• 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

钙信号与卵巢癌的潜在治疗靶点(综述)。

Calcium signals and potential therapy targets in ovarian cancer (Review).

机构信息

Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, P.R. China.

Department of Obstetrics and Gynecology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, P.R. China.

出版信息

Int J Oncol. 2023 Nov;63(5). doi: 10.3892/ijo.2023.5573. Epub 2023 Sep 15.

DOI:10.3892/ijo.2023.5573
PMID:37711071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10552713/
Abstract

Ovarian cancer (OC) is a deadly disease. The poor prognosis and high lethality of OC are attributed to its high degrees of aggressiveness, resistance to chemotherapy and recurrence rates. Calcium ion (Ca) signaling has received attention in recent years, as it appears to form an essential part of various aspects of cancer pathophysiology and is a potential therapeutic target for OC treatment. Disruption of normal Ca signaling pathways can induce changes in cell cycle progression, apoptosis, proliferation and migration and invasion, leading to the development of the malignant phenotype of tumors. In the present review, the main roles of ion channel/receptor/pump‑triggered Ca signaling pathways located at the plasma membrane and organelle Ca transport in OC are summarized. In addition, the potential of Ca signaling as a novel target for the development of effective treatment strategies for OC was discussed. Furthering the understanding into the role of Ca signaling in OC is expected to facilitated the identification of novel therapeutic targets and improved clinical outcomes for patients.

摘要

卵巢癌(OC)是一种致命的疾病。OC 的预后不良和高致死率归因于其高度侵袭性、对化疗的耐药性和复发率。近年来,钙离子(Ca)信号受到关注,因为它似乎是癌症病理生理学各个方面的重要组成部分,是治疗 OC 的潜在治疗靶点。破坏正常的 Ca 信号通路可诱导细胞周期进程、细胞凋亡、增殖和迁移及侵袭的改变,导致肿瘤恶性表型的发展。在本综述中,总结了位于质膜和细胞器 Ca 转运的离子通道/受体/泵触发的 Ca 信号通路在 OC 中的主要作用。此外,还讨论了 Ca 信号作为开发 OC 有效治疗策略的新靶点的潜力。深入了解 Ca 信号在 OC 中的作用有望促进鉴定新的治疗靶点,并改善患者的临床结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef1/10552713/3d0434d2dc83/ijo-63-05-05573-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef1/10552713/dbbe000a36e7/ijo-63-05-05573-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef1/10552713/b27f5c6d4170/ijo-63-05-05573-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef1/10552713/3d0434d2dc83/ijo-63-05-05573-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef1/10552713/dbbe000a36e7/ijo-63-05-05573-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef1/10552713/b27f5c6d4170/ijo-63-05-05573-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef1/10552713/3d0434d2dc83/ijo-63-05-05573-g02.jpg

相似文献

1
Calcium signals and potential therapy targets in ovarian cancer (Review).钙信号与卵巢癌的潜在治疗靶点(综述)。
Int J Oncol. 2023 Nov;63(5). doi: 10.3892/ijo.2023.5573. Epub 2023 Sep 15.
2
The anti-tumor effect of OP-B on ovarian cancer in vitro and in vivo, and its mechanism: An investigation using network pharmacology-based analysis.基于网络药理学分析的 OP-B 对卵巢癌的体内外抗肿瘤作用及其机制研究。
J Ethnopharmacol. 2022 Jan 30;283:114706. doi: 10.1016/j.jep.2021.114706. Epub 2021 Oct 3.
3
RAD6 promotes DNA repair and stem cell signaling in ovarian cancer and is a promising therapeutic target to prevent and treat acquired chemoresistance.RAD6促进卵巢癌中的DNA修复和干细胞信号传导,是预防和治疗获得性化疗耐药的一个有前景的治疗靶点。
Oncogene. 2017 Nov 30;36(48):6680-6690. doi: 10.1038/onc.2017.279. Epub 2017 Aug 14.
4
Research progress on traditional Chinese medicine-induced apoptosis signaling pathways in ovarian cancer cells.中药诱导卵巢癌细胞凋亡信号通路的研究进展。
J Ethnopharmacol. 2024 Jan 30;319(Pt 2):117299. doi: 10.1016/j.jep.2023.117299. Epub 2023 Oct 8.
5
DMBT1 suppresses cell proliferation, migration and invasion in ovarian cancer and enhances sensitivity to cisplatin through galectin-3/PI3k/Akt pathway.DMBT1 通过半乳糖凝集素-3/PI3k/Akt 通路抑制卵巢癌细胞增殖、迁移和侵袭,并增强顺铂敏感性。
Cell Biochem Funct. 2020 Aug;38(6):801-809. doi: 10.1002/cbf.3549. Epub 2020 May 19.
6
HIF-2α-dependent TGFBI promotes ovarian cancer chemoresistance by activating PI3K/Akt pathway to inhibit apoptosis and facilitate DNA repair process.缺氧诱导因子-2α(HIF-2α)依赖性 TGFBI 通过激活 PI3K/Akt 通路来抑制细胞凋亡和促进 DNA 修复过程,从而促进卵巢癌的化疗耐药性。
Sci Rep. 2024 Feb 16;14(1):3870. doi: 10.1038/s41598-024-53854-y.
7
β-Sitosterol targets ASS1 for Nrf2 ubiquitin-dependent degradation, inducing ROS-mediated apoptosis via the PTEN/PI3K/AKT signaling pathway in ovarian cancer.β-谷甾醇靶向精氨酸琥珀酸合成酶1(ASS1)以进行Nrf2泛素依赖性降解,通过PTEN/PI3K/AKT信号通路诱导卵巢癌中活性氧(ROS)介导的细胞凋亡。
Free Radic Biol Med. 2024 Mar;214:137-157. doi: 10.1016/j.freeradbiomed.2024.02.004. Epub 2024 Feb 15.
8
Emerging Roles for Ion Channels in Ovarian Cancer: Pathomechanisms and Pharmacological Treatment.离子通道在卵巢癌中的新作用:发病机制与药物治疗
Cancers (Basel). 2021 Feb 7;13(4):668. doi: 10.3390/cancers13040668.
9
Role of CXCL12-CXCR4 axis in ovarian cancer metastasis and CXCL12-CXCR4 blockade with AMD3100 suppresses tumor cell migration and invasion in vitro.CXCL12-CXCR4 轴在卵巢癌转移中的作用及 AMD3100 阻断 CXCL12-CXCR4 抑制肿瘤细胞体外迁移和侵袭。
J Cell Physiol. 2019 Apr;234(4):3897-3909. doi: 10.1002/jcp.27163. Epub 2018 Sep 7.
10
Combination of Niraparib, Cisplatin and Twist Knockdown in Cisplatin-Resistant Ovarian Cancer Cells Potentially Enhances Synthetic Lethality through ER-Stress Mediated Mitochondrial Apoptosis Pathway.尼拉帕利联合顺铂和 Twist 敲低在顺铂耐药卵巢癌细胞中通过内质网应激介导的线粒体凋亡途径增强合成致死作用。
Int J Mol Sci. 2021 Apr 10;22(8):3916. doi: 10.3390/ijms22083916.

引用本文的文献

1
Integration of Bulk and Single-Cell RNA Sequencing to Identify RNA Modifications-Related Prognostic Signature in Ovarian Cancer.整合批量和单细胞RNA测序以鉴定卵巢癌中与RNA修饰相关的预后特征
Int J Gen Med. 2025 May 20;18:2629-2647. doi: 10.2147/IJGM.S523878. eCollection 2025.

本文引用的文献

1
Saikosaponin D alleviates cancer cachexia by directly inhibiting STAT3.柴胡皂苷D通过直接抑制信号转导和转录激活因子3(STAT3)来减轻癌症恶病质。
Phytother Res. 2023 Mar;37(3):809-819. doi: 10.1002/ptr.7676. Epub 2022 Nov 29.
2
Role of TRPV1 ion channel in cervical squamous cell carcinoma genesis.瞬时受体电位香草酸亚型1离子通道在宫颈鳞状细胞癌发生中的作用。
Front Mol Biosci. 2022 Aug 22;9:980262. doi: 10.3389/fmolb.2022.980262. eCollection 2022.
3
The effect of iron on the expression levels of calcium related gene in cisplatin resistant epithelial ovarian cancer cells.
铁对顺铂耐药的上皮性卵巢癌细胞中钙相关基因表达水平的影响。
Explor Target Antitumor Ther. 2021;2(4):309-322. doi: 10.37349/etat.2021.00048. Epub 2021 Aug 30.
4
PLAA suppresses ovarian cancer metastasis via METTL3-mediated mA modification of TRPC3 mRNA.PLAA 通过 METTL3 介导的 TRPC3 mRNA 的 mA 修饰抑制卵巢癌细胞转移。
Oncogene. 2022 Aug;41(35):4145-4158. doi: 10.1038/s41388-022-02411-w. Epub 2022 Jul 22.
5
TRPs in Ovarian Serous Cystadenocarcinoma: The Expression Patterns, Prognostic Roles, and Potential Therapeutic Targets.卵巢浆液性囊腺癌中的瞬时受体电位通道:表达模式、预后作用及潜在治疗靶点
Front Mol Biosci. 2022 Jun 24;9:915409. doi: 10.3389/fmolb.2022.915409. eCollection 2022.
6
GRP75-faciliated Mitochondria-associated ER Membrane (MAM) Integrity controls Cisplatin-resistance in Ovarian Cancer Patients.GRP75 介导的线粒体相关内质网膜(MAM)完整性控制卵巢癌患者对顺铂的耐药性。
Int J Biol Sci. 2022 Apr 11;18(7):2914-2931. doi: 10.7150/ijbs.71571. eCollection 2022.
7
Regulation and role of CAMKK2 in prostate cancer.CAMKK2 在前列腺癌中的调控作用及角色。
Nat Rev Urol. 2022 Jun;19(6):367-380. doi: 10.1038/s41585-022-00588-z. Epub 2022 Apr 26.
8
CaMKK2 Promotes the Progression of Ovarian Carcinoma through the PI3K/PDK1/Akt Axis.钙调蛋白激酶激酶 2 通过 PI3K/PDK1/Akt 轴促进卵巢癌的进展。
Comput Math Methods Med. 2022 Mar 11;2022:7187940. doi: 10.1155/2022/7187940. eCollection 2022.
9
Calcium/calmodulin-dependent protein kinase kinase 2 mediates pleiotropic effects of epidermal growth factor in cancer cells.钙/钙调蛋白依赖性蛋白激酶激酶 2 介导表皮生长因子在癌细胞中的多效性作用。
Biochim Biophys Acta Mol Cell Res. 2022 Jul;1869(7):119252. doi: 10.1016/j.bbamcr.2022.119252. Epub 2022 Mar 7.
10
TRPC3 shapes the ER-mitochondria Ca transfer characterizing tumour-promoting senescence.TRPC3 塑造了促进肿瘤发生的衰老特征性的内质网-线粒体 Ca 转移。
Nat Commun. 2022 Feb 17;13(1):956. doi: 10.1038/s41467-022-28597-x.