Characterization of a Novel Mouse Model of Spontaneous Human Lung Cancer Metastasis
Characterization of a Novel Mouse Model of Spontaneous Human Lung Cancer Metastasis
Author Info
Dong M Shin Dongsheng Wang Georgia Z. Chen Guoqing Qian Nabil F Saba Sreenivas Nannapaneni Susan Müller
Corresponding Author
Georgia Z. ChenDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA
A B S T R A C T
To identify new strategies against lung metastasis and understand the underlying mechanisms, a highly metastatic pulmonary large cell carcinoma cell line model (801BL) was established through two rounds of in vivo selection using a nude mouse xenograft model. Satellite tandem repeat (STR) analysis confirmed the same genomic background of the newly established metastatic cell line 801BL as the non-metastatic 801C and low-metastatic 801D counterparts. Our study showed that 100% of mice (8 out of 8) injected subcutaneously with 801BL cells developed lung metastatic tumors, while none of the mice injected with 801C cells had lung metastasis (p<0.0001). Highly metastatic 801BL cells showed alterations in morphology and invasion capability when compared with 801C and/or 801D cell lines A comparative proteomic analysis between 801BL and 801C followed by bioinformatics analysis revealed significant alterations in several dominant cell signalling networks in the highly metastatic cell line. Western blot confirmed the proteomic findings for several proteins from each signalling network. Since the highly metastatic cell line and its non-metastatic counterpart share the identical genetic background, this model provides a powerful tool for study of the mechanisms underlying lung cancer metastasis.
Article Info
Article Type
Research ArticlePublication history
Received: Thu 10, Oct 2019Accepted: Tue 29, Oct 2019
Published: Mon 25, Nov 2019
Copyright
© 2023 Georgia Z. Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Hosting by Science Repository.DOI: 10.31487/j.COR.2019.5.13