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SIRT6 将癌症代谢置于主导地位。

SIRT6 puts cancer metabolism in the driver's seat.

机构信息

Department of Signal Transduction, Division of Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA.

出版信息

Cell. 2012 Dec 7;151(6):1155-6. doi: 10.1016/j.cell.2012.11.020.

DOI:10.1016/j.cell.2012.11.020
PMID:23217699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3757516/
Abstract

The rewiring of metabolism in cancer is thought to result from hyperactivation of signaling pathways that instruct cells to grow. Sebastian et al. show that loss of the tumor suppressor SIRT6 transforms cells by activating tumor metabolism. This occurs independently of mutations in canonical growth signaling pathways and reveals a tumorigenic role for cancer metabolism.

摘要

肿瘤代谢的重编程被认为是由于指导细胞生长的信号通路的过度激活所致。Sebastian 等人表明,肿瘤抑制因子 SIRT6 的缺失通过激活肿瘤代谢来转化细胞。这一过程独立于经典生长信号通路的突变发生,并揭示了肿瘤代谢在肿瘤发生中的致癌作用。

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SIRT6 puts cancer metabolism in the driver's seat.SIRT6 将癌症代谢置于主导地位。
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The histone deacetylase SIRT6 is a tumor suppressor that controls cancer metabolism.组蛋白去乙酰化酶 SIRT6 是一种肿瘤抑制因子,可控制癌症代谢。
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2
Oncogenic Kras maintains pancreatic tumors through regulation of anabolic glucose metabolism.致癌性 Kras 通过调节合成代谢葡萄糖代谢维持胰腺肿瘤。
Cell. 2012 Apr 27;149(3):656-70. doi: 10.1016/j.cell.2012.01.058.
3
Glycine decarboxylase activity drives non-small cell lung cancer tumor-initiating cells and tumorigenesis.
工程化外泌体靶向抑制 SIRT6 可抑制前列腺癌的肿瘤发生和转移。
Theranostics. 2021 Apr 26;11(13):6526-6541. doi: 10.7150/thno.53886. eCollection 2021.
4
SIRT6, a novel direct transcriptional target of FoxO3a, mediates colon cancer therapy.SIRT6,FoxO3a 的一个新型直接转录靶标,介导结肠癌治疗。
Theranostics. 2019 Apr 13;9(8):2380-2394. doi: 10.7150/thno.29724. eCollection 2019.
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