Yasen Aimaiti, Wang Maolin, Ran Bo, Lv Guodong, Aji Tuerganaili, Xiao Hui, Shao Yingmei, Wen Hao
Hepatobiliary and Hydatid Disease Department, Digestive and Vascular Surgery Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830054 Xinjiang People's Republic of China.
The First Clinical College of Xinjiang Medical University, Urumqi, 830011 Xinjiang People's Republic of China.
Cytotechnology. 2021 Feb;73(1):13-22. doi: 10.1007/s10616-020-00437-0. Epub 2020 Nov 8.
There may exist a connection between infection and cancer development. Here, it is aimed to investigate specific effects of protoscoleces (PSCs) on the proliferation and invasion capacities of hepatocellular carcinoma (HCC) cells in vitro and ex vitro. HepG2 cells were cultured with different quantities of PSCs in vitro. MTT analysis was used to evaluate effects of PSCs on the proliferation of HepG2 cells. Besides, scratch and transwell assays were respectively used for the detection of HepG2 cells migration and invasion capacities after co-culture with PSCs. Then, HepG2 cells were subcutaneously transplanted into nude mice with or without PSCs. From the 25th day of transplantation, the volume of subcutaneous lesions was measured every four days. At the 37th day, subcutaneous lesions were removed and their weight was evaluated. H&E staining was used for detecting basic pathological changes. HepG2 cells grew well without obvious morphological changes. Proliferation rate and migration capacity of HepG2 cells were higher in the co-culture group than the control group, which was closely associated with quantities of PSCs and co-culture time length. Moreover, HepG2 cells co-cultured with PSCs had stronger invasion ability than the control HepG2 cells. Importantly, there existed significant differences in the volume and weight of subcutaneous lesions after transplanting HepG2 cells with PSCs than the control group. HepG2 cells were also more pathologically heterogeneous in morphology after transplantation with PSCs. Thus, PSCs may promote proliferation and invasion of HCC cells.
感染与癌症发展之间可能存在联系。在此,旨在研究原头节(PSCs)在体外和离体条件下对肝癌(HCC)细胞增殖和侵袭能力的具体影响。在体外将HepG2细胞与不同数量的PSCs共培养。采用MTT分析法评估PSCs对HepG2细胞增殖的影响。此外,划痕实验和Transwell实验分别用于检测与PSCs共培养后HepG2细胞的迁移和侵袭能力。然后,将HepG2细胞皮下移植到有或没有PSCs的裸鼠体内。从移植第25天起,每四天测量一次皮下病变的体积。在第37天,取出皮下病变组织并评估其重量。采用苏木精-伊红(H&E)染色检测基本病理变化。HepG2细胞生长良好,无明显形态变化。共培养组中HepG2细胞的增殖率和迁移能力高于对照组,这与PSCs的数量和共培养时间长短密切相关。此外,与PSCs共培养的HepG2细胞比对照HepG2细胞具有更强的侵袭能力。重要的是,移植有PSCs的HepG2细胞后,皮下病变的体积和重量与对照组相比存在显著差异。移植有PSCs的HepG2细胞在形态上也具有更多的病理异质性。因此,PSCs可能促进HCC细胞的增殖和侵袭。