• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

正常及(癌)前卵巢表面上皮中的丝裂原活化蛋白激酶

Mitogen-activated protein kinases in normal and (pre)neoplastic ovarian surface epithelium.

作者信息

Choi Kyung-Chul, Auersperg Nelly, Leung Peter C K

机构信息

Department of Obstetrics and Gynaecology, BC Children's and Women's Hospital, University of British Columbia, Vancouver, British Columbia, Canada V6H 3V5.

出版信息

Reprod Biol Endocrinol. 2003 Oct 7;1:71. doi: 10.1186/1477-7827-1-71.

DOI:10.1186/1477-7827-1-71
PMID:14577832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC239898/
Abstract

Mitogen-activated protein kinases (MAPKs) are a group of serine/threonine kinases which are activated in response to a diverse array of extracellular stimuli and mediate signal transduction from the cell surface to the nucleus. It has been demonstrated that MAPKs are activated by external stimuli including chemotherapeutic agents, growth factors and reproductive hormones in ovarian surface epithelial cells. Thus, the MAPK signaling pathway may play an important role in the regulation of proliferation, survival and apoptosis in response to these external stimuli in ovarian cancer. In this article, an activation of the MAPK signaling cascade by several key reproductive hormones and growth factors in epithelial ovarian cancer is reviewed.

摘要

丝裂原活化蛋白激酶(MAPKs)是一类丝氨酸/苏氨酸激酶,可响应多种细胞外刺激而被激活,并介导从细胞表面到细胞核的信号转导。已有研究表明,在卵巢表面上皮细胞中,MAPKs可被包括化疗药物、生长因子和生殖激素在内的外部刺激激活。因此,MAPK信号通路可能在卵巢癌中响应这些外部刺激调节细胞增殖、存活和凋亡方面发挥重要作用。本文综述了上皮性卵巢癌中几种关键生殖激素和生长因子对MAPK信号级联的激活作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/91c2dae3ef9f/1477-7827-1-71-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/d6f4fd42ca78/1477-7827-1-71-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/b1f453f9ebee/1477-7827-1-71-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/bc89f3444f18/1477-7827-1-71-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/f9d0555dffa5/1477-7827-1-71-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/6645645a7f3e/1477-7827-1-71-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/91c2dae3ef9f/1477-7827-1-71-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/d6f4fd42ca78/1477-7827-1-71-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/b1f453f9ebee/1477-7827-1-71-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/bc89f3444f18/1477-7827-1-71-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/f9d0555dffa5/1477-7827-1-71-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/6645645a7f3e/1477-7827-1-71-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/239898/91c2dae3ef9f/1477-7827-1-71-6.jpg

相似文献

1
Mitogen-activated protein kinases in normal and (pre)neoplastic ovarian surface epithelium.正常及(癌)前卵巢表面上皮中的丝裂原活化蛋白激酶
Reprod Biol Endocrinol. 2003 Oct 7;1:71. doi: 10.1186/1477-7827-1-71.
2
Indomethacin induces apoptosis in 786-O renal cell carcinoma cells by activating mitogen-activated protein kinases and AKT.吲哚美辛通过激活丝裂原活化蛋白激酶和AKT诱导786-O肾癌细胞凋亡。
Eur J Pharmacol. 2007 Jun 1;563(1-3):49-60. doi: 10.1016/j.ejphar.2007.01.071. Epub 2007 Feb 8.
3
Profiling of protein kinases in the neoplastic transformation of human ovarian surface epithelium.人卵巢表面上皮肿瘤转化过程中蛋白激酶的分析
Gynecol Oncol. 2001 Aug;82(2):305-11. doi: 10.1006/gyno.2001.6280.
4
Follicle-stimulating hormone activates mitogen-activated protein kinase in preneoplastic and neoplastic ovarian surface epithelial cells.促卵泡激素激活癌前和肿瘤性卵巢表面上皮细胞中的丝裂原活化蛋白激酶。
J Clin Endocrinol Metab. 2002 May;87(5):2245-53. doi: 10.1210/jcem.87.5.8506.
5
Activation of extracellular signal-regulated kinase and c-Jun-NH(2)-terminal kinase but not p38 mitogen-activated protein kinases is required for RRR-alpha-tocopheryl succinate-induced apoptosis of human breast cancer cells.RRR-α-生育酚琥珀酸酯诱导人乳腺癌细胞凋亡需要细胞外信号调节激酶和c-Jun氨基末端激酶的激活,而p38丝裂原活化蛋白激酶则不需要。
Cancer Res. 2001 Sep 1;61(17):6569-76.
6
Activation and role of MAP kinase-dependent pathways in retinal pigment epithelial cells: ERK and RPE cell proliferation.丝裂原活化蛋白激酶(MAPK)依赖性通路在视网膜色素上皮细胞中的激活及其作用:细胞外信号调节激酶(ERK)与视网膜色素上皮细胞增殖
Invest Ophthalmol Vis Sci. 2002 Sep;43(9):3091-8.
7
XIAP regulates Akt activity and caspase-3-dependent cleavage during cisplatin-induced apoptosis in human ovarian epithelial cancer cells.X连锁凋亡抑制蛋白(XIAP)在顺铂诱导的人卵巢上皮癌细胞凋亡过程中调节Akt活性和半胱天冬酶-3依赖性切割。
Cancer Res. 2001 Mar 1;61(5):1862-8.
8
Adenosine triphosphate activates mitogen-activated protein kinase in pre-neoplastic and neoplastic ovarian surface epithelial cells.三磷酸腺苷激活肿瘤前和肿瘤性卵巢表面上皮细胞中的丝裂原活化蛋白激酶。
Biol Reprod. 2003 Jan;68(1):309-15. doi: 10.1095/biolreprod.102.006551.
9
Activation of mitogen-activated protein kinases by cisplatin and their role in cisplatin-resistance.顺铂对丝裂原活化蛋白激酶的激活及其在顺铂耐药中的作用。
Cancer Lett. 2007 Jun 18;251(1):1-16. doi: 10.1016/j.canlet.2006.10.007. Epub 2006 Nov 27.
10
Inhibition of BAD phosphorylation either at serine 112 via extracellular signal-regulated protein kinase cascade or at serine 136 via Akt cascade sensitizes human ovarian cancer cells to cisplatin.通过细胞外信号调节蛋白激酶级联反应抑制BAD在丝氨酸112位点的磷酸化,或通过Akt级联反应抑制BAD在丝氨酸136位点的磷酸化,可使人卵巢癌细胞对顺铂敏感。
Cancer Res. 2000 Nov 1;60(21):5988-94.

引用本文的文献

1
In-silico docking analysis of bioactive compounds sourced from Punica granatum peel extract: Approaching a precision solution for ovarian cancer.石榴皮提取物中生物活性化合物的计算机对接分析:寻求卵巢癌的精准解决方案。
J Ayurveda Integr Med. 2025 Jul 2;16(4):101125. doi: 10.1016/j.jaim.2025.101125.
2
Aberrant miR-3135b and miR-1273g-3p expression in the peripheral blood samples of BRCA1/2 (±) ovarian cancer patients.BRCA1/2(±)卵巢癌患者外周血样本中miR-3135b和miR-1273g-3p的异常表达。
Heliyon. 2023 Dec 20;10(1):e23876. doi: 10.1016/j.heliyon.2023.e23876. eCollection 2024 Jan 15.
3
Prognostic and immune correlation analysis of mitochondrial autophagy and aging-related genes in lung adenocarcinoma.

本文引用的文献

1
Gonadotropin-releasing hormone signaling pathways in an experimental ovarian tumor.实验性卵巢肿瘤中的促性腺激素释放激素信号通路
Endocrinology. 2003 Jul;144(7):2957-66. doi: 10.1210/en.2003-0011.
2
Sustained activation of JNK/p38 MAPK pathways in response to cisplatin leads to Fas ligand induction and cell death in ovarian carcinoma cells.顺铂刺激下JNK/p38丝裂原活化蛋白激酶(MAPK)信号通路的持续激活会导致卵巢癌细胞中Fas配体的诱导表达及细胞死亡。
J Biol Chem. 2003 May 23;278(21):19245-56. doi: 10.1074/jbc.M208134200. Epub 2003 Mar 12.
3
Paclitaxel induces inactivation of p70 S6 kinase and phosphorylation of Thr421 and Ser424 via multiple signaling pathways in mitosis.
肺腺癌中线粒体自噬和衰老相关基因的预后和免疫相关性分析。
J Cancer Res Clin Oncol. 2023 Dec;149(18):16311-16335. doi: 10.1007/s00432-023-05390-x. Epub 2023 Sep 12.
4
Arctigenin attenuates paraquat-induced human lung epithelial A549 cell injury by suppressing ROS/p38 mitogen-activated protein kinases-mediated apoptosis.牛蒡子苷元通过抑制活性氧/ p38丝裂原活化蛋白激酶介导的细胞凋亡减轻百草枯诱导的人肺上皮A549细胞损伤。
World J Emerg Med. 2022;13(5):373-378. doi: 10.5847/wjem.j.1920-8642.2022.086.
5
Applications of Proteomics in Ovarian Cancer: Dawn of a New Era.蛋白质组学在卵巢癌中的应用:新时代的曙光。
Proteomes. 2022 May 9;10(2):16. doi: 10.3390/proteomes10020016.
6
Current and Futuristic Roadmap of Ovarian Cancer Management: An Overview.当前和未来的卵巢癌管理路线图:概述。
Adv Exp Med Biol. 2021;1330:1-19. doi: 10.1007/978-3-030-73359-9_1.
7
Dual Inhibitors-Loaded Nanotherapeutics that Target Kinase Signaling Pathways Synergize with Immune Checkpoint Inhibitor.靶向激酶信号通路的双抑制剂负载纳米疗法与免疫检查点抑制剂协同作用。
Cell Mol Bioeng. 2019 May 21;12(5):357-373. doi: 10.1007/s12195-019-00576-1. eCollection 2019 Oct.
8
Effect of CXCR4 silencing with shRNA on MAPK signaling in ovarian cancer.使用短发夹RNA(shRNA)沉默CXCR4对卵巢癌中丝裂原活化蛋白激酶(MAPK)信号传导的影响。
Oncol Lett. 2018 Jun;15(6):10026-10030. doi: 10.3892/ol.2018.8550. Epub 2018 Apr 20.
9
Inhibitory effects of delphinidin on the proliferation of ovarian cancer cells via PI3K/AKT and ERK 1/2 MAPK signal transduction.飞燕草素通过PI3K/AKT和ERK 1/2 MAPK信号转导对卵巢癌细胞增殖的抑制作用。
Oncol Lett. 2017 Jul;14(1):810-818. doi: 10.3892/ol.2017.6232. Epub 2017 May 23.
10
Gene Expression Profiling of Chemokines and Their Receptors in Low and High Grade Astrocytoma.低级别和高级别星形细胞瘤中趋化因子及其受体的基因表达谱分析
Asian Pac J Cancer Prev. 2017 May 1;18(5):1307-1313. doi: 10.22034/APJCP.2017.18.5.1307.
紫杉醇在有丝分裂中通过多种信号通路诱导p70 S6激酶失活以及苏氨酸421和丝氨酸424的磷酸化。
Oncogene. 2003 Jan 30;22(4):484-97. doi: 10.1038/sj.onc.1206175.
4
Adenosine triphosphate activates mitogen-activated protein kinase in pre-neoplastic and neoplastic ovarian surface epithelial cells.三磷酸腺苷激活肿瘤前和肿瘤性卵巢表面上皮细胞中的丝裂原活化蛋白激酶。
Biol Reprod. 2003 Jan;68(1):309-15. doi: 10.1095/biolreprod.102.006551.
5
Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases.由细胞外信号调节激酶(ERK)、应激活化蛋白激酶(JNK)和p38蛋白激酶介导的丝裂原活化蛋白激酶信号通路。
Science. 2002 Dec 6;298(5600):1911-2. doi: 10.1126/science.1072682.
6
Telomerase is regulated by c-Jun NH2-terminal kinase in ovarian surface epithelial cells.端粒酶在卵巢表面上皮细胞中受c-Jun氨基末端激酶调控。
Cancer Res. 2002 Aug 15;62(16):4575-8.
7
Akt activation induced by lysophosphatidic acid and sphingosine-1-phosphate requires both mitogen-activated protein kinase kinase and p38 mitogen-activated protein kinase and is cell-line specific.溶血磷脂酸和1-磷酸鞘氨醇诱导的Akt激活既需要丝裂原活化蛋白激酶激酶,也需要p38丝裂原活化蛋白激酶,并且具有细胞系特异性。
Mol Pharmacol. 2002 Sep;62(3):660-71. doi: 10.1124/mol.62.3.660.
8
Gamma-synuclein promotes cancer cell survival and inhibits stress- and chemotherapy drug-induced apoptosis by modulating MAPK pathways.
J Biol Chem. 2002 Sep 20;277(38):35050-60. doi: 10.1074/jbc.M201650200. Epub 2002 Jul 16.
9
Proliferation of rhesus ovarian surface epithelial cells in culture: lack of mitogenic response to steroid or gonadotropic hormones.恒河猴卵巢表面上皮细胞在培养中的增殖:对类固醇或促性腺激素缺乏促有丝分裂反应。
Endocrinology. 2002 Jun;143(6):2198-207. doi: 10.1210/endo.143.6.8848.
10
Follicle-stimulating hormone activates mitogen-activated protein kinase in preneoplastic and neoplastic ovarian surface epithelial cells.促卵泡激素激活癌前和肿瘤性卵巢表面上皮细胞中的丝裂原活化蛋白激酶。
J Clin Endocrinol Metab. 2002 May;87(5):2245-53. doi: 10.1210/jcem.87.5.8506.