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Pancreatic cancer
by
Kleeff, Jorg
, La Vecchia, Carlo
, Tempero, Margaret
, Neale, Rachel E.
, Tuveson, David A.
, Neoptolemos, John P.
, Johnson, Colin D.
, Hruban, Ralph H.
, Apte, Minoti
, Biankin, Andrew V.
, Korc, Murray
in
631/67/1059/99
/ 631/67/327
/ 692/699/1503/1504/1713
/ 692/700/565/545/546
/ Animals
/ Animals, Genetically Modified - immunology
/ Biomarkers, Tumor - analysis
/ Biomarkers, Tumor - blood
/ Cancer Research
/ Diabetes Mellitus - etiology
/ Drug development
/ Early Detection of Cancer - standards
/ Epidemiology
/ Humans
/ Internal Medicine
/ Jaundice - etiology
/ Magnetic Resonance Imaging - methods
/ Medical Microbiology
/ Medical prognosis
/ Medicine
/ Medicine & Public Health
/ Mice
/ Models, Animal
/ Neoplasm Proteins - analysis
/ Neoplasm Proteins - blood
/ Pancreatic cancer
/ Pancreatic Neoplasms - epidemiology
/ Pancreatic Neoplasms - immunology
/ Pancreatic Neoplasms - physiopathology
/ primer
/ Prognosis
/ Proto-Oncogene Proteins p21(ras) - analysis
/ Proto-Oncogene Proteins p21(ras) - blood
/ Quality of Life Research
/ Risk Factors
/ Tomography, X-Ray Computed - methods
/ Tumors
/ Weight Loss - immunology
2016
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Pancreatic cancer
by
Kleeff, Jorg
, La Vecchia, Carlo
, Tempero, Margaret
, Neale, Rachel E.
, Tuveson, David A.
, Neoptolemos, John P.
, Johnson, Colin D.
, Hruban, Ralph H.
, Apte, Minoti
, Biankin, Andrew V.
, Korc, Murray
in
631/67/1059/99
/ 631/67/327
/ 692/699/1503/1504/1713
/ 692/700/565/545/546
/ Animals
/ Animals, Genetically Modified - immunology
/ Biomarkers, Tumor - analysis
/ Biomarkers, Tumor - blood
/ Cancer Research
/ Diabetes Mellitus - etiology
/ Drug development
/ Early Detection of Cancer - standards
/ Epidemiology
/ Humans
/ Internal Medicine
/ Jaundice - etiology
/ Magnetic Resonance Imaging - methods
/ Medical Microbiology
/ Medical prognosis
/ Medicine
/ Medicine & Public Health
/ Mice
/ Models, Animal
/ Neoplasm Proteins - analysis
/ Neoplasm Proteins - blood
/ Pancreatic cancer
/ Pancreatic Neoplasms - epidemiology
/ Pancreatic Neoplasms - immunology
/ Pancreatic Neoplasms - physiopathology
/ primer
/ Prognosis
/ Proto-Oncogene Proteins p21(ras) - analysis
/ Proto-Oncogene Proteins p21(ras) - blood
/ Quality of Life Research
/ Risk Factors
/ Tomography, X-Ray Computed - methods
/ Tumors
/ Weight Loss - immunology
2016
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Pancreatic cancer
by
Kleeff, Jorg
, La Vecchia, Carlo
, Tempero, Margaret
, Neale, Rachel E.
, Tuveson, David A.
, Neoptolemos, John P.
, Johnson, Colin D.
, Hruban, Ralph H.
, Apte, Minoti
, Biankin, Andrew V.
, Korc, Murray
in
631/67/1059/99
/ 631/67/327
/ 692/699/1503/1504/1713
/ 692/700/565/545/546
/ Animals
/ Animals, Genetically Modified - immunology
/ Biomarkers, Tumor - analysis
/ Biomarkers, Tumor - blood
/ Cancer Research
/ Diabetes Mellitus - etiology
/ Drug development
/ Early Detection of Cancer - standards
/ Epidemiology
/ Humans
/ Internal Medicine
/ Jaundice - etiology
/ Magnetic Resonance Imaging - methods
/ Medical Microbiology
/ Medical prognosis
/ Medicine
/ Medicine & Public Health
/ Mice
/ Models, Animal
/ Neoplasm Proteins - analysis
/ Neoplasm Proteins - blood
/ Pancreatic cancer
/ Pancreatic Neoplasms - epidemiology
/ Pancreatic Neoplasms - immunology
/ Pancreatic Neoplasms - physiopathology
/ primer
/ Prognosis
/ Proto-Oncogene Proteins p21(ras) - analysis
/ Proto-Oncogene Proteins p21(ras) - blood
/ Quality of Life Research
/ Risk Factors
/ Tomography, X-Ray Computed - methods
/ Tumors
/ Weight Loss - immunology
2016
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Journal Article
Pancreatic cancer
2016
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Overview
Pancreatic cancer is a major cause of cancer-associated mortality, with a dismal overall prognosis that has remained virtually unchanged for many decades. Currently, prevention or early diagnosis at a curable stage is exceedingly difficult; patients rarely exhibit symptoms and tumours do not display sensitive and specific markers to aid detection. Pancreatic cancers also have few prevalent genetic mutations; the most commonly mutated genes are
KRAS
,
CDKN2A
(encoding p16),
TP53
and
SMAD4
— none of which are currently druggable. Indeed, therapeutic options are limited and progress in drug development is impeded because most pancreatic cancers are complex at the genomic, epigenetic and metabolic levels, with multiple activated pathways and crosstalk evident. Furthermore, the multilayered interplay between neoplastic and stromal cells in the tumour microenvironment challenges medical treatment. Fewer than 20% of patients have surgically resectable disease; however, neoadjuvant therapies might shift tumours towards resectability. Although newer drug combinations and multimodal regimens in this setting, as well as the adjuvant setting, appreciably extend survival, ∼80% of patients will relapse after surgery and ultimately die of their disease. Thus, consideration of quality of life and overall survival is important. In this Primer, we summarize the current understanding of the salient pathophysiological, molecular, translational and clinical aspects of this disease. In addition, we present an outline of potential future directions for pancreatic cancer research and patient management.
In 2015, an estimated 367,000 new cases of pancreatic cancer were diagnosed worldwide; this disease is aggressive and patients face a dismal overall prognosis. In this Primer, the current understanding of pathophysiological, molecular, translational and clinical aspects of pancreatic cancer are described.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Animals
/ Animals, Genetically Modified - immunology
/ Biomarkers, Tumor - analysis
/ Diabetes Mellitus - etiology
/ Early Detection of Cancer - standards
/ Humans
/ Magnetic Resonance Imaging - methods
/ Medicine
/ Mice
/ Neoplasm Proteins - analysis
/ Pancreatic Neoplasms - epidemiology
/ Pancreatic Neoplasms - immunology
/ Pancreatic Neoplasms - physiopathology
/ primer
/ Proto-Oncogene Proteins p21(ras) - analysis
/ Proto-Oncogene Proteins p21(ras) - blood
/ Tomography, X-Ray Computed - methods
/ Tumors
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