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低剂量顺铂周期化疗促进肿瘤特异性免疫应答降低宫颈癌再发的实验研究[J]. 肿瘤防治研究, 2014, 41(01): 13-15. DOI: 10.3971/j.issn.1000-8578.2014.01.004
引用本文: 低剂量顺铂周期化疗促进肿瘤特异性免疫应答降低宫颈癌再发的实验研究[J]. 肿瘤防治研究, 2014, 41(01): 13-15. DOI: 10.3971/j.issn.1000-8578.2014.01.004
Enhancement of Anti-tumor Immune Response and Decrease of Recurrence Rate of Cervical Cancer by Low Dose Metronomic Chemotherapy of Cisplatin[J]. Cancer Research on Prevention and Treatment, 2014, 41(01): 13-15. DOI: 10.3971/j.issn.1000-8578.2014.01.004
Citation: Enhancement of Anti-tumor Immune Response and Decrease of Recurrence Rate of Cervical Cancer by Low Dose Metronomic Chemotherapy of Cisplatin[J]. Cancer Research on Prevention and Treatment, 2014, 41(01): 13-15. DOI: 10.3971/j.issn.1000-8578.2014.01.004

低剂量顺铂周期化疗促进肿瘤特异性免疫应答降低宫颈癌再发的实验研究

Enhancement of Anti-tumor Immune Response and Decrease of Recurrence Rate of Cervical Cancer by Low Dose Metronomic Chemotherapy of Cisplatin

  • 摘要: 目的 探讨低剂量顺铂周期化疗对机体抗肿瘤免疫应答及宫颈癌再发率的影响。方法 建立TC-1肿瘤细胞C57BL/6小鼠模型,分为3组(n=5):对照组、低剂量组、高剂量组,绘制3组肿瘤生长曲线,用药结束后7 d检测3组小鼠外周血单核细胞(peripheral blood mononuclear cells,PBMCs)中HPV-E7特异性CD8+T细胞的数目。同法建立小鼠肿瘤模型、分组、治疗,治疗结束后7 d,切除肿瘤组织,下腹部对侧接种TC-1细胞,观察肿瘤再发率和小鼠生存率。结果 (1)顺铂低剂量周期疗法和高剂量疗法抗肿瘤作用相似。(2)低剂量周期疗法组PBMC中HPV-E7阳性的CD8+T数量显著高于高剂量组和对照组。(3)低剂量周期疗法组肿瘤再发率显著低于高剂量组和对照组;(4)低剂量周期疗法组肿瘤小鼠生存率显著高于高剂量组和对照组。结论 顺铂低剂量周期疗法能有效抑制肿瘤生长,其通过促进肿瘤特异性免疫应答,在一定程度上降低肿瘤再发,提高宿主生存率。

     

    Abstract: Objective To explore the effect of low dose metronomic chemotherapy of cisplatin on specifi c anti-tumor immune response and recurrence rate of cervical cancer. Methods Establish C57BL/6 mouse tumor model with TC-1 cells was established, the mice were divided into 3 groups (n=5) (control, low dose and high dose group). The tumor growth curve was drawn and the HPV-E7 specifi c CD8+ T cells number in PBMC were determined. The tumor model establishment, grouping and treatment were same as above, after 7 days treatment, the tumor was removed and the TC-1 cells were reinjected in the contralateral hypogastrium after 2 days of surgery. The tumor recurrence rate and survival rate were checked. Results (1)The antitumor effect was similar after low dose or high dose cisplatin treatment.(2) The HPV-E7 specifi c CD8+T cells in low dose group were significantly higher than that in control or high dose group.(3)The tumor recurrence rate in the low dose group was lower than that in control or high dose group.(4)The survival rate in low dose group was higher than that in control or high dose group. Conclusion Low dose metronomic chemotherapy of cisplatin can inhibit tumor growth effectively, through enhancing specific antitumor immune response, decrease the recurrence of tumor and increase the host survival rate in a certain extent.

     

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