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Ferroptosis inhibition by lysosome-dependent catabolism of extracellular protein.铁死亡通过溶酶体依赖的细胞外蛋白分解代谢抑制。
Cell Chem Biol. 2022 Nov 17;29(11):1588-1600.e7. doi: 10.1016/j.chembiol.2022.10.006. Epub 2022 Oct 27.
2
Combinatorial GxGxE CRISPR screen identifies SLC25A39 in mitochondrial glutathione transport linking iron homeostasis to OXPHOS.组合型 GxGxE CRISPR 筛选鉴定出在线粒体谷胱甘肽转运中连接铁稳态与 OXPHOS 的 SLC25A39。
Nat Commun. 2022 May 5;13(1):2483. doi: 10.1038/s41467-022-30126-9.
3
Macropinocytosis is an alternative pathway of cysteine acquisition and mitigates sorafenib-induced ferroptosis in hepatocellular carcinoma.巨胞饮作用是半胱氨酸获取的替代途径,并减轻索拉非尼诱导的肝细胞癌中的铁死亡。
J Exp Clin Cancer Res. 2022 Mar 14;41(1):98. doi: 10.1186/s13046-022-02296-3.
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GLUT5-KHK axis-mediated fructose metabolism drives proliferation and chemotherapy resistance of colorectal cancer.GLUT5-KHK 轴介导的果糖代谢促进结直肠癌细胞的增殖和化疗耐药性。
Cancer Lett. 2022 May 28;534:215617. doi: 10.1016/j.canlet.2022.215617. Epub 2022 Mar 4.
5
SLC25A1 promotes tumor growth and survival by reprogramming energy metabolism in colorectal cancer.SLC25A1 通过重塑结直肠癌的能量代谢促进肿瘤生长和存活。
Cell Death Dis. 2021 Nov 27;12(12):1108. doi: 10.1038/s41419-021-04411-2.
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SLC25A39 is necessary for mitochondrial glutathione import in mammalian cells.SLC25A39 是哺乳动物细胞中线粒体谷胱甘肽导入所必需的。
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7
Dietary fructose improves intestinal cell survival and nutrient absorption.饮食中的果糖可改善肠道细胞的存活率和营养物质吸收。
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Sorafenib fails to trigger ferroptosis across a wide range of cancer cell lines.索拉非尼未能在广泛的癌细胞系中引发铁死亡。
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S100P contributes to promoter demethylation and transcriptional activation of SLC2A5 to promote metastasis in colorectal cancer.S100P 通过促进 SLC2A5 的启动子去甲基化和转录激活促进结直肠癌的转移。
Br J Cancer. 2021 Aug;125(5):734-747. doi: 10.1038/s41416-021-01306-z. Epub 2021 Jun 29.
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PRPF19 promotes tongue cancer growth and chemoradiotherapy resistance.PRPF19 促进舌癌生长和放化疗抵抗。
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营养转运蛋白:将癌症代谢与治疗机会联系起来。

Nutrient transporters: connecting cancer metabolism to therapeutic opportunities.

机构信息

Department of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, USA.

Rogel Cancer Center, University of Michigan, Ann Arbor, MI, USA.

出版信息

Oncogene. 2023 Mar;42(10):711-724. doi: 10.1038/s41388-023-02593-x. Epub 2023 Feb 4.

DOI:10.1038/s41388-023-02593-x
PMID:36739364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10266237/
Abstract

Cancer cells rely on certain extracellular nutrients to sustain their metabolism and growth. Solute carrier (SLC) transporters enable cells to acquire extracellular nutrients or shuttle intracellular nutrients across organelles. However, the function of many SLC transporters in cancer is unknown. Determining the key SLC transporters promoting cancer growth could reveal important therapeutic opportunities. Here we summarize recent findings and knowledge gaps on SLC transporters in cancer. We highlight existing inhibitors for studying these transporters, clinical trials on treating cancer by blocking transporters, and compensatory transporters used by cancer cells to evade treatment. We propose targeting transporters simultaneously or in combination with targeted therapy or immunotherapy as alternative strategies for effective cancer therapy.

摘要

癌细胞依赖某些细胞外营养物质来维持其新陈代谢和生长。溶质载体 (SLC) 转运蛋白使细胞能够获取细胞外营养物质或在细胞器之间转运细胞内营养物质。然而,许多 SLC 转运蛋白在癌症中的功能尚不清楚。确定促进癌症生长的关键 SLC 转运蛋白可能会揭示重要的治疗机会。在这里,我们总结了 SLC 转运蛋白在癌症中的最新发现和知识空白。我们强调了用于研究这些转运蛋白的现有抑制剂、通过阻断转运蛋白治疗癌症的临床试验,以及癌细胞用来逃避治疗的代偿性转运蛋白。我们建议同时或与靶向治疗或免疫治疗联合靶向转运蛋白作为有效癌症治疗的替代策略。