Molecular Drivers of Pancreatic Cancer Pathogenesis: Looking Inward to Move Forward
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 understa...
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doaj-bb69902b8b434371b58d68285ee885662020-11-24T22:04:12ZengMDPI AGInternational Journal of Molecular Sciences1422-00672017-04-0118477910.3390/ijms18040779ijms18040779Molecular Drivers of Pancreatic Cancer Pathogenesis: Looking Inward to Move ForwardMohammad Aslam Khan0Shafquat Azim1Haseeb Zubair2Arun Bhardwaj3Girijesh Kumar Patel4Moh’d Khushman5Seema Singh6Ajay Pratap Singh7Department of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USADepartment of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USADepartment of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USADepartment of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USADepartment of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USADepartments of Interdisciplinary Clinical Oncology, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USADepartment of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USADepartment of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USAPancreatic 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.http://www.mdpi.com/1422-0067/18/4/779pancreatic ductal adenocarcinomamolecular pathogenesistumor microenvironmentnon-coding RNAsmutationsmicroRNA |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mohammad Aslam Khan Shafquat Azim Haseeb Zubair Arun Bhardwaj Girijesh Kumar Patel Moh’d Khushman Seema Singh Ajay Pratap Singh |
spellingShingle |
Mohammad Aslam Khan Shafquat Azim Haseeb Zubair Arun Bhardwaj Girijesh Kumar Patel Moh’d Khushman Seema Singh Ajay Pratap Singh Molecular Drivers of Pancreatic Cancer Pathogenesis: Looking Inward to Move Forward International Journal of Molecular Sciences pancreatic ductal adenocarcinoma molecular pathogenesis tumor microenvironment non-coding RNAs mutations microRNA |
author_facet |
Mohammad Aslam Khan Shafquat Azim Haseeb Zubair Arun Bhardwaj Girijesh Kumar Patel Moh’d Khushman Seema Singh Ajay Pratap Singh |
author_sort |
Mohammad Aslam Khan |
title |
Molecular Drivers of Pancreatic Cancer Pathogenesis: Looking Inward to Move Forward |
title_short |
Molecular Drivers of Pancreatic Cancer Pathogenesis: Looking Inward to Move Forward |
title_full |
Molecular Drivers of Pancreatic Cancer Pathogenesis: Looking Inward to Move Forward |
title_fullStr |
Molecular Drivers of Pancreatic Cancer Pathogenesis: Looking Inward to Move Forward |
title_full_unstemmed |
Molecular Drivers of Pancreatic Cancer Pathogenesis: Looking Inward to Move Forward |
title_sort |
molecular drivers of pancreatic cancer pathogenesis: looking inward to move forward |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1422-0067 |
publishDate |
2017-04-01 |
description |
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. |
topic |
pancreatic ductal adenocarcinoma molecular pathogenesis tumor microenvironment non-coding RNAs mutations microRNA |
url |
http://www.mdpi.com/1422-0067/18/4/779 |
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