Ontology highlight
ABSTRACT: Background
Treatment of human lung squamous cell carcinoma (LUSC) using current targeted therapies is limited because of their diverse somatic mutations without any specific dominant driver mutations. These mutational diversities preventing the use of common targeted therapies or the combination of available therapeutic modalities would require a preclinical animal model of this tumor to acquire improved clinical responses. Patient-derived xenograft (PDX) models have been recognized as a potentially useful preclinical model for personalized precision medicine. However, whether the use of LUSC PDX models would be appropriate enough for clinical application is still controversial.Methods
In the process of developing PDX models from Korean patients with LUSC, the authors investigated the factors influencing the successful initial engraftment of tumors in NOD scid gamma mice and the retainability of the pathological and genomic characteristics of the parental patient tumors in PDX tumors.Conclusions
The authors have developed 62 LUSC PDX models that retained the pathological and genomic features of parental patient tumors, which could be used in preclinical and co-clinical studies. Trial registration Tumor samples were obtained from 139 patients with LUSC between November 2014 and January 2019. All the patients provided signed informed consents. This study was approved by the institutional review board (IRB) of Samsung Medical Center (2018-03-110).
SUBMITTER: Jung HY
PROVIDER: S-EPMC7409653 | biostudies-literature | 2020 Aug
REPOSITORIES: biostudies-literature
Jung Hae-Yun HY Kim Tae Ho TH Lee Jong-Eun JE Kim Hong Kwan HK Cho Jong Ho JH Choi Yong Soo YS Shin Sumin S Lee Se-Hoon SH Rhee Hwanseok H Lee Hee Kyung HK Choi Hyun Jung HJ Jang Hye Yoon HY Lee Seungjae S Kang Jung Hee JH Choi Young Ae YA Lee Sanghyuk S Lee Jinseon J Choi Yoon La Y Kim Jhingook J
Journal of translational medicine 20200806 1
<h4>Background</h4>Treatment of human lung squamous cell carcinoma (LUSC) using current targeted therapies is limited because of their diverse somatic mutations without any specific dominant driver mutations. These mutational diversities preventing the use of common targeted therapies or the combination of available therapeutic modalities would require a preclinical animal model of this tumor to acquire improved clinical responses. Patient-derived xenograft (PDX) models have been recognized as a ...[more]