A 3D culture system for evaluating the combined effects of cisplatin and anti-fibrotic drugs on the growth and invasion of lung cancer cells co-cultured with fibroblasts.
Huei-Jyuan PanChia-Wei LeeLi-Yu WuHeng-Hua HsuYi-Chung TungWei-Yu LiaoChau-Hwang LeePublished in: APL bioengineering (2023)
Fibrosis and fibroblast activation usually occur in the tissues surrounding a malignant tumor; therefore, anti-fibrotic drugs are used in addition to chemotherapy. A reliable technique for evaluating the combined effects of anti-fibrotic drugs and anticancer drugs would be beneficial for the development of an appropriate treatment strategy. In this study, we manufactured a three-dimensional (3D) co-culture system of fibroblasts and lung cancer cell spheroids in Matrigel supplemented with fibrin (fibrin/Matrigel) that simulated the tissue microenvironment around a solid tumor. We compared the efficacy of an anticancer drug (cisplatin) with or without pretreatments of two anti-fibrotic drugs, nintedanib and pirfenidone, on the growth and invasion of cancer cells co-cultured with fibroblasts. The results showed that the addition of nintedanib improved cisplatin's effects on suppressing the growth of cancer cell spheroids and the invasion of cancer cells. In contrast, pirfenidone did not enhance the anticancer activity of cisplatin. Nintedanib also showed higher efficacy than pirfenidone in reducing the expression of four genes in fibroblasts associated with cell adhesion, invasion, and extracellular matrix degradation. This study demonstrated that the 3D co-cultures in fibrin/Matrigel would be useful for assessing the effects of drug combinations on tumor growth and invasion.
Keyphrases
- idiopathic pulmonary fibrosis
- extracellular matrix
- cell migration
- interstitial lung disease
- systemic sclerosis
- cell adhesion
- drug induced
- stem cells
- magnetic resonance imaging
- endothelial cells
- squamous cell carcinoma
- magnetic resonance
- rheumatoid arthritis
- computed tomography
- binding protein
- dna methylation
- smoking cessation
- contrast enhanced
- transcription factor
- bioinformatics analysis