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C-MYC和MXI1在晚期肺腺癌组织中的表达及其临床意义 被引量:1

C-MYC and MXI1 Protein Expressions in the Advanced Lung Adenocarcinoma
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摘要 目的观察C-MYC和MXI1在晚期肺腺癌组织中的表达,同时探讨两者的相关性及其临床意义。方法使用免疫组化S-P法检测C-MYC和MXI1在100例晚期肺腺癌组织中表达情况,并分析其与晚期肺腺癌临床病理特征的关系。结果 C-MYC和MXI1在晚期肺腺癌组织中的阳性表达率分别为60.00%和55.00%。晚期肺腺癌组织中C-MYC、MXI1的表达呈负相关(r=-0.206,P<0.05)。C-MYC阴性患者比C-MYC阳性患者具有较长的生存时间(21.00个月vs 15.00个月),差异有统计学意义(χ~2=10.890,P<0.001);而MXI1阳性患者比MXI1阴性患者具有较长的生存时间(21.00个月vs 13.00个月),差异有统计学意义(χ~2=15.080,P<0.001)。结论 C-MYC和MXI1的异常表达可能与晚期肺腺癌的预后密切相关。 Objective To investigate the expressions of C-MYC and MXI1 protein and the clinical significance in the advanced lung adenocarcinoma. Methods The expressions of C-MYC and MXI1 in the advanced lung adeno-carcinoma were detected by immunohistochemistry, and the relationship between two proteins and clinicopathologic feature was analyzed. Results The positive expression rates of C-MYC and MXI1 in the advanced lung adenocarcinoma were 60.00% and 55.00% respectively. C-MYC was negatively related with MXI1 in the advanced lung adenocarcinoma( r = - 0. 206 ,P 〈 0.05 ). The overall survival of the patients with negative C-MYC were longer than the patients with positive C-MYC (21.00 vs 15. 00 months ; X2 = 10. 890, P 〈 0. 001 ). The overall survival of the patients with positive MXI1 were longer than the patients with negative MXI1 (21.00 vs 13.00 months; X2 = 15. 080, P 〈 0.001 ). Conclusion Abnormal expressions of C-MYC and MXI1 may be related to prognosis of advanced lung adenocarcinoma.
出处 《肿瘤基础与临床》 2017年第6期476-480,共5页 journal of basic and clinical oncology
关键词 C—MYC MXI1 晚期肺腺癌 免疫组化 C-MYC MXI1 advanced lung adenocarcinoma immunohistochemistry
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  • 1毛杰,海健,舒衡平,邬玉辉,欧慧英,罗沙阳,王守满.乳腺癌组织中Survivin和nm23蛋白的表达及其与腋淋巴结转移的关系[J].中南大学学报(医学版),2005,30(3):312-314. 被引量:5
  • 2Singh M, Bleile MJ, Shroyer AL, et al. Analysis of survivin expres- sion in a spectrum of benign to malignant lesions of the breast[J]. ADD1 Immunohistochem Mol Morohol,2004. 12(4): 296-304.
  • 3A1-Joudi FS, Iskandar ZA. Autoantibodies to survivin in the sera of patients with infiltrating ductal carcinoma of the breast[J]. Med J Malaysia, 2006, 61 (3): 302-306.
  • 4Pennati M, Folini M, Zaffaroni N. Targeting survivin in cancer therapy: fulfilled promises and open questions[J]. Carcinogenesis, 2007, 28(6): 1133-1139.
  • 5宁连胜,方志沂,主泽.现代乳腺疾病治疗学[M].第二版.北京:人民卫生出版社,2007:59-61.
  • 6Kohlberger PD, Breitenecker F, Kaider A, et al. Modified true-color computer-assisted image analysis versus subjective scoring of estrogen receptor expression in breast cancer: a comparison[J]. Anticancer Res, 1999, 19(3B): 2189-2193.
  • 7Afify A, Purnell P, Nguyen L. Role of CD44s and CD44v6 on human breast cancer cell adhesion, migration, and invasion[J]. Exp Mol Pathol, 2009, 86(2): 95-100.
  • 8Ponta H, Sherman L, Herrlich PA. CD44: from adhesion molecules to signalling regulators[J]. Nat Rev Mol Cell BioI, 2003, 4(1): 33-45.
  • 9Kaufmann M, Heider KH, Sinn HP, et al. CD44 variant exon epitopes in primary breast cancer and length of survival[J]. Lancet, 1995, 345 (8950): 615-619.
  • 10Yu P, Zhou L, Ke W, et al. Clinical significance of pAKT and CD44v6 overexpression with breast cancer[J].J Cancer Res Clin Oncol, 2010,136(8): 1283-1292.

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