Optimized Animal Model of Cyclophosphamide-induced Bone Marrow Suppression

被引:53
作者
Feng, Lizhi [1 ,2 ]
Huang, Qiuju [1 ]
Huang, Zhiying [1 ]
Li, Hang [1 ,2 ]
Qi, Xiaoxiao [1 ]
Wang, Ying [1 ]
Liu, Zhongqiu [1 ]
Liu, Xiaohong [1 ,2 ]
Lu, Linlin [1 ]
机构
[1] Guangzhou Univ Chinese Med, Int Inst Translat Chinese Med, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangzhou Univ Chinese Med, Dept Resp Med, Affiliated Hosp 1, Guangzhou 510405, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
HEMATOPOIETIC STEM-CELLS; MULTIPLE-MYELOMA; CHEMOTHERAPY; MYELOSUPPRESSION; MICE; DIFFERENTIATION; TRANSPLANTATION; RECOVERY; CANCER;
D O I
10.1111/bcpt.12600
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Myelosuppression is one of the serious side effects of anticancer chemotherapeutic drugs that deteriorate the bodily functions of patients, thereby affecting the quality of life considerably. Prevention of myelosuppression in anticancer chemotherapy is an important research topic. A stabilized chemotherapy-induced myelosuppression animal model is necessary in experimental research. This study aimed to establish an optimized animal model of chemotherapy-induced bone marrow suppression. After C57BL/6 mice were treated with intermediate- and high-dose (25/50 mg/kg) cyclophosphamide (CTX) for 10 days, the body-weight, changes in thymus and spleen, number of white blood cells (WBCs), red blood cells (RBCs), and platelets (PLTs) and changes in bone marrow in the mice were systematically evaluated at the next 2, 7 and 14 days. Our results demonstrated that CTX treatments could significantly decrease the body-weight of mice, as well as the ratios of the weights of thymus and spleen to body-weight. The physiological structures of thymus and spleen were destroyed by CTX treatments. The number of WBCs and RBCs significantly declined after CTX treatments; however, the number of PLTs increased. Moreover, the expression of Sca1 in bone marrow cells decreased on Day 2 but increased on Day 14. The expression of CD34 decreased in bone marrow cells after CTX treatments. In conclusion, mice models, with high-dose CTX treatments for 10 days, can be an optimized animal model for chemotherapy-induced bone marrow suppression.
引用
收藏
页码:428 / 435
页数:8
相关论文
共 29 条
[1]  
[Anonymous], 2013, EPOETIN DARBEPOETIN
[2]   Long term follow-up of allogeneic stem cell transplantation in patients with myelodysplastic syndromes using busulfan, cytosine arabinoside, and cyclophosphamide [J].
Atallah, Ehab ;
Abrams, Judith ;
Ayash, Lois ;
Bentley, Gail ;
Abidi, Muneer ;
Ratanatharathorn, Voravit ;
Uberti, Joseph .
AMERICAN JOURNAL OF HEMATOLOGY, 2010, 85 (08) :579-583
[3]  
Balducci Lodovico, 2003, Oncology (Williston Park), V17, P27
[4]   Prevention of myelosuppression and genotoxicity induced by cisplatin in murine bone marrow cells: effect of an organovanadium compound vanadium(III)-L-cysteine [J].
Basu, Abhishek ;
Ghosh, Prosenjit ;
Bhattacharjee, Arin ;
Patra, Arup Ranjan ;
Bhattacharya, Sudin .
MUTAGENESIS, 2015, 30 (04) :509-517
[5]  
BEAR HD, 1986, SOUTHERN MED J, V79, P1596, DOI 10.1097/00007611-198612000-00032
[6]  
BOTNICK LE, 1981, CANCER RES, V41, P2338
[7]  
Cichon T, 2012, ACTA BIOCHIM POL, V59, P377
[8]   Immunosuppressive Myeloid Cells Induced by Chemotherapy Attenuate Antitumor CD4+ T-Cell Responses through the PD-1-PD-L1 Axis [J].
Ding, Zhi-Chun ;
Lu, Xiaoyun ;
Yu, Miao ;
Lemos, Henrique ;
Huang, Lei ;
Chandler, Phillip ;
Liu, Kebin ;
Walters, Matthew ;
Krasinski, Antoni ;
Mack, Matthias ;
Blazar, Bruce R. ;
Mellor, Andrew L. ;
Munn, David H. ;
Zhou, Gang .
CANCER RESEARCH, 2014, 74 (13) :3441-3453
[9]  
GALLICCHIO VS, 1986, EXP HEMATOL, V14, P395
[10]   EVIDENCE THAT HEMATOPOIETIC STEM-CELLS EXPRESS MOUSE C-KIT BUT DO NOT DEPEND ON STEEL FACTOR FOR THEIR GENERATION [J].
IKUTA, K ;
WEISSMAN, IL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (04) :1502-1506