TY - JOUR
T1 - Pancreatic adenocarcinoma
T2 - Unconventional approaches for an unconventional disease
AU - Gromisch, Christopher
AU - Qadan, Motaz
AU - Machado, Mariana Albuquerque
AU - Liu, Kebin
AU - Colson, Yolonda
AU - Grinstaff, Mark W.
N1 - Funding Information:
This work was supported, in part, by NIH (F30 CA220843 to C. Gromisch; R01 CA227433 and R01 CA232056 to M.W. Grinstaff and Y. Colson; CA133085 to K. Liu), Veterans Administration (CX001364 to K. Liu), and Boston University.
Publisher Copyright:
© 2020 American Association for Cancer Research.
PY - 2020/8/15
Y1 - 2020/8/15
N2 - This review highlights current treatments, limitations, and pitfalls in the management of pancreatic cancer and discusses current research in novel targets and drug development to overcome these clinical challenges. We begin with a review of the clinical landscape of pancreatic cancer, including genetic and environmental risk factors, as well as limitations in disease diagnosis and prevention. We next discuss current treatment paradigms for pancreatic cancer and the shortcomings of targeted therapy in this disease. Targeting major driver mutations in pancreatic cancer, such as dysregulation in the KRAS and TGFb signaling pathways, have failed to improve survival outcomes compared with nontargeted chemotherapy; thus, we describe new advances in therapy such as Ras-binding pocket inhibitors. We then review next-generation approaches in nanomedicine and drug delivery, focusing on preclinical advancements in novel optical probes, antibodies, small-molecule agents, and nucleic acids to improve surgical outcomes in resectable disease, augment current therapies, expand druggable targets, and minimize morbidity. We conclude by summarizing progress in current research, identifying areas for future exploration in drug development and nanotechnology, and discussing future prospects for management of this disease.
AB - This review highlights current treatments, limitations, and pitfalls in the management of pancreatic cancer and discusses current research in novel targets and drug development to overcome these clinical challenges. We begin with a review of the clinical landscape of pancreatic cancer, including genetic and environmental risk factors, as well as limitations in disease diagnosis and prevention. We next discuss current treatment paradigms for pancreatic cancer and the shortcomings of targeted therapy in this disease. Targeting major driver mutations in pancreatic cancer, such as dysregulation in the KRAS and TGFb signaling pathways, have failed to improve survival outcomes compared with nontargeted chemotherapy; thus, we describe new advances in therapy such as Ras-binding pocket inhibitors. We then review next-generation approaches in nanomedicine and drug delivery, focusing on preclinical advancements in novel optical probes, antibodies, small-molecule agents, and nucleic acids to improve surgical outcomes in resectable disease, augment current therapies, expand druggable targets, and minimize morbidity. We conclude by summarizing progress in current research, identifying areas for future exploration in drug development and nanotechnology, and discussing future prospects for management of this disease.
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U2 - 10.1158/0008-5472.CAN-19-2731
DO - 10.1158/0008-5472.CAN-19-2731
M3 - Review article
C2 - 32220831
AN - SCOPUS:85089787307
SN - 0008-5472
VL - 80
SP - 3179
EP - 3192
JO - Cancer Research
JF - Cancer Research
IS - 16
ER -