Zebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis

Abstract Background Brain metastasis (BM) is thought to be related to the mortality and poor prognosis of non-small cell lung cancer (NSCLC). Despite promising development of NSCLC treatment, the treatment of NSCLC BM is still not optimistic due to the existence of the blood-brain barrier (BBB) that...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Ruo-Yue Fan, Jia-Qi Wu, Yu-Yang Liu, Xiang-Yu Liu, Si-Tong Qian, Chong-Yong Li, Ping Wei, Zhe Song, Ming-Fang He
Formato: article
Lenguaje:EN
Publicado: BMC 2021
Materias:
Acceso en línea:https://doaj.org/article/f5b6b1a9f7e749c680f23c14c95fbbd0
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:f5b6b1a9f7e749c680f23c14c95fbbd0
record_format dspace
spelling oai:doaj.org-article:f5b6b1a9f7e749c680f23c14c95fbbd02021-11-21T12:13:00ZZebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis10.1186/s13046-021-02173-51756-9966https://doaj.org/article/f5b6b1a9f7e749c680f23c14c95fbbd02021-11-01T00:00:00Zhttps://doi.org/10.1186/s13046-021-02173-5https://doaj.org/toc/1756-9966Abstract Background Brain metastasis (BM) is thought to be related to the mortality and poor prognosis of non-small cell lung cancer (NSCLC). Despite promising development of NSCLC treatment, the treatment of NSCLC BM is still not optimistic due to the existence of the blood-brain barrier (BBB) that prevent drug penetration, as well as the short median survival time of the patients left for treatment. In this context, further development of quick and effective pre-clinical models is needed in NSCLC BM treatment. Here, we report a model system using zebrafish to promote the development of drugs for patients with NSCLC BM. Methods Three different NSCLC cell lines (H1975, A549 and H1299) were used to establish zebrafish BM models. The embryo age and cell number for injection were first optimized. Metastatic cells were observed in the brain blood vessels of zebrafish and were verified by hematoxylin-eosin (HE) staining. Then, the metastasis potentials of H1975 and A549 with manipulated microRNA-330-3p (miR-330-3p) expression were also investigated. Finally, sensitivities of H1975 and A549 to osimertinib and gefitinib were tested. Results This zebrafish BM model could distinguish NSCLC cell lines with different BM potential. Over-expressed miR-330-p significantly improved the BM potential of the A549 cells while knockdown miR-330-p reduced the BM ability of the H1975 cells. Both osimertinib and gefitinib showed inhibition effect in zebrafish BM model with the inhibition rate higher than 50 %. H1975 cell showed much higher sensitivity to osimertinib rather than gefitinib both in vivo and in vitro. Conclusions We established zebrafish brain metastasis model for studying mechanism and treatment of NSCLC BM. This study provided a useful model for NSCLC brain metastasis that could be used to study the mechanism that drive NSCLC cells to the brain as well as identify potential therapeutic options.Ruo-Yue FanJia-Qi WuYu-Yang LiuXiang-Yu LiuSi-Tong QianChong-Yong LiPing WeiZhe SongMing-Fang HeBMCarticleZebrafishBrain metastasisXenograftNon-small cell lung cancerNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENJournal of Experimental & Clinical Cancer Research, Vol 40, Iss 1, Pp 1-15 (2021)
institution DOAJ
collection DOAJ
language EN
topic Zebrafish
Brain metastasis
Xenograft
Non-small cell lung cancer
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Zebrafish
Brain metastasis
Xenograft
Non-small cell lung cancer
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Ruo-Yue Fan
Jia-Qi Wu
Yu-Yang Liu
Xiang-Yu Liu
Si-Tong Qian
Chong-Yong Li
Ping Wei
Zhe Song
Ming-Fang He
Zebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis
description Abstract Background Brain metastasis (BM) is thought to be related to the mortality and poor prognosis of non-small cell lung cancer (NSCLC). Despite promising development of NSCLC treatment, the treatment of NSCLC BM is still not optimistic due to the existence of the blood-brain barrier (BBB) that prevent drug penetration, as well as the short median survival time of the patients left for treatment. In this context, further development of quick and effective pre-clinical models is needed in NSCLC BM treatment. Here, we report a model system using zebrafish to promote the development of drugs for patients with NSCLC BM. Methods Three different NSCLC cell lines (H1975, A549 and H1299) were used to establish zebrafish BM models. The embryo age and cell number for injection were first optimized. Metastatic cells were observed in the brain blood vessels of zebrafish and were verified by hematoxylin-eosin (HE) staining. Then, the metastasis potentials of H1975 and A549 with manipulated microRNA-330-3p (miR-330-3p) expression were also investigated. Finally, sensitivities of H1975 and A549 to osimertinib and gefitinib were tested. Results This zebrafish BM model could distinguish NSCLC cell lines with different BM potential. Over-expressed miR-330-p significantly improved the BM potential of the A549 cells while knockdown miR-330-p reduced the BM ability of the H1975 cells. Both osimertinib and gefitinib showed inhibition effect in zebrafish BM model with the inhibition rate higher than 50 %. H1975 cell showed much higher sensitivity to osimertinib rather than gefitinib both in vivo and in vitro. Conclusions We established zebrafish brain metastasis model for studying mechanism and treatment of NSCLC BM. This study provided a useful model for NSCLC brain metastasis that could be used to study the mechanism that drive NSCLC cells to the brain as well as identify potential therapeutic options.
format article
author Ruo-Yue Fan
Jia-Qi Wu
Yu-Yang Liu
Xiang-Yu Liu
Si-Tong Qian
Chong-Yong Li
Ping Wei
Zhe Song
Ming-Fang He
author_facet Ruo-Yue Fan
Jia-Qi Wu
Yu-Yang Liu
Xiang-Yu Liu
Si-Tong Qian
Chong-Yong Li
Ping Wei
Zhe Song
Ming-Fang He
author_sort Ruo-Yue Fan
title Zebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis
title_short Zebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis
title_full Zebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis
title_fullStr Zebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis
title_full_unstemmed Zebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis
title_sort zebrafish xenograft model for studying mechanism and treatment of non-small cell lung cancer brain metastasis
publisher BMC
publishDate 2021
url https://doaj.org/article/f5b6b1a9f7e749c680f23c14c95fbbd0
work_keys_str_mv AT ruoyuefan zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
AT jiaqiwu zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
AT yuyangliu zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
AT xiangyuliu zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
AT sitongqian zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
AT chongyongli zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
AT pingwei zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
AT zhesong zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
AT mingfanghe zebrafishxenograftmodelforstudyingmechanismandtreatmentofnonsmallcelllungcancerbrainmetastasis
_version_ 1718419162346291200