前列腺癌组织中ING4与VEGF的表达及相关性研究
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南充市科技局资助项目(14A0071)


Study of expression and correlation of ING4 and VEGF in prostate cancer
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    【摘要】 目的 探讨生长抑制因子4(ING4)与血管内皮生长因子(VEGF)在前列腺癌中表达及其对肿瘤发生发展的作用。方法 采用免疫组织化学ElivsionTM Plus二步法检测ING4及VEGF在28例前列腺癌及32例良性前列腺增生组织的表达,比较其在不同前列腺组织中表达差异,并将结果与前列腺癌病理分级、临床分期及PSA值进行分析。结果 ING4在良性前列腺增生组织中阳性表达率明显高于前列腺癌组织,差异具有统计学意义(P<005)。随肿瘤病理分级、临床分期及PSA值增加,ING4表达降低或缺失。VEGF在前列腺癌及良性前列腺增生组织中阳性表达率并无差异(P>005),但其强阳性表达率在前列腺癌中明显高于前列腺增生组织,且随肿瘤病理分级、临床分期及PSA增加而升高。前列腺癌中ING4表达与VEGF呈负相关(r=-0655,P<005)。结论 前列腺癌组织中ING4基因的异常表达是前列腺癌发生、发展的重要因素之一,可能通过促进新生血管生成发挥促癌作用;ING4可能成为前列腺癌诊断及治疗的生物学指标。

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    【Abstract】 Objective To investigate the expressions of ING4 and VEGF in prostate cancer and relationship of ING4 and VEGF in the development of tumor. Methods Expression of ING4 and VEGF in 28 cases of prostate cancer and 32 cases of benign prostatic hyperplasia were detected by EliVisionTM plus immunohistochemical stain. The immunoassay results were analyzed in relation to the tumor pathological grade, clinical stage and the different PSA. Results The positive expression rate of ING4 gene in prostate cancer tissues was significantly lower than that of benign prostatic hyperplasia, and decreased with the increase of tumor pathological grade, clinical stage and PSA. There was no difference in the positive expression rate of VEGF in prostate cancer and benign prostatic hyperplasia (P>005). But the strong positive expression rate in prostate cancer was significantly higher than that in benign prostatic hyperplasia, and increased with the pathological grade, clinical stage and PSA. The expression of ING4 was negatively correlated with VEGF in prostate cancer, which was statistically significant(P<005).Conclusion Abnormal expressions of ING4 is one of the significant factor of the increasing of the degree of the occurrence and progression of prostate cancer, and possibly play a role in tumor promotion by promoting tumor angiogenesis. ING4 may be a biological index for diagnosis and treatment of prostate cancer.

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  • 在线发布日期: 2017-05-22
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