Fibroblasts in cancer

被引:3663
作者
Kalluri, R [1 ]
Zeisberg, M
机构
[1] Beth Israel Deaconess Med Ctr, Ctr Matrix Biol, Boston, MA 02215 USA
[2] Harvard Mit Div Hlth Sci & Technol, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nrc1877
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumours are known as wounds that do not heal - this implies that cells that are involved in angiogenesis and the response to injury, such as endothelial cells and fibroblasts, have a prominent role in the progression, growth and spread of cancers. Fibroblasts are associated with cancer cells at all stages of cancer progression, and their structural and functional contributions to this process are beginning to emerge. Their production of growth factors, chemokines and extracellular matrix facilitates the angiogenic recruitment of endothelial cells and pericytes. Fibroblasts are therefore a key determinant in the malignant progression of cancer and represent an important target for cancer therapies.
引用
收藏
页码:392 / 401
页数:10
相关论文
共 134 条
[61]   Bone-marrow-derived myofibroblasts contribute to the cancer-induced stromal reaction [J].
Ishii, G ;
Sangai, T ;
Oda, T ;
Aoyagi, Y ;
Hasebe, T ;
Kanomata, N ;
Endoh, Y ;
Okumura, C ;
Okuhara, Y ;
Magae, J ;
Emura, M ;
Ochiya, T ;
Ochiai, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 309 (01) :232-240
[62]   Evidence that fibroblasts derive from epithelium during tissue fibrosis [J].
Iwano, M ;
Plieth, D ;
Danoff, TM ;
Xue, C ;
Okada, H ;
Neilson, EG .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 110 (03) :341-350
[63]   Epithelial-mesenchymal transition and its implications for fibrosis [J].
Kalluri, R ;
Neilson, EG .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (12) :1776-1784
[64]   Basement membranes: Structure, assembly and role in tumour angiogenesis [J].
Kalluri, R .
NATURE REVIEWS CANCER, 2003, 3 (06) :422-433
[65]   INHIBITION OF VASCULAR ENDOTHELIAL GROWTH FACTOR-INDUCED ANGIOGENESIS SUPPRESSES TUMOR-GROWTH INVIVO [J].
KIM, KJ ;
LI, B ;
WINER, J ;
ARMANINI, M ;
GILLETT, N ;
PHILLIPS, HS ;
FERRARA, N .
NATURE, 1993, 362 (6423) :841-844
[66]   Growth inhibition and apoptosis in liver myofibroblasts promoted by hepatocyte growth factor leads to resolution from liver cirrhosis [J].
Kim, WH ;
Matsumoto, K ;
Bessho, K ;
Nakamura, T .
AMERICAN JOURNAL OF PATHOLOGY, 2005, 166 (04) :1017-1028
[67]   GENETIC PREDISPOSITION TO CANCER IN MAN - INVITRO STUDIES [J].
KOPELOVICH, L .
INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1982, 77 :63-88
[68]   Reconstruction of functionally normal and malignant human breast tissues in mice [J].
Kuperwasser, C ;
Chavarria, T ;
Wu, M ;
Magrane, G ;
Gray, JW ;
Carey, L ;
Richardson, A ;
Weinberg, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :4966-4971
[69]   Frequent somatic mutations in PTEN and TP53 are mutually exclusive in the stroma of breast carcinomas [J].
Kurose, K ;
Gilley, K ;
Matsumoto, S ;
Watson, PH ;
Zhou, XP ;
Eng, C .
NATURE GENETICS, 2002, 32 (03) :355-357
[70]   COLLAGEN BIOSYNTHESIS IN NONFIBROBLASTIC CELL LINES [J].
LANGNESS, U ;
UDENFRIEND, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (01) :50-51