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báo cáo khoa học: In vivo Molecular targeting effects of anti-Sp17ICG-Der-02 on hepatocellular carcinoma evaluated by an optical imaging system
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Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: In vivo Molecular targeting effects of anti-Sp17ICG-Der-02 on hepatocellular carcinoma evaluated by an optical imaging system
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báo cáo khoa học: "In vivo Molecular targeting effects of anti-Sp17ICG-Der-02 on hepatocellular carcinoma evaluated by an optical imaging system"Li et al. Journal of Experimental & Clinical Cancer Research 2011, 30:25http://www.jeccr.com/content/30/1/25 RESEARCH Open AccessIn vivo Molecular targeting effects of anti-Sp17-ICG-Der-02 on hepatocellular carcinomaevaluated by an optical imaging systemFang-qiu Li1*, Shi-xin Zhang1, Lian-xiao An2, Yue-qing Gu2* Abstract Background: As the expression of human sperm protein 17 (Sp17) in normal tissue is limited and the function is obscure, its aberrant expression in malignant tumors makes it to be a candidated molecular marker for tumor imaging diagnosis and targeting therapy of the diseases.The aim of this research is to evaluate the targeting effects of anti-sperm protein 17 monoclonal antibody (anti-Sp17) on cancer in vivo and investigate its usefulness as a reagent for molecular imaging diagnosis. Methods: Immunohistochemistry was used to identify the expression of Sp17 in a hepatocellular carcinoma cell line and tumor xenograft specimens. A near infrared fluorescence dye, ICG-Der-02, was covalently linked to anti- Sp17 for in vivo imaging. The immuno-activity of the anti-Sp17-ICG-Der-02 complex was tested in vitro by ELISA; it was then injected into tumor-bearing nude mice through the caudal vein to evaluate its tumor targeting effect by near infrared imaging system. Results: Overexpression of Sp17 on the surface of the hepatocellular carcinoma cell line SMMC-7721 was demonstrated. Anti-Sp17-ICG-Der-02 with immuno-activity was successfully synthesized. The immuno-activity and photo stability of anti-Sp17- ICG-Der-02 showed good targeting capability for Sp17 expressing tumor models (SMMC-7721) in vivo, and its accumulation in the tumor lasted for at least 7 days. Conclusions: Anti-Sp17 antibody targeted and accumulated in Sp17 positive tumors in vivo, which demonstrated its capability of serving as a diagnostic reagent.Introduction recognition of early biomarker and anatomical changes before manifestation of gross pathological changes [3-6].Cancer remains one of the leading causes of death in The development of novel approaches for in vivo ima-the world. Despite advances in our understanding of ging and personalized treatment of cancers is urgentlymolecular and cancer biology, the discovery of cancer needed to find cancer-specific markers, but there is stillbiomarkers and the refinement of conventional surgical limited knowledge of suitable biomarkers.procedures, radiotherapy, and chemotherapy, the overall Sperm protein 17 (Sp17) was originally reported to besurvival rate from cancer has not significantly improved expressed exclusively in the testis. Its primary function isin the past two decades [1,2]. Early noninvasive detec- binding to the zona pellucida and playing a critical roletion and characterization of solid tumors is a fundamen- in successful fertilization [7]. Expression of Sp17 intal prerequisite for effective therapeutic intervention. malignant cells was first described by Dong et al, whoEmerging molecular imaging techniques now allow found the mouse homologue of Sp17 to be highly expressed in metastatic cell lines derived from a murine* Correspondence: njlifq@163.com; cupyueqing@163.com model of squamous cell carcinoma but not in the nonme-1 Laboratory of Molecular Biology, Institute of Medical Laboratory Sciences, tastatic parental line [8]. Various researchersJinling Hospital, School of Medicine, Nanjing University, Nanjing 210002, have demonstrated the aberrant expression of Sp17 inChina2 Department of Biomedical Engineering, School of Life Science and malignant tumors including myeloma [9], primary ovar-Technology, China Pharmaceutical University, Nanjing, 210009, China ian tumors [10,11], neuroectodermal and meningealFull list of author information is available at the end of the article © 2011 Li et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrest ...
Nội dung trích xuất từ tài liệu:
báo cáo khoa học: "In vivo Molecular targeting effects of anti-Sp17ICG-Der-02 on hepatocellular carcinoma evaluated by an optical imaging system"Li et al. Journal of Experimental & Clinical Cancer Research 2011, 30:25http://www.jeccr.com/content/30/1/25 RESEARCH Open AccessIn vivo Molecular targeting effects of anti-Sp17-ICG-Der-02 on hepatocellular carcinomaevaluated by an optical imaging systemFang-qiu Li1*, Shi-xin Zhang1, Lian-xiao An2, Yue-qing Gu2* Abstract Background: As the expression of human sperm protein 17 (Sp17) in normal tissue is limited and the function is obscure, its aberrant expression in malignant tumors makes it to be a candidated molecular marker for tumor imaging diagnosis and targeting therapy of the diseases.The aim of this research is to evaluate the targeting effects of anti-sperm protein 17 monoclonal antibody (anti-Sp17) on cancer in vivo and investigate its usefulness as a reagent for molecular imaging diagnosis. Methods: Immunohistochemistry was used to identify the expression of Sp17 in a hepatocellular carcinoma cell line and tumor xenograft specimens. A near infrared fluorescence dye, ICG-Der-02, was covalently linked to anti- Sp17 for in vivo imaging. The immuno-activity of the anti-Sp17-ICG-Der-02 complex was tested in vitro by ELISA; it was then injected into tumor-bearing nude mice through the caudal vein to evaluate its tumor targeting effect by near infrared imaging system. Results: Overexpression of Sp17 on the surface of the hepatocellular carcinoma cell line SMMC-7721 was demonstrated. Anti-Sp17-ICG-Der-02 with immuno-activity was successfully synthesized. The immuno-activity and photo stability of anti-Sp17- ICG-Der-02 showed good targeting capability for Sp17 expressing tumor models (SMMC-7721) in vivo, and its accumulation in the tumor lasted for at least 7 days. Conclusions: Anti-Sp17 antibody targeted and accumulated in Sp17 positive tumors in vivo, which demonstrated its capability of serving as a diagnostic reagent.Introduction recognition of early biomarker and anatomical changes before manifestation of gross pathological changes [3-6].Cancer remains one of the leading causes of death in The development of novel approaches for in vivo ima-the world. Despite advances in our understanding of ging and personalized treatment of cancers is urgentlymolecular and cancer biology, the discovery of cancer needed to find cancer-specific markers, but there is stillbiomarkers and the refinement of conventional surgical limited knowledge of suitable biomarkers.procedures, radiotherapy, and chemotherapy, the overall Sperm protein 17 (Sp17) was originally reported to besurvival rate from cancer has not significantly improved expressed exclusively in the testis. Its primary function isin the past two decades [1,2]. Early noninvasive detec- binding to the zona pellucida and playing a critical roletion and characterization of solid tumors is a fundamen- in successful fertilization [7]. Expression of Sp17 intal prerequisite for effective therapeutic intervention. malignant cells was first described by Dong et al, whoEmerging molecular imaging techniques now allow found the mouse homologue of Sp17 to be highly expressed in metastatic cell lines derived from a murine* Correspondence: njlifq@163.com; cupyueqing@163.com model of squamous cell carcinoma but not in the nonme-1 Laboratory of Molecular Biology, Institute of Medical Laboratory Sciences, tastatic parental line [8]. Various researchersJinling Hospital, School of Medicine, Nanjing University, Nanjing 210002, have demonstrated the aberrant expression of Sp17 inChina2 Department of Biomedical Engineering, School of Life Science and malignant tumors including myeloma [9], primary ovar-Technology, China Pharmaceutical University, Nanjing, 210009, China ian tumors [10,11], neuroectodermal and meningealFull list of author information is available at the end of the article © 2011 Li et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrest ...
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