Therapeutic Potential of Hongjam in A Diethylnitrosamine and Thioacetamide-induced Hepatocellular Carcinoma Mouse Model.

IF 2.5 Q3 ONCOLOGY Journal of Cancer Prevention Pub Date : 2024-12-30 DOI:10.15430/JCP.24.029
Young-Min Han, Hye-Rin Ahn, Da-Young Lee, Moon-Young Song, Seung-Won Lee, You-Kyung Jang, Byeong Yeob Jeon, Eun-Hee Kim
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Abstract

Hepatocellular carcinoma (HCC) is the most common and lethal type of primary liver cancer, frequently arising from chronic liver injury and inflammation. Despite treatment advancements, HCC prognosis remains poor, emphasizing the need for effective preventive and therapeutic strategies. This study investigates the hepatoprotective and anti-tumor effects of Hongjam, a steamed freeze-dried silkworm powder, in a diethylnitrosamine (DEN) and thioacetamide (TAA)-induced HCC mouse model. Mice were administered DEN intraperitoneally for 8 weeks, followed by TAA in drinking water for 9 weeks, with Hongjam supplementation (0.01, 0.1, and 1 g/kg) provided daily through food. Hongjam markedly reduced the tumor incidence, the size, and the histological lesions compared to the DEN/TAA group. Serum biochemical analysis revealed reduction in liver damage markers, including alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, and total bilirubin, with a notable decrease in total bilirubin surpassing. Immunohistochemical and Western blot analyses demonstrated that Hongjam downregulated expression of proliferation markers, including Ki67, phosphorylation of protein kinase B, and proliferating cell nuclear antigen, while upregulating the pro-apoptotic protein Bcl-2-associated X protein, indicating its dual role in suppressing proliferation and promoting apoptosis. Furthermore, Hongjam inhibited angiogenesis by suppressing the expression of key markers, including interleukin 6, VEGF, hypoxia-inducible factor-1 subunit alpha, platelet-derived growth factor subunit beta, matrix metalloproteinase-2, and cluster of differentiation 31, thereby disrupting the tumor microenvironment. These findings suggest that Hongjam exerts multifaceted protective effects against HCC by targeting proliferation, apoptosis, and angiogenesis pathways, while also mitigating liver damage. This study highlights the potential of Hongjam as a functional food or a complementary therapeutic agent for HCC prevention and management.

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红果酱对二乙基亚硝胺和硫代乙酰胺诱导肝癌小鼠模型的治疗作用。
肝细胞癌(HCC)是原发性肝癌中最常见和最致命的类型,通常由慢性肝损伤和炎症引起。尽管治疗进展,HCC预后仍然很差,强调需要有效的预防和治疗策略。本研究探讨了蒸熟冻干蚕粉红酱对二乙基亚硝胺(DEN)和硫乙酰胺(TAA)诱导的肝癌小鼠模型的肝保护和抗肿瘤作用。小鼠腹腔注射DEN 8周,随后在饮用水中添加TAA 9周,每天通过食物补充红果酱(0.01、0.1和1 g/kg)。与DEN/TAA组相比,Hongjam显著降低了肿瘤发生率、肿瘤大小和组织学病变。血清生化分析显示肝损伤标志物,包括碱性磷酸酶、丙氨酸转氨酶、天冬氨酸转氨酶和总胆红素降低,其中总胆红素显著降低。免疫组织化学和Western blot分析显示,红jam下调Ki67、蛋白激酶B磷酸化和增殖细胞核抗原等增殖标志物的表达,上调促凋亡蛋白bcl -2相关X蛋白的表达,表明其具有抑制增殖和促进凋亡的双重作用。此外,红jam通过抑制关键标志物的表达,包括白细胞介素6、VEGF、缺氧诱导因子-1亚基α、血小板衍生生长因子亚基β、基质金属蛋白酶-2和分化簇31,从而破坏肿瘤微环境,抑制血管生成。这些发现表明,红果酱通过靶向增殖、凋亡和血管生成途径对HCC具有多方面的保护作用,同时还能减轻肝损伤。本研究强调了红果酱作为HCC预防和治疗的功能性食品或补充治疗剂的潜力。
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