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FoxM1、c-myc蛋白在基底细胞样型乳腺癌中的表达及其临床意义 被引量:3

Clinical significance of protein expressions of FoxM1 and c-myc in basal-like breast cancer
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摘要 目的 探讨FoxM1和c-myc蛋白在基底细胞样型乳腺癌(BLBC)、非基底细胞样型乳腺癌(non-BLBC)及癌旁正常乳腺组织中的表达情况及二者之间的相互关系.方法 采用免疫组织化学法检测66例BLBC及其癌旁正常乳腺组织、70例non-BLBC组织FoxM1和c-myc蛋白的表达情况,采用Spearman相关分析法分析其与病理临床特征的关系.结果 BLBC、non-BLBC及癌旁正常乳腺组织中FoxM1蛋白阳性表达率分别为77.3%(51/66)、60.0%(42/70)和13.6%(9/66),c-myc蛋白阳性表达率分别为71.2%(47/66)、54.3%(38/70)和22.7%(15/66),FoxM1和c-myc蛋白在BLBC和non-BLBC组织中表达率均明显高于癌旁正常乳腺组织,且在BLBC组织中的表达明显高于non-BLBC组织,差异均有统计学意义(均P< 0.05).在BLBC中FoxM1和c-myc蛋白表达呈正相关(r=0.294,P< 0.05),且FoxM1和c-myc蛋白的表达与BLBC淋巴结转移及临床分期有关(P<0.05).结论 FoxM1和c-myc蛋白参与了BLBC的发生、发展,并且FoxM1和c-myc蛋白有一定的协同作用. Objective To detect the protein expressions of FoxM1 and c-myc in basal-like breast carcinoma and explore their correlation.Methods The expression of FoxM1 and c-myc was detected in 66 cases of BLBC,70 cases of non-BLBC and 66 cases of normal adjacent breast tissue by immunohistochemistry.The relationship of them was analyzed.Rusults The expression rates of FoxM1 and c-myc protein in BLBC [77.3 % (51/66),71.2 % (47/66)] was significant increased than that in normal breast tissue [13.6 % (9/66),22.7 % (15/66)],and higher than that in non-BLBC [60.0 % (42/70),54.3 % (38/70)].The expression of FoxM1 and c-myc positively correlated with lymph nodes metastasis and TNM staging of BLBC (P 〈 0.05).Positive expressions correlation could be found between the expression of FoxM1 and that of c-myc as well (r =0.294,P 〈 0.05).Conclusion FoxM1 and c-myc may play important roles in the carcinogenesis and development of BLBC and the study supports the positive feedback effect between the expressions of FoxM1 and c-myc furthermore.
出处 《肿瘤研究与临床》 CAS 2013年第11期726-729,共4页 Cancer Research and Clinic
关键词 乳腺肿瘤 原癌基因蛋白质类 FOXM1 C-MYC 基底细胞样 肿瘤 Breast neoplasms Proto-oncogene proteins FoxM1 c-myc Basal cell like,neoplasms
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  • 1李昂,闫文生,梁启万,刘继红,王家祥,赵松,方嬿.应用寡核苷酸芯片鉴别肺鳞癌Ⅰb期特异相关基因[J].中华医学杂志,2005,85(37):2623-2628. 被引量:2
  • 2彭玉华,拉莱.苏祖克,陈文彬,古丽娜.库尔班.子宫颈上皮细胞癌变中树突状细胞分布、TNF-α、c-myc的表达及其临床意义[J].新疆医科大学学报,2006,29(7):576-579. 被引量:6
  • 3Danielle Queiroz Calcagno,Mariana Ferreira Leal,Aline Damaceno Seabra,Andre Salim Khayat,Elizabeth Suchi Chen,Samia Demachki,Paulo Pimentel Assumpcao,Mario Henrique Girao Faria,Silvia Helena Barem Rabenhorst,Márcia Valéria Pitombeira Ferreira,Marília de Arruda Cardoso Smith,Rommel Rodríguez Burbano.Interrelationship between chromosome 8 aneuploidy,C-MYC amplification and increased expression in individuals from northern Brazil with gastric adenocarcinoma[J].World Journal of Gastroenterology,2006,12(38):6207-6211. 被引量:9
  • 4Kalinichenko VV, Major ML, Wang X, et al. Foxmlb transcription factor is essential for development of hepatocellular carcinomas and is negatively regulated by the pl9ARF tumor suppressor. Genes Dev, 2004, 18: 830-850.
  • 5Madureira PA, Varshochi R, Constantinidou D, et al. The Forkhead box M1 protein regulates the transcription of the estrogen receptor alpha in breast cancer cells. J Biol Chem, 2006, 281: 25167-25176.
  • 6Liu M, Dai B, Kang SH, et al. FoxM1B is overexpressed in human glioblastomas and critically regulates the tumorigenicity of glioma cells. Cancer Res, 2006, 66 : 3593-3602.
  • 7Wang Z, Banerjee S, Kong D, et al. Down-regulation of Forkhead Box M1 transcription factor leads to the inhibition of invasion and angiogenesis of pancreatic cancer cells. Cancer Res, 2007, 67: 8293-8300.
  • 8Kim IM, Ackerson T, Ramakrishna S, et al. The Forkhead Box M1 transcription factor stimulates the proliferation of tumor cells during development of lung cancer. Cancer Res, 2006, 66 : 2153-2161.
  • 9Radhakrishnan SK, Bhat UG, Hughes DE, et al. Identification of a chemical inhibitor of the oncogenic transcription factor Forkhead Box M1. Cancer Res, 2006, 66: 9731-9735.
  • 10Gusarova GA, Wang IC, Major ML, et al. A cell-penetrating ARF peptide inhibitor of FoxM1 in mouse hepatocellular carcinoma treatment. Clin Invest, 2007, 117: 99-111.

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  • 1苗芳,李劲松.EZH2和Ki-67在胃癌中的表达及其临床意义[J].泰山医学院学报,2008,29(2):87-89. 被引量:6
  • 2于世风.口腔组织病理学[M].6版.北京.人民卫生出版社,2007:55-57.
  • 3Kim SS. Assessment of long term endocrine function after transplantion of frozen-thawed human ovarian tissue to the heterotopic site:10 year longitudinal follow-up study[J]. J Assist Reprod Genet, 2012, 29: 489- 493.
  • 4Bracken AP, Pasini D, Capra M, et al. EZH2 is down stream of the pRB-E2F pathway, essential for proliferation and amplified in cancer [J]. EMBO J, 2003, 22: 5323-5335.
  • 5Kleer CG, Cao Q, Varambally S, et al. EZH2 is a marker of aggressive breast cancer and promotes neoplastie transform at ion of breast epithelial cells [J]. Proc Nad Acad Sci U S A, 2003, 100: 11606- 11611.
  • 6杨学财,尚伟,钟凤,等.PLAU基因变异与舌癌的关系研究[J].肿瘤研究与临床,2012,24:259-261.
  • 7Fan L,Strasser-Weippl K,Li JJ,et al.Breast cancer in China[J].Lancet Oncol,2014,15(7):e279-e289.
  • 8Kalinina OA,Kalinin SA,Polack EW,et al.Sustained hepatic expression of FoxM1Bin transgenic mice has minimal effects on hepatocellular carcinoma development but increases cell proliferation rates in preneoplastic and early neoplastic lesions[J].Oncogene,2003,22(40):6266-6276.
  • 9Wang Z,Ahmad A,Li Y,et al.Forkhead box M1transcription factor:a novel target for cancer therapy[J].Cancer Treat Rev,2010,36(2):151-156.
  • 10Semenza GL,Wang GL.A nuclear factor induced by hypoxia via de novo protein synthesis binds to the human erythropoietin gene enhancer at a site required for transcriptional activation[J].Mol cell Biol,1992,12(12):5447-5454.

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