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Fas和Ki-67在非小细胞肺癌组织中的表达 被引量:4

EXPRESSION OF Fas AND Ki-67 IN NON-SMALL CELL LUNG CANCER
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摘要 目的 探讨Fas和Ki-67在非小细胞肺癌(NSCLC)组织中的表达及临床意义。方法 采用免疫组化EnVison法检测Fas和Ki-67在60例NSCLC及18例癌旁正常肺组织中的表达。结果 在NSCLC组织中,Fas表达率显著低于癌旁正常肺组织(χ^2=6.94、14.30,P〈0.05),并与NSCLC的病理分级、临床分期及淋巴结转移有关(χ^2=7.17~10.90,P〈0.05);Ki-67表达率显著高于癌旁正常肺组织(χ^2=18.80、14.20,P〈0.01),并与NSCLC的病理分级、临床分期及淋巴结转移有关(=8.47~13.10,P〈0.05)。分化程度低、已发生转移的肺癌Fas表达水平显著降低,而Ki-67表达水平显著升高。在NSCLC组织中,Fas和Ki-67表达水平呈负相关(χ^2=3.93,P〈0.05)。结论 Fas和Ki-67表达异常与肺癌发生、发展及转移关系密切,对判断肺癌恶性程度及预后有重要参考价值。 Objective To observ the expression of Fas and Ki-67 in non-small cell lung cancer (NSCLC) and discuss the related clinical significance. Methods EnVison immunohistochemical method was applied to investigate the expression of Fas and Ki-67 in the tissue of NSCLC (n= 60) and the normal neighboring lung tissue (n=18). Results The level of Fas expression in NSCLC was significantly/ower than that in adjacent normal tissues (χ^2=6.94,14.30; P〈0. 05), and was correlated with pathological grading, clinical staging and lymphatic metastasis (χ^2=7.17- 10.90,P〈0.05). The level of Ki-67 expression in NSCLC was significantly higher than that in adjacent normal tissues (χ^2= 18. 80,14.20 ; P〈0.01 ), and was also correlated to pathology (χ^2=8.47- 13.10,P〈0.05). NSCLC in the advanced stage with poor differentiation and lymph node metastasis possessed lower Fas expression but higher Ki-67 expression (χ^2=3.93,P〈0.05). Conclusion Abnormal expression of Fas and Ki-67 is related to the occurrence, development, whether or not metastasis of NSCLC, and is of importance in the evaluation of malignancy and prognosis of the disease.
出处 《齐鲁医学杂志》 2007年第3期212-214,共3页 Medical Journal of Qilu
基金 青岛市科技局资助项目(03-1-NY-14-2)
关键词 抗原 CD95 KI-67抗原 非小细胞肺 免疫组织化学 antigens, CD95 Ki-67 antigen carcinoma, non-small cell lung immunohistochemistry
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参考文献4

  • 1VIARD LEVEUGLE I,VEYRENC S,FRENCH L E,et al.Frequent loss of Fas expression and function in human lung tumors with over expression of Fas in small cell lung carcinoma[J].Pathol,2003,201(2):268-277.
  • 2阎丽平,罗兵,王笑峰,赵鹏,黄葆华.EBV相关胃癌组织中bcl-2和Ki-67蛋白表达的检测[J].青岛大学医学院学报,2004,40(1):57-59. 被引量:7
  • 3NAMBU Y,HUGHES S J,REHEMTULLA,et al.Lack of cell surface Fas/Apo-1 expression in pulmonary adenocarcinoma[J].Clin Invest,1998,101(10):1102-1110.
  • 4SHIN M S,KIM H S,LEE S H,et al.Alterations of Fas pathway genes associated with nodal metastasis in non small cell lung cancer[J].Oncogene,2002,21 (26):4129-4136.

二级参考文献8

  • 1[2]Kume T , Oshins K , Shinohara T, et al. Low rate of apoptosis and overexpression of bcl-2 in Epstein-Barr virus-associated gastric carcinoma[J]. Histopatology, 1999,34:502.
  • 2[3]Ishii H, Gobe G, Kawakubo Y, et al. Interrelationship between Epstein-Barr virus infection in gastric carcinomas and the expression of apoptosis-associated proteins[J]. Histopathology, 2001,38:111.
  • 3[4]Tokamage M, Land CE, Uenura Y, et al. Epstein-Barr virus in gastric carcimona[J]. Am J Pathol, 1993,143(5):1250.
  • 4[5]Shibata D,Tokunaga M,Uenura Y,et al. Association of Epstein-Barr virus with undifferentiated gastric carcinomas with intense lymphoid infiltration[J]. Am J Pathol,1991,139:469.
  • 5[6]Henderson S,Rowe M,Gregory C,et al. Induction of bcl-2 experssion Epstein-Barr virus latent membrane protein 1 protects infected B cells from programmed cell death[J]. Cell, 1991,65:1107.
  • 6[7]Gulley ML, Pulitzer DR, Eagan PA,et al. Epstein-Barr virus infection is an early event in gastric carcinogenesis and is independent of bcl-2 expression and p53 accunulation[J]. Human Pathology,1996,27:20.
  • 7[8]Ohfuji S, Osaki M, Tsujitani S, et al. Low frequency of apoptosis in Epstein-Barr virus-associated gastric carcinoma with lymphoid stroma[J]. Int J Cancer, 1996,68:710.
  • 8罗兵,村上雅尚,柳原五吉,西连寺刚.EB病毒对人胃癌细胞系HSC-39感染的研究[J].中华微生物学和免疫学杂志,2002,22(4):379-384. 被引量:14

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