Acute and Chronic Pancreatitis, Luis Rodrigo, Editör, IntechOpen, London, ss.1-20, 2025
Pancreatic
cancer is characterised by high metastatic potential and poor survival rates. The major reason for this
is the failure of the therapeutic agent to reach the target cells due to the
dense desmoplastic microenvironment formed in pancreatic tumour. The formation
of an immunosuppressive tumour microenvironment due to disruption of matrix
morphology reduces the success rate of immunotherapy, chemotherapy and targeted
therapy methods used in the treatment of Pancreatic Adenoductal Carcinoma
(PDAC). In this chapter, the components of the pancreatic tumour
microenvironment; cancer cells, stromal cells (mesenchymal stem cells,
fibroblasts, pancreatic stellate cells, cancer-associated fibroblasts), immune
system cells and extracellular components (ECM, cytokines, growth factors, DNA
and small RNAs) are explained. This
stroma is a vital dynamic structure that regulates tumour growth, metabolism,
vascularisation, drug resistance, immune tolerance and metastasis pathways. To
comprehend and manage the intense desmoplastic stroma, it is crucial to
elucidate the behaviour of the microenvironment components in pancreatic
cancer. The microenvironment of PDAC, the most common type of pancreatic
cancer, and microenvironment-targeted therapeutic approaches are then presented
as in vitro, in vivo and clinical phase studies.