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胞嘧啶脱氨酶/5-氟胞嘧啶基因治疗与放疗联合用于前列腺癌的潜在益处:实验研究

Potential benefits of combining cytosine deaminase/5-fluorocytosine gene therapy and irradiation for prostate cancer: experimental study.

作者信息

Kato Hiroaki, Koshida Kiyoshi, Yokoyama Kunihiko, Mizokami Atsushi, Namiki Mikio

机构信息

Departments of Urology and Nuclear Medicine, Kanazawa University School of Medicine, Kanazawa, Japan.

出版信息

Int J Urol. 2002 Oct;9(10):567-76. doi: 10.1046/j.1442-2042.2002.00513.x.

Abstract

BACKGROUND

The purpose of this study was to investigate the potential of combining cytosine deaminase/5-fluorocytosine (CD/5-FC) gene therapy and radiation therapy (either external beam radiation or radioimmunotherapy [RIT]), for the treatment of prostate cancer.

METHODS

Tumor xenografts of CD-transduced LNCaP cells grown in the testes of severe combined immunodeficiency (SCID) mice were used to evaluate antitumor effect. The mice were injected intraperitoneally with 500 mg/kg of 5-FC, or with 5, 15 or 30 mg/kg of 5-fluorouracil (5-FU), for 9 days. The tumors were treated with fractionated radiation at a dose of 1 or 3 Gy/day for 3 days, or I-131 labelled anti-prostate specific antigen (anti-PSA) monoclonal antibody (mAb) administration at a subtherapeutic dose of 20 or 80 micro Ci. Intratumoral and serum concentrations of 5-FU were measured using high performance liquid chromatography.

RESULTS

Mice treated with CD/5-FC gene therapy presented a significant tumor growth inhibition comparable to that obtained with 15 mg/kg, 5-FU systemic administration without marked weight loss. Treatment with CD/5-FC gene therapy resulted in higher tumor but lower serum concentrations of 5-FU than treatment with systemic 5-FU chemotherapy. An additive antitumor effect was obtained when CD/5-FC therapy was combined with 1 Gy irradiation, which by itself did not produce a significant antitumor effect. However, the efficacy of CD/5-FC therapy was not enhanced when combined with RIT, probably due to poor accumulation of the mAb as the tumor/blood ratio never exceeded 1.

CONCLUSION

These findings indicate that CD/5-FC gene therapy for prostate cancer may function with enhanced antitumor effect when combined with external beam radiation. However, combining CD/5-FC gene therapy and RIT using an anti-PSA mAb may not be effective because of insufficient accumulation of the mAb at the target tumors.

摘要

背景

本研究旨在探讨胞嘧啶脱氨酶/5-氟胞嘧啶(CD/5-FC)基因治疗与放射治疗(外照射放疗或放射免疫治疗[RIT])联合用于治疗前列腺癌的潜力。

方法

将转导了CD的LNCaP细胞接种到严重联合免疫缺陷(SCID)小鼠睾丸中形成肿瘤异种移植物,用于评估抗肿瘤效果。给小鼠腹腔注射500mg/kg的5-FC,或5、15或30mg/kg的5-氟尿嘧啶(5-FU),持续9天。肿瘤接受分次放疗,剂量为每天1或3Gy,共3天,或给予亚治疗剂量20或80微居里的I-131标记抗前列腺特异性抗原(抗-PSA)单克隆抗体(mAb)。使用高效液相色谱法测量肿瘤内和血清中的5-FU浓度。

结果

接受CD/5-FC基因治疗的小鼠出现了显著的肿瘤生长抑制,与15mg/kg 5-FU全身给药的效果相当,且无明显体重减轻。与全身5-FU化疗相比,CD/5-FC基因治疗导致肿瘤内5-FU浓度更高但血清中5-FU浓度更低。当CD/5-FC治疗与1Gy照射联合时获得了相加的抗肿瘤效果,而1Gy照射本身并未产生显著的抗肿瘤效果。然而,CD/5-FC治疗与RIT联合时疗效未增强,可能是由于mAb积累不佳,因为肿瘤/血液比值从未超过1。

结论

这些发现表明,前列腺癌的CD/5-FC基因治疗与外照射放疗联合时可能具有增强的抗肿瘤作用。然而,使用抗-PSA mAb将CD/5-FC基因治疗与RIT联合可能无效,因为mAb在靶肿瘤处积累不足。

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