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PPAR-γ,COX-2在尖锐湿疣和鲍温样丘疹病的表达及相关性研究 被引量:1

The Expressions of PPAR-γ,COX-2 in the Lesions of Patients with Condyloma Acuminatum and Bowenoid Papulosis
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摘要 目的探讨过氧化物酶体增殖因子激活受体γ(PPAR-γ)和环氧合酶-2(COX-2)在尖锐湿疣(CA)和鲍温样丘疹病(BP)的表达,并进行相关性分析。方法CA、BP皮损和正常成年人包皮组织各17例,采用免疫组化法检测PPAR-γ、COX-2蛋白表达。结果PPAR-γ、COX-2在CA组和BP组中阳性表达均高于正常对照组(P<0.01),在CA和BP皮损中PPAR-γ的表达与COX-2呈正相关(r=0.505,P=0.038;r=0.562,P=0.019)。结论PPAR-γ、COX-2在HPV感染相关的增殖性皮肤病的发生发展中可能有重要作用。 Objective To investigate the expression of PPAR-γ, COX-2 in the skin lesion of eondyloma acuminatum and bowenoid papulosis. Methods The expression levels of PPAR-γ, COX-2 were measured by immunohistochemistry in 17 cases of condyloma acuminatum, 17 cases of bowenoid papulosis, as well as 17 cases of normal foreskin lesions. Results The immunohistochemical study showed that PPAR-γ and COX-2 weakly expressed in normal foreskin, but overexepressed in the skin lesions of both condyloma acuminatum and bowenoid papulosis(P〈0.01). There was straight linear correlation between the expressions of PPAR-γ and COX-2 not only in condyloma acuminatum(r= 0. 505, P= 0. 038) but also in bowenoid papulosis (r= 0.562, P= 0.019). Conclusion PPAR-γ and COX-2 may have important roles in proliferative dermatosis associated with human papilloma virus.
出处 《四川大学学报(医学版)》 CAS CSCD 北大核心 2009年第3期439-441,共3页 Journal of Sichuan University(Medical Sciences)
关键词 尖锐湿疣 鲍温样丘疹病 PPAR-Γ COX-2 Condyloma aeuminatum Bowenoid papulosis PPAR-γ COX-2
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  • 1Satoh T, Tovoda M, Hoshino H, et al. Activation of peroxisome proliferators-activated receptor gamma stimulates the growth arrest and DNA-damage indueible 153 gene in non-small cell lung carcinoma cells. Ontogene, 2002,21(14) :2171- 2180.
  • 2Howe LR, Dannenberg AJ. A role for cyelooxygenase-2 inhibitors in the prevention and treatment of cancer. Semin Oncol, 2002;29(3 Suppl-11):111-119.
  • 3Axiotis CA, Monteagudo C, Merino MJ, et al. Tmmunohistochemical detection of P-glycoprotein in endometrial adenocarcinoma. Am J Pathol, 1991,138 (4) : 799- 806.
  • 4Gaffney DK, Holden J, Zempolich K, et al. Elevated COX-2 expression in cervical carcinoma : reduced cause-specific survival and pelvic control. Am J Clin Oncol,2001 ;24(5):443-446.
  • 5董育玮,王兴鹏.PPARs在消化道肿瘤发生中的作用及其机制[J].国外医学(消化系疾病分册),2002,22(2):95-98. 被引量:5
  • 6Nijsten T, Geluyckens E, Colpaert C, et al. Peroxisome proliferator-activated receptors in squamous cell carcinoma and its precursors. J Cutan Pathol, 2005 , 32(5): 340-347.
  • 7Freudlsperger C, Moll I, Schumacher U, et al. Anti-proliferative effect of peroxlsome proliferator-activated receptor-gamma agonists on human malignant melanoma cells in vitro. Antieancer Drugs,2006,17(3) ,325-332.
  • 8罗玉琴,吴开春,孙安华,潘伯荣,张学庸,樊代明.浅表性胃炎、胃粘膜不典型增生及胃癌组织中COX-1、COX-2、iNOS表达的意义[J].中华消化杂志,2000,20(4):223-226. 被引量:71
  • 9Gateyly S. Comibutions of cyclooxygenase-2 tumor angiogenesis. Cancer Metastasis Rev,2000,19(1-2) : 19-27.
  • 10Buskens CJ, Ristimaki A, Offerhaus GJ, et al. Role of eyclooxygenase-2 in the development and treatment of oesophageal adenoeareinoma. Stand J Gastroenterol Suppl, 2003,23(9) :87-93.

二级参考文献31

  • 1陈望忠.两种新的选择性环氧合酶-2抑制剂[J].国外医学(药学分册),1997,24(3):168-171. 被引量:38
  • 2[1]Issemann I et al. Nature, 1990; 347(6294): 645~650
  • 3[2]Kersten S et al. Nature, 2000; 405(25): 421~424
  • 4[3]Ricote M et al. Proc Natl Acad Sci USA, 1998; 95(13):76147~76149
  • 5[4]Lin Q et al. Biochemistry, 1999; 38(1): 185~190
  • 6[5]Forman BM et al. Cell, 1995; 83(5): 803~812
  • 7[6]Ma HW et al. J Biol Chem; 1998; 273(46): 30131~30138
  • 8[7]Sato H et al. Bri J Cancer, 2000; 83(10): 1394~1400
  • 9[8]Kitamura S et al. Biol Biop Res Com, 1999; 265(2): 453~456
  • 10[9]Galli A et al. Arch Bioc Bioph, 1998; 354(2): 288~294

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  • 1Wang R,Lin F,Wang X,et al.Silencing Livin gene expression to inhibit proliferation and enhance chemosensitivity in tumor cells[J].Cancer Gene Ther,2008,15(6):402-412.
  • 2Moon PD,Koo HN,Jeong HJ,et al.Haeamtang induces apoptosis of colon cancer HT-29 cells through activation of caspase-3[J].Am J Chinese Med,2007,35(5):897-909.
  • 3Wang QL,Huang YH,Ni YH,et al.siRNA targeting midkine inhibits gastric cancer cells growth and induces apoptosis involved caspase-3,8,9 activation and mitochondrial depolarization[J].J Biomed Sci,2007,(14)6:783-795.
  • 4Chien SY,Wu YC,Chung JG,et al.Quercetin-induced apoptosis acts through mitochondrial and caspase3-dependent pathways in human breast cancerMDA-MB-231 cell[J].Hum Exp Toxicol,2009,28(8):493-503.
  • 5Kasof GM,Gomes BC.Livin,a Novel Inhibitor of Apoptosis Protein Family Member[J].J Biol Chem,2001,276(5):3238-3246.
  • 6Haferkamp A,Bedke J,Vetter C,et al.High nuclear Livin expression is a favourable prognostic indicator in renal cell carcinoma[J].BJU Int,2008,102(11):1700-1706.
  • 7Wagener N,Crnkovic-Mertens I,Vetter C,et at.Expression of inhibitor of apoptosis protein Livin in renal cell carcinoma and non-tumorous adult kidney[J].Br J Cancer,2007,97(9):1271-1276.
  • 8Liu B,Han M,Wen JK,et al.Livin/ML-IAP as a new target for cancer treatment[J].Cancer Lett,2007,250(2):168-176.
  • 9Chang H,Schinmer AD.Livin/melanoma inhibitor of apoptosis protein as a potential therapeutic target for the treatment of malignancy[J].Mol Cancer Ther,2007,6(1):24-30.
  • 10Putt KS,Chen GW,Pearson JM,et al.Small molecule activation of procaspase-3 to caspase-3 as a personalized anticancer strategy[J].Nat Chem Biol,2006,2(10):543-550.

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