TY - JOUR
T1 - Molecular drivers of pancreatic cancer pathogenesis
T2 - Looking inward to move forward
AU - Khan, Mohammad Aslam
AU - Azim, Shafquat
AU - Zubair, Haseeb
AU - Bhardwaj, Arun
AU - Patel, Girijesh Kumar
AU - Khushman, Moh’D
AU - Singh, Seema
AU - Singh, Ajay Pratap
N1 - Funding Information:
This work was supported in part by National Institute of Health (NIH) grants to Ajay Pratap Singh (R01CA175772). The authors have also received funding and resource support from the University of South Alabama Mitchell Cancer Institute.
Publisher Copyright:
© 2017 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2017/4/6
Y1 - 2017/4/6
N2 - Pancreatic cancer (PC) continues to rank among the most lethal cancers. The consistent increase in incidence and mortality has made it the seventh leading cause of cancer-associated deaths globally and the third in the United States. The biggest challenge in combating PC is our insufficient understanding of the molecular mechanism(s) underlying its complex biology. Studies during the last several years have helped identify several putative factors and events, both genetic and epigenetic, as well as some deregulated signaling pathways, with implications in PC onset and progression. In this review article, we make an effort to summarize our current understanding of molecular and cellular events involved in the pathogenesis of pancreatic malignancy. Specifically, we provide up-to-date information on the genetic and epigenetic changes that occur during the initiation and progression of PC and their functional involvement in the pathogenic processes. We also discuss the impact of the tumor microenvironment on the molecular landscape of PC and its role in aggressive disease progression. It is envisioned that a better understanding of these molecular factors and the mechanisms of their actions can help unravel novel diagnostic and prognostic biomarkers and can also be exploited for future targeted therapies.
AB - Pancreatic cancer (PC) continues to rank among the most lethal cancers. The consistent increase in incidence and mortality has made it the seventh leading cause of cancer-associated deaths globally and the third in the United States. The biggest challenge in combating PC is our insufficient understanding of the molecular mechanism(s) underlying its complex biology. Studies during the last several years have helped identify several putative factors and events, both genetic and epigenetic, as well as some deregulated signaling pathways, with implications in PC onset and progression. In this review article, we make an effort to summarize our current understanding of molecular and cellular events involved in the pathogenesis of pancreatic malignancy. Specifically, we provide up-to-date information on the genetic and epigenetic changes that occur during the initiation and progression of PC and their functional involvement in the pathogenic processes. We also discuss the impact of the tumor microenvironment on the molecular landscape of PC and its role in aggressive disease progression. It is envisioned that a better understanding of these molecular factors and the mechanisms of their actions can help unravel novel diagnostic and prognostic biomarkers and can also be exploited for future targeted therapies.
KW - MicroRNA
KW - Molecular pathogenesis
KW - Mutations
KW - Non-coding RNAs
KW - Pancreatic ductal adenocarcinoma
KW - Tumor microenvironment
UR - http://www.scopus.com/inward/record.url?scp=85017205279&partnerID=8YFLogxK
U2 - 10.3390/ijms18040779
DO - 10.3390/ijms18040779
M3 - Review article
C2 - 28383487
AN - SCOPUS:85017205279
SN - 1661-6596
VL - 18
JO - International journal of molecular sciences
JF - International journal of molecular sciences
IS - 4
M1 - 779
ER -