Establishment of a small-cell lung cancer (SCLC) mouse model using enhanced cancer stem-cell-functioning 3D SCLC spheroids

Authors
Jung, Yong HunKim, In KyoungEom, So YoungKim, HyunsooPark, KyungwonChung, SeokLee, Sang HaakYeo, Chang DongKim, Hye JoungKang, Hye Seon
Issue Date
2024-03
Publisher
대한독성 유전단백체 학회
Citation
Molecular & Cellular Toxicology
Abstract
BackgroundDespite its low incidence rate, small-cell lung cancer (SCLC), which accounts for approximately 10%-15% of all lung cancers, is concerningly characterized by its rapid progression, strong metastatic potential, and high fatality rate. Therefore, an effective predictive model for SCLC treatment is imperative for early intervention.ObjectiveIn this study, we aimed to enhance the cancer stem cell (CSC) capabilities of SCLC through a three-dimensional (3D) culturing approach and to evaluate its potential as a predictive model for therapeutic response in SCLC by transplanting the spheroids into mice.ResultsTo achieve uniform and scalable production of 3D SCLC spheroids, the SpheroFILM culture platform was employed and the expression of CSC markers was verified at the gene and protein levels within the spheroids cultured onboard. Moreover, spheroids were transplanted into mice to confirm gene and protein expression of CSC markers, tumor-formation capacity, proliferation ability, and invasion potential through histological staining.ConclusionBased on our results, the transplantation of enhanced CSC-functioning 3D SCLC cell lines into mice led to a significant increase in tumor-formation capacity along with elevated expression of CSC markers. Thus, the results collectively suggest that the augmentation of CSC properties in 3D cultured cell lines, when transplanted into animal models, reduces necrosis and enhances tumor formation, proliferation, and invasion.
Keywords
Small-cell lung cancer; Spheroids; Cancer stem cells; Mouse models; Transplantation
ISSN
1738-642X
URI
https://pubs.kist.re.kr/handle/201004/149634
DOI
10.1007/s13273-024-00435-9
Appears in Collections:
KIST Article > 2024
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