Sharma Supriya, Chhimwal Jyoti, Patial Vikram, Sk Ugir Hossain
Pharmacology and Toxicology Laboratory , Institute of Himalayan Bioresource Technology , Palampur , H.P. , India . Email:
Academy of Scientific & Innovative Research , Institute of Himalayan Bioresource Technology , Palampur , H.P. , India.
Toxicol Res (Camb). 2019 May 22;8(4):560-567. doi: 10.1039/c9tx00103d. eCollection 2019 Jul 1.
Podophyllotoxin has been explored as an anticancer, antiviral, and antibacterial agent; however, its low water solubility and toxicity limit its use. In this study, the efficacy of a more soluble and less toxic polyamidoamine (PAMAM) dendrimer-conjugated podophyllotoxin (DPODO) was evaluated against chemically induced hepatocellular carcinoma (HCC) in mice. HCC was induced by giving 0.01% diethylnitrosamine (DENA) in drinking water for 16 weeks. The HCC-induced mice were treated with 10 or 20 mg per kg body weight DPODO. The DENA administration led to HCC development, characterized by anisocytosis, karyomegaly, inflammation and degenerative changes in the liver. The DPODO treatment at 10 mg and 20 mg doses significantly reduced the histopathological changes in liver tissue. The DPODO treatment also significantly lowered the levels of inflammatory markers IL-6 and NF-κB in serum and tissue, respectively. Further, the treatment also significantly reduced fibrous tissue deposition in the liver, which was further confirmed by the reduced mRNA levels and tissue expression of fibrogenic markers TGF-β and α-SMA in the liver. The results of the present study indicate that DPODO treatment suppresses the progression of HCC by modulating the inflammatory and fibrogenic factors, which play important roles in HCC development.
鬼臼毒素已被作为一种抗癌、抗病毒和抗菌剂进行研究;然而,其低水溶性和毒性限制了它的应用。在本研究中,评估了一种更具溶解性且毒性较小的聚酰胺-胺(PAMAM)树枝状大分子偶联鬼臼毒素(DPODO)对化学诱导的小鼠肝细胞癌(HCC)的疗效。通过在饮用水中给予0.01%的二乙基亚硝胺(DENA)16周来诱导HCC。用每千克体重10或20毫克的DPODO对诱导出HCC的小鼠进行治疗。给予DENA导致了HCC的发生,其特征为肝脏中细胞大小不均、核肿大、炎症和退行性变化。10毫克和20毫克剂量的DPODO治疗显著减少了肝组织的组织病理学变化。DPODO治疗还分别显著降低了血清和组织中炎症标志物IL-6和NF-κB的水平。此外,该治疗还显著减少了肝脏中的纤维组织沉积,肝脏中促纤维化标志物TGF-β和α-SMA的mRNA水平及组织表达降低进一步证实了这一点。本研究结果表明,DPODO治疗通过调节在HCC发展中起重要作用的炎症和促纤维化因子来抑制HCC的进展。