The Niche Component Periostin Is Produced by Cancer-Associated Fibroblasts, Supporting Growth of Gastric Cancer through ERK Activation

被引:90
作者
Kikuchi, Yoshinao [1 ]
Kunita, Akiko [1 ]
Iwata, Caname [2 ]
Komura, Daisuke [1 ]
Nishiyama, Takashi [3 ]
Shimazu, Kazuhiro [1 ]
Takeshita, Kimiko [1 ]
Shibahara, Junji [1 ]
Kii, Isao [3 ]
Morishita, Yasuyuki [1 ,2 ]
Yashiro, Masakazu [4 ]
Hirakawa, Kosei [4 ]
Miyazono, Kohei [2 ]
Kudo, Akira [3 ]
Fukayama, Masashi [1 ]
Kashima, Takeshi G. [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Pathol, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo, Japan
[3] Tokyo Inst Technol, Dept Biol Informat, Yokohama, Kanagawa 227, Japan
[4] Osaka City Univ, Sch Med, Dept Surg Oncol, Osaka 545, Japan
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; EXTRACELLULAR-MATRIX; INCREASED EXPRESSION; PROGNOSTIC MARKER; FACTOR-BETA; CELL; PROTEIN; MICE; CARCINOMA; MICROENVIRONMENT;
D O I
10.1016/j.ajpath.2013.11.012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Overexpression of periostin (POSTN), an extraceaular matrix protein, has been observed in several cancers. We investigated the importance of POSTN in gastric cancer. Genome-wide gene expression analysis using publicly available microarray data sets revealed significantly high POSTN expression in cancer tissues from stage II-IV gastric cancer, compared with background normal tissues. The POSTN/vimentin mRNA expression ratio was highly associated with gene groups that regulate the cell cycle and cell proliferation. IHC showed that periglandular POSTN deposition, comprising Linear deposition abutting the glandular epithelial cells in normal mucosa, disappeared during intestinal gastric cancer progression. Stromal POSTN deposition was also detected at the invasive front of intestinal-type and diffuse-type cancers. In situ hybridization confirmed POSTN mRNA in cancer-associated fibroblasts, but not in tumor cells themselves. POSTN enhanced the in vitro growth of OCUM-2MLN and OCUM-12 diffuse-type gastric cancer cell lines, accompanied by the activation of ERK. Furthermore, coinoculation of gastric cancer cells with POSTN-expressing NIH3T3 mouse fibroblast cells facilitated tumor formation. The OCUM-2MLN orthotopic inoculation model demonstrated that tumors of the gastric wall in Postn(-/-) mice were significantly smaller than those in wild-type mice. Ki-67 and p-ERK positive rates were both lower in Postn(-/-) mice. These findings suggest that POSTN produced by cancerassociated fibroblasts constitutes a growth-supportive microenvironment for gastric cancer.
引用
收藏
页码:859 / 870
页数:12
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