Targeting the mechano-microenvironment and liver cancer stem cells: a promising therapeutic strategy for liver cancer

被引:11
作者
Fu, Xiaorong [1 ,2 ,3 ]
Zhang, Yi [3 ]
Luo, Qing [2 ]
Ju, Yang [3 ]
Song, Guanbin [2 ]
机构
[1] Guizhou Med Univ, Sch Biol & Engn, Guiyang 550000, Peoples R China
[2] Chongqing Univ, Coll Bioengn, Chongqing 400030, Peoples R China
[3] Nagoya Univ, Dept Mech Sci & Engn, Nagoya 4648603, Japan
基金
中国国家自然科学基金; 日本学术振兴会;
关键词
Liver cancer; mechano-microenvironment; cancer stem cells; tumor heterogeneity; mechanotherapy; EPITHELIAL-MESENCHYMAL TRANSITION; HEPATOCELLULAR-CARCINOMA; TRANSIENT ELASTOGRAPHY; STIFFNESS MEASUREMENT; MATRIX STIFFNESS; INITIATING CELLS; FIBROSIS; BETA; CHEMORESISTANCE; PROGRESSION;
D O I
10.20892/j.issn.2095-3941.2023.0229
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Over the past 2 decades, cancer stem cells (CSCs) have been identified as the root cause of cancer occurrence, progression, chemoradioresistance, recurrence, and metastasis. Targeting CSCs is a novel therapeutic strategy for cancer management and treatment. Liver cancer (LC) is a malignant disease that can endanger human health. Studies are increasingly suggesting that changes in the liver mechanical microenvironment are a primary driver triggering the occurrence and development of liver cancer. In this review, we summarize current understanding of the roles of the liver mechano-microenvironment and liver cancer stem cells (LCSCs) in liver cancer progression. We also discuss the relationship between the mechanical heterogeneity of liver cancer tissues and LCSC recruitment and metastasis. Finally, we highlight potential mechanosensitive molecules in LCSCs and mechanotherapy in liver cancer. Understanding the roles and regulatory mechanisms of the mechano-microenvironment and LCSCs may provide fundamental insights into liver cancer progression and aid in further development of novel therapeutic strategies.
引用
收藏
页码:816 / 829
页数:14
相关论文
共 109 条
[1]   Generation of functionally distinct T-cell populations by altering the viscoelasticity of their extracellular matrix [J].
Adu-Berchie, Kwasi ;
Liu, Yutong ;
Zhang, David K. Y. ;
Freedman, Benjamin R. ;
Brockman, Joshua M. ;
Vining, Kyle H. ;
Nerger, Bryan A. ;
Garmilla, Andrea ;
Mooney, David J. .
NATURE BIOMEDICAL ENGINEERING, 2023, 7 (11) :1374-+
[2]   The Role of Cancer-Associated Fibroblasts and Fibrosis in Liver Cancer [J].
Affo, Silvia ;
Yu, Le-Xing ;
Schwabe, Robert F. .
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 12, 2017, 12 :153-186
[3]   Tumor-associated fibroblasts predominantly come from local and not circulating precursors [J].
Arina, Ainhoa ;
Idel, Christian ;
Hyjek, Elizabeth M. ;
Alegre, Maria-Luisa ;
Wang, Ying ;
Bindokas, Vytautas P. ;
Weichselbaum, Ralph R. ;
Schreiber, Hans .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (27) :7551-7556
[4]   A comparison of FibroMeter™ NAFLD Score, NAFLD fibrosis score, and transient elastography as noninvasive diagnostic tools for hepatic fibrosis in patients with biopsy-proven non-alcoholic fatty liver disease [J].
Aykut, Umut Emre ;
Akyuz, Umit ;
Yesil, Atakan ;
Eren, Fatih ;
Gerin, Fatma ;
Ergelen, Rabia ;
Celikel, Cigdem Ataizi ;
Yilmaz, Yusuf .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2014, 49 (11) :1343-1348
[5]   The Role of Fibrosis and Liver-Associated Fibroblasts in the Pathogenesis of Hepatocellular Carcinoma [J].
Baglieri, Jacopo ;
Brenner, David A. ;
Kisseleva, Tatiana .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (07)
[6]   LIVER FIBROSIS AND EXTRACELLULAR-MATRIX [J].
BIAGINI, G ;
BALLARDINI, G .
JOURNAL OF HEPATOLOGY, 1989, 8 (01) :115-124
[7]   Cancer Stem Cells in Squamous Cell Carcinoma Switch between Two Distinct Phenotypes That Are Preferentially Migratory or Proliferative [J].
Biddle, Adrian ;
Liang, Xiao ;
Gammon, Luke ;
Fazil, Bilal ;
Harper, Lisa J. ;
Emich, Helena ;
Costea, Daniela Elena ;
Mackenzie, Ian C. .
CANCER RESEARCH, 2011, 71 (15) :5317-5326
[8]   The ever-increasing importance of cancer as a leading cause of premature death worldwide [J].
Bray, Freddie ;
Laversanne, Mathieu ;
Weiderpass, Elisabete ;
Soerjomataram, Isabelle .
CANCER, 2021, 127 (16) :3029-3030
[9]   Tumor microenvironment and the response to anticancer therapy [J].
Brown, JM .
CANCER BIOLOGY & THERAPY, 2002, 1 (05) :453-458
[10]   Intercellular crosstalk of hepatic stellate cells in liver fibrosis: New insights into therapy [J].
Cai, Xuanyan ;
Wang, Jiajia ;
Wang, Jincheng ;
Zhou, Qian ;
Yang, Bo ;
He, Qiaojun ;
Weng, Qinjie .
PHARMACOLOGICAL RESEARCH, 2020, 155