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Personalized medicine modality based on patient-derived xenografts from a malignant transformed GCTB harboring H3F3A G34W mutation.

Authors :
Yafei J
Haoran M
Wenyan J
Linghang X
Kai T
Gangyang W
Zhuoying W
Jing H
Mengkai Y
Yujie T
Yingqi H
Zhengdong C
Source :
Journal of orthopaedic translation [J Orthop Translat] 2021 Jun 01; Vol. 29, pp. 106-112. Date of Electronic Publication: 2021 Jun 01 (Print Publication: 2021).
Publication Year :
2021

Abstract

Background: The function of H3F3A G43W mutation, which has been observed in almost all GCTB, remains poorly characterized. Breakthrough in malignant GCTB has been trapped by the lack of clinical available drugs, limited canonical patient samples and paucity of fidelity preclinical models.<br />Methods: Tumor samples obtained from a malignant GCTB was implanted in immunodeficient mice for the generation of PDX. Histological examination and short tandem repeat (STR) were used for inherited features analyses. An epigenetic/transcriptional targeted compound library was selected for drug screening. The in vivo effects of selected drug were validated in PDX model.<br />Results: We established the PDX model with recurrent malignant GCTB specimens, histological examination and STR analyses revealed that PDX and their corresponding parental patients shared the same STRs and histologic features, suggesting common origins. ITF-2357 was the most significant compound with an IC50 lower than 0.1 uM. The results of the drug screening and in vivo PDX validation demonstrated that ITF-2357 might be a promising drug targeted H3F3A G34W mutation MGCTBs.<br />Conclusion: Our study demonstrates that PDX model maintained the same histologic and genetic features as those in the original patient. targeting HDAC through ITF-2357 effectively overcomes malignant GCTB progression in vitro and in vivo.<br />Translational Potential Statement: As PDX retain the principal histologic and genetic characteristics of the primary tumors, mad it a valuable research tool in predictive clinical efficacy. In this study, we first established a malignant GCTB PDX model, which might further accelerate the progress of drug development in malignant GCTB.<br />Competing Interests: All authors declare that they have no conflicts of interest concerning this article.<br /> (© 2021 Department of Orthopaedic, Shanghai General Hospital, Shanghai JiaoTong Univeraity school of medicine.)

Details

Language :
English
ISSN :
2214-031X
Volume :
29
Database :
MEDLINE
Journal :
Journal of orthopaedic translation
Publication Type :
Academic Journal
Accession number :
34136349
Full Text :
https://doi.org/10.1016/j.jot.2021.04.004