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裸鼠作为宫颈癌原位模型。

The nude rat as an orthotopic model for cervical cancer.

作者信息

Hamada Katsuyuki, Ueda Norifumi, Ito Masaharu, Roth Jack A, Follen Michele

机构信息

Section of Thoracic Molecular Oncology, Department of Thoracic and Cardiovascular Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Gynecol Oncol. 2005 Dec;99(3 Suppl 1):S159-65. doi: 10.1016/j.ygyno.2005.07.073. Epub 2005 Sep 26.

DOI:10.1016/j.ygyno.2005.07.073
PMID:16185752
Abstract

OBJECTIVE

The purposes of this study were to establish intracervical tumors of the nude rat as an orthotopic experimental model for human cervical cancer and to preliminary evaluate the effects of the adenoviral vector, Ad5CMV-p53, on orthotopic cervical tumor size.

METHODS

Human cervical cancer SiHa and ME-180 cells were injected into the cervix of the nude rat. Four days later, 1 x 10(9) plaque forming units (PFU) of Ad5CMV-p53 were injected into the cervix. The rats were later sacrificed to determine cervical tumor size.

RESULTS

Eight of ten nude rats developed SiHa cell tumors; all ten nude rats developed ME-180 cell tumors. Four of ten SiHa cell tumors metastasized to the pelvic cavity; no ME-180 cell tumors did. The growth of Ad5CMV-p53-infected cells was greatly suppressed. The ad5CMV-p53 treatment significantly reduced both cell tumor volumes in nude rat cervixes.

CONCLUSION

The nude rat cervix grows tumors similar to human cervical cancer tumors and makes an excellent experimental model. Transfection of cervical cancer cells with the wild-type p53 gene via Ad5CMV-p53 is a potential therapeutic approach to cervical cancer.

摘要

目的

本研究的目的是建立裸鼠宫颈原位肿瘤作为人类宫颈癌的原位实验模型,并初步评估腺病毒载体Ad5CMV-p53对原位宫颈肿瘤大小的影响。

方法

将人宫颈癌SiHa和ME-180细胞注入裸鼠宫颈。4天后,将1×10⁹ 空斑形成单位(PFU)的Ad5CMV-p53注入宫颈。随后处死大鼠以确定宫颈肿瘤大小。

结果

10只裸鼠中有8只发生SiHa细胞肿瘤;10只裸鼠均发生ME-180细胞肿瘤。10只SiHa细胞肿瘤中有4只转移至盆腔;ME-180细胞肿瘤均未转移。Ad5CMV-p53感染细胞的生长受到极大抑制。Ad5CMV-p53治疗显著减小了裸鼠宫颈中两种细胞肿瘤的体积。

结论

裸鼠宫颈生长的肿瘤与人宫颈癌肿瘤相似,是一种优良的实验模型。通过Ad5CMV-p53将野生型p53基因转染至宫颈癌细胞是一种潜在的宫颈癌治疗方法。

相似文献

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The nude rat as an orthotopic model for cervical cancer.裸鼠作为宫颈癌原位模型。
Gynecol Oncol. 2005 Dec;99(3 Suppl 1):S159-65. doi: 10.1016/j.ygyno.2005.07.073. Epub 2005 Sep 26.
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Adenovirus-mediated transfer of a wild-type p53 gene and induction of apoptosis in cervical cancer.
Cancer Res. 1996 Jul 1;56(13):3047-54.
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Recombinant adenovirus-p53 gene transfer and cell-specific growth suppression of human cervical cancer cells in vitro and in vivo.重组腺病毒-p53基因转导及人宫颈癌细胞在体外和体内的细胞特异性生长抑制
Gynecol Oncol. 2004 Feb;92(2):611-21. doi: 10.1016/j.ygyno.2003.10.033.
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Adenoviral p53 effects and cell-specific E7 protein-protein interactions of human cervical cancer cells.腺病毒p53对人宫颈癌细胞的作用及细胞特异性E7蛋白-蛋白相互作用
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Growth inhibition of human cervical cancer cells with the recombinant adenovirus p53 in vitro.重组腺病毒p53体外抑制人宫颈癌细胞生长
Gynecol Oncol. 1996 Mar;60(3):373-9. doi: 10.1006/gyno.1996.0057.
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Adenovirus-mediated transfer of human papillomavirus 16 E6/E7 antisense RNA and induction of apoptosis in cervical cancer.腺病毒介导的人乳头瘤病毒16 E6/E7反义RNA的转移及对子宫颈癌细胞凋亡的诱导作用
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Gene silencing with siRNA targeting E6/E7 as a therapeutic intervention in a mouse model of cervical cancer.在宫颈癌小鼠模型中,以靶向E6/E7的小干扰RNA进行基因沉默作为一种治疗干预手段。
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Adenovirus carrying TIMP-3: a potential tool for cervical cancer treatment.携带金属蛋白酶组织抑制因子-3的腺病毒:一种用于宫颈癌治疗的潜在工具。
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[Adenovirus-delivered tissue inhibitor of metalloproteinases-3 transfection increases the sensitivity of cervical cancer cells to cisplatin].腺病毒介导的金属蛋白酶组织抑制剂-3转染增加宫颈癌细胞对顺铂的敏感性
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