乳腺癌的基因治疗与核素靶向治疗

宋进华

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乳腺癌的基因治疗与核素靶向治疗

    作者简介: 宋进华(1976-),男,住院医师,硕士研究生,主要从事核素治疗的研究。;
  • 基金项目:

    国家自然科学基金资助项目(30070229)

  • 中图分类号: R817.5

Gene therapy and radionuclides targeting therapy in mammary carcinoma

  • CLC number: R817.5

  • 摘要: 乳腺癌的基因治疗是近年来肿瘤治疗研究的热点,目前处于实验或临床初步应用的基因治疗方法主要有免疫基因治疗、多药耐药基因治疗、反义寡核苷酸治疗、自杀基因治疗等方法,而将基因治疗与射核素相结合的基因靶向近距离放射治疗的方法具有放射性核素与自杀基因对肿瘤细胞的双重杀灭作用,为肿瘤基因治疗开辟了一条崭新的途径,在这一领域进一步研究必将加快基因靶向治疗向临床应用迈进的步伐。
  • [1] Amornmarn R, Bui MM. Molecular predictive factors for local recurrence and distant metastasis of breast cancer after lumpectomy with postoperative radiation therapy[J]. Ann Clin Labo Sci, 2000, 30(1):33-40.
    [2] Kurihara T, Brough DE, Kovesdi I, et al. Selectivity of a replication-competent adenovirus for human breast carcinoma cells expressing the MUC1 antige[J]. Journal Clin Invest,2000, 106(6):763-771.
    [3] Indraccolo S, Cola E, Rosato A, et al. Differential effects of angiostatin endostatin and interferon-alpha(1) gene transfer on in vivo growth of human breast cancer cells[J]. Gene Therapy, 2002, 9(13):867-878.
    [4] Lichtor T, Moser R, Cohen EP. Immunogene therapy with interleukin-2-secreting fibroblasts for intracerebrally metastasizing breast cancer in mice[J]. J Neurosurg, 2001, 94(2):287-292.
    [5] Obermiller PS, Tait DL, Holt JT. Gene therapy for carcinoma of the breast:Therapeutic genetic correction strategies[J]. Breast Cancer Res, 2000, 2(1):28-31.
    [6] Lesoom, Wood LA, Kim WH, et al. Systemic gene therapy with p53 reduces growth and metastastase so famalignant human breast cancer in nude mice[J]. Hum Gene Ther,1995, 6(4):39-52.
    [7] Wang SC, Zhang L, Hortobagyi GN, et al. Targeting HER2:recent developments and future directions for breast cancer patients[J]. Semin Oncol, 2001, 28(6 Supp118):21-29.
    [8] Springer CJ, Niculescu-Duvazl I. Prodrug activating systems in suicide gene theraphy[J]. J Clin Inves, 2000, 105(9):1161-1167.
    [9] Morimoto J, Otsuki Y. Suppression of murine mammary carcinoma growth and metastasis by HSVtk/GCV gene therapy using in vivo electroporation[J]. Cancer Gene Ther, 2002, 9(1):16-27.
    [10] Grignet-Debrus C, Cool V, Baudson N, et al. The role of cellular-and prodrug-associated factors in the bystander effect induced by the varicella zoster and herpes simplex viral thymidine kinases in suicide gene therapy[J]. Cancer Gene Ther, 2000, 7(11):1456-1468.
    [11] Balzarini J, Ostrowski T, Goslinski T, et al. Pronounced cytostatic activity and bystander effect of a novel series of fluorescent tricyclic acyclovir and ganciclovir derivatives in herpes simplex virus thymidine kinase gene-transduced tumor cell lines[J]. Gene Ther, 2002, 9(17):1173-1182.
    [12] Guha C, Guha U, Tribius S, et al. Antisence ATM gene therapy:as trategy to increase the radios ensitivity of human tumors[J]. Gene Ther, 2000, 7(10):852-858.
    [13] Majumdar AS, Zolotorev A, Samuel S, et al. Efficacy of herpes simplex virus thymidine kinase in combination with cytokine gene therapy in an experimental metastatic breast cancer model[J]. Cancer Gene Ther, 2000,7(7):1086-1099.
    [14] Braiden V, Ohtsuru A, Kawashita Y, et al. Eradication of breast cancer xenografts by hyperthermic suicide gene therapy under the control of the heat shock protein promoter[J].Hum Gene Ther, 2000, 11(18):2453-2463.
    [15] Wu Q, Moyana T, Xiang J. Cancer gene therapy by adenovirus-mediated gene transfer[J]. Cur Gene Ther, 2001,1(1):101-122.
    [16] Vlachaki MT, Chhikara M, Aguilar L, et al. Enhanced therapeutic effect of multiple injections of HSV-TK+GCV gene therapy in combination with ionizing radiation in a mouse mammary tumor model[J]. Int J Radiat Oncol Biol Phys,2001, 51(4):1008-1017.
    [17] Larson SM, Tjuvajev J, Biasberg R. Triumph qver mischance:a role for nuclear medicine in gene theraphy[J]. J Nucl Med, 1997, 38:1230-1233.
    [18] Mairs R J, Cunningham SH, Boyd M, et al. Application sof gene transfer to targeted radiotherapy[J]. Curr Pharm Des,2000, 6(14):1419-1432.
    [19] Boland A, Ricard M, Opolon P, et al. Adenovirus-mediated transfer of the thyroid sodium/iodide symporter gene into tumors for a targeted radiotherapy[J]. Cancer Res, 2000, 60(13):3484-3492.
    [20] Larnmering G, Hewit TH. Epidermal growth factor receptor as a genetic therapy target for carcinoma cell radiosensitization[J]. J Nat Cancer Inst, 2001, 93(12):921-929.
    [21] Germann C, Shields AF, Griersion JR, et al. 5 Fluoro 1(2,deoxy 2, fluorobeta Dribofuranosyl) uraciil trapping in morris hepatoma cell sex pressing the herpes simple the herpes simplex virus thymid ine kinase gene[J]. J Nucl Med,1998, 39(8):1418-1423.
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    [10] 柳江燕陈雪红 . 肿瘤受体显像及介导靶向治疗的研究进展. 国际放射医学核医学杂志, 2005, 29(6): 258-260.
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  • 收稿日期:  2003-05-06

乳腺癌的基因治疗与核素靶向治疗

    作者简介:宋进华(1976-),男,住院医师,硕士研究生,主要从事核素治疗的研究。
  • 210009 南京, 东南大学医学院
基金项目:  国家自然科学基金资助项目(30070229)

摘要: 乳腺癌的基因治疗是近年来肿瘤治疗研究的热点,目前处于实验或临床初步应用的基因治疗方法主要有免疫基因治疗、多药耐药基因治疗、反义寡核苷酸治疗、自杀基因治疗等方法,而将基因治疗与射核素相结合的基因靶向近距离放射治疗的方法具有放射性核素与自杀基因对肿瘤细胞的双重杀灭作用,为肿瘤基因治疗开辟了一条崭新的途径,在这一领域进一步研究必将加快基因靶向治疗向临床应用迈进的步伐。

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