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HMGB-1基因及其受体RAGE在宫颈鳞癌中的表达及临床意义 被引量:5

Gene expression and clinical significance of HMGB-1 and RAGE in cervical squamous epithelial carcinoma
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摘要 目的:检测高迁移率族蛋白-1(HMGB-1) mRNA和晚期糖基化终产物受体(RAGE) mRNA在宫颈鳞癌(CSEC)组织中的表达及其与临床病理参数间的关系,探讨它们与CSEC发生、侵袭和转移的关系。方法:采用实时荧光定量PCR(qRT-PCR)检测CSEC、癌旁及正常宫颈组织中HMGB-1 mRNA和RAGE mRNA的表达情况。结果:(1)HMGB-1 mRNA在CSES、癌旁组织表达水平均高于正常宫颈组织(P<0.05)。其表达与肿瘤分期、淋巴转移明显相关(P<0.05),而与肿瘤直径、分级无关(P>0.05)。(2)RAGE mRNA在CSES、癌旁及正常的宫颈组织中的表达水平无明显的统计差异(P>0.05),其表达与肿瘤直径、分级、分期无关(P>0.05),仅与淋巴转移相关(P<0.05)。结论:HMGB-1可作为判断宫颈肿瘤侵袭、转移的生物指标,RAGE与CSEC转移相关,HMGB-1/RAGE可能是促进CSEC转移发生的重要信号通路,它们将有可能成为治疗宫颈癌淋巴转移的新靶点。 Objective: To investigate the expression and clinico - pathological findings of high mobility group box-1( HMGB-1)mRNA and receptor for advanced glycation end products (RAGE)mRNA in cervical squamous epithelial carcinoma, to explore their roles during the carcinoma process, invasion and metastasis. Methods: Real time quantitative polymerase chain reaction (qRT-PCR)were employed to detect the expression of HMGB-1 mRNA and RAGE in CSEC and nomal cervical tissues. Results: The expression of HMGB-1 mRNA in the CSEC and their paraneoplastic tissues was higher than that in normal cervix tissues. And the overexpression of HMGB-1 mRNA in the CESC tissues was significantly correlated with the stage, the presence of metastasis, but not correlated with the diameter and grade of tumor. And expression of RAGE was no significantly differences between the CSEC ,paraneoplastic and normal cervical tissues.Statistical analysis showed that RAGE mRNA had a relation with the metastasis.But no relation in stage, diameter and grade of CSEC. Conclusion:HMGB-1 could be a prognostic predictor of malignant degree in the evaluation of CSEC patients. The pathway of HMGB-1/RAGE is the main mechanism correlated with the metastasis of CESC and they may become new targets for treating CSEC lyphatic metastasis.
出处 《天津医科大学学报》 2008年第1期30-33,共4页 Journal of Tianjin Medical University
基金 天津医科大学肿瘤医院院级课题基金资助(2007)
关键词 高迁移率族蛋白-1 晚期糖基化终产物受体 宫颈鳞癌 High mobility group box-1 (HMGB-1) Advanced glycation end products(RAGE) Cervical squamous epithelial carcinoma(CSEC)
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参考文献15

  • 1Tagnchi A, Blood DC, del Toro G, et al.Blockstage of RAGE amphoterin signalling suppresses tumour growth and matastasis[J].Nature, 2000,405 ( 6784 ) :354 被引量:1
  • 2Andersson U ,Erlandsson Harris H ,Yang H, et al. HMGB1 as a DNA-binding cytokine[J ]. J Leukoc Biol,2002 ,72 (6) :1084 被引量:1
  • 3Bonaldi T, Langst G, strohner R,et al. The DNA chaperone HMGB 1 facilitates ACF/CHRAC-dependent nucleosome sliding[J].EMBO J, 2002,21(24) :6865 被引量:1
  • 4Volp K, Brezniceanu ML, Bosser S,et al. Increased expression of high mobility group box 1 (HMGB 1 ) is associated with an elevated level of the antiapoptotic c-IAP2 protein in human colon carcinomas[J]. Colon Cancer, 2006,55(2):234 被引量:1
  • 5Pardo M, Garcia A, Thomas B, et al. The characterization of the invasion phenotype of uveal melanoma tumour ceils shows the presence of MUC18 and HMG-1 metastasis markers and leads to the identification of DJ-1 as a potential serum biomarker [J]. Int J Cancer, 2006,119(5):1014 被引量:1
  • 6Ishiguro H. Receptor for advanced glycation end products (RAGE) and its ligand, amphoterin are overexpressed and associated with prostate cancer development[J]. Prostate, 2005,64( 1):92 被引量:1
  • 7Choi YR, Kim H, Kang HJ, et al. Overexpression of high mobility group box 1 in gastrointestinal stromal tumors with KIT mutation [J].Cancer Res ,2003,63 ( 9 ) :2188 被引量:1
  • 8Hirata K, Takada M, Suzuki Y, et al. Expression of receptor for advanced glycation end products (RAGE) in human biliary cancer cells[J].Hepatogastroenterology,2003,50 ( 53 ): 1205 被引量:1
  • 9Evans A,Thomas W,Barry R,et al.Metastasis-associated or metastasis-inducing [J]. J Surg Oncol, 2004,88 ( 1):86 被引量:1
  • 10Ranvala H, Huttunen HJ, Fstages C, et al.Heparin-blinding proteins HB-GAM (pleiotrophin) and amphotefin in the regulation of cell mobility [J].Martrix Biol,2000,19 ( 5 ) :377 被引量:1

二级参考文献11

  • 1Taguchi A, Blood DC, del Toro G, et al. Blockage of RAGE amphoterin signalling suppresses tumour growth and metastasis [J]. Nature, 2000, 405(6784): 354- 360. 被引量:1
  • 2Rauvala H, Huttunen HJ, Fages C, et al. Heparin binding proteins HB GAM (pleiotrophin) and amphoterin in the regulation of cell mobility [J]. Matrix Biol, 2000, 19(5): 377- 387. 被引量:1
  • 3J萨姆布鲁克 E F 弗里奇 T 曼尼阿蒂斯 16-392.分子克隆实验指南 [M](第 2版)[M].北京:科学出版社,1999.. 被引量:1
  • 4Zi X, Grasso AW, Kung HJ, et al. A flavonoid antioxidant, silymarin, inhibits activation of erbB1 signaling and induces cyclin dependent kinase inhibitors, G1 arrest, and anticarcinogenic effects in human prostate carcinoma DU145 cells[J]. Cancer Res, 1998, 58(9): 1920 1929. 被引量:1
  • 5Heussen C, Dowdle EB. Electrophoretic analysis of plasminogen activation in polyacrylamide gels containing sodium dodecyl sulfate and copolymerized substrates [J]. Anal Biochem, 1980, 102(1): 196- 202. 被引量:1
  • 6Albini A, Iwamoto Y, Kleinman HK, et al. A rapid in vitro assay for quantitating the invasion potential of tumor cells [J]. Cancer Res, 1987, 47(12): 3239- 3245. 被引量:1
  • 7Thomas JO, Travers AA. HMG1 and 2, and related architectural DNA binding proteins [J]. Trends Biochem Sci, 2001, 26(3): 167- 174. 被引量:1
  • 8Kuniyasu H, Chihara Y, Kondo H, et al. Differential effects between amphoterin and advanced glycation end products on colon cancer cell [J]. Int J Cancer, 2003, 104(6): 722- 727. 被引量:1
  • 9Sternlicht MD, Werb Z. How matrix metalloproteinases regulate cell behavior [J]. Annu Rev Cell Dev Biol, 2001, 17: 463- 516. 被引量:1
  • 10Hag M, Shafii A, Zervos EE, et al. Addition of Matrix Metalloproteinase Inhibition to Conventional Cytotoxic Therapy Reduces Tumor Implantation and Prolongs Survival in a Murine Model of Human Pancreatic Cancer [J]. Cancer Res, 2000, 60(12): 3207- 3211. 被引量:1

共引文献15

同被引文献64

  • 1上官翰京,李志春,张晖萍.RAGE在恶性肿瘤中的研究进展[J].海南医学院学报,2007,13(1):79-82. 被引量:4
  • 2辛海,耿明,陈诵芬,陈秀芳,徐增祥.宫颈癌及其癌前病变组织中p16^(INK4a)和PCNA的表达及临床意义[J].中华肿瘤防治杂志,2007,14(20):1563-1567. 被引量:12
  • 3Kuniyasu H,Oue N,Wakikawa A,et al.Expression of receptors for advanced glycationend-products (RAGE) is closely associated with the invasive and metastatic activity of gastric cancer[J].Pathol,2002,196(2):163-170. 被引量:1
  • 4Ishiguro H,Nakaigawa N,Miyoshi Y,et al.Receptor for advanced glycation end products (RAGE) and its ligand,amphoterin are over expressed and associated with prostate cancer development[J].Prostate,2005,64 (1):92-100. 被引量:1
  • 5Kuniyasu H,Chijhara Y,Takahashi T.Co-expression of receptor for advanced glycation end products and the ligand amphoterin associates closely with metastasis of colorectal cancer[J].Oncol Rep,2003,10(2):445-448. 被引量:1
  • 6Takada M,Hirata K,Ajiki T,et al.Expression of receptor for advanced glycation end products (RAGE) and MMP-9 in human pancreatic cancer cells[J].Hepatogastroenterology,2004,51 (58):928-930. 被引量:1
  • 7Taguchi A,Blood DC,del Toro G,et al.Blockade of RAGE-am-photerin signalling suppresses tumour growth and metastases[J].Nature,2000,405 (6784):354-360. 被引量:1
  • 8Sims GP,Rowe DC,Rietdijk ST,et al.HMGB-1 and RAGE in inflammation and cancer[J].Annu Rev Immunol,2010,28(1):367-388. 被引量:1
  • 9Heikki Rauvala,Ari Rouhiainen.RAGE as a receptor of HMGBI (Amphoterin):Roles in Health and Disease[J].Curr Mol Med,2007,7:725-734. 被引量:1
  • 10Craig D,Logsdon,Maren K,et al.RAGE and RAGE Ligands in Cancer[J].Curr Mol Med,2007,7:777-789. 被引量:1

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