Risk factors and therapeutic targets in pancreatic cancer

被引:42
作者
Woermann, Sonja Maria [1 ]
Alguel, Hana [1 ]
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Med Klin 2, Munich, Germany
来源
FRONTIERS IN ONCOLOGY | 2013年 / 3卷
关键词
pancreatic ductal adenocarcinoma; risk factors; hereditary cancer syndromes; therapeutic targets; signal-transduction pathways; immune response; stroma reaction; epigenetic changes;
D O I
10.3389/fonc.2013.00282
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic cancer (PC) is one of the most challenging tumor entities worldwide, characterized as a highly aggressive disease with dismal overall prognosis and an incidence rate equalling mortality rate. Over the last decade, substantial progress has been made to define the morphological changes and key genetic events in pancreatic carcinogenesis. And yet, it is still unclear what factors trigger PC. Some risk factors appear to be associated with sex, age, race/ethnicity, or other rare genetic conditions. Additionally, modifying factors such as smoking, obesity, diabetes, occupational risk factors, etc., increase the potential for acquiring genetic mutations that may result in PC. Another hallmark of PC is its poor response to radio- and chemo-therapy. Current chemotherapeutic regimens could not provide substantial survival benefit with a clear increase in overall survival. Recently, several new approaches to significantly improve the clinical outcome of PC have been described involving downstream signaling cascades desmoplasia and stromal response as well as tumor microenvironment, immune response, vasculature, and angiogenesis. This review summarizes major risk factors for PC and tries to illuminate relevant targets considerable for new therapeutic approaches.
引用
收藏
页数:17
相关论文
共 269 条
  • [1] Determination of fs/fd for 7 TeV pp Collisions and Measurement of the B0 → D-K+ Branching Fraction
    Aaij, R.
    Adeva, B.
    Adinolfi, M.
    Adrover, C.
    Affolder, A.
    Ajaltouni, Z.
    Albrecht, J.
    Alessio, F.
    Alexander, M.
    Alkhazov, G.
    Cartelle, P. Alvarez
    Alves, A. A., Jr.
    Amato, S.
    Amhis, Y.
    Amoraal, J.
    Anderson, J.
    Appleby, R. B.
    Gutierrez, O. Aquines
    Arrabito, L.
    Artamonov, A.
    Artuso, M.
    Aslanides, E.
    Auriemma, G.
    Bachmann, S.
    Back, J. J.
    Bailey, D. S.
    Balagura, V.
    Baldini, W.
    Barlow, R. J.
    Barschel, C.
    Barsuk, S.
    Barter, W.
    Bates, A.
    Bauer, C.
    Bauer, Th.
    Bay, A.
    Bediaga, I.
    Belous, K.
    Belyaev, I.
    Ben-Haim, E.
    Benayoun, M.
    Bencivenni, G.
    Benson, S.
    Benton, J.
    Bernet, R.
    Bettler, M. -O.
    van Beuzekom, M.
    Bien, A.
    Bifani, S.
    Bizzeti, A.
    [J]. PHYSICAL REVIEW LETTERS, 2011, 107 (21)
  • [2] Abe N, 2000, CANCER RES, V60, P3117
  • [3] ACS (American Cancer Society), 2011, GLOB CANC FACTS FIG
  • [4] THE EFFECTS OF SUCROSE, FRUCTOSE, AND HIGH-FRUCTOSE CORN SYRUP MEALS ON PLASMA-GLUCOSE AND INSULIN IN NON-INSULIN-DEPENDENT DIABETIC SUBJECTS
    AKGUN, S
    ERTEL, NH
    [J]. DIABETES CARE, 1985, 8 (03) : 279 - 283
  • [5] Molecular targeting of angiogenesis
    Alessi, P
    Ebbinghaus, C
    Neri, D
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2004, 1654 (01): : 39 - 49
  • [6] Allison DC, 1998, J SURG ONCOL, V67, P151, DOI 10.1002/(SICI)1096-9098(199803)67:3<151::AID-JSO2>3.0.CO
  • [7] 2-8
  • [8] MOST HUMAN CARCINOMAS OF THE EXOCRINE PANCREAS CONTAIN MUTANT C-K-RAS GENES
    ALMOGUERA, C
    SHIBATA, D
    FORRESTER, K
    MARTIN, J
    ARNHEIM, N
    PERUCHO, M
    [J]. CELL, 1988, 53 (04) : 549 - 554
  • [9] American Cancer Society (ACS), 2013, CANC FACTS FIG 2015
  • [10] Anderson KE, 2006, CANC EPIDEMIOLOGY PR, P721