4.7 Article

The anticancer effects of cyanidin 3-O-glucoside combined with 5-fluoro- uracil on lung large-cell carcinoma in nude mice

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 151, 期 -, 页码 -

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ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2022.113128

关键词

Apoptosis; Cyanidin 3-O-glucoside; 5-Fluorouracil; Lung large-cell carcinoma; Inflammation

资金

  1. Ministry of Science and Technology (Taiwan) [109-2320-B-303-004-MY3]
  2. Chang Gung Memorial Hospital (Taiwan) [CMRPG5J0191]

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This study found that cyanidin-3-O-glucoside (C3G) can inhibit the growth of lung large-cell carcinoma (LCC), and its inhibitory effects can be enhanced when used in combination with 5-fluorouracil (5-FU). C3G can induce tumor cell apoptosis, reduce inflammation, and affect the expression of tumor microenvironment-related factors.
The haskap (Lonicera caerulea L., Caprifoliaceae) berry has been widely used in traditional medicine in Kuril Islands, Russia, Japan, and China. Cyanidin-3-O-glucoside (C3G) is the most abundant anthocyanin in haskap berries, and C3G induces antiproliferative pharmacological activity in various cancer cells. However, no study has investigated its anti-lung large-cell carcinoma (LCC) pharmacological role. Therefore, this study determined whether C3G alone or C3G combined with 5-fluorouracil (5-FU) inhibits human lung LCC. We determined the tumor growth, apoptosis, inflammation, and metastasis in the H661 lung LCC lines xenografted into BALB/c nude mice. The mice were administered saline (control), 5-FU, C3G, or both C3G and 5-FU. Relative to the control mice, those treated with C3G alone or both C3G and 5-FU exhibited impaired tumor growth; increased tumor apoptosis; decreased inflammatory cytokine levels (e.g., IL-1 beta, TNF-alpha, C-reactive protein, and IL-6); decreased inflammation-related factors, including cyclooxygenase-2 protein and nuclear factor-kappa B (NF-kappa B) mRNA; increased inhibition of NF-kappa B kinase alpha mRNA; and downregulated metastasis-related factors, such as transforming growth factor-beta, CD44, epidermal growth factor receptor, and vascular endothelial growth factor. In addition, C3G alone or combined with 5-FU affected the expression of the tumor microenvironment-related factors Ki67, CD45, PDL1, and CD73. Compared with the mice treated with 5-FU or C3G alone, those treated with both C3G and 5-FU exhibited significantly impaired tumor growth, decreased tumor sizes, and increased tumor inhibition. This in vivo study demonstrated that C3G alone or combined with 5-FU may impair the growth of lung LCC and inhibit tumorigenesis. The findings indicate that C3G alone or C3G combined with 5-FU may be beneficial for treating human lung LCC.

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