• 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

共同靶向线粒体钙稳态和自噬可增强癌细胞的化疗敏感性。

Co-targeting Mitochondrial Ca Homeostasis and Autophagy Enhances Cancer Cells' Chemosensitivity.

作者信息

Dubois Charlotte, Kondratskyi Artem, Bidaux Gabriel, Noyer Lucile, Vancauwenberghe Eric, Farfariello Valério, Toillon Robert-Allain, Roudbaraki Morad, Tierny Dominique, Bonnal Jean-Louis, Prevarskaya Natalia, Vanden Abeele Fabien

机构信息

Univ. Lille, Inserm, U1003 - PHYCEL - Physiologie Cellulaire, 59000 Lille, France.

Univ. Lille, Inserm, U1003 - PHYCEL - Physiologie Cellulaire, 59000 Lille, France.

出版信息

iScience. 2020 Jul 24;23(7):101263. doi: 10.1016/j.isci.2020.101263. Epub 2020 Jun 12.

DOI:10.1016/j.isci.2020.101263
PMID:32585596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7322071/
Abstract

Mitochondria are important cell death checkpoints, and mitochondrial Ca overload is considered as a potent apoptotic intrinsic pathway inducer. Here, we report that this Ca apoptosis link is largely ineffective in inducing cell-death just by itself and required a concomitant inhibition of autophagy to counteract its pro-survival action. In such condition, an acute mitochondrial stress revealed by a DRP1-mediated mitochondrial dynamic remodeling is observed concomitantly with mitochondrial depolarization, release of cytochrome c, and efficient apoptosis induction. We also uncover that mitochondrial Ca status modulates the function of autophagy as a sensitizer for chemotherapies. This priming mediated by mitochondrial Ca overload and inhibition of autophagy sensitizes many cancer cells types to different chemotherapies with independent mechanisms of action. Collectively, our results redefine an important cell signaling pathway, uncovering new combined therapies for the treatment of diseases associated with mitochondrial Ca homeostasis disorders such as cancer.

摘要

线粒体是重要的细胞死亡检查点,线粒体钙超载被认为是一种强大的凋亡内在途径诱导剂。在此,我们报告,这种钙凋亡联系仅靠自身在诱导细胞死亡方面大多无效,需要同时抑制自噬以抵消其促生存作用。在这种情况下,伴随着线粒体去极化、细胞色素c释放和有效的凋亡诱导,观察到由动力蛋白1(DRP1)介导的线粒体动态重塑所揭示的急性线粒体应激。我们还发现线粒体钙状态调节自噬作为化疗敏化剂的功能。由线粒体钙超载和自噬抑制介导的这种预处理使许多癌细胞类型对具有独立作用机制的不同化疗敏感。总体而言,我们的结果重新定义了一条重要的细胞信号通路,揭示了用于治疗与线粒体钙稳态紊乱相关疾病(如癌症)的新联合疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/fa4dc528b98e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/19fc446e8970/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/b726502fb4dd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/66808c85a533/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/17648a682bd0/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/0e29c4198d6c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/0b526d139263/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/fa4dc528b98e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/19fc446e8970/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/b726502fb4dd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/66808c85a533/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/17648a682bd0/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/0e29c4198d6c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/0b526d139263/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db9/7322071/fa4dc528b98e/gr6.jpg

相似文献

1
Co-targeting Mitochondrial Ca Homeostasis and Autophagy Enhances Cancer Cells' Chemosensitivity.共同靶向线粒体钙稳态和自噬可增强癌细胞的化疗敏感性。
iScience. 2020 Jul 24;23(7):101263. doi: 10.1016/j.isci.2020.101263. Epub 2020 Jun 12.
2
Deficiency in the mitochondrial apoptotic pathway reveals the toxic potential of autophagy under ER stress conditions.线粒体凋亡途径的缺陷揭示了内质网应激条件下自噬的潜在毒性。
Autophagy. 2014;10(11):1921-36. doi: 10.4161/15548627.2014.981790.
3
Cytoprotective role of autophagy during paclitaxel-induced apoptosis in Saos-2 osteosarcoma cells.自噬在紫杉醇诱导 Saos-2 骨肉瘤细胞凋亡过程中的细胞保护作用。
Int J Oncol. 2013 Jun;42(6):1985-92. doi: 10.3892/ijo.2013.1884. Epub 2013 Apr 5.
4
PD98059 protects the brain against mitochondrial-mediated apoptosis and autophagy in a cardiac arrest rat model.PD98059 可保护心脏骤停大鼠模型的大脑免受线粒体介导的细胞凋亡和自噬。
Life Sci. 2019 Sep 1;232:116618. doi: 10.1016/j.lfs.2019.116618. Epub 2019 Jun 29.
5
Novel Role of Carbon Monoxide in Improving Neurological Outcome After Cardiac Arrest in Aged Rats: Involvement of Inducing Mitochondrial Autophagy.一氧化碳在改善老龄大鼠心脏骤停后神经预后中的新作用:诱导线粒体自噬的参与。
J Am Heart Assoc. 2019 May 7;8(9):e011851. doi: 10.1161/JAHA.118.011851.
6
ROS-mediated activation and mitochondrial translocation of CaMKII contributes to Drp1-dependent mitochondrial fission and apoptosis in triple-negative breast cancer cells by isorhamnetin and chloroquine.ROS 介导线粒体钙调蛋白依赖性激酶 II 的激活和易位促进山奈酚和氯喹诱导的三阴性乳腺癌细胞中依赖于动力相关蛋白 1 的线粒体裂变和细胞凋亡。
J Exp Clin Cancer Res. 2019 May 28;38(1):225. doi: 10.1186/s13046-019-1201-4.
7
Morusin induces paraptosis-like cell death through mitochondrial calcium overload and dysfunction in epithelial ovarian cancer.桑色素通过线粒体钙超载和功能障碍诱导上皮性卵巢癌细胞发生类副凋亡性细胞死亡。
Chem Biol Interact. 2018 Mar 1;283:59-74. doi: 10.1016/j.cbi.2018.02.003. Epub 2018 Feb 5.
8
Silibinin triggers yeast apoptosis related to mitochondrial Ca influx in Candida albicans.水飞蓟宾引发白色念珠菌中与线粒体钙内流相关的酵母凋亡。
Int J Biochem Cell Biol. 2016 Nov;80:1-9. doi: 10.1016/j.biocel.2016.09.008. Epub 2016 Sep 14.
9
IP Receptor-Mediated Calcium Signaling and Its Role in Autophagy in Cancer.IP受体介导的钙信号传导及其在癌症自噬中的作用
Front Oncol. 2017 Jul 5;7:140. doi: 10.3389/fonc.2017.00140. eCollection 2017.
10
Mitochondria autophagy is induced after hypoxic/ischemic stress in a Drp1 dependent manner: the role of inhibition of Drp1 in ischemic brain damage.线粒体自噬在缺氧/缺血应激后以依赖动力相关蛋白1(Drp1)的方式被诱导:Drp1抑制在缺血性脑损伤中的作用
Neuropharmacology. 2014 Nov;86:103-15. doi: 10.1016/j.neuropharm.2014.07.002. Epub 2014 Jul 10.

引用本文的文献

1
Modulating Nitric Oxide: Implications for Cytotoxicity and Cytoprotection.调节一氧化氮:对细胞毒性和细胞保护的影响
Antioxidants (Basel). 2024 Apr 23;13(5):504. doi: 10.3390/antiox13050504.
2
Gemcitabine in combination with epibrassinolide enhanced the apoptotic response in an ER stress-dependent manner and reduced the epithelial-mesenchymal transition in pancreatic cancer cells.吉西他滨与表油菜素内酯联合使用以内质网应激依赖的方式增强了凋亡反应,并减少了胰腺癌细胞中的上皮-间质转化。
Turk J Biol. 2022 Sep 19;46(6):439-457. doi: 10.55730/1300-0152.2630. eCollection 2022.
3
Transient Receptor Potential Ankyrin 1 (TRPA1) Channel as a Sensor of Oxidative Stress in Cancer Cells.

本文引用的文献

1
Calcium, mitochondria and cell metabolism: A functional triangle in bioenergetics.钙、线粒体和细胞代谢:生物能量学中的功能三角形。
Biochim Biophys Acta Mol Cell Res. 2019 Jul;1866(7):1068-1078. doi: 10.1016/j.bbamcr.2018.10.016. Epub 2018 Oct 26.
2
Short-Term Mitochondrial Permeability Transition Pore Opening Modulates Histone Lysine Methylation at the Early Phase of Somatic Cell Reprogramming.短期线粒体通透性转换孔开放调节体细胞重编程早期阶段组蛋白赖氨酸甲基化。
Cell Metab. 2018 Dec 4;28(6):935-945.e5. doi: 10.1016/j.cmet.2018.08.001. Epub 2018 Aug 30.
3
The regulation of autophagy by calcium signals: Do we have a consensus?
瞬时受体电位锚蛋白 1(TRPA1)通道作为癌细胞氧化应激的传感器。
Cells. 2023 Apr 26;12(9):1261. doi: 10.3390/cells12091261.
4
Exploring the relationship between autophagy and Gefitinib resistance in NSCLC by silencing PDLIM5 using ultrasound-targeted microbubble destruction technology.利用超声靶向微泡破坏技术沉默PDLIM5,探讨非小细胞肺癌中自噬与吉非替尼耐药性之间的关系。
Cancer Cell Int. 2022 Sep 25;22(1):293. doi: 10.1186/s12935-022-02718-4.
5
FAM172A supervises ER (endoplasmic reticulum) stress-triggered autophagy in the epidural fibrosis process.FAM172A在硬膜外纤维化过程中调控内质网应激引发的自噬。
JOR Spine. 2022 May 1;5(2):e1203. doi: 10.1002/jsp2.1203. eCollection 2022 Jun.
6
Chemotherapy Resistance: Role of Mitochondrial and Autophagic Components.化疗耐药性:线粒体和自噬成分的作用
Cancers (Basel). 2022 Mar 12;14(6):1462. doi: 10.3390/cancers14061462.
7
Targeting autophagy in prostate cancer: preclinical and clinical evidence for therapeutic response.靶向前列腺癌中的自噬:治疗反应的临床前和临床证据。
J Exp Clin Cancer Res. 2022 Mar 22;41(1):105. doi: 10.1186/s13046-022-02293-6.
8
Mipsagargin: The Beginning-Not the End-of Thapsigargin Prodrug-Based Cancer Therapeutics.米帕沙卡丁:他泊沙卡丁前药类癌症治疗的开始——而非结束。
Molecules. 2021 Dec 9;26(24):7469. doi: 10.3390/molecules26247469.
钙信号对自噬的调控:我们是否达成共识?
Cell Calcium. 2018 Mar;70:32-46. doi: 10.1016/j.ceca.2017.08.005. Epub 2017 Aug 19.
4
Chloroquine and hydroxychloroquine for cancer therapy.氯喹和羟氯喹用于癌症治疗。
Mol Cell Oncol. 2014 Jul 15;1(1):e29911. doi: 10.4161/mco.29911. eCollection 2014.
5
Comprehensive analysis of mitochondrial permeability transition pore activity in living cells using fluorescence-imaging-based techniques.利用基于荧光成像技术对活细胞中线粒体通透性转换孔活性进行综合分析。
Nat Protoc. 2016 Jun;11(6):1067-80. doi: 10.1038/nprot.2016.064. Epub 2016 May 12.
6
Mipsagargin, a novel thapsigargin-based PSMA-activated prodrug: results of a first-in-man phase I clinical trial in patients with refractory, advanced or metastatic solid tumours.米普司他丁,一种新型的基于毒胡萝卜素的前列腺特异性膜抗原激活前药:难治性、晚期或转移性实体瘤患者的首次人体I期临床试验结果。
Br J Cancer. 2016 Apr 26;114(9):986-94. doi: 10.1038/bjc.2016.72.
7
Targeting mitochondrial biogenesis to overcome drug resistance to MAPK inhibitors.靶向线粒体生物合成以克服对MAPK抑制剂的耐药性。
J Clin Invest. 2016 May 2;126(5):1834-56. doi: 10.1172/JCI82661. Epub 2016 Apr 4.
8
Mitochondrial calcium uniporter regulator 1 (MCUR1) regulates the calcium threshold for the mitochondrial permeability transition.线粒体钙单向转运体调节因子1(MCUR1)调节线粒体通透性转换的钙阈值。
Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):E1872-80. doi: 10.1073/pnas.1602264113. Epub 2016 Mar 14.
9
The calcium-signaling toolkit: Updates needed.钙信号传导工具包:需要更新。
Biochim Biophys Acta. 2016 Jun;1863(6 Pt B):1337-43. doi: 10.1016/j.bbamcr.2015.11.033. Epub 2015 Nov 30.
10
Thapsigargin, Origin, Chemistry, Structure-Activity Relationships and Prodrug Development.毒胡萝卜素、来源、化学、构效关系及前药开发
Curr Pharm Des. 2015;21(38):5501-17. doi: 10.2174/1381612821666151002112824.