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骨肉瘤基因治疗进展

Advances in Gene Therapy of Osteosarcoma
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摘要 目的:骨肉瘤是20岁以下儿童、青少年好发的骨原性发恶性肿瘤,恶性度高、预后差.目前骨肉瘤治疗主要以大剂量辅助化疗和手术治疗为主,但治疗后仍具有病情进展快、病灶转移早、肿瘤易复发特点.人类基因组学研究进展表明,骨肉瘤的产生是由宿主基因组体的体细胞介导异常而产生的.基因治疗是一种新的治疗方法,通过基因转移技术将外源正常基因导入到靶细胞中,以纠正或补偿遗传缺陷或疾病异常.随着转基因技术的发展应用,基因治疗骨肉瘤备受学者关注,通过基因治疗有望进一步提高骨肉瘤患者的生存率和预后.本文就近几年骨肉瘤的基因治疗的进展、现状综述. Osteosarcoma is a primary malignant tumor of bone in children and adolescents under the age of 20,with high malignancy and poor prognosis.At present,the treatment of osteosarcoma is mainly based on high-dose individualized neoadjuvant chemotherapy(preoperative chemotherapy)and surgical treatment,but after treatment,it still has the characteristics of rapid disease progression,early metastasis,tumor recurrence,and difficulty in treatment.Gene therapy is a new and new treatment method,which intends to introduce foreign normal genes into target cells through gene transfer technology to correct or compensate genetic defects or disease abnormalities.With the development and application of transgenic technology,gene therapy for osteosarcoma has attracted much attention from scholars,and gene therapy is expected to further improve the survival rate and prognosis of osteosarcoma patients.This article reviews the progress and current status of gene therapy for osteosarcoma in recent years.
作者 李哲宏 甘新天 白磊鹏 吕家兴 曹海营 徐莹 金宇 LI Zhe-hong;GAN Xin-tian;BAI Lei-peng(Postgraduate school of Chengde medical university,Chengde 067000)
出处 《中国伤残医学》 2021年第21期98-100,共3页 Chinese Journal of Trauma and Disability Medicine
关键词 基因治疗 骨肉瘤 进展 Gene therapy Osteosarcoma
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  • 1王燕,丘钜世,乔慧,汪睿,彭挺生,李扬,EG Van Meir.缺氧对HRE-TK/GCV系统杀伤骨肉瘤细胞的增强作用[J].中国肿瘤临床,2005,32(2):68-72. 被引量:2
  • 2王燕,汪睿,乔慧,李晋云,彭挺生,李扬,张萌,梁惠珍,丘钜世.缺氧反应元件启动子表达反义血管内皮生长因子(VEGF)_(165)cDNA靶向性抑制骨肉瘤细胞VEGF表达[J].中华病理学杂志,2005,34(9):588-591. 被引量:6
  • 3Muramaki M, Miyaka H, Hara H, et al. Synergistic inhibition of tumor growth and metastasis by combined treatment with TNP-470 and gemcitabine in a human bladder cancer kotcc-1 model. J Urol, 2004,172(4 Pt 1):1485-1489.
  • 4He R, Liu B, Yang C, et al. Inhibition of K562 leukemia angiogenesis and growth by expression of antisense vascular endothelial growth factor (VEGF) sequence. Cancer Gene Ther,2003,10 ( 12 ) :879-886.
  • 5Saleh M, Stacker SA, Wilks AF, et al. Inhibition of growth of C6 glioma cells in vivo by expression of antisense vascular endothelial growth factor sequence. Cancer Res, 1996,56 (2) : 393-401.
  • 6Okada T, Caplen N J, Ramsey WJ, et al. In situ generation of pseudotyped retroviral progeny by adenovirus-mediated transduction of tumor cells enhances the killing effect of HSV-tk suicide gene therapy in vitro and in vivo. J Gene Med, 2004,6(3) :288-299.
  • 7Springer CJ, Niculescu-Duvaz I. Prodrug-activating systems insuicide gene therapy. J Clin Invest, 2000,105(9): 1161-1167.
  • 8Vaupel P. The role of hypoxia-induced factors in tumor progression. Oncologist, 2004,9 ( suppl 5 ) : 10-17.
  • 9Post DE, Van Meir EG. Generation of bidirectional hypoxia/HIF-responsive expression vectors to target gene expression to hypoxia cells. Gene Ther, 2001,8(23) :1801-1807.
  • 10鄂征.组织培养和分子细胞学技术.3版.北京:北京出版社,1999:155—158.

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