Hypothesis: are neoplastic macrophages/microglia present in glioblastoma multiforme?

被引:44
作者
Huysentruyt, Leanne C. [2 ]
Akgoc, Zeynep [1 ]
Seyfried, Thomas N. [1 ]
机构
[1] Boston Coll, Dept Biol, Chestnut Hill, MA 02167 USA
[2] Univ Calif San Francisco, Dept Med Hematol & Oncol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
fusion; glioblastoma multiforme; glioma; macrophage; microglia; phagocytosis; TUMOR-ASSOCIATED MACROPHAGES; GENE-EXPRESSION ANALYSIS; MARROW-DERIVED CELLS; CANCER-CELLS; BREAST-CANCER; BRAIN-TUMORS; EXTRACRANIAL METASTASIS; CARCINOMA CELLS; MOUSE MODEL; STEM-CELLS;
D O I
10.1042/AN20110011
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Most malignant brain tumours contain various numbers of cells with characteristics of activated or dysmorphic macrophages/microglia. These cells are generally considered part of the tumour stroma and are often described as TAM (tumour-associated macrophages). These types of cells are thought to either enhance or inhibit brain tumour progression. Recent evidence indicates that neoplastic cells with macrophage characteristics are found in numerous metastatic cancers of non-CNS (central nervous system) origin. Evidence is presented here suggesting that sub-populations of cells within human gliomas, specifically GBM (glioblastoma multiforme), are neoplastic macrophages/microglia. These cells are thought to arise following mitochondrial damage in fusion hybrids between neoplastic stem cells and macrophages/microglia.
引用
收藏
页码:183 / 193
页数:11
相关论文
共 140 条
[1]
Fusion of microglia with pyramidal neurons after retroviral infection [J].
Ackman, James B. ;
Siddiqi, Faez ;
Walikonis, Randall S. ;
LoTurco, Joseph J. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (44) :11413-11422
[2]
Fusion of bone-marrow-derived cells with Purkinje neurons, cardiomyocytes and hepatocytes [J].
Alvarez-Dolado, M ;
Pardal, R ;
Garcia-Vardugo, JM ;
Fike, JR ;
Lee, HO ;
Pfeffer, K ;
Lois, C ;
Morrison, SJ ;
Alvarez-Buylla, A .
NATURE, 2003, 425 (6961) :968-973
[3]
Amat JA, 1996, GLIA, V16, P368, DOI 10.1002/(SICI)1098-1136(199604)16:4<368::AID-GLIA9>3.0.CO
[4]
2-W
[5]
Flow cytometric characterization of tumor-associated macrophages in experimental gliomas [J].
Badie, B ;
Schartner, JM .
NEUROSURGERY, 2000, 46 (04) :957-961
[6]
A transient microenvironment loaded mainly with macrophages in the early developing human pancreas [J].
Banaei-Bouchareb, L ;
Peuchmaur, M ;
Czernichow, P ;
Polak, M .
JOURNAL OF ENDOCRINOLOGY, 2006, 188 (03) :467-480
[7]
The role of tumour-associated macrophages in tumour progression: implications for new anticancer therapies [J].
Bingle, L ;
Brown, NJ ;
Lewis, CE .
JOURNAL OF PATHOLOGY, 2002, 196 (03) :254-265
[8]
Why don't we get more cancer? A proposed role of the microenvironment in restraining cancer progression [J].
Bissell, Mina J. ;
Hines, William C. .
NATURE MEDICINE, 2011, 17 (03) :320-329
[9]
Plasticity of macrophage function during tumor progression: Regulation by distinct molecular mechanisms [J].
Biswas, Subhra K. ;
Sica, Antonio ;
Lewis, Claire E. .
JOURNAL OF IMMUNOLOGY, 2008, 180 (04) :2011-2017
[10]
BJERKNES R, 1987, JNCI-J NATL CANCER I, V78, P279