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维甲酸受体α和β在胰腺癌组织中的表达及意义 被引量:1

Expression of retinoic acid recepter α and β in pancreatic cancer and its clinical significance
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摘要 目的:探讨维甲酸受体-α、β在正常胰腺和胰腺癌组织中的表达及其临床意义,通过分析其表达了解维甲酸受体-α、β在胰腺癌发生发展中的作用。方法:采用免疫组织化学方法观察维甲酸受体-α、β在10例正常胰腺组织及30例胰腺癌组织中的表达情况,并分析其表达与胰腺癌临床病理特点之间的关系。结果:维甲酸受体-α在正常组织中的表达低于胰腺癌组织(P<0.05),在胰腺癌组织中随临床病理分期的升高表达量增加,并且随着肿瘤组织分化程度的降低,表达量增加(P<0.05),在远处转移和淋巴结转移的胰腺癌组织中的表达高于无转移组(P<0.05),但与患者年龄无关(P>0.05)。维甲酸受体-β在正常胰腺组织中的表达明显高于胰腺癌组织(P<0.05),在胰腺癌组织中的表达与临床病理分期、肿瘤组织分化程度及年龄无关(P>0.05),远处转移和淋巴结转移组中维甲酸受体-β的表达与未转移组差异亦无统计学意义(P>0.05)。结论:维甲酸受体-α和维甲酸受体-β与胰腺癌发生相关;维甲酸受体-α高表达提示预后不良;维甲酸受体-β在胰腺癌中起抑癌基因的作用。 Objective: To study the expression of retinoic acid recepter a and β(RAR- a andβ )in normal pancreatic tissue and pancreatic cancer and its clinical significance. To understand the role of RAR- a, β in occurrence and development of pancreatic cancer through analyzing its ex- pression. Method: The expression of RAR-a and βin the samples from 10 cases of normal pancreatic tissues and 30 cases of pancreatic cancer tissues was detected by using immunohisto- chemical method, and the relationship between RAR- a and β expression and the clinicopathologi- cal characters of pancreatic caneer was analyzed. Results: The expression of RAR-a in normal pancreatic tissue was inferior to in pancreatic cancer tissues(P〈 0.05). RAR- a expression was in- creased with the increase of surgery clinical pathologic stage and histological grades in pancreatic cancer tissues(P 〈 0.05). RAR-a expression of metastasis and lymph node metastasis was higher than no metastasis in pancreatic cancer tissues(P〈 0.05), but its expression was unrelated to age (P 〉 0.05). The expression of RAR-β in normal pancreatic tissue was higher than in pancreatic cancer tissues (P 〈 0.05). RAR- β expression was unrelated to clinical pathologic stage, histological grades and age in pancreatic cancer tissues(P〉 0.05). There was no statistically differences of RAR- β expression between metastasis or lymph node metastasis groups and no metastasis groups in pan- creatic cancer tissues. Conclusion: RAR- a and β is related to the occurrence of pancreatic can- cer. The high expression of RAR- a prompt the poor prognosis in pancreatic cancer. RAR- β plays the role of cancer suppressor gene in pancreatic cancer.
出处 《中国现代普通外科进展》 CAS 2014年第11期872-876,共5页 Chinese Journal of Current Advances in General Surgery
关键词 胰腺肿瘤 维甲酸受体-α 维甲酸受体-β Pancreatic neoplasms RAR- a RAR-β
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  • 1Maisonneuve P,Lowenfels AB.Epidemiology of pancreatic cancer:anupdate[J].Dig Dis 2010,28(4-5):645-656.
  • 2Barker SS,Poulsom R,Wright NA,et al.Expression of estrogen re- ceptor and estrogen-inducible genes in pancreatic cancer[J].Br J Surg,]997,84:1085-1089.
  • 3Cash DE,Bock CB,Schughart K,et al.Retinoic acid receptor alpha function in vertebrate limb skeletogenesis:a modulator of chondro- genesis[J].Cell Biology,1997,136(2):445-457.
  • 4Yu Z,Han J,Lin J,et al.Apoptosis induced by atRA in MEPM cells is mediated through activation of caspase and RAR[J].Toxico- logical Sciences,2006,89(2):504-509.
  • 5Hua S,Kittler R,White K P.Genomic antagonism between retinoic acid and estrogen signaling in breast cancer[J].Cell,2009,137(7):1259-1271.
  • 6Vuillemenot BRl,Pulling LC,Palmisano WA,et al.Carcinogen ex- posure differentially modulates RAR-b promoter hypermethylation,an early and frequent event in mouse lung carcinogenesis[J].Car- cinogenesis,2004,25(4):623-629.
  • 7Soprano DR,Qin P,Soprano KJ.Retinoic acid receptors and can- cers[J].Annu Rev Nutr,2004,24:201-221.
  • 8Lee KC,Li J,Cole PA,et al.Transcriptional activation by thyroid hormone receptor -beta involves chromatin remodeling,histone acetylation,and synergistic stimulation by p300 and steroid receptor coactivators[J].Mol Endocrinol,2003,17(5):908-922.
  • 9Bastien J,Rochette -Egly C.Nuclear retinoid receptors and the transcription of retinoid-target genes[J].Gene,2004,328:1-16.
  • 10Ren M,Pozzi S,Bistulfi G,et al.Impaired retinoic acid(RA)sig- nal leads to RARbeta2 epigenetic silencing and RA resis- tance[J].Mol Cell Biol,2005,25(3):10591-10603.

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