SERPINE1: Role in Cholangiocarcinoma Progression and a Therapeutic Target in the Desmoplastic Microenvironment.
Ralf-Peter CzekayCraig E HigginsHasan Basri AydinRohan SamarakoonNusret Bekir SubasiStephen P HigginsHwajeong LeePaul J HigginsPublished in: Cells (2024)
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.
Keyphrases
- poor prognosis
- papillary thyroid
- long non coding rna
- idiopathic pulmonary fibrosis
- systemic sclerosis
- stem cells
- induced apoptosis
- bone marrow
- single cell
- randomized controlled trial
- squamous cell
- genome wide
- oxidative stress
- cell therapy
- gene expression
- childhood cancer
- epithelial mesenchymal transition
- mesenchymal stem cells
- extracellular matrix
- endoplasmic reticulum stress
- cell death
- genome wide identification