Exogenous Expression of Caspase-14 Induces Tumor Suppression in Human Salivary Cancer Cells by Inhibiting Tumor Vascularization

被引:0
|
作者
Wu, Mengjie [2 ]
Kodani, Isamu [3 ]
Dickinson, Douglas [1 ]
Huff, Frank [1 ]
Ogbureke, Kalu U. E. [1 ]
Qin, Haiyan [1 ]
Arun, Senthil [1 ]
Dulebohn, Rachel [1 ]
Al-Shabrawey, Mohamed [1 ]
Tawfik, Amany [1 ]
Prater, Susan [1 ]
Lewis, Jill [1 ]
Wataha, John [4 ]
Messer, Regina [1 ]
Hsu, Stephen [1 ]
机构
[1] Med Coll Georgia, Sch Dent, Dept Oral Biol, Augusta, GA 30912 USA
[2] Zhejiang Univ, Hosp Stomotol, Dept Orthodont, Hangzhou 310027, Peoples R China
[3] Tottori Univ, Fac Med, Tottori Univ Hosp, Dept Oral & Maxillofacial Surg, Yonago, Tottori 683, Japan
[4] Univ Washington, Dept Restorat Dent, Seattle, WA 98195 USA
关键词
Caspase-14; salivary gland cancer; vascularization; gene therapy; HUMAN SJOGRENS-SYNDROME; KERATINOCYTE DIFFERENTIATION; EPIDERMAL-KERATINOCYTES; MURINE MODEL; SKIN-CANCER; INDUCTION; GENE; APOPTOSIS; PATHWAYS; THERAPY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Current therapeutic approaches to salivary gland cancer are often associated with severe disfigurement and loss of glandular function, which are traumatic to the patients. Exploration of novel treatment approaches, such as gene therapy, is needed. Materials and Methods: The human salivary gland cancer cell line HSG was transiently transfected with full length human caspase-14 cDNA. Photomicroscopy, BrdU assay, cell counting, MTT assay, and TUNEL assay were applied. To determine the tumorigenicity, tumor volume, tumor pathology and vascularization were analyzed in vivo. Results: Cell growth and viability were inhibited significantly by transient caspase-14 expression. Caspase-14 expression resulted in a significant reduction of tumorigenicity. Importantly, a significant decrease in tumor blood vessel formation was observed. Conclusion: Salivary gland cancer cells underwent growth inhibition, cell death, and reduced tumorigenicity in vivo when exogenous caspase-14 was expressed, which could be due, in part, to an inhibitory effect of caspase-14 on tumor vascularization.
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页码:3811 / 3818
页数:8
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