Establishment of humanised xenograft models as in vivo study for lung metastasis of osteosarcoma

被引:0
|
作者
Khamarudin, Farhana [1 ,2 ]
Muhamad, Mudiana
Ibahim, Mohamad Johari
Zain, Wan Nor I'zzah Wan Mohamad
Aziz, Mardiana Abdul [3 ]
Ridzuan, Nurul Raudzah Adib
Ab-Rahim, Sharaniza [1 ,4 ]
机构
[1] Univ Teknol MARA, Dept Biochem & Mol Med, Sungai Buloh 47000, Selangor, Malaysia
[2] Univ Teknol MARA, Inst Med Mol Biotechnol, Sungai Buloh 47000, Selangor, Malaysia
[3] Univ Teknol MARA, Dept Pathol, Sungai Buloh 47000, Selangor, Malaysia
[4] Univ Teknol MARA, Fac Med, Dept Biochem & Mol Med, Sungai Buloh Campus,Jalan Hosp, Sungai Buloh 47000, Selangor, Malaysia
来源
IMMUNOTHERAPY ADVANCES | 2024年 / 4卷 / 01期
关键词
xenograft; osteosarcoma; lung metastasis; mouse model; PULMONARY METASTASIS; PROGNOSTIC-FACTORS; SARCOMA;
D O I
10.1093/immadv/ltae002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Humanised xenograft models and cancer cell lines are widely used for preclinical drug evaluation, biological studies, and targeted therapy strategies in cancer research. A humanised mouse model is a laboratory mouse that has been genetically modified to contain specific human genes, cells, or tissues. By introducing human-specific elements into rodents, researchers can create a more accurate representation of human physiological and pathological processes. Lacking an appropriate animal model for osteosarcoma (OS), hindered understanding of underlying mechanisms in OS metastasis progression. Markedly, metastasis influences the prognosis and treatment of osteosarcoma. Gaining insight into the mechanisms and occurrences of metastasis could potentially facilitate oncologists in improving therapies. Hence, it is important to develop a lung metastatic OS model to study the basic biology of its progression. This study has established a tumour-bearing mouse model using HOS-143B cell line which was injected into male NOD.SCID gamma (NSG) mice at two locations; intramuscularly (hind leg) and subcutaneously (back) respectively. The primary and metastatic tumour size was monitored by palpating the area of tumour induced and quantified using digital calliper. H&E staining was performed by pathologist to confirm metastasis. Our results showed that mice injected with 1 million cancer cells were unable to produce tumours. Meanwhile, mice injected with three million cancer cells showed tumour development and lung metastasis after 25 days of cancer cell inoculation. In conclusion, this study has successfully established a lung metastatic OS mouse model that could be useful for biological studies of OS. These findings imply that this model is essential for safety and efficacy before clinical trials, accelerate the translation from basic research to therapeutic applications. Graphical Abstract
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页数:9
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