Evaluation of cisplatin-hydrogel for improving localized antitumor efficacy in gastric cancer

被引:13
作者
Qian, Keyang [1 ]
Qian, Hanqing [2 ,3 ]
Cai, Juan [1 ]
Yue, Wuheng [4 ]
Yu, Xiaoxiao [5 ]
Liu, Baorui [2 ,3 ]
机构
[1] Nanjing Med Univ, Clin Coll, Comprehens Canc Ctr, Nanjing Drum Tower Hosp, Nanjing 210008, Jiangsu, Peoples R China
[2] Nanjing Univ, Med Sch, Comprehens Canc Ctr, Nanjing Drum Tower Hosp, 321 Zhongshan Rd, Nanjing 210008, Jiangsu, Peoples R China
[3] Nanjing Univ, Clin Canc Inst, 321 Zhongshan Rd, Nanjing 210008, Jiangsu, Peoples R China
[4] Nanjing Univ Chinese Med, Comprehens Canc Ctr, Nanjing Drum Tower Hosp, Clin Coll Tradit Chinese & Western Med, Nanjing 210008, Jiangsu, Peoples R China
[5] China Pharmaceut Univ, Sch Basic Med & Clin Pharm, Nanjing 210000, Jiangsu, Peoples R China
关键词
Orthotopic; Gastric cancer; Cisplatin; Hydrogel; Toxicity;
D O I
10.1016/j.prp.2019.01.005
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Gastric cancer, one of the most common disease, has become a major public health problem worldwide. Cisplatin (DDP) has been a widely used drug for the treatment of cancer, also usually applied in gastric cancer in clinic. However, the side effects including toxicity and drug-resistance restricted the usage of DDP in clinic, so we prepared a DDP-complexed hydrogel (DDP-Gel) and investigated its efficacy in gastric cancer. For in vivo studies, MKN45-Luc cells were injected into BLAB/C node mice subcutaneously to establish gastric cancer with orthotopically grown tumors. Mice bearing tumors were treated with normal saline, DDP and DDP-Gel. Body weight and survival condition were observed and recorded. The treatment efficacy in vivo was detected by luciferase imaging and histological evaluation was performed by H&E staining of different organs. Additionally, normal ICR mice were treated with different doses of DDP/DDP-Gel to calculate their LD50 in vivo. The results showed that DDP-Gel prolonged survival time and ameliorated body weight changes of mice bearing tumors. DDP-Gel exhibited higher efficacy to inhibit tumor growth and metastasis, compared to DDP. Besides, LD50 of DDP-Gel was 166.0 mg/kg, 13.2 folds higher than DDP. As a conclusion, DDP-Gel showed a more effective and safer function than DDP in gastric cancer, which indicating that DDP-Gel might be a novel strategy for gastric cancer therapy.
引用
收藏
页码:755 / 760
页数:6
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