Xenograft models for undifferentiated pleomorphic sarcoma not otherwise specified are essential for preclinical testing of therapeutic agents

被引:6
作者
Becker, Marc [1 ,2 ]
Graf, Claudine [3 ]
Tonak, Marcus [2 ,4 ]
Radsak, Markus P. [5 ]
Bopp, Tobias [5 ]
Bals, Robert [6 ]
Bohle, Rainer M. [1 ]
Theobald, Matthias [3 ]
Rommens, Pol-Maria [2 ]
Proschek, Dirk [2 ]
Wehler, Thomas C. [3 ]
机构
[1] Univ Saarland, Med Ctr, Inst Pathol, D-66421 Homburg, Saarland, Germany
[2] Johannes Gutenberg Univ Mainz, Ctr Orthopaed & Trauma Surg, Interdisciplinary Sarcoma Working Grp, D-55131 Mainz, Rhineland Palat, Germany
[3] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Internal Med 3, D-55131 Mainz, Rhineland Palat, Germany
[4] Univ Hosp Mannheim, Dept Orthopaed & Trauma Surg, D-68167 Mannheim, Baden Wurttembe, Germany
[5] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Immunol, D-55131 Mainz, Rhineland Palat, Germany
[6] Univ Saarland, Med Ctr, Dept Internal Med Pulmonol Allergol & Resp Crit C, D-66421 Homburg, Saarland, Germany
关键词
pleomorphic sarcoma; doxorubicin; pazopanib; HDAC inhibitor; xenograft; animal model; MALIGNANT FIBROUS HISTIOCYTOMA; SOFT-TISSUE SARCOMA; CELL-LINE; ESTABLISHMENT; PAZOPANIB; CLASSIFICATION; HYBRIDIZATION; CHEMOTHERAPY; THERAPIES; PALETTE;
D O I
10.3892/ol.2016.4784
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Undifferentiated pleomorphic sarcoma not otherwise specified belongs to the heterogeneous group of soft tissue tumors. It is preferentially located in the upper and lower extremities of the body, and surgical resection remains the only curative treatment. Preclinical animal models are crucial to improve the development of novel chemotherapeutic agents for the treatment of undifferentiated pleomorphic sarcoma. However, this approach has been hampered by the lack of reproducible animal models. The present study established two xenograft animal models generated from stable non-clonal cell cultures, and investigated the difference in chemotherapeutic effects on tumor growth between undifferentiated pleomorphic sarcoma in vivo and in vitro. The cell cultures were generated from freshly isolated tumor tissues of two patients with undifferentiated pleomorphic sarcoma. For the in vivo analysis, these cells were injected subcutaneously into immunodeficient mice. The mice were monitored for tumor appearance and treated with the most common or innovative chemotherapeutic agents available to date. Furthermore, the same drugs were administered to in vitro cell cultures. The most effective tumor growth inhibition in vitro was observed with doxorubicin and the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA), also known as vorinostat. In the in vivo xenograft mouse model, the combination of doxorubicin and the tyrosine kinase inhibitor pazopanib induced a significant tumor reduction. By contrast, treatment with vorinostat did not reduce the tumor growth. Taken together, the results obtained from drug testing in vitro differed significantly from the in vivo results. Therefore, the novel and reproducible xenograft animal model established in the present study demonstrated that in vivo models are required to test potential chemotherapeutic agents for the treatment of undifferentiated pleomorphic sarcoma prior to clinical use, since animal models are more similar to humans, compared with in vitro cell cultures.
引用
收藏
页码:1257 / 1264
页数:8
相关论文
共 34 条
[1]   Malignant fibrous histiocytoma-pleomorphic sarcoma, NOS gene expression, histology, and clinical course. A pilot study [J].
Adrien, Daigeler ;
Ludger, Klein-Hitpass ;
Ingo, Stricker ;
Oliver, Mueller ;
Cornelius, Kuhnen ;
Michael, Chromik Ansgar ;
Lars, Steinstraesser ;
Ole, Goertz ;
Hans-Ulrich, Steinau ;
Marcus, Lehnhardt .
LANGENBECKS ARCHIVES OF SURGERY, 2010, 395 (03) :261-275
[2]  
Al-Agha OM, 2008, ARCH PATHOL LAB MED, V132, P1030, DOI 10.1043/1543-2165(2008)132[1030:MFHBTP]2.0.CO
[3]  
2
[4]  
[Anonymous], 2013, WHO CLASSIFICATION T, DOI DOI 10.1001/JAMAOTO.2016.2670
[5]   Soft tissue sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Casali, P. G. ;
Blay, J. -Y. .
ANNALS OF ONCOLOGY, 2010, 21 :v198-v203
[6]  
Fletcher C DM., 2002, World Health Organisation Classification of tumours: Tumours of Soft Tissue and Bone, V3rd
[7]  
Grimer Robert, 2010, Sarcoma, V2010, P1, DOI 10.1155/2010/506182
[8]  
Hakozaki M, 2006, ANTICANCER RES, V26, P3393
[9]   Prognostic Factors and Impact of Adjuvant Treatments on Local and Metastatic Relapse of Soft-Tissue Sarcoma Patients in the Competing Risks Setting [J].
Italiano, Antoine ;
Le Cesne, Axel ;
Mendiboure, Jean ;
Blay, Jean-Yves ;
Piperno-Neumann, Sophie ;
Chevreau, Christine ;
Delcambre, Corinne ;
Penel, Nicolas ;
Terrier, Philippe ;
Ranchere-Vince, Dominique ;
Lae, Marick ;
Le Guellec, Sophie ;
Michels, Jean-Jacques ;
Robin, Yves Marie ;
Bellera, Carine ;
Bonvalot, Sylvie .
CANCER, 2014, 120 (21) :3361-3369
[10]   Trends in Survival for Patients With Metastatic Soft-Tissue Sarcoma [J].
Italiano, Antoine ;
Mathoulin-Pelissier, Simone ;
Le Cesne, Axel ;
Terrier, Philippe ;
Bonvalot, Sylvie ;
Collin, Francoise ;
Michels, Jean-Jacques ;
Blay, Jean-Yves ;
Coindre, Jean-Michel ;
Bui, Binh .
CANCER, 2011, 117 (05) :1049-1054