Kim Dokyeong, Park Young Jin, Hwang Young Sun
Precision Medicine Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Oral Cancer Research Institute, Department of Oral Pathology, Yonsei University, College of Dentistry, Seoul, Republic of Korea.
Anticancer Res. 2024 Dec;44(12):5337-5349. doi: 10.21873/anticanres.17361.
BACKGROUND/AIM: Accumulated evidence indicates that interactions among various stromal cells within the tumor microenvironment (TME) significantly influence cancer progression. Oral cancers not diagnosed at early stages are associated with low five-year survival rates, highlighting the need for substantial improvements in patient outcomes. Understanding the interactions between cancer cells and the tumor microenvironment is crucial for identifying methods and developing treatment strategies that more effectively inhibit tumor progression and metastasis.
This study investigated the roles of cancer-associated fibroblasts (CAFs) and THP-1 monocytes in tumor growth and invasion, observing changes in cancer biological characteristics through interactions with stromal cells. HSC2 oral squamous cell carcinoma (OSCC) cells were co-cultured with normal fibroblasts (NF), cancer-associated fibroblasts (CAF), or THP-1 cells. Changes in cancer cell invasion were investigated using Matrigel-coated transwell assays, collagen-based dermal equivalent assays, and in vivo mouse studies.
HSC2 cells co-cultured with CAFs or THP-1 exhibited increased invasion compared to those co-cultured with normal fibroblasts (NF) in the dermal equivalent. In a mouse gingival xenograft model, cancer cells co-implanted with CAFs or THP-1 showed significantly increased tumor growth compared to those co-implanted with NF. Micro-CT (μCT) analysis revealed significant alveolar bone resorption around the mandible in tumors grown with CAFs or THP-1 cells. Conditioned media (CM) from CAFs or THP-1 significantly increased HSC2 invasion and migration, an effect that was inhibited by the protein secretion inhibitor Brefeldin (BFA). Furthermore, QuantSeq 3' mRNA sequencing indicated increased expression of IGFBP3, closely associated with cancer invasion, in HSC2 cells co-cultured with CAFs or THP-1.
These findings suggest that cancer cells enhance their invasive characteristics through close interactions with the surrounding stromal cells.
背景/目的:越来越多的证据表明,肿瘤微环境(TME)中各种基质细胞之间的相互作用会显著影响癌症进展。早期未被诊断出的口腔癌与较低的五年生存率相关,这凸显了大幅改善患者预后的必要性。了解癌细胞与肿瘤微环境之间的相互作用对于确定更有效抑制肿瘤进展和转移的方法及制定治疗策略至关重要。
本研究调查了癌症相关成纤维细胞(CAFs)和THP-1单核细胞在肿瘤生长和侵袭中的作用,通过与基质细胞的相互作用观察癌症生物学特性的变化。将HSC2口腔鳞状细胞癌(OSCC)细胞与正常成纤维细胞(NF)、癌症相关成纤维细胞(CAF)或THP-1细胞共培养。使用基质胶包被的Transwell实验、基于胶原蛋白的真皮替代物实验和体内小鼠研究来研究癌细胞侵袭的变化。
与在真皮替代物中与正常成纤维细胞(NF)共培养的HSC2细胞相比,与CAFs或THP-1共培养的HSC2细胞侵袭能力增强。在小鼠牙龈异种移植模型中,与NF共植入的癌细胞相比,与CAFs或THP-1共植入的癌细胞肿瘤生长显著增加。显微CT(μCT)分析显示,在与CAFs或THP-1细胞共同生长的肿瘤中,下颌骨周围有明显的牙槽骨吸收。来自CAFs或THP-1的条件培养基(CM)显著增加了HSC2的侵袭和迁移,蛋白质分泌抑制剂布雷菲德菌素(BFA)可抑制这种作用。此外,QuantSeq 3' mRNA测序表明,在与CAFs或THP-1共培养的HSC2细胞中,与癌症侵袭密切相关的IGFBP3表达增加。
这些发现表明,癌细胞通过与周围基质细胞的密切相互作用增强了其侵袭特性。