 May 8;518(1-3):154-8. doi: 10.1016/s0014-5793(02)02689-3.

Abstract

Prostaglandin E2 (PGE2)-dependent effects on various cell responses are regulated by respective PGE2 receptors (EP1, EP2, EP3, EP4) expressing in target cells. Alveolar type II cell (a main progenitor cell of lung adenocarcinoma) expressed only EP4, while human lung adenocarcinoma cells (A549) expressed EP3 as well as EP4. An antagonistic effect of EP3 against EP4 through the modulation of cyclic AMP level is required for PGE2-mediated activation of Ras signal pathway in A549 cells. These results suggest that the expression of EP3 may be a critical factor for the PGE2-mediated activation of Ras signal pathway in A549 cells.

摘要

前列腺素E2(PGE2)对各种细胞反应的依赖性作用由靶细胞中表达的各自的PGE2受体(EP1、EP2、EP3、EP4)调节。II型肺泡细胞(肺腺癌的主要祖细胞)仅表达EP4,而人肺腺癌细胞(A549)同时表达EP3和EP4。在A549细胞中,PGE2介导的Ras信号通路激活需要EP3通过调节环磷酸腺苷水平对EP4产生拮抗作用。这些结果表明,EP3的表达可能是PGE2介导的A549细胞中Ras信号通路激活的关键因素。

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