RETRACTED: Characterization of Phosphoglycerate Kinase-1 Expression of Stromal Cells Derived from Tumor Microenvironment in Prostate Cancer Progression (Retracted Article)

被引:65
|
作者
Wang, Jianhua [1 ,4 ]
Ying, Gigi [3 ]
Wang, Jingchen [4 ]
Jung, Younghun [4 ]
Lu, Jian [1 ]
Zhu, Jiang [2 ]
Pienta, Kenneth J. [3 ]
Taichman, Russell S. [4 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Inst Med Sci, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Rui Jin Hosp, Shanghai Inst Hematol, Shanghai 200025, Peoples R China
[3] Univ Michigan, Sch Med, Dept Internal Med, Div Hematol Oncol, Ann Arbor, MI USA
[4] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
关键词
MATRIX METALLOPROTEINASES; GROWTH; FIBROBLASTS; ANGIOGENESIS; METASTASIS; CARCINOMAS; SECRETION; OVEREXPRESSION; MYOFIBROBLASTS; TUMORIGENESIS;
D O I
10.1158/0008-5472.CAN-09-2863
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor and stromal interactions in the tumor microenvironment are critical for oncogenesis and cancer progression. Our understanding of the molecular events by which reactive stromal fibroblasts-myofibroblast or cancer-associated fibroblasts (CAF)-affect the growth and invasion of prostate cancer remains unclear. Laser capture microdissection and cDNA microarray analysis of CAFs in prostate tumors revealed strong up-regulation of phosphoglycerate kinase-1 (PGK1), an ATP-generating glycolytic enzyme that forms part of the glycolytic pathway and is directly involved in CXCL12-CXCR4 signaling. Normal fibroblasts overexpressing PGK1 resembled myofibroblasts in their expression of smooth muscle a-actin, vimentin, and high levels of CXCL12. These cells also displayed a higher proliferative index and the capability to contribute to prostate tumor cell invasion in vitro, possibly through expression of MMP-2 and MMP-3 and activation of the AKT and ERK pathways. Coimplantation of PGK1-overexpressing fibroblasts with prostate tumor cells promoted tumor cell growth in vivo. Collectively, these observations suggest that PGK1 helps support the interactions between cancer and its microenvironment. Cancer Res; 70(2); 471-80. (C)2010 AACR.
引用
收藏
页码:471 / 480
页数:10
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