• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

曲格列酮诱导结肠癌细胞系分化及过氧化物酶体增殖物激活受体γ表达

Induction of differentiation and peroxisome proliferator-activated receptor gamma expression in colon cancer cell lines by troglitazone.

作者信息

Kato Masashi, Kusumi Tomomi, Tsuchida Shigeki, Tanaka Masanori, Sasaki Mutsuo, Kudo Hajime

机构信息

Second Department of Pathology, Hirosaki University School of Medicine, 5 Zaifu-cho, 036-8562, Japan.

出版信息

J Cancer Res Clin Oncol. 2004 Feb;130(2):73-9. doi: 10.1007/s00432-003-0510-2. Epub 2003 Nov 21.

DOI:10.1007/s00432-003-0510-2
PMID:14634802
Abstract

PURPOSE

We investigated the relationship between the effects of troglitazone (TGZ) on cellular growth, differentiation and apoptosis induction, and the induction of peroxisome proliferator-activated receptor (PPAR) gamma in three human colon cancer cell lines, HCT-15, DLD-1and LoVo.

METHODS

Viable cell number was evaluated by the Alamar blue assay and apoptotic cell death by TUNEL methods. Expression of PPARgamma mRNA and protein was examined by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot, respectively. The differentiation markers of colonic mucosa, villin and MUC2 mRNAs, were analyzed by real-time RT-PCR.

RESULTS

HCT-15 and DLD-1 cells proliferated rapidly while LoVo cells grew slowly. TGZ dose-dependently inhibited the proliferation of all the cell lines, and also induced apoptotic cell death. High expression of PPARgamma mRNA and protein was demonstrated in DLD-1 and LoVo cells before TGZ treatment. After the treatment, PPARgamma mRNA and protein levels were increased in HCT-15 and LoVo cells. Villin and MUC2 mRNAs were increased by TGZ treatment in HCT-15 cells while villin mRNA was repressed in LoVo cells. Changes in expression of PPARgamma, villin or MUC2 mRNAs were not observed in DLD-1 cells.

CONCLUSIONS

These results suggest that PPARgamma levels are not correlated with the rates of cell proliferation. Differentiation induction by TGZ was only observed in the cell lines with enhanced PPARgamma expression.

摘要

目的

我们研究了曲格列酮(TGZ)对三种人结肠癌细胞系HCT-15、DLD-1和LoVo细胞生长、分化及凋亡诱导的影响,以及过氧化物酶体增殖物激活受体(PPAR)γ的诱导情况之间的关系。

方法

通过alamar蓝分析法评估活细胞数量,用TUNEL法检测凋亡细胞死亡情况。分别通过逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测PPARγ mRNA和蛋白质的表达。通过实时RT-PCR分析结肠黏膜的分化标志物villin和MUC2 mRNA。

结果

HCT-15和DLD-1细胞增殖迅速,而LoVo细胞生长缓慢。TGZ剂量依赖性地抑制所有细胞系的增殖,并诱导凋亡细胞死亡。在TGZ处理前,DLD-1和LoVo细胞中PPARγ mRNA和蛋白质高表达。处理后,HCT-15和LoVo细胞中PPARγ mRNA和蛋白质水平升高。TGZ处理使HCT-15细胞中villin和MUC2 mRNA增加,而LoVo细胞中villin mRNA受到抑制。DLD-1细胞中未观察到PPARγ、villin或MUC2 mRNA表达的变化。

结论

这些结果表明PPARγ水平与细胞增殖速率无关。TGZ仅在PPARγ表达增强的细胞系中观察到分化诱导作用。

相似文献

1
Induction of differentiation and peroxisome proliferator-activated receptor gamma expression in colon cancer cell lines by troglitazone.曲格列酮诱导结肠癌细胞系分化及过氧化物酶体增殖物激活受体γ表达
J Cancer Res Clin Oncol. 2004 Feb;130(2):73-9. doi: 10.1007/s00432-003-0510-2. Epub 2003 Nov 21.
2
Peroxisome proliferator-activated receptor-gamma agonists cause growth arrest and apoptosis in human ovarian carcinoma cell lines.过氧化物酶体增殖物激活受体γ激动剂可导致人卵巢癌细胞系生长停滞和凋亡。
Int J Gynecol Cancer. 2007 Mar-Apr;17(2):418-25. doi: 10.1111/j.1525-1438.2006.00866.x. Epub 2007 Feb 19.
3
Peroxisome proliferator-activated receptor gamma induces growth arrest and differentiation markers of human colon cancer cells.过氧化物酶体增殖物激活受体γ诱导人结肠癌细胞的生长停滞和分化标志物。
Jpn J Cancer Res. 1999 Jan;90(1):75-80. doi: 10.1111/j.1349-7006.1999.tb00668.x.
4
Characteristics of the peroxisome proliferator activated receptor gamma (PPARgamma) ligand induced apoptosis in colon cancer cells.过氧化物酶体增殖物激活受体γ(PPARγ)配体诱导结肠癌细胞凋亡的特征。
Gut. 2002 May;50(5):658-64. doi: 10.1136/gut.50.5.658.
5
Expression of NAG-1, a transforming growth factor-beta superfamily member, by troglitazone requires the early growth response gene EGR-1.曲格列酮对转化生长因子-β超家族成员NAG-1的表达需要早期生长反应基因EGR-1。
J Biol Chem. 2004 Feb 20;279(8):6883-92. doi: 10.1074/jbc.M305295200. Epub 2003 Dec 8.
6
Troglitazone, a peroxisome proliferator-activated receptor gamma (PPAR gamma ) ligand, selectively induces the early growth response-1 gene independently of PPAR gamma. A novel mechanism for its anti-tumorigenic activity.曲格列酮是一种过氧化物酶体增殖物激活受体γ(PPARγ)配体,可独立于PPARγ选择性诱导早期生长反应-1基因。这是其抗肿瘤活性的一种新机制。
J Biol Chem. 2003 Feb 21;278(8):5845-53. doi: 10.1074/jbc.M208394200. Epub 2002 Dec 9.
7
[Effects of peroxisome proliferator-activated receptor-gamma ligand troglitazone on colon cancer cell growth].过氧化物酶体增殖物激活受体γ配体曲格列酮对结肠癌细胞生长的影响
Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Aug 18;38(4):385-8.
8
Peroxisome proliferator-activated receptor gamma1 (PPARgamma1) expresses in rat mesangial cells and PPARgamma agonists modulate its differentiation.过氧化物酶体增殖物激活受体γ1(PPARγ1)在大鼠系膜细胞中表达,且PPARγ激动剂可调节其分化。
Biochim Biophys Acta. 2000 Jun 2;1497(1):148-54. doi: 10.1016/s0167-4889(00)00054-9.
9
Troglitazone inhibits cell growth and induces apoptosis of B-cell acute lymphoblastic leukemia cells with t(14;18).曲格列酮可抑制伴有t(14;18)的B细胞急性淋巴细胞白血病细胞的生长并诱导其凋亡。
Acta Haematol. 2006;116(1):30-40. doi: 10.1159/000092345.
10
Combined treatment with TRAIL and PPARγ ligands overcomes chemoresistance of ovarian cancer cell lines.联合使用 TRAIL 和 PPARγ 配体可克服卵巢癌细胞系的化疗耐药性。
J Cancer Res Clin Oncol. 2011 May;137(5):875-86. doi: 10.1007/s00432-010-0952-2. Epub 2010 Sep 29.

引用本文的文献

1
Addressing chemically-induced obesogenic metabolic disruption: selection of chemicals for human PPARα, PPARγ transactivation, and adipogenesis test methods.针对化学诱导的肥胖代谢紊乱的干预:用于人类 PPARα、PPARγ 转录激活和脂肪生成测试方法的化学物质选择。
Front Endocrinol (Lausanne). 2024 Jul 8;15:1401120. doi: 10.3389/fendo.2024.1401120. eCollection 2024.
2
Peroxisome Proliferator-Activated Receptor Gamma in Obesity and Colorectal Cancer: the Role of Epigenetics.过氧化物酶体增殖物激活受体 γ 在肥胖与结直肠癌中的作用:表观遗传学视角。
Sci Rep. 2017 Sep 6;7(1):10714. doi: 10.1038/s41598-017-11180-6.
3
The arachidonic acid metabolite 11β-ProstaglandinF2α controls intestinal epithelial healing: deficiency in patients with Crohn's disease.

本文引用的文献

1
Apoptosis induced by activation of peroxisome-proliferator activated receptor-gamma is associated with Bcl-2 and NF-kappaB in human colon cancer.过氧化物酶体增殖物激活受体γ激活诱导的细胞凋亡与人类结肠癌中的Bcl-2和核因子κB相关。
Life Sci. 2002 Apr 19;70(22):2631-46. doi: 10.1016/s0024-3205(02)01510-2.
2
Characteristics of the peroxisome proliferator activated receptor gamma (PPARgamma) ligand induced apoptosis in colon cancer cells.过氧化物酶体增殖物激活受体γ(PPARγ)配体诱导结肠癌细胞凋亡的特征。
Gut. 2002 May;50(5):658-64. doi: 10.1136/gut.50.5.658.
3
Differential expression of the chromosome 11 mucin genes in colorectal cancer.
花生四烯酸代谢产物11β-前列腺素F2α调控肠道上皮愈合:克罗恩病患者存在该物质缺乏
Sci Rep. 2016 May 3;6:25203. doi: 10.1038/srep25203.
4
Chemotherapy and chemoprevention by thiazolidinediones.噻唑烷二酮类药物的化疗与化学预防
Biomed Res Int. 2015;2015:845340. doi: 10.1155/2015/845340. Epub 2015 Mar 19.
5
Can an oral antidiabetic (rosiglitazone) be of benefit in leukemia treatment?一种口服抗糖尿病药物(罗格列酮)是否对白血病的治疗有益?
Saudi Pharm J. 2015 Jan;23(1):14-21. doi: 10.1016/j.jsps.2013.12.009. Epub 2013 Dec 22.
6
Genetic variants within obesity-related genes are associated with tumor recurrence in patients with stages II/III colon cancer.肥胖相关基因内的遗传变异与II/III期结肠癌患者的肿瘤复发相关。
Pharmacogenet Genomics. 2015 Jan;25(1):30-7. doi: 10.1097/FPC.0000000000000101.
7
Antiproliferative and apoptotic effects of telmisartan in human colon cancer cells.替米沙坦对人结肠癌细胞的抗增殖和凋亡作用。
Oncol Lett. 2014 Dec;8(6):2681-2686. doi: 10.3892/ol.2014.2592. Epub 2014 Oct 9.
8
Regulation of epithelial differentiation in rat intestine by intraluminal delivery of an adenoviral vector or silencing RNA coding for Schlafen 3.通过腺病毒载体腔内递送或编码 Schlafen 3 的沉默 RNA 对大鼠肠道上皮分化的调节。
PLoS One. 2013 Nov 11;8(11):e79745. doi: 10.1371/journal.pone.0079745. eCollection 2013.
9
Glucagonlike peptide 2 analogue teduglutide: stimulation of proliferation but reduction of differentiation in human Caco-2 intestinal epithelial cells.胰高血糖素样肽 2 类似物特迪格鲁肽:刺激人 Caco-2 肠上皮细胞增殖但减少分化。
JAMA Surg. 2013 Nov;148(11):1037-42. doi: 10.1001/jamasurg.2013.3731.
10
Combinational effect of PPARγ agonist and RXR agonist on the growth of SGC7901 gastric carcinoma cells in vitro.PPARγ激动剂与RXR激动剂对SGC7901胃癌细胞体外生长的联合作用。
Tumour Biol. 2013 Aug;34(4):2409-18. doi: 10.1007/s13277-013-0791-2. Epub 2013 Apr 20.
11号染色体黏蛋白基因在结直肠癌中的差异表达。
J Pathol. 2001 Oct;195(3):327-35. doi: 10.1002/path.951.
4
Activation of the PPAR pathway induces apoptosis and COX-2 inhibition in HT-29 human colon cancer cells.PPAR 信号通路的激活可诱导 HT-29 人结肠癌细胞凋亡并抑制 COX-2。
Carcinogenesis. 2001 Sep;22(9):1379-83. doi: 10.1093/carcin/22.9.1379.
5
Autophagy delays sulindac sulfide-induced apoptosis in the human intestinal colon cancer cell line HT-29.自噬延缓舒林酸硫化物诱导的人结肠癌细胞系HT-29凋亡。
Exp Cell Res. 2001 Aug 15;268(2):139-49. doi: 10.1006/excr.2001.5285.
6
Ligands for peroxisome proliferator-activated receptor gamma inhibit growth and induce apoptosis of human papillary thyroid carcinoma cells.过氧化物酶体增殖物激活受体γ的配体可抑制人甲状腺乳头状癌细胞的生长并诱导其凋亡。
J Clin Endocrinol Metab. 2001 May;86(5):2170-7. doi: 10.1210/jcem.86.5.7493.
7
Troglitazone induces apoptosis via the p53 and Gadd45 pathway in vascular smooth muscle cells.曲格列酮通过p53和Gadd45途径诱导血管平滑肌细胞凋亡。
Eur J Pharmacol. 2000 Nov 3;407(3):227-35. doi: 10.1016/s0014-2999(00)00758-5.
8
Roles of PPARs in health and disease.过氧化物酶体增殖物激活受体(PPARs)在健康与疾病中的作用。
Nature. 2000 May 25;405(6785):421-4. doi: 10.1038/35013000.
9
The PPARs: from orphan receptors to drug discovery.过氧化物酶体增殖物激活受体:从孤儿受体到药物发现
J Med Chem. 2000 Feb 24;43(4):527-50. doi: 10.1021/jm990554g.
10
Nonapoptotic cell death associated with S-phase arrest of prostate cancer cells via the peroxisome proliferator-activated receptor gamma ligand, 15-deoxy-delta12,14-prostaglandin J2.通过过氧化物酶体增殖物激活受体γ配体15-脱氧-Δ12,14-前列腺素J2与前列腺癌细胞S期阻滞相关的非凋亡性细胞死亡。
Cell Growth Differ. 2000 Jan;11(1):49-61.