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Pancreatic ductal adenocarcinoma: From genetics to biology to radiobiology to oncoimmunology and all the way back to the clinic

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER
Volume 1855, Issue 1, Pages 61-82

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbcan.2014.12.001

Keywords

Pancreatic cancer; Genetics; Biology; Chemotherapy; Radiobiology; Oncoimmunology

Funding

  1. Cancer Research UK [CRUK C5255/A15935]
  2. Medical Research Council [MRC MC_PC_12004]
  3. Kidani Memorial Trust
  4. Oxford Cancer Imaging Centre [OCIC C5255/A16466]
  5. Oxford Cancer Research Centre
  6. Cancer Research UK [19277] Funding Source: researchfish
  7. Medical Research Council [MC_PC_12004] Funding Source: researchfish
  8. National Institute for Health Research [CL-2014-13-002] Funding Source: researchfish
  9. MRC [MC_PC_12004] Funding Source: UKRI

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Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer death. Despite improvements in the clinical management, the prognosis of PDAC remains dismal. In the present comprehensive review, we will examine the knowledge of PDAC genetics and the new insights into human genome sequencing and clonal evolution. Additionally, the biology and the role of the stroma in tumour progression and response to treatment will be presented. Furthermore, we will describe the evidence on tumour chemoresistance and radioresistance and will provide an overview on the recent advances in PDAC metabolism and circulating tumour cells. Next, we will explore the characteristics and merits of the different mouse models of PDAC. The inflammatory milieu and the immunosuppressive microenvironment mediate tumour initiation and treatment failure. Hence, we will also review the inflammatory and immune escaping mechanisms and the new immunotherapies tested in PDAC. A better understanding of the different mechanisms of tumour formation and progression will help us to identify the best targets for testing in future clinical studies of PDAC. (C) 2014 Elsevier B.V. All rights reserved.

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