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本文引用的文献

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Triglycerides Promote Lipid Homeostasis during Hypoxic Stress by Balancing Fatty Acid Saturation.三酰甘油通过平衡脂肪酸饱和度促进缺氧应激下的脂质稳态。
Cell Rep. 2018 Sep 4;24(10):2596-2605.e5. doi: 10.1016/j.celrep.2018.08.015.
2
Single-cell transcriptomes from human kidneys reveal the cellular identity of renal tumors.人类肾脏的单细胞转录组揭示了肾脏肿瘤的细胞特征。
Science. 2018 Aug 10;361(6402):594-599. doi: 10.1126/science.aat1699.
3
Resistance to Systemic Therapies in Clear Cell Renal Cell Carcinoma: Mechanisms and Management Strategies.透明细胞肾细胞癌的系统治疗耐药:机制与管理策略。
Mol Cancer Ther. 2018 Jul;17(7):1355-1364. doi: 10.1158/1535-7163.MCT-17-1299.
4
Genetic and metabolic hallmarks of clear cell renal cell carcinoma.透明细胞肾细胞癌的遗传和代谢特征。
Biochim Biophys Acta Rev Cancer. 2018 Aug;1870(1):23-31. doi: 10.1016/j.bbcan.2018.06.003. Epub 2018 Jun 28.
5
Impairment of gamma-glutamyl transferase 1 activity in the metabolic pathogenesis of chromophobe renal cell carcinoma.γ-谷氨酰转移酶 1 活性在嗜铬细胞瘤肾细胞癌代谢发病机制中的损害。
Proc Natl Acad Sci U S A. 2018 Jul 3;115(27):E6274-E6282. doi: 10.1073/pnas.1710849115. Epub 2018 Jun 11.
6
The glutathione redox system is essential to prevent ferroptosis caused by impaired lipid metabolism in clear cell renal cell carcinoma.谷胱甘肽氧化还原系统对于防止由于透明细胞肾细胞癌中脂质代谢受损引起的铁死亡是至关重要的。
Oncogene. 2018 Oct;37(40):5435-5450. doi: 10.1038/s41388-018-0315-z. Epub 2018 Jun 5.
7
PPARγ is dispensable for clear cell renal cell carcinoma progression.过氧化物酶体增殖物激活受体 γ(PPARγ)对于透明细胞肾细胞癌的进展是可有可无的。
Mol Metab. 2018 Aug;14:139-149. doi: 10.1016/j.molmet.2018.05.013. Epub 2018 May 21.
8
Arginase 2 Suppresses Renal Carcinoma Progression via Biosynthetic Cofactor Pyridoxal Phosphate Depletion and Increased Polyamine Toxicity.精氨酸酶 2 通过生物合成辅因子吡哆醛磷酸耗竭和增加多胺毒性来抑制肾癌进展。
Cell Metab. 2018 Jun 5;27(6):1263-1280.e6. doi: 10.1016/j.cmet.2018.04.009. Epub 2018 May 10.
9
Metabolomics and Metabolic Reprogramming in Kidney Cancer.代谢组学与肾癌的代谢重编程
Semin Nephrol. 2018 Mar;38(2):175-182. doi: 10.1016/j.semnephrol.2018.01.006.
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Orellanine specifically targets renal clear cell carcinoma.奥雷拉宁专门针对肾透明细胞癌。
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谷氨酰转移酶 1 促进透明细胞肾细胞癌的发生和进展。

Gamma-Glutamyltransferase 1 Promotes Clear Cell Renal Cell Carcinoma Initiation and Progression.

机构信息

Abramson Family Cancer Research Institute, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

Department of Cell and Developmental Biology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Mol Cancer Res. 2019 Sep;17(9):1881-1892. doi: 10.1158/1541-7786.MCR-18-1204. Epub 2019 May 31.

DOI:10.1158/1541-7786.MCR-18-1204
PMID:31151999
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6726546/
Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common subtype of kidney cancer. While the localized form of this disease can be treated surgically, advanced and metastatic stages are resistant to chemotherapies. Although more innovative treatments, such as targeted or immune-based therapies, exist, the need for new therapeutic options remains. ccRCC presents unique metabolic signatures and multiple studies have reported a significant increase in levels of reduced glutathione (GSH) and its precursors in ccRCC tumor samples compared with normal kidney tissues. These observations led us to investigate the effects of blocking the GSH pathway, particularly the gamma-glutamyltransferase 1 (GGT1) enzyme, in multiple ccRCC cell lines. In this study, we provide and evidence that GGT1/GSH pathway inhibition impacts ccRCC cell growth, through increased cell-cycle arrest. Of note, GGT1 inhibition also impairs ccRCC cell migration. Finally, pharmacologic GSH pathway inhibition decreases ccRCC cell proliferation and increases sensitivity to standard chemotherapy. Our results suggest that GGT1/GSH pathway inhibition represents a new strategy to overcome ccRCC chemoresistance. IMPLICATIONS: GGT1/GSH pathway inhibition represents a promising therapeutic strategy to overcome chemoresistance and inhibit progression of ccRCC tumors.

摘要

透明细胞肾细胞癌(ccRCC)是最常见的肾癌亚型。虽然这种疾病的局限性形式可以通过手术治疗,但晚期和转移性阶段对化疗有抵抗力。尽管存在更具创新性的治疗方法,如靶向或免疫疗法,但仍需要新的治疗选择。ccRCC 表现出独特的代谢特征,多项研究报告称,与正常肾脏组织相比,ccRCC 肿瘤样本中还原型谷胱甘肽(GSH)及其前体的水平显著增加。这些观察结果促使我们研究阻断 GSH 途径,特别是γ-谷氨酰转移酶 1(GGT1)酶,对多种 ccRCC 细胞系的影响。在这项研究中,我们提供了 和 证据表明,GGT1/GSH 途径抑制通过增加细胞周期停滞来影响 ccRCC 细胞生长。值得注意的是,GGT1 抑制也会损害 ccRCC 细胞迁移。最后,药物 GSH 途径抑制可降低 ccRCC 细胞增殖并增加对标准化疗的敏感性。我们的研究结果表明,GGT1/GSH 途径抑制代表了克服 ccRCC 化疗耐药性的一种新策略。

启示

GGT1/GSH 途径抑制代表了克服化疗耐药性和抑制 ccRCC 肿瘤进展的有前途的治疗策略。