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PDX models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications

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...

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Autores principales: Jung, Hae-Yun, Kim, Tae Ho, Lee, Jong-Eun, Kim, Hong Kwan, Cho, Jong Ho, Choi, Yong Soo, Shin, Sumin, Lee, Se-Hoon, Rhee, Hwanseok, Lee, Hee Kyung, Choi, Hyun Jung, Jang, Hye Yoon, Lee, Seungjae, Kang, Jung Hee, Choi, Young Ae, Lee, Sanghyuk, Lee, Jinseon, Choi, Yoon La, Kim, Jhingook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409653/
https://www.ncbi.nlm.nih.gov/pubmed/32762722
http://dx.doi.org/10.1186/s12967-020-02473-y
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author Jung, Hae-Yun
Kim, Tae Ho
Lee, Jong-Eun
Kim, Hong Kwan
Cho, Jong Ho
Choi, Yong Soo
Shin, Sumin
Lee, Se-Hoon
Rhee, Hwanseok
Lee, Hee Kyung
Choi, Hyun Jung
Jang, Hye Yoon
Lee, Seungjae
Kang, Jung Hee
Choi, Young Ae
Lee, Sanghyuk
Lee, Jinseon
Choi, Yoon La
Kim, Jhingook
author_facet Jung, Hae-Yun
Kim, Tae Ho
Lee, Jong-Eun
Kim, Hong Kwan
Cho, Jong Ho
Choi, Yong Soo
Shin, Sumin
Lee, Se-Hoon
Rhee, Hwanseok
Lee, Hee Kyung
Choi, Hyun Jung
Jang, Hye Yoon
Lee, Seungjae
Kang, Jung Hee
Choi, Young Ae
Lee, Sanghyuk
Lee, Jinseon
Choi, Yoon La
Kim, Jhingook
author_sort Jung, Hae-Yun
collection PubMed
description 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)
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spelling pubmed-74096532020-08-10 PDX models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications Jung, Hae-Yun Kim, Tae Ho Lee, Jong-Eun Kim, Hong Kwan Cho, Jong Ho Choi, Yong Soo Shin, Sumin Lee, Se-Hoon Rhee, Hwanseok Lee, Hee Kyung Choi, Hyun Jung Jang, Hye Yoon Lee, Seungjae Kang, Jung Hee Choi, Young Ae Lee, Sanghyuk Lee, Jinseon Choi, Yoon La Kim, Jhingook J Transl Med Research 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) BioMed Central 2020-08-06 /pmc/articles/PMC7409653/ /pubmed/32762722 http://dx.doi.org/10.1186/s12967-020-02473-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jung, Hae-Yun
Kim, Tae Ho
Lee, Jong-Eun
Kim, Hong Kwan
Cho, Jong Ho
Choi, Yong Soo
Shin, Sumin
Lee, Se-Hoon
Rhee, Hwanseok
Lee, Hee Kyung
Choi, Hyun Jung
Jang, Hye Yoon
Lee, Seungjae
Kang, Jung Hee
Choi, Young Ae
Lee, Sanghyuk
Lee, Jinseon
Choi, Yoon La
Kim, Jhingook
PDX models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications
title PDX models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications
title_full PDX models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications
title_fullStr PDX models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications
title_full_unstemmed PDX models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications
title_short PDX models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications
title_sort pdx models of human lung squamous cell carcinoma: consideration of factors in preclinical and co-clinical applications
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409653/
https://www.ncbi.nlm.nih.gov/pubmed/32762722
http://dx.doi.org/10.1186/s12967-020-02473-y
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