期刊文献+

血小板源性生长因子-D在膀胱癌中的表达及其临床意义 被引量:3

Expression and clinical significance of PDGF-D in bladder cancer
原文传递
导出
摘要 目的观察廊小板源性生长因子-D(PDGF—D)在膀胱移行细胞癌(BTCC)中的表达,探讨PDGF—D与膀胱移行细胞癌的发生发展之间的关系及其临床意义。方法分别采用实时定量逆转录一聚合酶链反应(real—timeRT—PCR)法和蛋白免疫印迹(Westernblot)法检测62例膀胱移行细胞癌组织、10例癌旁正常膀胱组织中PDGF—DmRNA和蛋白的表达,并分析其与临床病理之间的关系。结果PDGF—DmRNA在BTCC中的表达量是正常对照组的1.89倍,PDGF—D蛋白在癌组织中的表达明显高于正常膀胱组织(相对吸光度比值:正常组0.231±0.041,癌症组0.689±0.083,P〈0.05)。而且随着肿瘤病理分级的升高及淋巴结转移的出现,PDGF—DmRNA和蛋白的表达水平均逐渐升高,各组间差异有统计学意义(P〈0.05)。但不同分期的癌组织中PDGF—DmRNA和蛋白的表达水平的差异无统计学意义(P〉0.05)。结论PDGF—D表达增强与膀胱癌的发生及分化、转移密切相关,可能在膀胱癌的发生发展中发挥重要作用。 Objective To investigate the expression of PDGF-D in bladder transitional cell carcinoma (BTCC) , and its clinical significance in tumorigenesis and progression of BTCC. Methods By using real-time reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting, the expression levels of PDGF-D mRNA and protein were detected in 62 cases of BTCC tissues, and 10 cases of the normal bladder tissues which were closely adjacent to the carcinoma. The relationship between PDGF-D expression and the clinicopathological features was analyzed. Results The expression levels of PDGF-D mRNA in BTCC were 1.89 times as much as those in the normal control group. PDGF-D protein expressed in tumor tissues was significantly higher than in normal bladder tissues (absorbance ratio in the normal bladder tissues was 0.231 ±0. 041, and that in the tumor tissues was 0. 689 ±0. 083, P 〈 0.05 ). Moreover, with the grades going up and appearance of lymph node metastasis, the expression levels of PDGF-D mRNA and protein were increased gradually (P 〈 0. 05 ). But in different clinical stages ,the expression levels of PDGF-D mRNA and protein had no significant difference ( P 〉 0.05 ). Conclusion The overexpression of PDGF-D is closely correlated with the occurrence, differentiation and lymphatic metastasis of BTCC, and may play an important role in carcinogenesis and progression of bladder cancer.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2010年第3期287-289,共3页 Chinese Journal of Experimental Surgery
关键词 膀胱肿瘤 血小板源性生长因子 Bladder neoplasm PDGF
  • 相关文献

参考文献7

  • 1Bergsten E,Uutela M,Li X,et al.PDGF-D is a specific,protease-activated ligand for the PDGF-β-receptor.Nat Cell Biod,2001,3,512-516.
  • 2Reigstad LJ,Varhaug.JE,Lillehaug JR.Structural and functional specificities of PDGF-C and PDGF-D,the novel members of the playletderived growth factors family.FEBS J,2005,272:5723-5741.
  • 3王爱民,王宝恩,江龙安,贾继东,韩涛,李培建.血小板衍生生长因子对肝星状细胞基质分解素-1及其抑制因子基因表达的调节[J].中华实验外科杂志,2000,17(3):241-242. 被引量:8
  • 4Yu J,Ustach C,Kim HR.Platelet-derived growth factor signaling and human cancer.J Biochem Mol Biol,2003,36:49-59.
  • 5Johanna A,Badiosa G,Christer B.Role of platelet-derived growth factots in physiology and medicine.Genes Dev,2008,22:1276-1312.
  • 6Heldin CH,Eriksson U,Ostman A.New members of the platelet-derived growth factor family of mitogens.Arch Biochem Biophys,2002,398:284-290.
  • 7Kong D,Wang Z,Sarkar SH,et al.Platelet-derivecl growth factor-D overexpression contributes to epithelial-mesenchymal transition of PC3 prostate cancel cells.Stem Cells,2008,26:1425-1435.

二级参考文献2

共引文献7

同被引文献24

  • 1丁国芳,李继承,李春生,徐银峰.nm23H1、VEGF表达与前列腺癌转移和生存率的关系[J].中华泌尿外科杂志,2005,26(9):619-621. 被引量:9
  • 2Karvinen H, Rutanen J, Leppnen O, Laeh R, Levonen AL, Eriksson U, Y1 - Herttuala S. PDGF - C and - D and their receptors PDGFR - alpha and PDGFR - beta in atherosclerotie human arteries[J]. Eur J Clin Invest, 2009, 39(4) : 320.
  • 3Wang Z, Kong D, Li Y, Sarkar F H. PDGF - D signaling : a novel target in cancer therapy[ J]. Curr Drug Targets. 2009, 10(1): 38,.
  • 4Wang Z, Ahmad A, Li Y, Kong D, Azmi A S, Banerjee S, Sarkar FH. Emerging roles of PDGF - D signaling pathway in tumor development and progression[ J]. Biochim Biophys Ac- ta. 2010, 1806(1): 122.
  • 5Reigstad L J, Varhaug J E, Lillehaug J R. Structural and functional specificities of PDGF - C and PDGF - D, the novel members of the platelet - derived growth factors family [ J ]. FEBS J, 2005, 272(22) : 5723.
  • 6Sun Z J, Chen G, Zhang W, Hu X, Liu Y, Zhou Q, Zhu LX, Zhao YF. Curcumin dually inhibits both mTOR and NF - KB pathways through a crossed/Akt/IKK signaling axis in ad- enoid cystic carcinoma. Mol Pharmacol. 2010 Oct 19. [ Epub ahead of print].
  • 7Ammoun S, Flaiz C, Ristic N, et al. Dissecting and targeting the growth factor dependent and growth factor independent ex- traeellular signal regulated kinase pathway in human schwan- noma[ J ]. Cancer Res, 2008, 68 ( 13 ) : 5236.
  • 8Zhao L, Zhang C, Liao G, Long J. RNAi - mediated inhibi- tion of PDGF - D leads to decreased cell growth, invasion and angiogenesis in the SGC - 7901 gastric cancer xenograft model [J]. CancerSiolTher, 2010, 9(1):42.
  • 9Kong D, Banerjee S, Huang W, Li Y, Wang Z, Kim HR, Sarkar FH. Mammalian target of rapamycin repression by 3,3 - diindolylmethane inhibits invasion and angiogenesis in platelet - derived growth factor - D - overexpressing PC3 cells [J]. Cancernes, 2008, 68(6): 1927.
  • 10Wang Z, Kong D, Li Y, et al. PDGF-D signaling: a novel target in cancer therapy. Curt Drug Targets, 2009, l0: 38-41.

引证文献3

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部