» Articles » PMID: 32641866

Cancer-associated Fibroblasts Mediate Cancer Progression and Remodel the Tumouroid Stroma

Overview
Journal Br J Cancer
Specialty Oncology
Date 2020 Jul 10
PMID 32641866
Citations 46
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Cancer-associated fibroblasts (CAFs) are highly differentiated and heterogeneous cancer-stromal cells that promote tumour growth, angiogenesis and matrix remodelling.

Methods: We utilised an adapted version of a previously developed 3D in vitro model of colorectal cancer, composed of a cancer mass and the surrounding stromal compartment. We compared cancer invasion with an acellular stromal surround, a "healthy" or normal cellular stroma and a cancerous stroma. For the cancerous stroma, we incorporated six patient-derived CAF samples to study their differential effects on cancer growth, vascular network formation and remodelling.

Results: CAFs enhanced the distance and surface area of the invasive cancer mass whilst inhibiting vascular-like network formation. These processes correlated with the upregulation of hepatocyte growth factor (HGF), metallopeptidase inhibitor 1 (TIMP1) and fibulin-5 (FBLN5). Vascular remodelling of previously formed endothelial structures occurred through the disruption of complex networks, and was associated with the upregulation of vascular endothelial growth factor (VEGFA) and downregulation in vascular endothelial cadherin (VE-Cadherin).

Conclusions: These results support, within a biomimetic 3D, in vitro framework, the direct role of CAFs in promoting cancer invasion, and their key function in driving vasculogenesis and angiogenesis.

Citing Articles

High-throughput non-homogenous 3D polycaprolactone scaffold for cancer cell and cancer-associated fibroblast mini-tumors to evaluate drug treatment response.

Malakpour-Permlid A, Rodriguez M, Untracht G, Andersen P, Oredsson S, Boisen A Toxicol Rep. 2025; 14:101863.

PMID: 39758801 PMC: 11699757. DOI: 10.1016/j.toxrep.2024.101863.


Stromal Expression Profiling Reveals Immune-Driven Adaption to Malignancy in Canine Melanoma Subtypes.

Beebe E, Krudewig C, Motamed Z, Malbon A, Markkanen E Vet Comp Oncol. 2024; 23(1):20-29.

PMID: 39420530 PMC: 11830460. DOI: 10.1111/vco.13021.


Dense Collagen I as a Biomimetic Material to Track Matrix Remodelling in Renal Carcinomas.

Upadhyay A, Bakkalci D, Micalet A, Butler M, Bergin M, Moeendarbary E ACS Omega. 2024; 9(40):41419-41432.

PMID: 39398183 PMC: 11465592. DOI: 10.1021/acsomega.4c04442.


Vascularized platforms for investigating cell communication via extracellular vesicles.

Kim J, Ro J, Cho Y Biomicrofluidics. 2024; 18(5):051504.

PMID: 39323481 PMC: 11421861. DOI: 10.1063/5.0220840.


Advances in targeting cancer-associated fibroblasts through single-cell spatial transcriptomic sequencing.

Lyu P, Gu X, Wang F, Sun H, Zhou Q, Yang S Biomark Res. 2024; 12(1):73.

PMID: 39075612 PMC: 11287900. DOI: 10.1186/s40364-024-00622-9.


References
1.
Robertson A . Urinary diversion in meningomyelocele. Australas Radiol. 1967; 11(2):155-9. DOI: 10.1111/j.1440-1673.1967.tb01516.x. View

2.
Shiga K, Hara M, Nagasaki T, Sato T, Takahashi H, Takeyama H . Cancer-Associated Fibroblasts: Their Characteristics and Their Roles in Tumor Growth. Cancers (Basel). 2015; 7(4):2443-58. PMC: 4695902. DOI: 10.3390/cancers7040902. View

3.
Attieh Y, Matic Vignjevic D . The hallmarks of CAFs in cancer invasion. Eur J Cell Biol. 2016; 95(11):493-502. DOI: 10.1016/j.ejcb.2016.07.004. View

4.
Reid S, Kay E, Neilson L, Henze A, Serneels J, McGhee E . Tumor matrix stiffness promotes metastatic cancer cell interaction with the endothelium. EMBO J. 2017; 36(16):2373-2389. PMC: 5556271. DOI: 10.15252/embj.201694912. View

5.
Mantovani A, Marchesi F, Malesci A, Laghi L, Allavena P . Tumour-associated macrophages as treatment targets in oncology. Nat Rev Clin Oncol. 2017; 14(7):399-416. PMC: 5480600. DOI: 10.1038/nrclinonc.2016.217. View