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1
Impact of monocarbonyl analogs of curcumin (MACs) C66 and B2BrBC on the expression of diabetes-associated genes in streptozotocin-treated rat pancreatic RIN-m cells-Quantitative RT-PCR array data.姜黄素单羰基类似物(MACs)C66和B2BrBC对链脲佐菌素处理的大鼠胰腺RIN-m细胞中糖尿病相关基因表达的影响——定量逆转录聚合酶链反应芯片数据
Data Brief. 2024 Sep 16;57:110952. doi: 10.1016/j.dib.2024.110952. eCollection 2024 Dec.
2
Monocarbonyl analogs of curcumin C66 and B2BrBC modulate oxidative stress, JNK activity, and pancreatic gene expression in rats with streptozotocin-induced diabetes.姜黄素 C66 和 B2BrBC 的单羰基类似物调节链脲佐菌素诱导糖尿病大鼠的氧化应激、JNK 活性和胰腺基因表达。
Biochem Pharmacol. 2024 Nov;229:116491. doi: 10.1016/j.bcp.2024.116491. Epub 2024 Aug 13.
3
Curcumin analogs (B2BrBC and C66) supplementation attenuates airway hyperreactivity and promote airway relaxation in neonatal rats exposed to hyperoxia.姜黄素类似物(B2BrBC 和 C66)补充可减轻新生大鼠暴露于高氧环境下的气道高反应性并促进气道松弛。
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4
Comparative study of the antioxidant properties of monocarbonyl curcumin analogues C66 and B2BrBC in isoproteranol induced cardiac damage.单羰基姜黄素类似物 C66 和 B2BrBC 的抗氧化性能在异丙肾上腺素诱导的心脏损伤中的比较研究。
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5
Antioxidant and anti-inflammatory effects of the monocarbonyl curcumin analogs B2BRBC and C66 in monocrotaline-induced right ventricular hypertrophy.单羰基姜黄素类似物 B2BRBC 和 C66 在野百合碱诱导的右心室肥厚中的抗氧化和抗炎作用。
J Biochem Mol Toxicol. 2019 Aug;33(8):e22353. doi: 10.1002/jbt.22353. Epub 2019 Jun 10.
6
Efficacy of the monocarbonyl curcumin analog C66 in the reduction of diabetes-associated cardiovascular and kidney complications.单羰基姜黄素类似物 C66 在减少糖尿病相关心血管和肾脏并发症方面的疗效。
Mol Med. 2022 Oct 31;28(1):129. doi: 10.1186/s10020-022-00559-5.
7
Anticancer perspectives of monocarbonyl analogs of curcumin: A decade (2014-2024) review.姜黄素单羰基类似物的抗癌作用:十年(2014-2024)回顾。
Arch Pharm (Weinheim). 2024 Sep;357(9):e2400197. doi: 10.1002/ardp.202400197. Epub 2024 Jun 19.
8
Heterocyclic cyclohexanone monocarbonyl analogs of curcumin can inhibit the activity of ATP-binding cassette transporters in cancer multidrug resistance.姜黄素的杂环环己酮单羰基类似物可抑制癌症多药耐药中ATP结合盒转运蛋白的活性。
Biochem Pharmacol. 2015 Feb 1;93(3):305-17. doi: 10.1016/j.bcp.2014.12.012. Epub 2014 Dec 25.
9
Synthesis and Anti-Inflammatory Evaluation of Novel C66 Analogs for the Treatment of LPS-Induced Acute Lung Injury.用于治疗脂多糖诱导的急性肺损伤的新型C66类似物的合成与抗炎评价
Chem Biol Drug Des. 2015 Oct;86(4):753-63. doi: 10.1111/cbdd.12548. Epub 2015 Mar 20.
10
Inhibition of JNK by compound C66 prevents pathological changes of the aorta in STZ-induced diabetes.化合物C66对JNK的抑制作用可预防链脲佐菌素诱导的糖尿病大鼠主动脉的病理变化。
J Cell Mol Med. 2014 Jun;18(6):1203-12. doi: 10.1111/jcmm.12267. Epub 2014 Apr 10.

本文引用的文献

1
Ameliorating potential of curcumin and its analogue in central nervous system disorders and related conditions: A review of molecular pathways.姜黄素及其类似物在中枢神经系统疾病及相关疾病中的改善作用:分子途径综述。
Phytother Res. 2022 Aug;36(8):3143-3180. doi: 10.1002/ptr.7522. Epub 2022 Jul 4.
2
Protective Effects of Curcumin in Cardiovascular Diseases-Impact on Oxidative Stress and Mitochondria.姜黄素在心血管疾病中的保护作用——对氧化应激和线粒体的影响。
Cells. 2022 Jan 20;11(3):342. doi: 10.3390/cells11030342.
3
Role of c-Jun N-terminal Kinase (JNK) in Obesity and Type 2 Diabetes.c-Jun N-末端激酶(JNK)在肥胖和 2 型糖尿病中的作用。
Cells. 2020 Mar 13;9(3):706. doi: 10.3390/cells9030706.
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A Review of Curcumin and Its Derivatives as Anticancer Agents.姜黄素及其衍生物作为抗癌剂的研究进展。
Int J Mol Sci. 2019 Feb 27;20(5):1033. doi: 10.3390/ijms20051033.
5
JNK at the crossroad of obesity, insulin resistance, and cell stress response.JNK 在肥胖、胰岛素抵抗和细胞应激反应的十字路口。
Mol Metab. 2016 Dec 8;6(2):174-184. doi: 10.1016/j.molmet.2016.12.001. eCollection 2017 Feb.
6
Therapeutic potential of curcumin in digestive diseases.姜黄素在消化疾病中的治疗潜力。
World J Gastroenterol. 2013 Dec 28;19(48):9256-70. doi: 10.3748/wjg.v19.i48.9256.
7
Curcumin and diabetes: a systematic review.姜黄素与糖尿病:系统评价。
Evid Based Complement Alternat Med. 2013;2013:636053. doi: 10.1155/2013/636053. Epub 2013 Nov 24.
8
Synthesis and biological evaluation of allylated and prenylated mono-carbonyl analogs of curcumin as anti-inflammatory agents.姜黄素烯丙基化和异戊烯基化单羰基类似物作为抗炎剂的合成及生物学评价
Eur J Med Chem. 2014 Mar 3;74:671-82. doi: 10.1016/j.ejmech.2013.10.061. Epub 2013 Nov 1.
9
Therapeutic roles of curcumin: lessons learned from clinical trials.姜黄素的治疗作用:临床试验获得的经验。
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Synthesis and anti-bacterial properties of mono-carbonyl analogues of curcumin.姜黄素单羰基类似物的合成及其抗菌性能
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姜黄素单羰基类似物(MACs)C66和B2BrBC对链脲佐菌素处理的大鼠胰腺RIN-m细胞中糖尿病相关基因表达的影响——定量逆转录聚合酶链反应芯片数据

Impact of monocarbonyl analogs of curcumin (MACs) C66 and B2BrBC on the expression of diabetes-associated genes in streptozotocin-treated rat pancreatic RIN-m cells-Quantitative RT-PCR array data.

作者信息

Stojchevski Radoslav, Velichkovikj Sara, Bogdanov Jane, Hadzi-Petrushev Nikola, Mladenov Mitko, Poretsky Leonid, Avtanski Dimiter

机构信息

Friedman Diabetes Institute, Lenox Hill Hospital, Northwell Health, New York, NY, USA.

Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA.

出版信息

Data Brief. 2024 Sep 16;57:110952. doi: 10.1016/j.dib.2024.110952. eCollection 2024 Dec.

DOI:10.1016/j.dib.2024.110952
PMID:39351132
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11440284/
Abstract

This paper presents a dataset obtained from an RT-qPCR array analysis of rat pancreatic RIN-m cells treated with two monocarbonyl analogs of curcumin (MACs), C66 and B2BrBC in the presence or absence of streptozotocin (STZ). The array quantified the expression of 84 genes associated with the onset, development, and progression of diabetes. This dataset provides information on the gene expression profiles of pancreatic cells modulated by two specific MACs in a diabetic context. The data can serve as a foundation for developing new hypotheses, designing follow-up experiments, and identifying novel targets for treatment. It can be used to investigate further the molecular mechanisms underlying the therapeutic effects of these MACs and in comparative studies using other experimental antidiabetic compounds.

摘要

本文展示了一个数据集,该数据集来自于对大鼠胰腺RIN - m细胞进行逆转录定量聚合酶链反应(RT - qPCR)阵列分析的结果。这些细胞在有或没有链脲佐菌素(STZ)存在的情况下,用两种姜黄素单羰基类似物(MACs),即C66和B2BrBC进行处理。该阵列定量了84个与糖尿病的发生、发展和进展相关的基因的表达。这个数据集提供了在糖尿病背景下,由两种特定MACs调节的胰腺细胞基因表达谱的信息。这些数据可作为开发新假设、设计后续实验以及确定新治疗靶点的基础。它可用于进一步研究这些MACs治疗效果背后的分子机制,以及用于使用其他实验性抗糖尿病化合物的比较研究。