Inhibitory Role of Pentraxin-3 in Esophageal Squamous Cell Carcinoma

被引:8
|
作者
Ma, Dan [1 ,2 ,3 ,4 ]
Zong, Ye [1 ,2 ,3 ,4 ]
Zhu, Sheng-Tao [1 ,2 ,3 ,4 ]
Wang, Yong-Jun [1 ,2 ,3 ,4 ]
Li, Peng [1 ,2 ,3 ,4 ]
Zhang, Shu-Tian [1 ,2 ,3 ,4 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Dept Gastroenterol, 95 Yong An Rd, Beijing 100050, Peoples R China
[2] Natl Clin Res Ctr Digest Dis, Beijing 100050, Peoples R China
[3] Beijing Digest Dis Ctr, Beijing 100050, Peoples R China
[4] Beijing Key Lab Precanc Les Digest Dis, Beijing 100050, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Apoptosis; Esophageal Squamous Cell Carcinoma; Pentraxin-3; Proliferation; C-REACTIVE PROTEIN; BREAST-CANCER; PTX3; INFLAMMATION; FAMILY; MEMBER; IMMUNITY; CLONING;
D O I
10.4103/0366-6999.189921
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Esophageal cancer is the sixth leading cause of cancer-related death worldwide. Pentraxin-3 (PTX3) is a member of the PTX superfamily. Here, we investigated the role of PTX3 in esophageal squamous cell carcinoma (ESCC). Methods: The effect of PTX3 on ESCC cell proliferation, colony formation, apoptosis, migration, and invasion was investigated using cell viability assays, colony formation assays, flow cytometry, and migration and invasion assays. The effect of PTX3 on the tumorigenicity of ESCC in vivo was investigated with xenograft studies in nude mice. Results: PTX3 overexpression in ESCC cells reduced cellular proliferation and colony formation (P 0.05) and increased the rate of apoptosis (P 0.05). PTX3 expression had no significant effect on the migratory or invasive potential of ESCC cells. In our mouse model of human ESCC, we achieved 100% successful tumor establishment. Compared with the control and empty vector-expressing groups, the PTX3-expressing group formed significantly smaller tumors (P 0.05). Conclusions: This study indicates that PTX3 might play an inhibitory role in ESCC.
引用
收藏
页码:2233 / 2240
页数:8
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