Fibroblast Subsets in Intestinal Homeostasis, Carcinogenesis, Tumor Progression, and Metastasis

被引:13
作者
Dang, Hao [1 ]
Harryvan, Tom J. [1 ]
Hawinkels, Lukas J. A. C. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Gastroenterol & Hepatol, Albinusdreef 2, NL-2333 Leiden, Netherlands
关键词
colorectal cancer; tumor stage; adenoma– carcinoma sequence; cancer-associated fibroblast;
D O I
10.3390/cancers13020183
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Colorectal cancer often develops via the adenoma-carcinoma sequence, a process which is accompanied by (epi) genetic alterations in epithelial cells and gradual phenotypic changes in fibroblast populations. Recent studies have made it clear that these fibroblast populations which, in the context of invasive cancers are termed cancer-associated fibroblasts (CAFs), play an important role in intestinal tumor progression. This review provides an overview on the emerging role of fibroblasts in various stages of colorectal cancer development, ranging from adenoma initiation to metastatic spread of tumor cells. As fibroblasts show considerable heterogeneity in subsets and phenotypes during cancer development, a better functional understanding of stage-specific (alterations in) fibroblast/CAF populations is key to increase the effectiveness of fibroblast-based prognosticators and therapies. In intestinal homeostasis, continuous renewal of the epithelium is crucial to withstand the plethora of stimuli which can damage the structural integrity of the intestines. Fibroblasts contribute to this renewal by facilitating epithelial cell differentiation as well as providing the structural framework in which epithelial cells can regenerate. Upon dysregulation of intestinal homeostasis, (pre-) malignant neoplasms develop, a process which is accompanied by (epi) genetic alterations in epithelial cells as well as phenotypic changes in fibroblast populations. In the context of invasive carcinomas, these fibroblast populations are termed cancer-associated fibroblasts (CAFs). CAFs are the most abundant cell type in the tumor microenvironment of colorectal cancer (CRC) and consist of various functionally heterogeneous subsets which can promote or restrain cancer progression. Although most previous research has focused on the biology of epithelial cells, accumulating evidence shows that certain fibroblast subsets can also importantly contribute to tumor initiation and progression, thereby possibly providing avenues for improvement of clinical care for CRC patients. In this review, we summarized the current literature on the emerging role of fibroblasts in various stages of CRC development, ranging from adenoma initiation to the metastatic spread of cancer cells. In addition, we highlighted translational and therapeutic perspectives of fibroblasts in the different stages of intestinal tumor progression.
引用
收藏
页码:1 / 22
页数:22
相关论文
共 167 条
[81]   Compartmentalized Epidermal Activation of β-Catenin Differentially Affects Lineage Reprogramming and Underlies Tumor Heterogeneity [J].
Kretzschmar, Kai ;
Weber, Christine ;
Driskell, Ryan R. ;
Calonje, Eduardo ;
Watt, Fiona M. .
CELL REPORTS, 2016, 14 (02) :269-281
[82]   Colorectal cancer [J].
Kuipers, Ernst J. ;
Grady, William M. ;
Lieberman, David ;
Seufferlein, Thomas ;
Sung, Joseph J. ;
Boelens, Petra G. ;
de Velde, Cornelis J. H. van ;
Watanabe, Toshiaki .
NATURE REVIEWS DISEASE PRIMERS, 2015, 1
[83]   Cellular and Molecular Mediators of Intestinal Fibrosis [J].
Lawrance, Ian C. ;
Rogler, Gerhard ;
Bamias, Giorgos ;
Breynaert, Christine ;
Florholmen, Jon ;
Pellino, Gianluca ;
Reif, Shimon ;
Speca, Silvia ;
Latella, Giovanni .
JOURNAL OF CROHNS & COLITIS, 2017, 11 (12) :1491-1503
[84]   Immunohistochemical analysis of pericryptal fibroblast sheath and proliferating epithelial cells in human colorectal adenomas and carcinomas with adenoma components [J].
Li, A ;
Hasui, K ;
Yonezawa, S ;
Tanaka, S ;
Sato, E .
PATHOLOGY INTERNATIONAL, 1999, 49 (05) :426-434
[85]   Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors [J].
Li, Huipeng ;
Courtois, Elise T. ;
Sengupta, Debarka ;
Tan, Yuliana ;
Chen, Kok Hao ;
Goh, Jolene Jie Lin ;
Kong, Say Li ;
Chua, Clarinda ;
Hon, Lim Kiat ;
Tan, Wah Siew ;
Wong, Mark ;
Choi, Paul Jongjoon ;
Wee, Lawrence J. K. ;
Hillmer, Axel M. ;
Tan, Iain Beehuat ;
Robson, Paul ;
Prabhakar, Shyam .
NATURE GENETICS, 2017, 49 (05) :708-+
[86]   Idiopathic pulmonary fibrosis will increase the risk of lung cancer [J].
Li Junyao ;
Yang Ming ;
Li Ping ;
Su Zhenzhong ;
Gao Peng ;
Zhang Jie .
CHINESE MEDICAL JOURNAL, 2014, 127 (17) :3142-3149
[87]   Cancer-associated fibroblasts promote PD-L1 expression in mice cancer cells via secreting CXCL5 [J].
Li, Ziqian ;
Zhou, Jiawang ;
Zhang, Junjie ;
Li, Shiying ;
Wang, Hongsheng ;
Du, Jun .
INTERNATIONAL JOURNAL OF CANCER, 2019, 145 (07) :1946-1957
[88]   Cancer-Associated Fibroblasts Build and Secure the Tumor Microenvironment [J].
Liu, Tianyi ;
Zhou, Linli ;
Liu, Danni ;
Andl, Thomas ;
Zhang, Yuhang .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2019, 7
[89]   Tumor progression in hepatocellular carcinoma: Relationship with tumor stroma and parenchymal disease [J].
Lockwood, DSR ;
Yeadon, TM ;
Clouston, AD ;
Crawford, DG ;
Fawcett, J ;
Callaghan, SA ;
Gotley, DC .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2003, 18 (06) :666-672
[90]   Periostin Promotes Colorectal Tumorigenesis through Integrin-FAK-Src Pathway-Mediated YAP/TAZ Activation [J].
Ma, Handong ;
Wang, Jing ;
Zhao, Xueli ;
Wu, Tiantian ;
Huang, Zhengjie ;
Chen, Dafan ;
Liu, Yingfu ;
Ouyang, Gaoliang .
CELL REPORTS, 2020, 30 (03) :793-+