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Aspartate Rescues S-phase Arrest Caused by Suppression of Glutamine Utilization in KRas-driven Cancer Cells.天冬氨酸可挽救KRas驱动的癌细胞中因谷氨酰胺利用受抑制而导致的S期阻滞。
J Biol Chem. 2016 Apr 22;291(17):9322-9. doi: 10.1074/jbc.M115.710145. Epub 2016 Feb 26.
2
Formation of Renal Cysts and Tumors in Vhl/Trp53-Deficient Mice Requires HIF1α and HIF2α.Vhl/Trp53 缺陷小鼠肾囊肿和肿瘤的形成需要 HIF1α 和 HIF2α。
Cancer Res. 2016 Apr 1;76(7):2025-36. doi: 10.1158/0008-5472.CAN-15-1859. Epub 2016 Jan 12.
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8-Chloroadenosine Sensitivity in Renal Cell Carcinoma Is Associated with AMPK Activation and mTOR Pathway Inhibition.肾细胞癌中8-氯腺苷敏感性与AMPK激活及mTOR通路抑制相关。
PLoS One. 2015 Aug 27;10(8):e0135962. doi: 10.1371/journal.pone.0135962. eCollection 2015.
4
Cell cycle status dictates effectiveness of rapamycin.细胞周期状态决定雷帕霉素的有效性。
Cell Cycle. 2015;14(16):2556-7. doi: 10.1080/15384101.2015.1060778. Epub 2015 Jun 30.
5
Apoptotic effects of high-dose rapamycin occur in S-phase of the cell cycle.高剂量雷帕霉素的凋亡作用发生在细胞周期的S期。
Cell Cycle. 2015;14(14):2285-92. doi: 10.1080/15384101.2015.1046653. Epub 2015 May 6.
6
HIF2α-Dependent Lipid Storage Promotes Endoplasmic Reticulum Homeostasis in Clear-Cell Renal Cell Carcinoma.缺氧诱导因子2α依赖性脂质储存促进透明细胞肾细胞癌的内质网稳态
Cancer Discov. 2015 Jun;5(6):652-67. doi: 10.1158/2159-8290.CD-14-1507. Epub 2015 Mar 31.
7
Rapamycin-induced G1 cell cycle arrest employs both TGF-β and Rb pathways.雷帕霉素诱导的G1期细胞周期阻滞同时利用了TGF-β和Rb信号通路。
Cancer Lett. 2015 May 1;360(2):134-40. doi: 10.1016/j.canlet.2015.01.043. Epub 2015 Feb 3.
8
Blocking anaplerotic entry of glutamine into the TCA cycle sensitizes K-Ras mutant cancer cells to cytotoxic drugs.阻断谷氨酰胺的回补性进入三羧酸循环会使K-Ras突变癌细胞对细胞毒性药物敏感。
Oncogene. 2015 May 14;34(20):2672-80. doi: 10.1038/onc.2014.207. Epub 2014 Jul 14.
9
Phospholipase D and the maintenance of phosphatidic acid levels for regulation of mammalian target of rapamycin (mTOR).磷脂酶D与维持磷脂酸水平以调节雷帕霉素哺乳动物靶蛋白(mTOR)
J Biol Chem. 2014 Aug 15;289(33):22583-22588. doi: 10.1074/jbc.R114.566091. Epub 2014 Jul 2.
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The multifaceted von Hippel-Lindau tumour suppressor protein.具有多方面功能的 von Hippel-Lindau 肿瘤抑制蛋白。
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一种在肾透明癌细胞中失调的G1晚期脂质检查点。

A Late G1 Lipid Checkpoint That Is Dysregulated in Clear Cell Renal Carcinoma Cells.

作者信息

Patel Deven, Salloum Darin, Saqcena Mahesh, Chatterjee Amrita, Mroz Victoria, Ohh Michael, Foster David A

机构信息

From the Department of Biological Sciences, Hunter College of the City University of New York, New York, New York 10065.

the Biochemistry Program and.

出版信息

J Biol Chem. 2017 Jan 20;292(3):936-944. doi: 10.1074/jbc.M116.757864. Epub 2016 Dec 12.

DOI:10.1074/jbc.M116.757864
PMID:27956548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5247665/
Abstract

Lipids are important nutrients that proliferating cells require to maintain energy homeostasis as well as to build plasma membranes for newly synthesized cells. Previously, we identified nutrient-sensing checkpoints that exist in the latter part of the G phase of the cell cycle that are dependent upon essential amino acids, Gln, and finally, a checkpoint mediated by mammalian target of rapamycin (mTOR), which integrates signals from both nutrients and growth factors. In this study, we have identified and temporally mapped a lipid-mediated G checkpoint. This checkpoint is located after the Gln checkpoint and before the mTOR-mediated cell cycle checkpoint. Intriguingly, clear cell renal cell carcinoma cells (ccRCC) have a dysregulated lipid-mediated checkpoint due in part to defective phosphatase and tensin homologue (PTEN). When deprived of lipids, instead of arresting in G, these cells continue to cycle and utilize lipid droplets as a source of lipids. Lipid droplets have been known to maintain endoplasmic reticulum homeostasis and prevent cytotoxic endoplasmic reticulum stress in ccRCC. Dysregulation of the lipid-mediated checkpoint forces these cells to utilize lipid droplets, which could potentially lead to therapeutic opportunities that exploit this property of ccRCC.

摘要

脂质是增殖细胞维持能量稳态以及为新合成细胞构建质膜所需的重要营养素。此前,我们鉴定了细胞周期G期后期存在的营养感应检查点,这些检查点依赖于必需氨基酸、谷氨酰胺,最后是由雷帕霉素哺乳动物靶标(mTOR)介导的检查点,mTOR整合来自营养物质和生长因子的信号。在本研究中,我们鉴定并在时间上绘制了一个脂质介导的G期检查点。该检查点位于谷氨酰胺检查点之后、mTOR介导的细胞周期检查点之前。有趣的是,透明细胞肾细胞癌(ccRCC)细胞的脂质介导检查点失调,部分原因是磷酸酶和张力蛋白同源物(PTEN)缺陷。当缺乏脂质时,这些细胞不会停滞在G期,而是继续循环并利用脂滴作为脂质来源。已知脂滴可维持内质网稳态并防止ccRCC中的细胞毒性内质网应激。脂质介导检查点的失调迫使这些细胞利用脂滴,这可能会带来利用ccRCC这一特性的治疗机会。