Int J Oral Biol.  2024 Mar;49(1):18-25. 10.11620/IJOB.2024.49.1.18.

Efficacy of biological inhibitors in three-dimensional culture models of oral squamous cell carcinoma

Affiliations
  • 1Division of Gastroenterology, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul 06273, Republic of Korea
  • 2Department of Dental Hygiene, Daejeon Health University, Daejeon 34504, Republic of Korea
  • 3Department of Dental Hygiene, Division of Health Science, Baekseok University, Cheonan 31065, Republic of Korea
  • 4Precision Medicine Research Center, Department of Biomedicine and Health Sciences, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea

Abstract

Despite advancements in therapeutic approaches, radiotherapy and cisplatin-based chemotherapy remain primary noninvasive treatments for patients with oral squamous cell carcinoma (OSCC). Moreover, the 5-year survival rate for patients with OSCC has remained almost unchanged for several decades, and many side effects of chemotherapy still exist. In this study, three-dimensional (3D) models of OSCC were established using fibroblasts, and the efficacy of various biological inhibitors was evaluated. A culture of epithelial cells with two types of fibroblasts (hTERT-hNOFs and cancer-associated fibroblasts) within a type I collagen matrix resulted in the formation of a continuous layer of tightly packed cells compared to models without fibroblasts. Furthermore, the effects of biological chemicals, including Y27632, latrunculin A, and verteporfin, on these models were investigated. The stratified formation of the epithelial layer and invasion in OSCC 3D-culture models were effectively inhibited by verteporfin, whereas invasion was weakly inhibited by Y27632 and latrunculin. Collectively, the developed OSCC 3D-culture models established with fibroblasts demonstrated the potential for drug screening, with verteporfin showing promising efficacy.

Keyword

Squamous cell carcinoma of head and neck; 3D cell culture; Y 27632; Latrunculin A; Verteporfin
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