Inhibition of CD147 gene expression via RNA interference reduces tumor cell proliferation, activation, adhesion, and migration activity in the human Jurkat T-lymphoma cell line

被引:28
作者
Chen, Xiang [1 ]
Su, Juan [1 ]
Chang, Jing [1 ]
Kanekura, Takuro [2 ]
Li, Ji [1 ]
Kuang, Ye Hong [1 ]
Peng, Sheng [1 ]
Yang, Fang [1 ]
Lu, Hui [1 ]
Zhang, Jiang Lin [1 ]
机构
[1] Cent S Univ, Xiang Ya Hosp, Dept Dermatol, Changsha 410008, Hunan, Peoples R China
[2] Kagoshima Univ, Grad Sch Med & Dent Sci, Field Sensory Organol, Dept Dermatol, Kagoshima 890, Japan
基金
中国国家自然科学基金;
关键词
CD147; siRNA; Jurkat; proliferation; activation; lymphoma;
D O I
10.1080/07357900701867892
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD147, a leukocyte surface molecule over-expressed in T-lymphoma cells, is reportedly associated with lymphocyte activation and proteinase production via interactions with fibroblasts and plays a role in stromal invasion by lymphoma cells. To determine the role of CD147 in the progression of T-lymphoma, we performed siRNA interference-mediated knockdown of CD147 in a CD147-expressing Jurkat T-cell line. CD147 knockdown resulted in the decreased proliferation and migration of Jurkat cells and reduced the adhesion of Jurkat cells to extracelluar matrix fibronectin in vitro. CD147-siRNA inhibited the activation of Jurkat cells via down-regulation of CD25 expression. Our results indicate that CD147 is involved in T-lymphoma progression, a finding useful in efforts to develop targeted therapies to treat patients with T-lymphoma.
引用
收藏
页码:689 / 697
页数:9
相关论文
共 40 条
[1]   Early activation of caspases during T lymphocyte stimulation results in selective substrate cleavage in nonapoptotic cells [J].
Alam, A ;
Cohen, LY ;
Aouad, S ;
Sékaly, RP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (12) :1879-1890
[2]   Interaction with glycosaminoglycans is required for cyclophilin B to trigger integrin-mediated adhesion of peripheral blood T lymphocytes to extracellular matrix [J].
Allain, F ;
Vanpouille, C ;
Carpentier, M ;
Slomianny, MC ;
Durieux, S ;
Spik, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (05) :2714-2719
[3]   A NOVEL METALLOPROTEINASE GENE SPECIFICALLY EXPRESSED IN STROMAL CELLS OF BREAST CARCINOMAS [J].
BASSET, P ;
BELLOCQ, JP ;
WOLF, C ;
STOLL, I ;
HUTIN, P ;
LIMACHER, JM ;
PODHAJCER, OL ;
CHENARD, MP ;
RIO, MC ;
CHAMBON, P .
NATURE, 1990, 348 (6303) :699-704
[4]  
BISWAS C, 1995, CANCER RES, V55, P434
[5]  
Bordador LC, 2000, INT J CANCER, V85, P347, DOI 10.1002/(SICI)1097-0215(20000201)85:3<347::AID-IJC9>3.0.CO
[6]  
2-#
[7]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[8]   EMMPRIN-mediated MMP regulation in tumor and endothelial cells [J].
Caudroy, S ;
Polette, M ;
Nawrocki-Raby, B ;
Cao, J ;
Toole, BP ;
Zucker, S ;
Birembaut, P .
CLINICAL & EXPERIMENTAL METASTASIS, 2002, 19 (08) :697-702
[9]   A small interfering CD147-targeting RNA inhibited the proliferation, invasiveness, and metastatic activity of malignant melanoma [J].
Chen, Xiang ;
Lin, Jing ;
Kanekura, Takuro ;
Su, Juan ;
Lin, Wei ;
Xie, Hongfu ;
Wu, Yixi ;
Li, Juan ;
Chen, Mingliang ;
Chang, Jing .
CANCER RESEARCH, 2006, 66 (23) :11323-11330
[10]   The functional interactions between CD98, β1-integrins, and CD147 in the induction of U937 homotypic aggregation [J].
Cho, JY ;
Fox, DA ;
Horejsi, V ;
Sagawa, K ;
Skubitz, KM ;
Katz, DR ;
Chain, B .
BLOOD, 2001, 98 (02) :374-382