• 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

鞘脂类/神经酰胺代谢通路与自噬在黑色素瘤发生发展中的作用:新的治疗靶点和机会

Sphingolipid/Ceramide Pathways and Autophagy in the Onset and Progression of Melanoma: Novel Therapeutic Targets and Opportunities.

机构信息

Retrovirus Center and Virology Section, Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, 56127 Pisa, Italy.

Virology Unit, Pisa University Hospital, 56127 Pisa, Italy.

出版信息

Int J Mol Sci. 2019 Jul 12;20(14):3436. doi: 10.3390/ijms20143436.

DOI:10.3390/ijms20143436
PMID:31336922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6678284/
Abstract

Melanoma is a malignant tumor deriving from neoplastic transformation of melanocytes. The incidence of melanoma has increased dramatically over the last 50 years. It accounts for most cases of skin cancer deaths. Early diagnosis leads to remission in 90% of cases of melanoma; conversely, for melanoma at more advanced stages, prognosis becomes more unfavorable also because dvanced melanoma is often resistant to pharmacological and radiological therapies due to genetic plasticity, presence of cancer stem cells that regenerate the tumor, and efficient elimination of drugs. This review illustrates the role of autophagy in tumor progression and resistance to therapy, focusing on molecular targets for future drugs.

摘要

黑色素瘤是一种恶性肿瘤,源自黑色素细胞的肿瘤性转化。在过去的 50 年中,黑色素瘤的发病率急剧上升。它占皮肤癌死亡病例的大多数。早期诊断可使 90%的黑色素瘤病例得到缓解;相反,对于更晚期的黑色素瘤,预后变得更加不利,这也是因为由于遗传可塑性、存在再生肿瘤的癌症干细胞以及药物的有效清除,晚期黑色素瘤通常对药物治疗和放射治疗具有抗性。本综述说明了自噬在肿瘤进展和对治疗的抗性中的作用,重点介绍了未来药物的分子靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/c3d8d2a02165/ijms-20-03436-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/569571717e13/ijms-20-03436-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/201322a28733/ijms-20-03436-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/59bb6ef9789c/ijms-20-03436-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/c3d8d2a02165/ijms-20-03436-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/569571717e13/ijms-20-03436-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/201322a28733/ijms-20-03436-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/59bb6ef9789c/ijms-20-03436-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1664/6678284/c3d8d2a02165/ijms-20-03436-g004.jpg

相似文献

1
Sphingolipid/Ceramide Pathways and Autophagy in the Onset and Progression of Melanoma: Novel Therapeutic Targets and Opportunities.鞘脂类/神经酰胺代谢通路与自噬在黑色素瘤发生发展中的作用:新的治疗靶点和机会
Int J Mol Sci. 2019 Jul 12;20(14):3436. doi: 10.3390/ijms20143436.
2
Acid Ceramidase in Melanoma: EXPRESSION, LOCALIZATION, AND EFFECTS OF PHARMACOLOGICAL INHIBITION.黑色素瘤中的酸性神经酰胺酶:表达、定位及药理学抑制作用
J Biol Chem. 2016 Jan 29;291(5):2422-34. doi: 10.1074/jbc.M115.666909. Epub 2015 Nov 9.
3
Ceramide metabolism alterations contribute to Tumor Necrosis Factor-induced melanoma dedifferentiation and predict resistance to immune checkpoint inhibitors in advanced melanoma patients.神经酰胺代谢改变导致肿瘤坏死因子诱导的黑色素瘤去分化,并预测晚期黑色素瘤患者对免疫检查点抑制剂的耐药性。
Front Immunol. 2024 Jul 29;15:1421432. doi: 10.3389/fimmu.2024.1421432. eCollection 2024.
4
Novel mechanisms of action of classical chemotherapeutic agents on sphingolipid pathways.经典化疗药物对鞘脂途径的新型作用机制。
Biol Chem. 2015 Jun;396(6-7):669-79. doi: 10.1515/hsz-2014-0302.
5
Acid ceramidase controls apoptosis and increases autophagy in human melanoma cells treated with doxorubicin.酸性鞘磷脂酶控制阿霉素处理的人黑色素瘤细胞凋亡和自噬。
Sci Rep. 2021 May 27;11(1):11221. doi: 10.1038/s41598-021-90219-1.
6
Ablation of Acid Ceramidase Impairs Autophagy and Mitochondria Activity in Melanoma Cells.酸 ceramidase 的消融会损害黑色素瘤细胞中的自噬和线粒体活性。
Int J Mol Sci. 2021 Mar 23;22(6):3247. doi: 10.3390/ijms22063247.
7
Tamoxifen regulation of sphingolipid metabolism--Therapeutic implications.他莫昔芬对鞘脂代谢的调节——治疗意义。
Biochim Biophys Acta. 2015 Sep;1851(9):1134-45. doi: 10.1016/j.bbalip.2015.05.001. Epub 2015 May 9.
8
Ceramide activates lysosomal cathepsin B and cathepsin D to attenuate autophagy and induces ER stress to suppress myeloid-derived suppressor cells.神经酰胺激活溶酶体组织蛋白酶B和组织蛋白酶D以减弱自噬,并诱导内质网应激以抑制髓源性抑制细胞。
Oncotarget. 2016 Dec 20;7(51):83907-83925. doi: 10.18632/oncotarget.13438.
9
The unfolding role of ceramide in coordinating retinoid-based cancer therapy.神经酰胺在协调视黄酸类癌症治疗中的作用不断显现。
Biochem J. 2021 Oct 15;478(19):3621-3642. doi: 10.1042/BCJ20210368.
10
Disruption of sphingolipid metabolism augments ceramide-induced autophagy in preeclampsia.鞘脂代谢紊乱增强了子痫前期中神经酰胺诱导的自噬。
Autophagy. 2015 Apr 3;11(4):653-69. doi: 10.1080/15548627.2015.1034414.

引用本文的文献

1
From Lipid Signatures to Cellular Responses: Unraveling the Complexity of Melanoma and Furthering Its Diagnosis and Treatment.从脂质特征到细胞反应:揭示黑色素瘤的复杂性并推进其诊断和治疗。
Medicina (Kaunas). 2024 Jul 25;60(8):1204. doi: 10.3390/medicina60081204.
2
Sphingolipid-Based Synergistic Interactions to Enhance Chemosensitivity in Lung Cancer Cells.基于神经鞘脂的协同作用增强肺癌细胞的化疗敏感性。
Cells. 2023 Nov 8;12(22):2588. doi: 10.3390/cells12222588.
3
Establishment of SLC7A11-knockout mouse and its preliminary investigation in melanoma.

本文引用的文献

1
Acid ceramidase promotes drug resistance in acute myeloid leukemia through NF-κB-dependent P-glycoprotein upregulation.酸性鞘磷脂酶通过 NF-κB 依赖性 P-糖蛋白上调促进急性髓系白血病的耐药性。
J Lipid Res. 2019 Jun;60(6):1078-1086. doi: 10.1194/jlr.M091876. Epub 2019 Apr 8.
2
Atg2 mediates direct lipid transfer between membranes for autophagosome formation.Atg2 介导膜之间的直接脂质转移,以形成自噬体。
Nat Struct Mol Biol. 2019 Apr;26(4):281-288. doi: 10.1038/s41594-019-0203-4. Epub 2019 Mar 25.
3
Co-delivery of Doxorubicin and Ceramide in a Liposomal Formulation Enhances Cytotoxicity in Murine B16BL6 Melanoma Cell Lines.
建立 SLC7A11 基因敲除小鼠及其在黑色素瘤中的初步研究。
In Vitro Cell Dev Biol Anim. 2023 Oct;59(9):729-737. doi: 10.1007/s11626-023-00819-6. Epub 2023 Nov 6.
4
Whole Transcriptome Analysis of Substantia Nigra in Mice with MPTP-Induced Parkinsonism Bearing Defective Glucocerebrosidase Activity.MPTP 诱导的葡萄糖脑苷脂酶活性缺陷帕金森病小鼠黑质全转录组分析。
Int J Mol Sci. 2023 Jul 29;24(15):12164. doi: 10.3390/ijms241512164.
5
Regulation of Autophagy via Carbohydrate and Lipid Metabolism in Cancer.癌症中通过碳水化合物和脂质代谢对自噬的调控
Cancers (Basel). 2023 Apr 7;15(8):2195. doi: 10.3390/cancers15082195.
6
Ceramide present in cholangiocarcinoma-derived extracellular vesicle induces a pro-inflammatory state in monocytes.胆管癌来源的细胞外囊泡中的神经酰胺诱导单核细胞产生促炎状态。
Sci Rep. 2023 May 12;13(1):7766. doi: 10.1038/s41598-023-34676-w.
7
Autophagy Paradox: Strategizing Treatment Modality in Melanoma.自噬悖论:黑色素瘤治疗模式的策略制定。
Curr Treat Options Oncol. 2023 Feb;24(2):130-145. doi: 10.1007/s11864-023-01053-8. Epub 2023 Jan 21.
8
New algorithms based on autophagy-related lncRNAs pairs to predict the prognosis of skin cutaneous melanoma patients.基于自噬相关 lncRNAs 对的新算法预测皮肤黑色素瘤患者的预后。
Arch Dermatol Res. 2023 Aug;315(6):1511-1526. doi: 10.1007/s00403-022-02522-0. Epub 2023 Jan 9.
9
Potential role of autophagy induced by FLT3-ITD and acid ceramidase in acute myeloid leukemia chemo-resistance: new insights.FLT3-ITD 诱导的自噬和酸性神经酰胺酶在急性髓系白血病化疗耐药中的潜在作用:新的见解。
Cell Commun Signal. 2022 Oct 31;20(1):172. doi: 10.1186/s12964-022-00956-7.
10
Transcriptional Differences in Lipid-Metabolizing Enzymes in Murine Sebocytes Derived from Sebaceous Glands of the Skin and Preputial Glands.皮肤和包皮腺来源的鼠类皮脂细胞中脂质代谢酶的转录差异。
Int J Mol Sci. 2021 Oct 27;22(21):11631. doi: 10.3390/ijms222111631.
脂质体剂型中多柔比星和神经酰胺的共递送增强了对小鼠 B16BL6 黑素瘤细胞系的细胞毒性。
AAPS PharmSciTech. 2019 Feb 4;20(3):99. doi: 10.1208/s12249-019-1316-0.
4
Molecular Mechanism of Inhibition of Acid Ceramidase by Carmofur.卡莫氟抑制酸性神经鞘氨醇酶的分子机制。
J Med Chem. 2019 Jan 24;62(2):987-992. doi: 10.1021/acs.jmedchem.8b01723. Epub 2018 Dec 19.
5
Targeting the Sphingosine 1-Phosphate Axis Exerts Potent Antitumor Activity in BRAFi-Resistant Melanomas.靶向鞘氨醇 1-磷酸轴在 BRAFi 耐药性黑色素瘤中发挥强大的抗肿瘤活性。
Mol Cancer Ther. 2019 Feb;18(2):289-300. doi: 10.1158/1535-7163.MCT-17-1141. Epub 2018 Nov 27.
6
Lysosomal acid ceramidase ASAH1 controls the transition between invasive and proliferative phenotype in melanoma cells.溶酶体酸性神经酰胺酶 ASAH1 控制黑色素瘤细胞侵袭和增殖表型之间的转变。
Oncogene. 2019 Feb;38(8):1282-1295. doi: 10.1038/s41388-018-0500-0. Epub 2018 Sep 25.
7
Role of sphingolipids in senescence: implication in aging and age-related diseases.鞘脂类在衰老中的作用:与衰老和与年龄相关疾病的关系。
J Clin Invest. 2018 Jul 2;128(7):2702-2712. doi: 10.1172/JCI97949.
8
Autophagic cell death participates in POMC-induced melanoma suppression.自噬性细胞死亡参与阿黑皮素原诱导的黑色素瘤抑制过程。
Cell Death Discov. 2018 Jul 10;4:11. doi: 10.1038/s41420-018-0070-5. eCollection 2018.
9
Sphingolipids as Regulators of Autophagy and Endocytic Trafficking.鞘脂作为自噬和内吞运输的调节剂。
Adv Cancer Res. 2018;140:27-60. doi: 10.1016/bs.acr.2018.04.008. Epub 2018 May 22.
10
Chloroquine inhibits autophagic flux by decreasing autophagosome-lysosome fusion.氯喹通过减少自噬体-溶酶体融合来抑制自噬流。
Autophagy. 2018;14(8):1435-1455. doi: 10.1080/15548627.2018.1474314. Epub 2018 Jul 20.