留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码
x

阿片受体及其药物与乳腺癌的关系的研究进展

周成茂 刘震 阮林

周成茂, 刘震, 阮林. 阿片受体及其药物与乳腺癌的关系的研究进展[J]. 分子影像学杂志, 2015, 38(4): 420-421. doi: 10.3969/j.issn.1674-4500.2015.04.35
引用本文: 周成茂, 刘震, 阮林. 阿片受体及其药物与乳腺癌的关系的研究进展[J]. 分子影像学杂志, 2015, 38(4): 420-421. doi: 10.3969/j.issn.1674-4500.2015.04.35
Chengmao Zhou, Zhen Liu, Lin Ruan. Advances in the Relationship between opioid drug and its receptor and breast cancer[J]. Journal of Molecular Imaging, 2015, 38(4): 420-421. doi: 10.3969/j.issn.1674-4500.2015.04.35
Citation: Chengmao Zhou, Zhen Liu, Lin Ruan. Advances in the Relationship between opioid drug and its receptor and breast cancer[J]. Journal of Molecular Imaging, 2015, 38(4): 420-421. doi: 10.3969/j.issn.1674-4500.2015.04.35

阿片受体及其药物与乳腺癌的关系的研究进展

doi: 10.3969/j.issn.1674-4500.2015.04.35
详细信息
    作者简介:

    周成茂,在读硕士研究生,E-mail: 564099474@qq.com

    通讯作者:

    阮林,博士研究生,主任医师,E-mail: RuanLin187@163.com

Advances in the Relationship between opioid drug and its receptor and breast cancer

  • 摘要: 阿片类药物是癌症患者常用的麻醉镇痛药,但有许多研究提示阿片受体及其药物与乳腺癌之间存在紧密关联。本文对阿片类药物对乳腺癌和阿片受体对乳腺癌以及μ阿片受体多态性A118G与乳腺癌的关系做一综述。

     

  • [1] 2012 G. IARC[C]//globocan.Lyon,France, 2013: 12-4.
    [2] 张敏璐, 黄哲宙, 郑莹. 中国2008年女性乳腺癌发病、死亡和患病情况的估计及预测[J]. 中华流行病学杂志, 2012, 33(10): 1049-51.
    [3] Satija A, Ahmed SM, Gupta R, et al. Breast Cancer pain management- A review of current & novel therapies[J]. Indian J Med Res, 2014, 139(2): 216-25.
    [4] Zagon IS, Mclaughlin PJ, Goodman SR, et al. Opioid receptors and endogenous opioids in diverse human and animal cancers[J]. J Natl Cancer Inst, 1987, 79(5): 1059-65.
    [5] Schreiber G, Campa MJ, Prabhakar S, et al. Molecular characterization of the human delta opioid receptor in lung Cancer[J]. Anticancer Res, 1998, 18(3A): 1787-92.
    [6] Scopsi L, Balslev E, Brunner N, et al. Immunoreactive opioid peptides in human breast Cancer[J]. Am J Pathol, 1989, 134(2): 473-9.
    [7] Gach K, Piestrzeniewicz M, Fichna J, et al. Opioid antagonist-induced regulation of the mu-opioid receptor expression in MCF-7 breast Cancer cell line[J]. Endocr Regul, 2009, 43(1): 23-8.
    [8] Gach K, Piestrzeniewicz M, Fichna JA, et al. Opioid-induced regulation of mu-opioid receptor gene expression in the MCF-7 breast Cancer cell line[J]. Biochem Cell Biol, 2008, 86(3): 217-26. doi: 10.1139/O08-001
    [9] Mclaughlin PJ, Zagon IS. Novel treatment for triple-negative breast and ovarian Cancer: endogenous opioid suppression of women's cancers[J]. Expert Rev Anticancer Ther, 2014, 14(3): 247-50. doi: 10.1586/14737140.2014.867234
    [10] Zagon IS, Porterfield NK, Mclaughlin PJ. Opioid growth factor - opioid growth factor receptor axis inhibits proliferation of triple negative breast Cancer[J]. Exp Biol Med (Maywood), 2013, 238 (6): 589-99. doi: 10.1177/1535370213489492
    [11] Hatzoglou A, Bakogeorgou E, Castanas E. The antiproliferative effect of opioid receptor agonists on the T47D human breast Cancer cell line,is partially mediated through opioid receptors[J]. Eur J Pharmacol, 1996, 296(2): 199-207. doi: 10.1016/0014-2999(95)00703-2
    [12] Afsharimani B, Baran JA, Watanabe SA, et al. Morphine and breast tumor metastasis: the role of matrix-degrading enzymes[J]. Clin Exp Metastasis, 2014, 31(2): 149-58. doi: 10.1007/s10585-013-9616-3
    [13] Doornebal CW, Vrijland K, Hau CS, et al. Morphine does not facilitate breast Cancer progression in two preclinical mouse models for invasive lobular and HER2+breast Cancer[J]. Pain, 2015(7): 85-8.
    [14] Ustun F, Durmus-Altun G, Altaner S, et al. Evaluation of morphine effect on tumour angiogenesis in mouse breast tumour model, EATC [J]. Med Oncol, 2011, 28(4): 1264-72. doi: 10.1007/s12032-010-9573-5
    [15] Ecimovic P, Murray D, Doran P, et al. Direct effect of morphine on breast Cancer cell function in vitro: role of the NET1 gene[J]. Br J Anaesth, 2011, 107(6): 916-23. doi: 10.1093/bja/aer259
    [16] Nguyen J, Luk K, Vang D, et al. Morphine stimulates Cancer progression and mast cell activation and impairs survival in transgenic mice with breast Cancer[J]. Br J Anaesth, 2014, 113(1, SI): 4-13. doi: 10.1093/bja/aeu013
    [17] Niu DG, Peng F, Zhang W, et al. Morphine promotes Cancer stem cell properties, contributing to chemoresistance in breast Cancer[J]. Oncotarget, 2015, 6(6): 3963-76. doi: 10.18632/oncotarget
    [18] Chou W, Wang C, Liu P, et al. Human opioid receptor A118G polymorphism affects intravenous patient-controlled analgesia morphine consumption after total abdominal hysterectomy[J]. Anesthesiology, 2006, 105(2): 334-7. doi: 10.1097/00000542-200608000-00016
    [19] De Gregori M, Diatchenko L, Belfer I, et al. OPRM1 receptor as new biomarker to help the prediction of post mastectomy pain and recurrence in breast cance[J]. Minerva Anestesiol, 2014(3): 63-5.
    [20] Bortsov AV, Millikan RC, Belfer IA, et al. mu-Opioid receptor gene a118G polymorphism predicts survival in patients with breast Cancer[J]. Anesthesiology, 2012, 116(4): 896-902. doi: 10.1097/ALN.0b013e31824b96a1
    [21] Cieslinska A, Sienkiewicz-Szlapka E, Kostyra E, et al. mu-Opioid receptor gene(OPRM1)polymorphism in patients with breast Cancer [J]. Tumour Biol, 2015(11): 125-7.
    [22] Tan EC, Tan CH, Karupathivan U, et al. Mu opioid receptor gene polymorphisms and heroin dependence in Asian populations[J]. Neuroreport, 2003, 14(4): 569-72. doi: 10.1097/00001756-200303240-00008
    [23] Smith JP, Bingaman SI, Mauger DT, et al. Opioid growth factor improves clinical benefit and survival in patients with advanced pancreatic Cancer[J]. Open Access J Clin Trials, 2010(2): 37-48
  • 加载中
计量
  • 文章访问数:  481
  • HTML全文浏览量:  200
  • PDF下载量:  2
  • 被引次数: 0
出版历程
  • 收稿日期:  2015-07-21
  • 刊出日期:  2015-12-01

目录

    /

    返回文章
    返回

    关于《分子影像学杂志》变更刊期通知

    各位专家、作者、读者:

    为了缩短出版时滞,促进科研成果的快速传播,我刊自2024年1月起,刊期由双月刊变更为月刊。本刊主要栏目有:基础研究、临床研究、技术方法、综述等。

    感谢各位专家、作者、读者长期以来对我刊的支持与厚爱!

    南方医科大学学报编辑部

    《分子影像学杂志》

    2023年12月27日