Cancer-Associated Fibroblasts: Challenges and Directions

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cell Microenvironment".

Deadline for manuscript submissions: 25 October 2024 | Viewed by 766

Special Issue Editors


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Guest Editor
Department of Regenerative & Cancer Cell Biology, Albany Medical College, Albany, NY 12208, USA
Interests: EGFR transactivation; TGF-β signaling; gene regulation; tumor progression; fibroproliferative disease; EMT; skin cancer; cell motility; PAI-1
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Guest Editor
Department of chemistry, Purdue University, West Lafayette, IN 47907, USA
Interests: design and development of targeted ligands and drugs; molecular imaging; preclinical development of FAP-targeted radioligands

Special Issue Information

Dear Colleagues,

Cancer-associated fibroblasts (CAFs) represent a significant cellular component within the tumor microenvironment (TME) and play a crucial role in facilitating tumor growth. They directly contribute to tumor progression by releasing various growth factors, including vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF), fibroblast growth factor (FGF), and various chemokines that stimulate angiogenesis and promote tumor development. Additionally, CAFs indirectly support tumor growth by secreting immune-suppressive cytokines like TGF-β, IL-8, and IL-10, and by remodeling the extracellular matrix (ECM), thereby rendering tumors resistant to various therapeutic interventions.

Cancer-associated fibroblasts (CAFs) are identified through several biomarkers, including α-SMA, PDGFRα/β, and fibroblast activation protein alpha (FAPα), among others. Notably, recent interest has grown around the reprogramming of the tumor microenvironment through the use of FAP-targeting ligand conjugates. This approach has gained prominence due to the exclusive overexpression of FAP in CAFs, with minimal to undetectable expression in healthy tissues. Currently, there are ongoing developments in the clinical use of 68Ga/177Lu-labeled FAP-targeting small molecules and peptide-based PET imaging agents, as well as radiotherapeutic agents.

This Special Issue will focus on original preclinical studies or comprehensive review articles. Topics can include the methods used to target CAF directly or indirectly until depletion of CAFs or elimination of tumor promotion, as well as the immunosuppressive function of CAFs using a combination of different therapeutic strategies for cancer treatment.

Dr. Paul J. Higgins
Dr. Ramesh Mukkamala
Guest Editors

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Keywords

  • cancer-associated fibroblast (CAFs)
  • tumor microenvironment (TME)
  • fibroblast activation protein alpha (FAPα)
  • immunotherapy
  • cytokines
  • angiogenesis
  • metastasis
  • FAP inhibitors
  • radioligands
  • imaging agents

Published Papers (1 paper)

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Review

16 pages, 2197 KiB  
Review
SERPINE1: Role in Cholangiocarcinoma Progression and a Therapeutic Target in the Desmoplastic Microenvironment
by Ralf-Peter Czekay, Craig E. Higgins, Hasan Basri Aydin, Rohan Samarakoon, Nusret Bekir Subasi, Stephen P. Higgins, Hwajeong Lee and Paul J. Higgins
Cells 2024, 13(10), 796; https://doi.org/10.3390/cells13100796 - 7 May 2024
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Abstract
A heterogenous population of inflammatory elements, other immune and nonimmune cells and cancer-associated fibroblasts (CAFs) are evident in solid malignancies where they coexist with the growing tumor mass. In highly desmoplastic malignancies, CAFs are the prominent mesenchymal cell type in the tumor microenvironment [...] Read more.
A heterogenous population of inflammatory elements, other immune and nonimmune cells and cancer-associated fibroblasts (CAFs) are evident in solid malignancies where they coexist with the growing tumor mass. In highly desmoplastic malignancies, CAFs are the prominent mesenchymal cell type in the tumor microenvironment (TME), where their presence and abundance signal a poor prognosis. CAFs play a major role in the progression of various cancers by remodeling the supporting stroma into a dense, fibrotic matrix while secreting factors that promote the maintenance of cancer stem-like characteristics, tumor cell survival, aggressive growth and metastasis and reduced sensitivity to chemotherapeutics. Tumors with high stromal fibrotic signatures are more likely to be associated with drug resistance and eventual relapse. Identifying the molecular underpinnings for such multidirectional crosstalk among the various normal and neoplastic cell types in the TME may provide new targets and novel opportunities for therapeutic intervention. This review highlights recent concepts regarding the complexity of CAF biology in cholangiocarcinoma, a highly desmoplastic cancer. The discussion focuses on CAF heterogeneity, functionality in drug resistance, contributions to a progressively fibrotic tumor stroma, the involved signaling pathways and the participating genes. Full article
(This article belongs to the Special Issue Cancer-Associated Fibroblasts: Challenges and Directions)
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