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EphB4和EphrinB2 mRNA在子宫颈癌组织中的表达及其与血管生成的关系 被引量:1

Expression of Eph B4 and Ephrin B2 mRNA in cervical cancer tissues and angiogenesis
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摘要 目的检测EphB4和EphrinB2 mRNA在子宫颈癌组织中的表达,探讨其在子宫颈癌发生、发展及血管生成过程中的作用。方法采用逆转录多聚酶链反应(RT-PCR)法检测90例子宫颈癌、15例子宫颈上皮内瘤样病变(CIN)和15例正常宫颈组织中EphB4和EphrinB2 mRNA的表达,同时利用链霉菌抗生物素蛋白-过氧化酶连接(SP)法检测上述组织的微血管密度(MVD),分析EphB4和EphrinB2 mRNA的表达与各种临床病理参数和血管生成的关系。结果尽管所有子宫颈组织中均可检测出EphB4和EphrinB2 mRNA的表达,但是EphB4 mRNA在子宫颈癌(125.59±16.63)和CIN(122.61±17.30)组织中的表达强度均高于其在正常宫颈组织中的表达(95.72±4.63)(P均<0.05)。EphrinB2 mRNA在子宫颈癌组织中的表达强度(111.11±22.86)明显高于其在CIN(94.48±6.30)和正常宫颈组织中的表达(93.56±7.89)(P均<0.05)。EphB4 mRNA在子宫颈癌组织中的表达强度与子宫颈癌的临床分期和肿瘤直径密切相关(P均<0.05)。EphrinB2 mRNA在子宫颈癌组织中的表达强度只与子宫颈癌的肿瘤直径密切相关(P<0.05)。正常宫颈组织、CIN和子宫颈癌组织中MVD逐渐增加,分别为(11.33±2.38),(26.47±7.47)和(42.97±9.99)。子宫颈癌组织中EphB4和EphrinB2 mRNA的表达均与MVD呈正相关。结论EphB4和EphrinB2在子宫颈癌的发生、发展及血管生成过程中可能起重要的作用。 [ Objective] To detect the expression of EphB4 and EphrinB2 mRNA in cervical cancer tissues to probe their role in the oncogenesis, development and angiogenesis of cervical cancer. [Methods] The expression of EphB4, EphrinB2 mRNA and its microvessel density (MVD) in 90 patients with cervical caner, 15 patients with cer- vical intraepithelial neoplasm (CIN) and 15 patients with normal cervix were detected by reverse transcription-poly- merase chain reaction (RT-PCR) method and immunohistochemistry of streptavidin-peroxidase (SP) method. [ Resuits] Although Eph B4 and Ephrin B2 mRNA expression were detected in all tissues, the relative amount of Eph B4 mRNA was higher in cervical cancer (125.59±16.63) or CIN (122.61±17.30) than in normal cervices (95.72± 4.63) (P 〈0.05). And the relative amount of Ephrin B2 mRNA was higher in cervical cancer (111.11±22.86) than in CIN (94.48±6.30) or normal cervices (93.56±7.89) (P 〈0.05). In patients with cervical cancer, the relative amount of Eph B4 mRNA was correlated with both clinical stage and tumor diameter whereas the relative amount of Ephrin B2 mRNA was only correlated with tumor diameter. Values of MVD were found to increase gradually from normal cervix (11.33±2.38), to CIN (26.47±7.47), and to cervical cancer (42.97±9.99). Relative amount of both Eph B4 and Ephrin B2 mRNA was shown to be positively eorrelated with MVD in patients with eervieal eaneer as well. [Conclusion] Eph B4 and Ephrin B2 interaetion may play an important role both in the oneogenesis and angiogenesis of eervieal eareinomas.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2008年第14期2003-2005,2025,共4页 China Journal of Modern Medicine
基金 国家自然科学基金(No:30672220)
关键词 子宫颈肿瘤 EPHB4 MRNA EPHRINB2 MRNA MVD cervix neoplasm EphB4 mRNA EphrinB2 mRNA MVD
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参考文献8

  • 1WEIDNER N, SEMPLE JP, WELCH WR, et al. Tumor angiogenesis and metastasis-correlation in invasive breast carcinoma[J]. N Engl J Med, 1991, 324: 1-8.
  • 2HUYNH-DO U, VINDIS C, LIU H, et al. Ephrin-B1 transduces signals to activate integrin-mediated migration, attachment and angiogenesis[J]. Journal of Cell Science, 2002, 115: 3073-3081.
  • 3TIM F u LLER, THOMAS KORFF, ADRIENNE KILIAN, et aL Forward EphB4 signaling in endothelial coils controls cellular repulsion and segregation from ephrinB2 positive coils[J]. Journal of Cell Science, 2003, 116: 2461-2470.
  • 4XU Z, LAI KO, ZHOU HM, et al. Ephrin-B1 reverse signaling activates JNK through a novel mechanism that is independent of tyroslne phesphorylation [J]. J Biol Chem, 2003, 278: 24767-24775.
  • 5BENBOW U, BRINCKERHOFF CE. The AP-1 site and MMP gene regulation: what is all the fuss about?[J]. Matrix Biol, 1997, 15: 519-526.
  • 6STEINLE JJ, MEININGER CJ, CHOWDHURY U, et al. Role of ephrin B2 in human retinal endothelial, cell proliferation and migration[J]. Cell Signal, 2003, 15: 1011-1017.
  • 7PALMER A, ZIMMER M, ERDMANN KS, et al. EphrinB phosphorylation and reverse signaling: regulation by Src kinases and PTP-BL phosphatase[J]. Mol Cell, 2002, 9: 725-737.
  • 8XIA G, KUMAR SR, MASOOD R, et al. EphB4 expression and biological significance in prostate cancer [J]. Cancer Res, 2005, 65: 4623-4632.

同被引文献9

  • 1Wang HU, Chen ZF, Anderson DJ. Molecular distinction and angiogenic interaction between embryonic arteries and veins revealed by ephrin-B2 and its receptor Eph-B4 [J]. Cell, 1998,93(5): 741-753.
  • 2Ftiller T, Korff T, Kilian A, et al. Forward EphB4 signaling in endothelial cells controls cellular repulsion and segregation from ephrinB2 positive cells[J]. J Cell Sci, 2003,116 (Pt 12) :2461-2470.
  • 3Kertesz N, Krasnoperov V, Reddy R, et al. The soluble extracellular domain of EphB4 (sEphB4) antagonizes EphB4- EphrinB2 interaction, modulates angiogenesis, and inhibits tumor growth[J]. Blood, 2006,107(6) : 2330-2338.
  • 4Wang Y, Nakayama M, Pitulescu ME, et al. Ephrin-B2 controls VEGF-induced angiogenesis and lymphangiogenesis [J]. Nature,2010,465 (7297):483-486.
  • 5Kawasaki H, Altieri DC, Lu CD, et al. Inhibition of apoptosis by survivin predicts shorter survival rates in colorectal caneer[J]. Cancer Res, 1998,58(22) :5071-5074.
  • 6Adams RH, Wilkinson GA, Weiss C, et al. Roles of ephrinB ligands and EphB receptors in cardiovascular development: demarcation of arterial/venous domains, vascular morphogenesis, and sprouting angiogenesis[J]. Genes Dev, 1999,13(3) : 295-306.
  • 7Noren NK, Lu M, Freeman AL, et al. Interplay between EphB4 on tumor cells and vascular ephrin-B2 regulates tumor growth[J]. Proc Natl Acad Sci USA, 2004,101(15):5583-5588.
  • 8Red-Horse K, Kapidzic M, Zhou Y, et al. EPHB4 regulates chemokine-evoked trophoblast responses: a mechanism for incorporating the human placenta into the maternal circulation [J]. Development,2005,132(18) :4097-4106.
  • 9Zhang J, Dong H, Wang B, et al. Dynamic changes occur in patterns of endometrial EFNB2/EPHB4 expression during the period of spiral arterial modification in mice [J]. Biol Reprod,2008,79(3) :450-458.

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