期刊文献+

C-ERBB2和MYC mRNA基因表达水平在乳腺癌诊断的临床应用 被引量:3

The Clinical Application of C-ERBB2 and MYC mRNA Expressions in Diagnosis of Breast Carcinoma
下载PDF
导出
摘要 目的采用逆转录聚合酶链反应(RT-PCR)检测C-ERBB2和核内原癌基因(c-MYC)在外周血循环肿瘤细胞(circulating tumor cell,CTC)的表达,探讨其在乳腺癌诊断中的应用。方法以β2-actin为内对照,采用RT-PCR检测40例健康体检者、79例乳腺癌、66例良性乳腺疾病和51例其它肿瘤患者外周血CTCs中C-ERBB2和MYC mRNA表达水平。结果外周血CTCs中C-ERBB2和MYC在乳腺癌组和良性乳腺疾病组的表达率比较,差异有统计学意义;在乳腺癌组和其它肿瘤组表达率比较,差异有统计学意义;而良性乳腺疾病组和其它肿瘤组的表达率比较,差异无统计学意义。C-ERBB2和MYC联合检测,可提高对乳腺癌诊断的灵敏度、特异性和一致率。结论 RT-PCR联合检测外周血CTCs的C-ERBB2和MYC基因表达水平,可提高对乳腺癌诊断的特异性,具有操作简便、价格便宜和标本来源容易等优点,可有效辅助诊断乳腺癌。 Objective To explore the clinical application of the expressions of C-ERBB2 and MYC in CTCs in diagnosis of breast carcinoma according to detecting the C-ERBB2 and c-MYC mRNA expressions in the circulating tumor cells by RT-PCR.Methods In internal contrast withβ2-action,the significant differences of the expressions of C-ERBB2 and MYC among the 40-health-people group,the 79-breast-carcinoma group,the 66-benign-breast-disease group and the 51-other-carcinoma group were detected by the RT-PCR.Results 1)There was significant difference in the expression rates of C-ERBB2 and MYC between breast-carcinoma group and the benign disease group;2)There was significant difference in the expression rates of those between the breast-carcinoma group and othercarcinoma group;3)There was no difference of those expression rates between the benign-breast-disease group and the other-carcinoma group.The sensitivity,specificity and concordance rate were improved by combining detection of C-ERBB2 and MYC.Conclusion The specificity of RT-PCR to diagnose the breast cancer can be improved by combining with the detection of the expressions of C-ERBB2 and MYC in CTCs.This combination also can be a useful back-up in diagnosis of the breast cancer because of some advantages,like simple operation,low price,easy sample source and so on.
出处 《成都医学院学报》 CAS 2014年第6期683-685,共3页 Journal of Chengdu Medical College
基金 四川省杰出青年基金资助项目(NO:2007-5-345)
关键词 C-ERBB2 MYC 乳腺癌 RT-PCR C-ERBB2 MYC Breast carcinoma RT-PCR
  • 相关文献

参考文献7

二级参考文献57

  • 1Pantel K, Brakenhoff RH. Dissecting the metastastic cascade [J] Nat Rev Cancer,2004,4(6) :448-456.
  • 2Lianidou ES,Markou A. Circulating tumor cells in breast canc- er : detection systems, molecular characterization, and future chal- lenges[J]. Clin Chem,2011,57(9) :1242-1255.
  • 3Marrinucci D,Bethel K,Bruce RH,et al. Case study of the mor- phologic variation of circulating tumor cells[J]. Hum Pathol, 2007,38(3) 514-519.
  • 4Meng SD, Tripathy D,Frenkel EP, et al. Circulating tumor cells in patients with breast cancer dormancy[J]. Clin Cancer Res, 2004,10(24) :8152-8162.
  • 5Chang YS,di Tomaso E,McDonald DM,et al. Mosaic blood ves- sels in tumors; frequency of cancer cells in contact with flowing blood[J],Proc Natl Acad Sci U S A,2000,97(26) : 14608-14613.
  • 6Glinsky V,Glinsky GV, Glinskii OV, et al. Intravascular meta- static cancer cell homotypic aggregation at the sites ot" primary attachment to the endothelium[J]. Cancer Res, 2003,63 (13)3805-3811.
  • 7Mfihes G, Witt A, Kubista E, et al. Circulating breast cancer cells are frequently apoptotie[J]. Am J Pathol,2001,159(1) 17-20.
  • 8Rossi E,Basso U,Celadin R, et al. M30 meoepitope expression in epithelial cancer: quantification of apoptosis in circulating tumor cells by cell search analysis[J]. Clin Cancer Res, 2010, 16(21) :5233-5243.
  • 9Miiller V, Stahmann N, Riethdorf S, et al. Circulating tumor cells in breast cancer:correlation to bone marrow micrometastases,heteroge- neous response to systemic therapy and low proliferative activity[J]. Clin Cancer Res,2005,11(10) :3678-3685.
  • 10Aktas B,Mtiller V,Tewes M,et al. Comparison of estrogen and progesterone receptor status of circulating tumor ceils and the primary tumor in metastatic breast cancer patients[J]. Gyneeol Oncol, 2011,122(2) : 356-360.

共引文献16

同被引文献33

  • 1Hofman J, Skarka A, Havrankova J, et al. Pharmacokinetic interactions of breast cancer chemotherapeutics with human doxorubicin reductases [J]. Biochem Pharmacol, 2015, 96(3) 168-178.
  • 2Kim KY, Kim SH, Yu SN, et al. Salinomycin enhances doxo- rubicin induced cytotoxicity in multidrug resistant MCF-7/ MDR human breast cancer cells via decreased efflux of doxoru- bicin [J]. Mol MedRep, 2015, 12(2) :1898-1904.
  • 3Lv J, Xia K, Xu P, et al. miRNA expression patterns in che- moresistant breast cancer tissues [J]. Biomed Pharmacother, 2014, 68(8) :935-942.
  • 4Achari C, Winslow S, Ceder Y, et al. Expression of miR-34c induces G2/M cell cycle arrest in breast cancer ceils [ [J]. BMC Cancer, 2014, 26(14): 538.
  • 5Navarro F, Lieberman J. miR-34 and p53: New Insights into a Complex Functional Relationship [J]. PLoS One, 2015, 10 (7) :e0132767.
  • 6Xiang S, Dauchy RT, Hauch A, et al. Doxorubicin resistance in breast cancer is driven by light at night induced disruption of the circadian melatonin signal [J]. J Pineal Res, 2015, 59 (1) 60-69.
  • 7Gezer U, Keskin S, I ci A, et al. Abundant circulating mi- croRNAs in breast cancer patients fluctuate considerably during neoadjuvant chemotherapy[J]. Oncol Lett, 2014, 8 (2) : 845- 848.
  • 8Medimegh I, Omrane I, Privat M, et al. MicroRNAs expres-sion in triple negative vs non triple negative breast cancer in Tunisia.. interaction with clinical outcome [J]. PLoS One, 2014, 9(11):e111877.
  • 9Li R, Shi X, Ling F, et al. MiR 34a suppresses ovarian cancer proliferation and motility by targeting AXL[J]. Tumour Biol, 2015, 36(9):7277- 7283.
  • 10Stahlhut C, Slack FJ. Combinatorial Action of MicroRNAs let- 7 and miR-34 Effectively Synergizes with Erlotinib to Suppress Non-small Cell Lung Cancer Cell Proliferation[J]. Cell Cycle, 2015, 14(13) :2171-2180.

引证文献3

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部