The distribution of liver cancer stem cells correlates with the mechanical heterogeneity of liver cancer tissue

被引:21
作者
Sun, Yuchuan [1 ]
Li, Hong [1 ]
Chen, Qiufang [1 ]
Luo, Qing [1 ]
Song, Guanbin [1 ]
机构
[1] Chongqing Univ, Minist Educ, Coll Bioengn, Key Lab Biorheol Sci & Technol, Chongqing 400030, Peoples R China
基金
中国国家自然科学基金;
关键词
Liver cancer; Mechanical heterogeneity; Liver cancer stem cells; Matrix stiffness; HEPATOCELLULAR-CARCINOMA; MATRIX STIFFNESS; TUMOR MICROENVIRONMENT; PROGRESSION; INVASION; METASTASIS; POPULATION; MIGRATION; STRESS; YAP;
D O I
10.1007/s00418-021-01979-w
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The survival of cancer stem cells is usually limited to a specific tumor microenvironment, and this microenvironment plays a vital role in the development of tumors. The mechanical properties of the microenvironment differ in different regions of solid tumors. However, in solid tumors, whether the distribution of cancer stem cells relates to the mechanical microenvironment of different regions is still unclear. In this study, we undertook a biophysical and biochemical assessment of the changes in the mechanical properties of liver tissue during the progression of liver cancer and explored the distribution of liver cancer stem cells in liver cancer tissues. Our analysis confirmed previous observations that the stiffness of liver tissue gradually increased with the progress of fibrosis. In liver cancer tissues, we found obvious mechanical heterogeneity: the core of the tumor was soft, the invasive front tissue was the hardest, and the para-cancer tissue was in an intermediate state. Interestingly, the greatest number of liver cancer stem cells was found in the invasive front part of the tumor. We finally established that stroma stiffness correlated with the number of liver cancer stem cells. These findings indicate that the distribution of liver cancer stem cells correlates with the mechanical heterogeneity of liver cancer tissue. This result provides a theoretical basis for the development of targeted therapies against the mechanical microenvironment of liver cancer stem cells.
引用
收藏
页码:47 / 58
页数:12
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