دورية أكاديمية

Pemetrexed Hinders Translation Inhibition upon Low Glucose in Non-Small Cell Lung Cancer Cells.

التفاصيل البيبلوغرافية
العنوان: Pemetrexed Hinders Translation Inhibition upon Low Glucose in Non-Small Cell Lung Cancer Cells.
المؤلفون: Piecyk M; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France.; Hospices Civils de Lyon, Biopathology of Tumours, CPE, GHE Hospital, F-69500 Bron, France., Triki M; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France., Laval PA; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France., Dragic H; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France., Cussonneau L; Université Clermont Auvergne, INRAE, Unité de Nutrition Humaine, UMR1019, 63122 Clermont-Ferrand, France., Fauvre J; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France., Duret C; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France., Aznar N; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France., Renno T; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France., Manié SN; Inserm U1242, Université de Rennes, Centre de Lutte Contre le Cancer Eugène Marquis, 35042 Rennes, France., Chaveroux C; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France., Ferraro-Peyret C; Université Lyon, Cancer Research Centre of Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France.; Hospices Civils de Lyon, Biopathology of Tumours, CPE, GHE Hospital, F-69500 Bron, France.
المصدر: Metabolites [Metabolites] 2021 Mar 26; Vol. 11 (4). Date of Electronic Publication: 2021 Mar 26.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101578790 Publication Model: Electronic Cited Medium: Print ISSN: 2218-1989 (Print) Linking ISSN: 22181989 NLM ISO Abbreviation: Metabolites Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Basel : MDPI
مستخلص: Genetic alterations in non-small cell lung cancers (NSCLC) stimulate the generation of energy and biomass to promote tumor development. However, the efficacy of the translation process is finely regulated by stress sensors, themselves often controlled by nutrient availability and chemotoxic agents. Yet, the crosstalk between therapeutic treatment and glucose availability on cell mass generation remains understudied. Herein, we investigated the impact of pemetrexed (PEM) treatment, a first-line agent for NSCLC, on protein synthesis, depending on high or low glucose availability. PEM treatment drastically repressed cell mass and translation when glucose was abundant. Surprisingly, inhibition of protein synthesis caused by low glucose levels was partially dampened upon co-treatment with PEM. Moreover, PEM counteracted the elevation of the endoplasmic reticulum stress (ERS) signal produced upon low glucose availability, providing a molecular explanation for the differential impact of the drug on translation according to glucose levels. Collectively, these data indicate that the ERS constitutes a molecular crosstalk between microenvironmental stressors, contributing to translation reprogramming and proteostasis plasticity.
References: FEBS J. 2019 Jan;286(2):241-278. (PMID: 30027602)
Genes Dev. 2004 Dec 1;18(23):2893-904. (PMID: 15545625)
Oncol Rep. 2016 May;35(5):2606-14. (PMID: 26985651)
Nat Cell Biol. 2016 Oct;18(10):1090-101. (PMID: 27617932)
Mol Biol Cell. 2005 Dec;16(12):5493-501. (PMID: 16176978)
BMC Syst Biol. 2010 May 06;4:58. (PMID: 20459610)
Mol Cell. 2013 Mar 28;49(6):1049-59. (PMID: 23395000)
Proc Natl Acad Sci U S A. 1998 Feb 17;95(4):1432-7. (PMID: 9465032)
EMBO J. 2017 Feb 1;36(3):252-259. (PMID: 28007895)
Cancer Res. 2015 Feb 1;75(3):544-53. (PMID: 25644265)
Science. 1987 Mar 20;235(4795):1492-5. (PMID: 3103217)
Nat Commun. 2020 May 19;11(1):2498. (PMID: 32427827)
J Med Chem. 1992 Nov 13;35(23):4450-4. (PMID: 1447744)
Trends Cancer. 2016 May;2(5):252-262. (PMID: 28741511)
Oncologist. 2010;15(12):1352-8. (PMID: 21148615)
Nat Cell Biol. 2013 May;15(5):481-90. (PMID: 23624402)
Cancer Res. 1997 Mar 15;57(6):1116-23. (PMID: 9067281)
Cancer Res. 2004 Jun 1;64(11):3892-9. (PMID: 15172999)
Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19345-50. (PMID: 18032601)
Cancer Res. 2010 Dec 15;70(24):10299-309. (PMID: 21159649)
Nat Cell Biol. 2011 Mar;13(3):184-90. (PMID: 21364565)
Proc Natl Acad Sci U S A. 2002 Dec 10;99(25):15920-5. (PMID: 12446838)
EMBO Rep. 2016 Oct;17(10):1374-1395. (PMID: 27629041)
Nat Commun. 2020 Jun 10;11(1):2936. (PMID: 32522993)
Cell Death Dis. 2014 Feb 20;5:e1067. (PMID: 24556682)
Elife. 2019 Apr 16;8:. (PMID: 30990168)
Oncotarget. 2017 Jul 15;8(40):68191-68207. (PMID: 28978108)
Apoptosis. 2009 Aug;14(8):996-1007. (PMID: 19360473)
Mol Cell Biol. 2002 Aug;22(15):5575-84. (PMID: 12101249)
Sci Rep. 2017 Jun 19;7(1):3831. (PMID: 28630443)
Mol Cell Biol. 2003 Feb;23(4):1292-303. (PMID: 12556489)
Nat Commun. 2017 May 26;8:15503. (PMID: 28548087)
Proc Natl Acad Sci U S A. 2010 May 11;107(19):8788-93. (PMID: 20421486)
Proc Natl Acad Sci U S A. 2017 Sep 12;114(37):E7697-E7706. (PMID: 28847964)
J Immunother Cancer. 2020 Nov;8(2):. (PMID: 33243934)
Br J Cancer. 1998;78 Suppl 3:27-34. (PMID: 9717988)
Am J Respir Cell Mol Biol. 2014 Jun;50(6):1005-9. (PMID: 24605820)
J Cancer Res Clin Oncol. 2012 Apr;138(4):545-54. (PMID: 22203472)
Cancer Res. 2009 Jul 1;69(13):5467-74. (PMID: 19549896)
Mol Biol Cell. 2010 Sep 15;21(18):3220-31. (PMID: 20660158)
Curr Opin Genet Dev. 2018 Feb;48:104-111. (PMID: 29179096)
Cell. 2005 Nov 18;123(4):569-80. (PMID: 16286006)
Nat Rev Mol Cell Biol. 2007 Jul;8(7):519-29. (PMID: 17565364)
Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):6658-63. (PMID: 9192621)
Science. 1997 Jul 4;277(5322):99-101. (PMID: 9204908)
Nat Methods. 2009 Apr;6(4):275-7. (PMID: 19305406)
Cancer Metab. 2015 May 28;3:6. (PMID: 26023330)
Oncologist. 2009 Sep;14(9):930-5. (PMID: 19737998)
فهرسة مساهمة: Keywords: ER stress signaling; NSCLC; glucose availability; pemetrexed; protein synthesis
تواريخ الأحداث: Date Created: 20210403 Latest Revision: 20210428
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC8067050
DOI: 10.3390/metabo11040198
PMID: 33810430
قاعدة البيانات: MEDLINE
الوصف
تدمد:2218-1989
DOI:10.3390/metabo11040198