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食管鳞癌组织中PTEN、PI3K和Paxillin的表达及其临床意义[J]. 肿瘤防治研究, 2010, 37(04): 425-427. DOI: 10.3971/j.issn.1000-8578.2010.04.015
引用本文: 食管鳞癌组织中PTEN、PI3K和Paxillin的表达及其临床意义[J]. 肿瘤防治研究, 2010, 37(04): 425-427. DOI: 10.3971/j.issn.1000-8578.2010.04.015
Expression and Clinical Significance of PTEN,PI3K and Paxillin Proteins in Esophageal Squamous Cell Carcinoma[J]. Cancer Research on Prevention and Treatment, 2010, 37(04): 425-427. DOI: 10.3971/j.issn.1000-8578.2010.04.015
Citation: Expression and Clinical Significance of PTEN,PI3K and Paxillin Proteins in Esophageal Squamous Cell Carcinoma[J]. Cancer Research on Prevention and Treatment, 2010, 37(04): 425-427. DOI: 10.3971/j.issn.1000-8578.2010.04.015

食管鳞癌组织中PTEN、PI3K和Paxillin的表达及其临床意义

Expression and Clinical Significance of PTEN,PI3K and Paxillin Proteins in Esophageal Squamous Cell Carcinoma

  • 摘要: 目的 研究PTEN、PI3K和Paxillin在食管鳞癌组织(esophageal squamous cell carcinoma,ESCC)中的表达及其与ESCC细胞发生、发展与转移的关系以及PTEN、PI3K和Paxillin三者之间的相关性。 方法 应用免疫组织化学SP法检测24例正常食管黏膜、94例ESCC组织中PTEN、PI3K和Paxillin的表达情况。 结果 食管癌组织中PTEN、PI3K和Paxillin的阳性表达率与正常食管黏膜组织相比差异均有统计学意义(P<0.01) 。PTEN表达与食管癌细胞的分化程度(P<0.05)、淋巴结转移(P<0.01)、浸润深度 (P<0.05)及临床分期(P<0.05)显著相关;PI3K表达与分化程度、淋巴结转移、浸润深度及临床分期显著相关(均P<0.01);Paxillin表达与淋巴结转移、浸润深度和临床分期等因素有关(均P<0.01);PTEN 分别与 PI3K、Paxillin表达之间均呈显著负相关(P<0.01);PI3K与Paxillin 表达呈显著正相关(P<0.05) 。 结论 PTEN、PI3K和Paxillin表达均与食管癌发生发展及侵袭转移有关,可作为评价ESCC生物学行为的指标。在食管癌的发生发展中 PI3K、PTEN 的作用可能互相拮抗,PI3K和Paxillin 协同促进肿瘤的恶性进展。

     

    Abstract: Objective To study the expression of PTEN, PI3K and Paxillin in esophageal squamous cell carcinoma(ESCC)and to investigate the relationship between the expression of PTEN,PI3K and Paxillin and carcinogenesis and progression of esophageal carcinoma and correlation among PTEN,PI3K and Paxillin expression each other . Methods PTEN,PI3K and Paxillin expression were detected in 24 normal esophageal mucosa, 94 ESCC with SP immunohistochemistry method. Results There were significant differences of PTEN,PI3K and Paxillin expressions between esophageal carcinoma and normal mucosa epithelium (all P<0.01). There were significant correlation between PTEN expression and the degrees of differentiation (P<0.05),invasive depth (P<0.05), clinical staging (P<0.05) and the metastasis of lymph node (P<0.01). There were significant correlation between PI3K expression and the degrees of differentiation,invasive depth, clinical staging and the metastasis of lymph node (all P<0.01).The positive expression rate of Paxillin had the relationship with invasive depth, clinical staging and metastasis of lymph node (all P<0.01). There was a negative relationship between PTEN and PI3K or Paxillin expression (P<0.01). A positive correlation was found between the expression of PI3K and Paxillin (P<0.05) . Conclusion PTEN,PI3K and Paxillin play important roles in carcinogenesis and progression of esophageal carcinoma,and can be used as valuable biomakers to evaluate biological characteristics in esophageal carcinoma. PTEN and PI3K may counteract with each other; PI3K and Paxillin may cooperate to promote malignant progress of esophageal carcinoma.

     

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