TY - JOUR
T1 - The Paradoxical Web of Pancreatic Cancer Tumor Microenvironment
AU - Lafaro, Kelly J.
AU - Melstrom, Laleh G.
N1 - Publisher Copyright:
© 2019 American Society for Investigative Pathology
PY - 2019/1
Y1 - 2019/1
N2 - Pancreatic ductal adenocarcinoma (PDAC) is increasing in incidence and is projected to become the second leading cause of cancer death in the United States. Despite significant advances in understanding the disease, there has been minimal increase in PDAC patient survival. PDAC tumors are unique in the fact that there is significant desmoplasia. This generates a large stromal compartment composed of immune cells, inflammatory cells, growth factors, extracellular matrix, and fibroblasts, comprising the tumor microenvironment (TME), which may represent anywhere from 15% to 85% of the tumor. It has become evident that the TME, including both the stroma and extracellular component, plays an important role in tumor progression and chemoresistance of PDAC. This review will discuss the multiple components of the TME, their specific impact on tumorigenesis, and the multiple therapeutic targets.
AB - Pancreatic ductal adenocarcinoma (PDAC) is increasing in incidence and is projected to become the second leading cause of cancer death in the United States. Despite significant advances in understanding the disease, there has been minimal increase in PDAC patient survival. PDAC tumors are unique in the fact that there is significant desmoplasia. This generates a large stromal compartment composed of immune cells, inflammatory cells, growth factors, extracellular matrix, and fibroblasts, comprising the tumor microenvironment (TME), which may represent anywhere from 15% to 85% of the tumor. It has become evident that the TME, including both the stroma and extracellular component, plays an important role in tumor progression and chemoresistance of PDAC. This review will discuss the multiple components of the TME, their specific impact on tumorigenesis, and the multiple therapeutic targets.
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U2 - 10.1016/j.ajpath.2018.09.009
DO - 10.1016/j.ajpath.2018.09.009
M3 - Review article
C2 - 30558722
AN - SCOPUS:85058003867
SN - 0002-9440
VL - 189
SP - 44
EP - 57
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 1
ER -