期刊文献+

miR-125b与浸润性乳腺癌研究进展 被引量:2

Research progress in roles of mi R-125b in invasive breast cancer
下载PDF
导出
摘要 微小RNA(micro RNAs)是一类重要的高度保守的内源性、非编码RNA,在转录后水平调节着基因的表达。micro RNAs的异常表达涉及肿瘤发生发展的各个过程,因具备成为肿瘤的生物学标志和治疗靶点的潜能而被广泛研究。在众多肿瘤细胞中,micro RNA-125b(mi R-125b)的异常表达被广泛证实,而研究相对深入的即为浸润性乳腺癌。作为在浸润性乳腺癌细胞系和在体肿瘤细胞中显著改变的micro RNA,学界对mi R-125b所担任的角色是抑癌基因还是促癌基因存在争论。在此笔者将概述现有关于mi R-125b在浸润性乳腺癌的发生、发展、诊断、预后及药物抗性中发挥的各类生物学作用。借此,更好的理解mi R-125b在浸润性乳腺癌基因网络中的角色,有助于探究mi R-125b在未来成为浸润性乳腺癌诊断标志或者治疗靶点的生物学前景,甚至探索其在肿瘤中的全部潜能。 MicroRNAs (miRNAs) are a critical class of evolutionarily conserved non-coding endogenous RNA molecules that regulate gene expression post-transcriptionally. Thousands of miRNAs are reported to play irreplaceable roles in normal cell homeostasis, cell metastasis and disease pathogensls and progression, and they have lately been widely studied due to their potential function as diagnostic biomarks and targets for cancer therapy. The link between miRNA-125b deregulation and many types of cancer has been validated, including invasive breast cancer. As a significant deregulated signature, miR-125b is reported to have paradoxical functions as either oncogene-like or tumor suppressor-like in invasive breast cancer or cell lines. In this review, we summarized the implication of miR-125b in various celluar biological activities including tumorigenesis, progression, diagnose, prognosis, chemoresistanc. Therefore, better understanding of miR-125b's role in gene network of invasive breast cancer may help exploit the potential of miR-125b in regards to cancer diagnosis, treatment, and chemoresistanc, even the full potential of miRNAs in all types of cancer.
出处 《中国现代医学杂志》 CAS 北大核心 2015年第13期48-53,共6页 China Journal of Modern Medicine
基金 中南大学研究生自主创新基金(No:2014zzts365)
关键词 MI R-125b 浸润性乳腺癌 病因学 治疗方法 miR-125b invasive breast cancer etiology therapy
  • 相关文献

参考文献32

  • 1BYLER S, GOLDGAR S, HEERBOTH S, et al. Genetic and epigenetic aspects of breast cancer progression and therapy[J]. Anticancer research, 2014, 34(3): 1071-1077.
  • 2SCOFF GK, GOGA A, BHAUMIK D, et al. Coordinate suppres- sion of ERBB2 and ERBB3 by enforced expression of mi- cro-RNA miR-125a or miR-125b[J]. The Journal of Biological Chemistry, 2007, 282(2): 1479-1486.
  • 3JIA HY, WANG YX, YAN WT, et al. MicroRNA-125b functions as a tumor suppressor in hepatocellular carcinoma cells[J]. Inter- national Journal of Molecular Sciences, 2012, 13(7): 8762-8774.
  • 4LIU LH, LI H, LI JP, et al. miR-125b suppresses the prolifera- tion and migration of osteosarcoma cells through down-regulation of STAT3[J]. Biochemical and Biophysical Research Communica- tions, 2011, 416(1-2): 31-38.
  • 5ZHANG H, LUO XQ, FENG DD, et al. Upregulation of microR- NA-125b contributes to leukemogenesis and increases drug resis- tance in pediatric acute promyelocytic leukemia [J]. Molecular Cancer, 2011, 10: 108.
  • 6OZEK NS, TUNA S, ERSON-BENSAN AE, et al. Characteriza- tion of microRNA-125b expression in MCF7 breast cancer cells by ATR-FTIR spectroscopy[J]. The Analyst, 2010, 135(12): 3094-3102.
  • 7MATTIE MD, BENZ CC, BOWERS J, et al. Optimized high-throughput microRNA expression profiling provides novel biomarker assessment of clinical prostate and breast cancer biop- sies[J]. Molecular Cancer, 2006, 5: 24.
  • 8BOCKMEYER CL, CHRISTGEN M, MULLER M, et al. MicroR- NA profiles of healthy basal and luminal mammary epithelial cells are distinct and reflected in different breast cancer subtypes [J]. Breast Cancer Research and Treatment, 2011, 130(3): 735-745.
  • 9LIU Z, LIU H, DESAI S, et al. miR-125b functions as a key mediator for snail-induced stem cell propagation and chemoresistance[J]. The Journal of Biological Chemistry, 2013, 288(6): 4334-4345.
  • 10ZHOU M, LIU Z, ZHAO Y, et al. MicmRNA-125b confers the resistance of breast cancer cells to paclitaxel through suppres- sion of pro-apoptotic Bcl-2 antagonist killer l(Bakl) expression [J]. The Journal of Biological Chemistry, 2010, 285(28): 21496- 21507.

二级参考文献41

  • 1Kovalchuk O, Filkowski J, Meservy J, et al. Involvement of microRNA-451 in resistance of the MCF-7 breast cancer cells to hemotherapeutic drug doxorubicin[J]. Mol Cancer Ther, 2008,7(7):2152-2159.
  • 2Xia L,Zhang D,Du R. miR-15b and miR-16 modulate muhidrug resistance by targetingBCL2 in human gastric cancer cells[J]. Int J Cancer, 2008,123 (2):372-379.
  • 3Zhu W,Shan X,Wang TS,et al. miR-181b modulates multidrug resistance by targeting BCL2 in human cancer cell lines[J ]. Int J Cancer, 2010,127(11) :2520-2529.
  • 4Li Y, Li W, Yang Y, et al. MicroRNA-21 targets LRRFIP1 and contributes to VM-26 resistance in glioblastoma multiforme[J]. Brain Res, 2009,1286(1 ) : 13-18.
  • 5Lippert TH,Ruoff HJ,Volm M. Intrinsic and acquired drug resistance in malignant tumors. The main reason for therapeutic failure [J]. Arzneimittelforschung, 2008,58 (6) :261-264.
  • 6Biedler JL, Riehm H. Cellular resistance to actinomycin D in Chinese hamster cells in vitro: cross-resistance, radioautographic, and cytogenetic studies[J]. Cancer Res, 1970, 30(4) : 1174-1184.
  • 7Rabik CA, Dolau ME. Molecular mechanisms of resistance and toxicity associated with platinating agents [J]. Cancer Treat Rev, 2007,33 ( 1 ) : 9-23.
  • 8Gottesman MM, Fojo T, Bates SE. Muhidrug resistance in cancer: role of ATP-dependent transporters [J]. Nat Rev Cancer, 2002,2 ( 1 ) : 48-58.
  • 9Johnstone RW,Ruefli AA,Lowe SW. Apoptosis:a link between cancer genetics and chemotherapy[J]. Ce11,2002,108 (2) : 153-164.
  • 10Wang X,Wang C,Qin YW,et al. Simultaneous suppression of muhidrug resistance and antiapoptotic cellular defense induces apoptosis in chemoresistant human acute myeloid leukemia cells [ J ]. Leuk Res, 2007,31 (7) : 989-994.

共引文献12

同被引文献10

引证文献2

二级引证文献5

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