侯新新, 赵萌, 王红霞, 张贵宇. PPARγ ERα和ERβ在子宫内膜癌的表达及其相关性分析[J]. 中国肿瘤临床, 2013, 40(17): 1029-1033. DOI: 10.3969/j.issn.1000-8179.20130449
引用本文: 侯新新, 赵萌, 王红霞, 张贵宇. PPARγ ERα和ERβ在子宫内膜癌的表达及其相关性分析[J]. 中国肿瘤临床, 2013, 40(17): 1029-1033. DOI: 10.3969/j.issn.1000-8179.20130449
Xinxin HOU, Meng ZHAO, Hongxia WANG, Guiyu ZHANG. Correlations among the expressions of PPARγ, ERα, and ERβ in endometrial carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2013, 40(17): 1029-1033. DOI: 10.3969/j.issn.1000-8179.20130449
Citation: Xinxin HOU, Meng ZHAO, Hongxia WANG, Guiyu ZHANG. Correlations among the expressions of PPARγ, ERα, and ERβ in endometrial carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2013, 40(17): 1029-1033. DOI: 10.3969/j.issn.1000-8179.20130449

PPARγ ERα和ERβ在子宫内膜癌的表达及其相关性分析

Correlations among the expressions of PPARγ, ERα, and ERβ in endometrial carcinoma

  • 摘要:
      目的   探讨PPARγ、ERα和ERβ在子宫内膜癌的表达情况,分析三者之间的相互联系及临床意义。
      方法  采用免疫组织化学法及Western blot法检测正常子宫内膜及高中低分化子宫内膜癌组织中PPARγ、ERα和ERβ的表达。
      结果  PPARγ在子宫内膜癌中表达量明显降低,且随病理分级的进展,呈递减趋势;ERα在正常子宫内膜及高分化子宫内膜癌中表达量无显著性差异(P>0.05),而在中、低分化子宫内膜癌中表达量降低(P < 0.05);ERβ表达量仅在低分化子宫内膜癌降低,在正常子宫内膜及高中分化子宫内膜癌中表达量无显著性差异(P>0.05)。Pearson相关分析提示ERα与PPARγ在不同子宫内膜组织中表达量呈正相关(P < 0.05),而ERα与ERβ、ERβ与PPARγ间无相关性。
      结论  PPARγ及ERα表达水平与子宫内膜癌的分化程度、临床分期相关,在子宫内膜癌的发生发展中可能起重要作用。

     

    Abstract:
      Objective  To investigate the expressions of peroxisome proliferator-activated receptor gamma (PPARγ), estrogen receptor alpha (ERα), and estrogen receptor beta (ERβ) in endometrial carcinoma and to analyze their correlations and clinical significance.
      Methods  Immunohistochemical assay and Western blot were used to detect the expressions of PPARγ, ERα, and ERβ in normal endometrial tissues and well-differentiated, moderately differentiated, and poorly differentiated endometrial carcinomas.
      Results  PPAR γ expression was significantly lower in endometrial carcinoma than in the normal endometrium and was intimately associated with clini- copathologic variables. ERα expression gradually decreased in moderately and poorly differenti-ated endometrial carcinomas. However, no significant differences were found between the normal endometrium and well-differentiated endometrial carcinoma. ERβ expression only decreased in the poorly differentiated endometrial carcinoma. No significant association was observed between ERβ and clinicopathologic variables. Pearson correlation analysis showed a significant positive cor-relation between the expressions of PPARγ and ERα. No correlations were observed between the expressions of ERα and ERβ and between that of ERβ and PPARγ.
      Conclusion  The expression lev-els of PPARγ and ERα were significantly associated with the clinicopathologic stage of endometrial carcinoma, and have essential functions in endometrial tumorigenesis and tumor progression.

     

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