Feng Ya-Xing, Li Wei, Wen Xu-Dong, Zhang Ning, Liu Wei-Hui, Yang Zhan-Yu
Department of Gastroenterology and Hepatology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, Sichuan Province, 610072, China.
Department of Basic Medical Science, The General Hospital of Western Theater Command, Chengdu, Sichuan Province, 610083, China.
Stem Cells Int. 2020 Nov 28;2020:8819523. doi: 10.1155/2020/8819523. eCollection 2020.
As sinusoidal endothelial cell progenitor cells (SEPCs) play a significant role in liver regeneration, it is necessary to elucidate whether SEPCs participate in tumour progression of hepatocellular carcinoma (HCC).
A total of 45 patients with primary HCC who underwent liver resection were included in this study. The liver tumours were removed from the patients, and partial tissues were prepared to identify SEPCs through double staining of CD133/CD45 and CD133/CD31 at the same location. Blood samples were collected to examine liver function parameters and tumour markers. The demographics and clinicopathological characteristics of the patients were collected for correlation analysis with SEPCs.
SEPCs were observed in several blood vessels within the HCC nodules of all 45 patients, but no SEPCs were detected in the tumour-adjacent tissues. The number of SEPCs was correlated with the expression levels of HCC tumour markers -fetoprotein (AFP) and CA199. There was a positive correlation between the expression of SEPC markers and diameter of HCC tumours in differently differentiated specimens ( < 0.01). The expression levels of SEPC markers were significantly higher in patients with poorly differentiated HCC than in patients with moderately and highly differentiated HCC ( < 0.05).
SEPCs are closely associated with HCC progression; therefore, SEPCs may be considered potential prognostic and metastatic biomarkers and therapeutic candidates for HCC.
由于窦状内皮细胞祖细胞(SEPCs)在肝脏再生中发挥重要作用,因此有必要阐明SEPCs是否参与肝细胞癌(HCC)的肿瘤进展。
本研究纳入了45例行肝切除术的原发性HCC患者。从患者身上切除肝脏肿瘤,并制备部分组织,通过在同一位置对CD133/CD45和CD133/CD31进行双重染色来鉴定SEPCs。采集血样以检测肝功能参数和肿瘤标志物。收集患者的人口统计学和临床病理特征,与SEPCs进行相关性分析。
在所有45例患者的HCC结节内的几条血管中观察到SEPCs,但在肿瘤邻近组织中未检测到SEPCs。SEPCs的数量与HCC肿瘤标志物甲胎蛋白(AFP)和CA199的表达水平相关。在不同分化程度的标本中,SEPC标志物的表达与HCC肿瘤直径呈正相关(<0.01)。低分化HCC患者中SEPC标志物的表达水平显著高于中高分化HCC患者(<0.05)。
SEPCs与HCC进展密切相关;因此,SEPCs可被视为HCC潜在的预后和转移生物标志物及治疗靶点。