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前列腺癌神经生长因子受体TrkA/p75NTR比值与临床分期、分级的关系 被引量:2

Expression ratio of the nerve growth factor receptor Trk A to p75NTR correlates with the clinical stage and pathological grade of prostate cancer
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摘要 目的:探讨神经生长因子(NGF)的两种受体(TrkA和p75NTR)在前列腺癌(PCa)发生、发展中的表达规律及作用机制。方法:采用免疫组化法研究62例PCa和35例良性前列腺增生(BPH)组织中TrkA及p75NTR蛋白的表达,并结合临床资料进行统计分析。结果:通过成组t检验,发现自BPH组织至低分化PCa组织(Gleason 8~10分),随着组织分化逐渐降低或临床分期逐渐增高,TrkA受体表达显著增强,p75NTR受体表达显著减低,TrkA/p75NTR比例显著增大。在BPH组织中两者比例为0.32,在Gleason评分6分的PCa组织中为0.52,在7分的组织中为1.65,而在8~10分的组织中为5.75;在pT2期组织中两者比例为0.89,在pT3a期为1.5,在pT3b期为3.75,在有淋巴结转移(pTxN1)的组织中为7.00。结论:TrkA/p75NTR比例的失调性增高,可能是前列腺细胞恶变后的基本特征之一。TrkA/p75NTR比值越高,组织分化程度越低,临床分级、分期越高,患者预后可能越差。 Objective: To investigate the expressions and action mechanisms of nerve growth factor (NGF) receptors TrkA and p75NTR in the oncogenesis and progression of prostate cancer (PCa). Methods: Using immunohistochemistry, we detected the expressions of TrkA and p75NTR in 62 PCa and 35 benign prostatic hyperplasia (BPH) samples, and conducted statistical analysis on the basis of clinical data. Results: Independent-samples t-test showed that, along with poorer tissue differentiation or higher clinical stage of PCa, the expression of TrkA was significantly up-regulated, that of p75NTR remarkably down-regulated, and the expression ra- tio of TrkA to p75NTR markedly increased. The TrkA/p75NTR ratio was 0.32 in the BPH, 0.52 in the PCa tissue with Gleason score of 6, 1.65 in the PCa tissue with Gleason score of 7, 5.75 in the PCa tissue with Gleason score ≥8, 0.89 in the clinical stage of pT2, 1.5 in pT3a, 3.75 in pT3b, and 7.00 in pTxN1. Conclusion : The abnormally increased expression ratio of TrkA to p75NTR might be one of the essential features of malignant transformation of prostate cells. A higher TrkA/p75NTR expression ratio may be associated with a lower tissue differentiation, a higher clinical stage or Gleason score, and therefore a poorer prognosis.
出处 《中华男科学杂志》 CAS CSCD 北大核心 2015年第11期982-987,共6页 National Journal of Andrology
关键词 前列腺癌 TRKA P75NTR 临床分期 GLEASON评分 prostate cancer TrkA p75 NTR clinical stage Gleason score
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参考文献16

  • 1Levi-Montalcini R. The nerve growth factor 35 years later. Sci- ence, 1987, 237 (4819): 1154-1162.
  • 2Micera A, Lambiase A, Aloe L, et al. Nerve growth factm" in- volvement in the visual system: Implications in allergic and neu- rodegenerative diseases. Cytokine Growth Factor Rev, 2004, 15 (6): 411-417.
  • 3Wehrman T, He X, Raab B, et al. Structural and mechanisticinsights into nerve growth factor interactions with the TrkA and p75 receptors. Neuron, 2007, 53 ( 1 ) : 25-38.
  • 4Sofroniew MV, Howe CL, Mobley WC. Nerve growth factor sig- naling, neuroprotection, and neural repair. Annu Rev Neurosei, 2001, 24(1) :1217-1281.
  • 5Liu F, Xuan A, Chen Y, et al. Combined effect of nerve growth factor and brain derived neurotrophic factor on neuronal differen- tiation of neural stem cells and the potential molecular mecha- nisms. Mol Med Rep, 2014, 10(4) : 1739-1745.
  • 6Culmsee C, Gerling N, Lehmann M, et al. Nerve growth factor survival signaling in cultured hippocampal neurons is mediated through TrkA and requires the common neurotrophin receptor p75. Neuroseience, 2002, 115(4) : 1089-1108.
  • 7Molloy NH, Read DE, Gorman AM. Nerve growth factor in can- cer cell death and survival. Cancers, 2011, 3( 1 ) : 510-530.
  • 8lacaruso MF, Galli S, Marti M, et al. Structural model for p75 (NTR)-TrkA intracellular domain interaction: A combined FRET and bioinformatics study. J Mol Biol, 2011, 414 (5) : 681-698.
  • 9Bradshaw RA, Pundavela J, Biare J, et al. NGF and ProNGF: Regulation of neuronal and neoplastic responses through receptor signaling. Adv Biol Regul, 2015, 58(14) : 16-27.
  • 10Wang W, Chen J, Guo X. The role of nerve growth factor and itsreceptors in tumorigenesis and cancer pain. Biosci Trends, 2014, 8(2) : 68-74.

二级参考文献10

  • 1Buckley PF, Mahadik S, Pillai A, et al. Neurotrophins and schizophrenia. Schizophr Res, 2007, 94(1-3) : 1-11.
  • 2Miller LJ, Fischer KA, Goralnick SJ, et al. Nerve growth factor and chronic prostatitis/chronic pelvic pain syndrome. Urology, 2002, 59(4) : 603-608.
  • 3Montano X, Djamgoz MB. Epidermal growth factor, neurotrophins and the metastatic cascade in prostate cancer. FEBS Lett, 2004, 571(1-3): 1-8.
  • 4Papatsoris AG, Liolitsa D, Deliveliotis C. Manipulation of the nerve growth factor network in prostate cancer. Expert Opin lnvestig Drugs, 2007, 16(3) : 303-309.
  • 5SigMa S, Bodei S, Missale C, et al. Gene expression profile of prostate cancer cell lines : Effect of nerve growth factor treatment. Mol Cell Endocrinol, 2008, 284(1-2) : 11-20.
  • 6Groth R, Aanonsen L. Spinal brain-derived neurotrophic factor (BDNF) produces hyperalgesia in normal mice while antisense directed against either BDNF or trkB, prevent inflammation- induced hyperalgesia. Pain, 2002, 100(1-2): 171-181.
  • 7Festuccia C, Muzi P, Gravina GL, et al. Tyrosine kinase inhibitor CEP-701 blocks the NTRK1/NGF receptor and limits the invasive capability of prostate cancer cells in vitro. Int J Oncol, 2007, 30(1) : 193-200.
  • 8Bronzetti E, Artico M, Forte F, et al. A possible role of BDNF in prostate cancer detection. Oncol Rep, 2008, 19 ( 4 ) : 969- 974.
  • 9Missale C, Boroni F, Losa M, et al. Nerve growth factor suppresses the transforming phenotype of human prolactinomas. Proc Natl Acad Sci U S A, 1993, 90(17) : 7961-7965.
  • 10陈昌杰.神经生长因子及其受体在前列腺癌中的表达[J].四川解剖学杂志,2007,15(4):6-8. 被引量:4

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