Ju Yeonuk, Kim Bu Gyeom, Gim Jeong-An, Bong Jun Woo, Cheong Chin Ock, Oh Sang Cheul, Kang Sang Hee, Min Byung Wook, Lee Sun Il
Division of Colon and Rectal Surgery, Department of Surgery, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Republic of Korea.
Institute of Convergence New Drug Development, Korea University College of Medicine, Seoul 08308, Republic of Korea.
Nutrients. 2025 Aug 12;17(16):2609. doi: 10.3390/nu17162609.
BACKGROUND/OBJECTIVES: Colorectal cancer (CRC) remains a significant global health concern, with limited treatment options for metastatic stage 4 CRC. Fibroblast Growth Factor Receptor (FGFR) is a promising therapeutic target in CRC, while cannabidiol (CBD) has shown potential for inducing cell death and overcoming drug resistance. This study evaluates the efficacy of FGFR inhibitors and explores the synergistic effects of combining FGFR inhibitors with CBD in inducing apoptosis in CRC cells.
Cannabidiol and FGFR inhibitors were applied, and protein expression was analyzed via Western blot. Cell viability was assessed using the WST-1 assay, while apoptosis was measured through flow cytometry using Annexin V-FITC/PI staining. CHOP-specific siRNA transfection was performed to study gene silencing effects, followed by RNA sequencing for differential expression and pathway analysis. Statistical significance was determined using ANOVA and -tests, with < 0.05.
FGFR expression patterns were confirmed in various cancer cell lines, with NCI-H716 showing high FGFR2 expression. Treatment with CBD (4 µM) and AZD4547 (10 nM) resulted in significant cell death, especially when used in combination, indicating the effectiveness of this combined therapy. Increased apoptosis in NCI-H716 cells was confirmed with the combined treatment. RNA sequencing and heatmap analysis suggested that ER stress might be related to the observed synergistic effect. The role of ER stress in the combination-induced apoptosis of NCI-H716 cells was further validated.
The combination of FGFR inhibitors and cannabidiol exhibited a synergistic effect in inducing cell death in colorectal cancer cells, likely through the ER stress pathway. This study supports the potential of combined FGFR inhibitor and CBD therapy as a promising strategy for enhancing anticancer effects in CRC.
背景/目的:结直肠癌(CRC)仍然是一个重大的全球健康问题,转移性4期CRC的治疗选择有限。成纤维细胞生长因子受体(FGFR)是CRC中有前景的治疗靶点,而大麻二酚(CBD)已显示出诱导细胞死亡和克服耐药性的潜力。本研究评估FGFR抑制剂的疗效,并探索FGFR抑制剂与CBD联合在诱导CRC细胞凋亡中的协同作用。
应用大麻二酚和FGFR抑制剂,并通过蛋白质印迹分析蛋白质表达。使用WST-1试验评估细胞活力,同时通过Annexin V-FITC/PI染色的流式细胞术测量细胞凋亡。进行CHOP特异性siRNA转染以研究基因沉默效果,随后进行RNA测序以进行差异表达和通路分析。使用方差分析和t检验确定统计学显著性,P<0.05。
在各种癌细胞系中证实了FGFR表达模式,NCI-H716显示高FGFR2表达。用CBD(4μM)和AZD4547(10 nM)处理导致显著的细胞死亡,尤其是联合使用时,表明这种联合疗法有效。联合处理证实NCI-H716细胞中细胞凋亡增加。RNA测序和热图分析表明内质网应激可能与观察到的协同效应有关。内质网应激在联合诱导的NCI-H716细胞凋亡中的作用得到进一步验证。
FGFR抑制剂和大麻二酚的联合在诱导结直肠癌细胞死亡中表现出协同作用,可能通过内质网应激途径。本研究支持联合FGFR抑制剂和CBD疗法作为增强CRC抗癌作用的有前景策略的潜力。