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The significance of the co-existence of osteopontin and tumor-associated macrophages in gastric cancer progression
被引:71
|作者:
Lin, Chang-Ni
[1
]
Wang, Chih-Jung
[2
,3
]
Chao, Ying-Jui
[2
,3
]
Lai, Ming-Derg
[1
]
Shan, Yan-Shen
[2
,3
]
机构:
[1] Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Surg, Tainan 70101, Taiwan
[3] Natl Cheng Kung Univ, Coll Med, Inst Clin Med, Tainan 70101, Taiwan
来源:
BMC CANCER
|
2015年
/
15卷
关键词:
Gastric cancer;
Osteopontin;
Tumor-associated macrophage;
Biomarker;
Cancer immunology;
BREAST-CANCER;
INFILTRATING MACROPHAGES;
HEPATOCELLULAR-CARCINOMA;
CLINICAL-IMPLICATIONS;
PANCREATIC-CANCER;
IN-VIVO;
METASTASIS;
EXPRESSION;
SURVIVAL;
INVASION;
D O I:
10.1186/s12885-015-1114-3
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Osteopontin (OPN) can recruit macrophages to the site of inflammation and promote tumorigenesis. M2 tumor-associated macrophages (M2-TAMs) also play an important role in cancer progression. This study aimed to clarify the role of OPN and M2-TAMs co-existence in gastric cancer. Methods: The levels of OPN and M2-TAMs were evaluated by immunohistochemical staining in 170 resected gastric cancer specimens that were collected from 1998 to 2012. M2-TAMs were identified by staining for an M2 marker, CD204. The prognostic significance and correlation between OPN and CD204 expression were analyzed. A co-culture system of OPN+-AGS and U937 cells was designed to study the effect of OPN on the skewing of macrophages toward M2-TAMs for gastric cancer progression in vitro and in vivo. Results: Patients with high expression (>50%) of OPN or CD204 exhibited poor 5-year overall survival rates (48.61%, p = 0.0055, and 52.14%, p = 0.0498, respectively). A positive correlation was observed between OPN and CD204 expression and high co-expression of OPN and CD204 demonstrated poor 5-year overall survival rates (48.90%, p = 0.0131). In the co-culture study, OPN was able to attract U937 cells and skew them toward M2-TAMs through paracrine action. The M2-TAMs could increase the invasiveness of OPN+-AGS cells and the growth rate of xenograft of a mixture of co-cultured OPN+-AGS and U937 cells. Conclusion: OPN can skew macrophages toward M2-TAMs during gastric cancer progression. The co-existence of OPN and infiltrating M2-TAMs correlates with disease progression and poor survival and thus can serve as a prognostic marker in gastric cancer.
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页数:10
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