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研究生: 陳國庭
Kuo-Ting Chen
論文名稱: 錸(I)-188三羰基標誌Trastuzumab單株抗體作為乳癌造影及治療劑之研究
Study on [188]Re(I)-Tricarbonyl Labeled Trastuzumab Monoclonal Antibody as Imaging and Therapeutic Agent for Breast Cancer with HER2-overexpression
指導教授: 羅建苗
Jem-Mau Lo
李德偉
Te-Wei Lee
口試委員:
學位類別: 碩士
Master
系所名稱: 原子科學院 - 生醫工程與環境科學系
Department of Biomedical Engineering and Environmental Sciences
論文出版年: 2007
畢業學年度: 95
語文別: 中文
論文頁數: 71
中文關鍵詞: 錸-188單株抗體
相關次數: 點閱:1下載:0
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  • Herceptin®是近年來常見的抗乳癌藥物,其中的主成分trastuzumab抗體是一種經過基因重組的人類化單株抗體 (humanized monoclonal antibody),其Fab端能辨識HER2,可取代生長因子結合HER2,終止其激酶信號功能,而抑制腫瘤細胞的分化與增生,臨床上用來治療有HER2大量表現的人類乳癌。
    錸-188的半衰期長達16.9小時,且能釋放高能的β-粒子 (2.12MeV)及高解析度的γ射線 (0.155MeV),用來標誌單株抗體,可兼具放射免疫治療及放射免疫造影之功效。本研究發展出新的錸-188標誌方式,先以無機化學合成方法在水相中製備錸-188(I)-三羰基離子,[188Re(OH2)3(CO)3]+,再將放射性核種錸-188標誌於trastuzumab單株抗體,作為HER2過量表現乳癌之造影及治療劑。
    在本實驗中,以高效能液相層析法、分子大小排阻層析法及蛋白質去性沉澱法測試188Re(I)-trastuzumab的標誌效率及穩定度。並將188Re(I)-trastuzumab注入植有BT-474 (大量表現HER2)或MCF-7 (低表現HER2)腫瘤細胞的實驗裸鼠,經生物分佈及藥物動力學的分析,證實188Re(I)-trastuzumab保有trastuzumab本身的藥物專一性及活性。在SPECT/CT造影的實驗中,188Re(I)-trastuzumab因為與HER2有高度的親和力,使放射性標誌藥物能累積在BT-474腫瘤中,使之顯影。然而,將188Re(I)-trastuzumab注入已植有MCF-7腫瘤的實驗裸鼠,放射性藥物累積於腫瘤的量相對較低,亦無SPECT/CT之顯影。由此研究所得結果可推論188Re(I)-trastuzumab在未來有發展為放射免疫治療藥物之潛力。


    Trastuzumab (Herceptin®), a humanized IgG1 monoclonal antibody directed against the extracellular domain of the HER2 protein, acts as an immunotherapeutic agent for HER2-overexpressing human breast cancers. In this study, 188Re, an emitter with 2.12MeV β- and 0.155MeV γ and t1/2 = 16.9h, was labeled to trastuzumab aiming for radioimmunotherapy of HER2/neu-positive breast cancer. The 188Re(I)-tricarbonyl ion, [188Re(OH2)3(CO)3]+, was employed as a precursor for direct labeling 188Re to the monoclonal antibody. The resultant 188Re(I)-trastuzumab was found to be very stable even challenging with histidine. The tumor and normal tissues localization properties of 188Re(I)-trastuzumab in athymic mice bearing BT-474 human breast cancer xenografts (HER2/neu-overexpressing) and bearing MCF-7 human breast cancer xenografts (HER2/neu-low expressing) were investigated. The in vivo biodistribution study demonstrated that 188Re(I)-trastuzumab was specifically accumulated in BT-474 tumor and the image of 188Re localized BT-474 tumor was clearly visualized within the useful lifetime of the radionuclide. By contrast, the 188Re(I)-trastuzumab uptakes in HER2-low expressing MCF-7 tumor was minimal so that the 188Re image localized at the tumor was not seen. It is revealed from the imaging study that 188Re(I)-trastuzumab may be a potential radioimmunotherapeutic agent for treatment of HER2/neu-overexpressing cancers.

    第一章、緒論 1.1 放射性分子影像藥物 1.2 放射免疫治療 1.3 ErbB家族及HER2 1.4 Herceptin® 1.5 [188Re(CO)3(OH2)3]+標誌 第二章、實驗材料與方法 2.1 試藥與耗材 2.2 儀器 2.3 [186Re(CO)3(OH2)3]及[188Re(CO)3(OH2)3]+之合成及特性分析 2.3.1 合成步驟 2.3.2 [186Re(CO)3(OH2)3]及[188Re(CO)3(OH2)3]+之分析 2.3.3反應中加入四氫硼酸鹽交換樹脂 2.4 Trastuzumab抗體之純化與定量 2.4.1 實驗步驟 2.5 [188Re(CO)3(OH2)3]+標誌trastuzumab 2.5.1 標誌步驟 2.5.2 188Re(I)-trastuzumab之分析 2.6 [99mTc(CO)3(OH2)3]+標誌trastuzumab 2.7 131I標誌trastuzumab 2.8 活體外實驗 2.8.1 原理 2.8.1.1 細胞受器親和力 2.8.1.2 細胞受器親和力競爭實驗方法 2.8.2 188Re(I)-/ 99mTc(I)-trastuzumab與BT-474細胞受器親和力實驗 2.8.3 188Re(I)-/ 99mTc(I)-trastuzumab與BT-474細胞受器結合競爭實驗 2.9 實驗動物腫瘤模式 2.10 生物分佈 2.11 動物造影 第三章、結果與討論 3.1 [188Re(CO)3(OH2)3]+之製備 3.1.1 反應條件之討論 3.1.2 [188Re(CO)3(OH2)3]+之穩定度 3.1.3 [188Re(CO)3(OH2)3]+與組胺酸配位鍵結合 3.1.4 四氫硼酸陰離子交換樹脂之使用 3.1.5 最佳[188Re(CO)3(OH2)3]+之製備條件 3.2 [188Re(CO)3(OH2)3]+標誌trastuzumab 3.2.1 Trastuzumab抗體之純化與定量 3.2.2 標誌反應條件 3.2.3 188Re(I)-trastuzumab之純化 3.2.4 188Re(I)-trastuzumab之穩定度 3.2.5 188Re(I)-trastuzumab標誌過程中之輻射分解 3.2.6 最佳188Re(I)-trastuzumab之製備條件 3.3 188Re(I)-trastuzumab對HER2之親和力 3.3.1 131I標誌trastuzumab測試藥物活性 3.3.2 188Re(I)-/ 99mTc(I)-trastuzumab之細胞飽和實驗 3.3.3 188Re(I)-/ 99mTc(I)-trastuzumab之細胞競爭實驗 3.3.4 188Re(I)-trastuzumab之特異性鍵結 3.3.5 188Re(I)-trastuzumab對BT-474之親和力 3.4 188Re(I)-trastuzumab之生物分佈及造影 3.4.1 動物模式建立 3.4.2 188Re(I)-trastuzumab之生物分佈 3.4.3 188Re(I)-trastuzumab之SPECT/CT造影 3.4.4 188Re(I)-trastuzumab於動物活體中之藥物動力學 3.4.5 188Re(I)-trastuzumab於生物活體中之特性 第四章、結論 第五章、參考文獻

    1. Goldenberg DM. Targeted therapy of cancer with radiolabeled antibodies. J Nucl Med. May 2002;43(5):693-713.

    2. John E, Wilder S, Thakur ML. Structural perturbations of monoclonal antibodies following radiolabelling: in vitro evaluation of different techniques. Nuclear medicine communications. Jan 1994;15(1):24-28.

    3. Park SH, Seifert S, Pietzsch HJ. Novel and efficient preparation of precursor [188Re(OH2)3(CO)3]+ for the labeling of biomolecules. Bioconjugate chemistry. Jan-Feb 2006;17(1):223-225.

    4. Koppe MJ, Bleichrodt RP, Soede AC, et al. Biodistribution and therapeutic efficacy of 125/131I-, 186Re-, 88/90Y-, or 177Lu-labeled monoclonal antibody MN-14 to carcinoembryonic antigen in mice with small peritoneal metastases of colorectal origin. J Nucl Med. Jul 2004;45(7):1224-1232.

    5. Tang Y, Scollard D, Chen P, Wang J, Holloway C, Reilly RM. Imaging of HER2/neu expression in BT-474 human breast cancer xenografts in athymic mice using [99mTc]-HYNIC-trastuzumab (Herceptin) Fab fragments. Nuclear medicine communications. May 2005;26(5):427-432.

    6. Lehmann J, Denardo GL, Yuan A, et al. Comparison of normal tissue pharmacokinetics with 111In/90Y monoclonal antibody m170 for breast and prostate cancer. International journal of radiation oncology, biology, physics. Nov 15 2006;66(4):1192-1198.

    7. Tang Y, Wang J, Scollard DA, et al. Imaging of HER2/neu-positive BT-474 human breast cancer xenografts in athymic mice using 111In-trastuzumab (Herceptin) Fab fragments. Nuclear medicine and biology. Jan 2005;32(1):51-58.

    8. Smith-Jones PM, Solit DB, Akhurst T, Afroze F, Rosen N, Larson SM. Imaging the pharmacodynamics of HER2 degradation in response to Hsp90 inhibitors. Nature biotechnology. Jun 2004;22(6):701-706.

    9. Adams GP, Weiner LM. Monoclonal antibody therapy of cancer. Nature biotechnology. Sep 2005;23(9):1147-1157.

    10. Harris M. Monoclonal antibodies as therapeutic agents for cancer. Lancet Oncol. May 2004;5(5):292-302.

    11. Hynes NE, Lane HA. ERBB receptors and cancer: the complexity of targeted inhibitors. Nat Rev Cancer. May 2005;5(5):341-354.

    12. Yarden Y, Sliwkowski MX. Untangling the ErbB signalling network. Nat Rev Mol Cell Biol. Feb 2001;2(2):127-137.

    13. Blume-Jensen P, Hunter T. Oncogenic kinase signalling. Nature. May 17 2001;411(6835):355-365.

    14. Gschwind A, Fischer OM, Ullrich A. The discovery of receptor tyrosine kinases: targets for cancer therapy. Nat Rev Cancer. May 2004;4(5):361-370.

    15. Cho HS, Mason K, Ramyar KX, et al. Structure of the extracellular region of HER2 alone and in complex with the Herceptin Fab. Nature. Feb 13 2003;421(6924):756-760.

    16. Plosker GL, Keam SJ. Trastuzumab: a review of its use in the management of HER2-positive metastatic and early-stage breast cancer. Drugs. 2006;66(4):449-475.

    17. Carter P, Presta L, Gorman CM, et al. Humanization of an anti-p185HER2 antibody for human cancer therapy. Proceedings of the National Academy of Sciences of the United States of America. May 15 1992;89(10):4285-4289.

    18. Borchardt PE, Yuan RR, Miederer M, McDevitt MR, Scheinberg DA. Targeted actinium-225 in vivo generators for therapy of ovarian cancer. Cancer research. Aug 15 2003;63(16):5084-5090.

    19. Li G, Wang Y, Huang K, Zhang H, Peng W, Zhang C. The experimental study on the radioimmunotherapy of the nasopharyngeal carcinoma overexpressing HER2/neu in nude mice model with intratumoral injection of 188Re-herceptin. Nuclear medicine and biology. Jan 2005;32(1):59-65.

    20. He J, Liu C, Vanderheyden JL, et al. Radiolabelling morpholinos with 188Re tricarbonyl provides improved in vitro and in vivo stability to re-oxidation. Nuclear medicine communications. Jul 2004;25(7):731-736.

    21. Schibli R, Katti KV, Higginbotham C, Volkert WA, Alberto R. In vitro and in vivo evaluation of bidentate, water-soluble phosphine ligands as anchor groups for the organometallic fac-[99mTc(CO)3]+-core. Nuclear medicine and biology. Aug 1999;26(6):711-716.

    22. Schibli R, Schwarzbach R, Alberto R, et al. Steps toward high specific activity labeling of biomolecules for therapeutic application: preparation of precursor [(188)Re(H(2)O)(3)(CO)(3)](+) and synthesis of tailor-made bifunctional ligand systems. Bioconjugate chemistry. Jul-Aug 2002;13(4):750-756.

    23. Mayfield S, Vaughn JP, Kute TE. DNA strand breaks and cell cycle perturbation in herceptin treated breast cancer cell lines. Breast cancer research and treatment. Nov 2001;70(2):123-129.

    24. Eckelman WC, Mathis CA. Targeting proteins in vivo: in vitro guidelines. Nuclear medicine and biology. Feb 2006;33(2):161-164.

    25. Lin WY, Tsai SC, Hsieh BT, Lee TW, Ting G, Wang SJ. Evaluation of three rhenium-188 candidates for intravascular radiation therapy with liquid-filled balloons to prevent restenosis. J Nucl Cardiol. Jan-Feb 2000;7(1):37-42.

    26. Palm S, Enmon RM, Jr., Matei C, et al. Pharmacokinetics and Biodistribution of 86Y-Trastuzumab for 90Y dosimetry in an ovarian carcinoma model: correlative MicroPET and MRI. J Nucl Med. Jul 2003;44(7):1148-1155.

    27.顏肇良,鎝99m(I)標誌Trastuzumab單株抗體作為乳癌細胞造影劑之研究,國立清華大學碩士論文,2006。

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