The Tumor Stroma of Squamous Cell Carcinoma: A Complex Environment That Fuels Cancer Progression.
Alexandra BuruianăBogdan-Alexandru GhebanIoana-Andreea Gheban-RoșcaCarmen GeorgiuDoința CrișanMaria CrișanPublished in: Cancers (2024)
The tumor microenvironment (TME), a complex assembly of cellular and extracellular matrix (ECM) components, plays a crucial role in driving tumor progression, shaping treatment responses, and influencing metastasis. This narrative review focuses on the cutaneous squamous cell carcinoma (cSCC) tumor stroma, highlighting its key constituents and their dynamic contributions. We examine how significant changes within the cSCC ECM-specifically, alterations in fibronectin, hyaluronic acid, laminins, proteoglycans, and collagens-promote cancer progression, metastasis, and drug resistance. The cellular composition of the cSCC TME is also explored, detailing the intricate interplay of cancer-associated fibroblasts (CAFs), mesenchymal stem cells (MSCs), endothelial cells, pericytes, adipocytes, and various immune cell populations. These diverse players modulate tumor development, angiogenesis, and immune responses. Finally, we emphasize the TME's potential as a therapeutic target. Emerging strategies discussed in this review include harnessing the immune system (adoptive cell transfer, checkpoint blockade), hindering tumor angiogenesis, disrupting CAF activity, and manipulating ECM components. These approaches underscore the vital role that deciphering TME interactions plays in advancing cSCC therapy. Further research illuminating these complex relationships will uncover new avenues for developing more effective treatments for cSCC.
Keyphrases
- extracellular matrix
- squamous cell carcinoma
- endothelial cells
- mesenchymal stem cells
- hyaluronic acid
- cell therapy
- immune response
- papillary thyroid
- adipose tissue
- lymph node metastasis
- type diabetes
- squamous cell
- young adults
- poor prognosis
- radiation therapy
- skeletal muscle
- dendritic cells
- cell proliferation
- long non coding rna
- inflammatory response
- cell cycle
- big data
- high glucose
- genetic diversity