Anti-Metastatic Effects of Crocodile Blood Powder through E-cadherin Activation and Matrix Metalloproteinase Inhibition in Hepatocellular Carcinoma Cells.
[BACKGROUND] Crocodile blood is a rich and valuable source of bioactive compounds derived from natural products.
APA
Rungarunlert S, Phonarknguen R, et al. (2026). Anti-Metastatic Effects of Crocodile Blood Powder through E-cadherin Activation and Matrix Metalloproteinase Inhibition in Hepatocellular Carcinoma Cells.. Asian Pacific journal of cancer prevention : APJCP, 27(1), 183-192. https://doi.org/10.31557/APJCP.2026.27.1.183
MLA
Rungarunlert S, et al.. "Anti-Metastatic Effects of Crocodile Blood Powder through E-cadherin Activation and Matrix Metalloproteinase Inhibition in Hepatocellular Carcinoma Cells.." Asian Pacific journal of cancer prevention : APJCP, vol. 27, no. 1, 2026, pp. 183-192.
PMID
41569186
Abstract
[BACKGROUND] Crocodile blood is a rich and valuable source of bioactive compounds derived from natural products. Crocodile blood powder (CP) has garnered significant attention for its potential applications in human health treatment.
[OBJECTIVE] This study aimed to investigate the effect of CP on the invasion and metastasis of hepatocellular carcinoma (HepG2) cells.
[METHODS] We analyzed the protein content of CP using MS/MS techniques. The effects of CP on cell proliferation, apoptosis, metastasis, and invasion were assessed using immunofluorescence, a wound healing assay, a transwell invasion assay, and Western blot analysis, respectively.
[RESULT] The findings indicated that CP could inhibit the proliferation of HepG2 cell lines. Additionally, CP increased caspase-3 expression, inducing apoptosis in HepG2 cells. CP treatment also reduced metastasis and invasion of HepG2 cells. Immunofluorescence and Western blot analyses revealed that CP upregulated E-cadherin expression, while downregulating MMP-2 and MMP-9 expression.
[CONCLUSION] Overall, this study demonstrated that CP inhibits HepG2 cell proliferation and promotes apoptosis. Furthermore, CP suppresses metastasis and invasion by increasing E-cadherin expression and downregulating MMP-2 and MMP-9. Thus, CP may serve as a promising candidate for hepatocellular carcinoma therapy.
[OBJECTIVE] This study aimed to investigate the effect of CP on the invasion and metastasis of hepatocellular carcinoma (HepG2) cells.
[METHODS] We analyzed the protein content of CP using MS/MS techniques. The effects of CP on cell proliferation, apoptosis, metastasis, and invasion were assessed using immunofluorescence, a wound healing assay, a transwell invasion assay, and Western blot analysis, respectively.
[RESULT] The findings indicated that CP could inhibit the proliferation of HepG2 cell lines. Additionally, CP increased caspase-3 expression, inducing apoptosis in HepG2 cells. CP treatment also reduced metastasis and invasion of HepG2 cells. Immunofluorescence and Western blot analyses revealed that CP upregulated E-cadherin expression, while downregulating MMP-2 and MMP-9 expression.
[CONCLUSION] Overall, this study demonstrated that CP inhibits HepG2 cell proliferation and promotes apoptosis. Furthermore, CP suppresses metastasis and invasion by increasing E-cadherin expression and downregulating MMP-2 and MMP-9. Thus, CP may serve as a promising candidate for hepatocellular carcinoma therapy.
MeSH Terms
Humans; Carcinoma, Hepatocellular; Liver Neoplasms; Cadherins; Cell Proliferation; Apoptosis; Alligators and Crocodiles; Animals; Cell Movement; Hep G2 Cells; Matrix Metalloproteinase Inhibitors; Matrix Metalloproteinase 9; Powders; Antigens, CD; Matrix Metalloproteinase 2; Neoplasm Invasiveness; Tumor Cells, Cultured