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本文引用的文献

1
Integrating miRNA and gene expression profiling analysis revealed regulatory networks in gastrointestinal stromal tumors.整合微小RNA(miRNA)和基因表达谱分析揭示了胃肠道间质瘤中的调控网络。
Epigenomics. 2016 Oct;8(10):1347-1366. doi: 10.2217/epi-2016-0030. Epub 2016 Sep 14.
2
Polymorphisms in DNA repair genes in gastrointestinal stromal tumours: susceptibility and correlation with tumour characteristics and clinical outcome.胃肠道间质瘤中DNA修复基因的多态性:易感性及其与肿瘤特征和临床结局的相关性
Tumour Biol. 2016 Oct;37(10):13413-13423. doi: 10.1007/s13277-016-5276-7. Epub 2016 Jul 27.
3
Inhibitor of Apoptosis Proteins (IAPs) are commonly dysregulated in GIST and can be pharmacologically targeted to enhance the pro-apoptotic activity of imatinib.凋亡抑制蛋白(IAPs)在胃肠道间质瘤(GIST)中通常表达失调,并且可以通过药物靶向作用来增强伊马替尼的促凋亡活性。
Oncotarget. 2016 Jul 5;7(27):41390-41403. doi: 10.18632/oncotarget.9159.
4
Pharmacogenetics of tyrosine kinase inhibitors in gastrointestinal stromal tumor and chronic myeloid leukemia.酪氨酸激酶抑制剂在胃肠道间质瘤和慢性髓性白血病中的药物遗传学
Expert Opin Drug Metab Toxicol. 2016 Jul;12(7):733-42. doi: 10.1080/17425255.2016.1184649. Epub 2016 May 17.
5
Autophagy and Apoptotic Crosstalk: Mechanism of Therapeutic Resistance in HER2-Positive Breast Cancer.自噬与凋亡的相互作用:HER2阳性乳腺癌治疗耐药的机制
Breast Cancer (Auckl). 2016 Mar 13;10:13-23. doi: 10.4137/BCBCR.S32791. eCollection 2016.
6
PIK3C2A is a gene-specific target of microRNA-518a-5p in imatinib mesylate-resistant gastrointestinal stromal tumor.PIK3C2A是甲磺酸伊马替尼耐药胃肠道间质瘤中微小RNA - 518a - 5p的基因特异性靶点。
Lab Invest. 2016 Jun;96(6):652-60. doi: 10.1038/labinvest.2015.157. Epub 2016 Mar 7.
7
The multifaceted role of autophagy in tumor evasion from immune surveillance.自噬在肿瘤逃避免疫监视中的多方面作用。
Oncotarget. 2016 Apr 5;7(14):17591-607. doi: 10.18632/oncotarget.7540.
8
Functional role of autophagy in gastric cancer.自噬在胃癌中的功能作用。
Oncotarget. 2016 Apr 5;7(14):17641-51. doi: 10.18632/oncotarget.7508.
9
The Emerging Hallmarks of Cancer Metabolism.癌症代谢的新特征
Cell Metab. 2016 Jan 12;23(1):27-47. doi: 10.1016/j.cmet.2015.12.006.
10
Inhibition effect of Peg-IFNα-2b and Imatinib alone or combination on imatinib-resistant gastrointestinal stromal tumors cell lines.聚乙二醇干扰素α-2b和伊马替尼单独或联合使用对伊马替尼耐药胃肠道间质瘤细胞系的抑制作用。
Int J Clin Exp Pathol. 2015 Sep 1;8(9):11340-7. eCollection 2015.

胃肠道间质瘤(GIST):面对自噬与凋亡之间的细胞死亡

Gastrointestinal stromal tumors (GIST): Facing cell death between autophagy and apoptosis.

作者信息

Ravegnini Gloria, Sammarini Giulia, Nannini Margherita, Pantaleo Maria A, Biasco Guido, Hrelia Patrizia, Angelini Sabrina

机构信息

a Department of Pharmacy and Biotechnology , University of Bologna , Bologna Italy.

b Department of Specialized , Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna , Bologna , Italy.

出版信息

Autophagy. 2017 Mar 4;13(3):452-463. doi: 10.1080/15548627.2016.1256522. Epub 2017 Jan 5.

DOI:10.1080/15548627.2016.1256522
PMID:28055310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5361605/
Abstract

Autophagy and apoptosis are 2 fundamental biological mechanisms that may cooperate or be antagonistic, although both are involved in deciding the fate of cells in physiological or pathological conditions. These 2 mechanisms coexist simultaneously in cells and share common upstream signals and stimuli. Autophagy and apoptosis play pivotal roles in cancer development. Autophagy plays a key function in maintaining tumor cell survival by providing energy during unfavorable metabolic conditions through its recycling mechanism, and supporting the high energy requirement for metabolism and growth. This review focuses on gastrointestinal stromal tumors and cell death through autophagy and apoptosis, taking into account the involvement of both of these processes in tumor development and growth and as mechanisms of drug resistance. We also focus on the crosstalk between autophagy and apoptosis as an emerging field with major implications for the development of novel therapeutic options.

摘要

自噬和凋亡是两种基本的生物学机制,它们可能相互协作或相互拮抗,尽管二者都参与决定细胞在生理或病理条件下的命运。这两种机制在细胞中同时存在,并共享共同的上游信号和刺激。自噬和凋亡在癌症发展中发挥着关键作用。自噬通过其循环机制在不利的代谢条件下提供能量,从而在维持肿瘤细胞存活方面发挥关键作用,并支持肿瘤代谢和生长对高能量的需求。本综述聚焦于胃肠道间质瘤以及通过自噬和凋亡导致的细胞死亡,同时考虑到这两个过程在肿瘤发展和生长中的作用以及作为耐药机制的情况。我们还将自噬与凋亡之间的相互作用作为一个新兴领域进行重点关注,这一领域对新型治疗方案的开发具有重大意义。