Cancer-associated fibroblasts and its derived exosomes: a new perspective for reshaping the tumor microenvironment

被引:39
作者
Peng, Zhiwei [1 ]
Tong, Zhiwei [1 ]
Ren, Zihao [1 ]
Ye, Manping [2 ]
Hu, Kongwang [1 ,3 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Dept Gen Surg, Hefei 230022, Anhui, Peoples R China
[2] Anhui Med Univ, Anhui Inst Innovat Drugs, Sch Pharm, Anhui Prov Key Lab Major Autoimmune Dis, Hefei 230032, Anhui, Peoples R China
[3] Anhui Med Univ, Fuyang Affiliated Hosp, Dept Gen Surg, Fuyang 236000, Anhui, Peoples R China
关键词
Cancer-associated fibroblasts; Exosomes; Tumor microenvironment; Diagnosis; Therapy; CARCINOMA-ASSOCIATED FIBROBLASTS; MESENCHYMAL STEM-CELLS; BREAST-CANCER; EXTRACELLULAR VESICLES; COLORECTAL-CANCER; PROGRESSION; ANGIOGENESIS; SECRETION; PROMOTE; PROLIFERATION;
D O I
10.1186/s10020-023-00665-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer-associated fibroblasts (CAFs) are the most abundant stromal cells within the tumor microenvironment (TME). They extensively communicate with the other cells. Exosome-packed bioactive molecules derived from CAFs can reshape the TME by interacting with other cells and the extracellular matrix, which adds a new perspective for their clinical application in tumor targeted therapy. An in-depth understanding of the biological characteristics of CAF-derived exosomes (CDEs) is critical for depicting the detailed landscape of the TME and developing tailored therapeutic strategies for cancer treatment. In this review, we have summarized the functional roles of CAFs in the TME, particularly focusing on the extensive communication mediated by CDEs that contain biological molecules such as miRNAs, proteins, metabolites, and other components. In addition, we have also highlighted the prospects for diagnostic and therapeutic applications based on CDEs, which could guide the future development of exosome-targeted anti-tumor drugs.
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页数:24
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共 222 条
[1]   Human breast cancer invasion and aggression correlates with ECM stiffening and immune cell infiltration [J].
Acerbi, I. ;
Cassereau, L. ;
Dean, I. ;
Shi, Q. ;
Au, A. ;
Park, C. ;
Chen, Y. Y. ;
Liphardt, J. ;
Hwang, E. S. ;
Weaver, V. M. .
INTEGRATIVE BIOLOGY, 2015, 7 (10) :1120-1134
[2]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[3]   Current perspectives on the crosstalk between lung cancer stem cells and cancer-associated fibroblasts [J].
Alguacil-Nunez, Cristina ;
Ferrer-Ortiz, Ines ;
Garcia-Verdu, Elena ;
Lopez-Pirez, Pilar ;
Maria Llorente-Cortijo, Irene ;
Sainz, Bruno, Jr. .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2018, 125 :102-110
[4]  
[Anonymous], CA CANC J CLIN, DOI DOI 10.3322/caac.21492
[5]   Altered p53 functionality in cancer-associated fibroblasts contributes to their cancer-supporting features [J].
Arandkar, Sharathchandra ;
Furth, Noa ;
Elisha, Yair ;
Nataraj, Nishanth Belugali ;
van der Kuip, Heiko ;
Yarden, Yosef ;
Aulitzky, Walter ;
Ulitsky, Igor ;
Geiger, Benjamin ;
Oren, Moshe .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (25) :6410-6415
[6]   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
[7]   Targeting Metabolism to Improve the Tumor Microenvironment for Cancer Immunotherapy [J].
Bader, Jackie E. ;
Voss, Kelsey ;
Rathmell, Jeffrey C. .
MOLECULAR CELL, 2020, 78 (06) :1019-1033
[8]   A FAK-Cas-Rac-Lamellipodin Signaling Module Transduces Extracellular Matrix Stiffness into Mechanosensitive Cell Cycling [J].
Bae, Yong Ho ;
Mui, Keeley L. ;
Hsu, Bernadette Y. ;
Liu, Shu-Lin ;
Cretu, Alexandra ;
Razinia, Ziba ;
Xu, Tina ;
Pure, Ellen ;
Assoian, Richard K. .
SCIENCE SIGNALING, 2014, 7 (330)
[9]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[10]   Exosomes in cancer: Use them or target them? [J].
Bastos, Nuno ;
Ruivo, Carolina F. ;
da Silva, Soraia ;
Melo, Sonia A. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2018, 78 :13-21