Stromal biology of pancreatic cancer

被引:266
作者
Chu, Gerald C.
Kimmelman, Alec C.
Hezel, Aram F.
DePinho, Ronald A. [1 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Ctr Appl Canc Sci, Belfer Fdn Inst Innovat Canc Sci, Boston, MA 02115 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Canc, Boston, MA USA
[4] Harvard Univ, Sch Med, Radiat Oncol Program, Boston, MA USA
[5] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[6] Harvard Univ, Sch Med, Dept Genet, Boston, MA USA
关键词
pancreatic cancer; tumor stroma; pancreatic ductal adenocarcinoma; tumor microenvironment;
D O I
10.1002/jcb.21209
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The genetic paradigm of cancer, focused largely on sequential molecular aberrations and associated biological impact in the neoplastic cell compartment of malignant tumors, has dominated Our view of cancer pathogenesis. For the most part, this conceptualization has overlooked the dynamic and complex contributions of the surrounding microenvironment comprised of non-tumor cells (stroma) that may resist, react to, and/or foster tumor development. Pancreatic ductal adenocarcinoma (PDAC) is a highly lethal disease in which a prominent tumor stroma compartment is a defining characteristic. Indeed, the bulk of PDAC tumor volume consists of non-neoplastic fibroblastic, vascular, and inflammatory cells surrounded by immense quantities of extracellular matrix, far exceeding that found in most other tumor types. Remarkably, little is known about the composition and physiology of the PDAC tumor microenvironment, in particular, the role of stroma in tumor initiation and progression. This review attempts to define key challenges, opportunities and state-of-know relating to the PDAC microenvironment research with an emphasis on how inflammatory processes and key cancer pathways may shape the ontogeny of the tumor stroma. Such knowledge may be used to understand the evolution and biology of this lethal cancer and may convert these insights into new points of therapeutic intervention.
引用
收藏
页码:887 / 907
页数:21
相关论文
共 152 条
  • [1] Activated Kras and Ink4a/Arf deficiency cooperate to produce metastatic pancreatic ductal adenocarcinoma
    Aguirre, AJ
    Bardeesy, N
    Sinha, M
    Lopez, L
    Tuveson, DA
    Horner, J
    Redston, MS
    DePinho, RA
    [J]. GENES & DEVELOPMENT, 2003, 17 (24) : 3112 - 3126
  • [2] Cyclooxygenase-2 expression associated with severity of PanIN lesions: A possible link between chronic pancreatitis and pancreatic cancer
    Albazaz, R
    Verbeke, CS
    Rahman, SH
    McMahon, MJ
    [J]. PANCREATOLOGY, 2005, 5 (4-5) : 361 - 369
  • [3] Clinicopathological correlates of pancreatic intraepithelial neoplasia: A comparative analysis of 82 cases with and 152 cases without pancreatic ductal adenocarcinoma
    Andea, A
    Sarkar, F
    Adsay, VN
    [J]. MODERN PATHOLOGY, 2003, 16 (10) : 996 - 1006
  • [4] Overexpression of TGF-β by infiltrated granulocytes correlates with the expression of collagen mRNA in pancreatic cancer
    Aoyagi, Y
    Oda, T
    Kinoshita, T
    Nakahashi, C
    Hasebe, T
    Ohkohchi, N
    Ochiai, A
    [J]. BRITISH JOURNAL OF CANCER, 2004, 91 (07) : 1316 - 1326
  • [5] Pancreatic stellate cells are activated by proinflammatory cytokines: implications for pancreatic fibrogenesis
    Apte, MV
    Haber, PS
    Darby, SJ
    Rodgers, SC
    McCaughan, GW
    Korsten, MA
    Pirola, RC
    Wilson, JS
    [J]. GUT, 1999, 44 (04) : 534 - 541
  • [6] Desmoplastic reaction in pancreatic cancer - Role of pancreatic stellate cells
    Apte, MV
    Park, S
    Phillips, PA
    Santucci, N
    Goldstein, D
    Kumar, RK
    Ramm, GA
    Buchler, M
    Friess, H
    McCarroll, JA
    Keogh, G
    Merrett, N
    Pirola, R
    Wilson, JS
    [J]. PANCREAS, 2004, 29 (03) : 179 - 187
  • [7] Stellate cell activation in alcoholic pancreatitis
    Apte, MV
    Wilson, JS
    [J]. PANCREAS, 2003, 27 (04) : 316 - 320
  • [8] Periacinar stellate shaped cells in rat pancreas: identification, isolation, and culture
    Apte, MV
    Haber, PS
    Applegate, TL
    Norton, ID
    McCaughan, GW
    Korsten, MA
    Pirola, RC
    Wilson, JS
    [J]. GUT, 1998, 43 (01) : 128 - 133
  • [9] Oncogenic H-ras stimulates tumor angiogenesis by two distinct pathways
    Arbiser, JL
    Moses, MA
    Fernandez, CA
    Ghiso, N
    Cao, YH
    Klauber, N
    Frank, D
    Brownlee, M
    Flynn, E
    Parangi, S
    Byers, HR
    Folkman, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (03) : 861 - 866
  • [10] Endothelial/pericyte interactions
    Armulik, A
    Abramsson, A
    Betsholtz, C
    [J]. CIRCULATION RESEARCH, 2005, 97 (06) : 512 - 523