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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Shandong First Med Univ, Hosp Shandong Acad Med Sci, Dept Gynaecol & Obstet, Affiliated Hosp 3, Jinan 750031, Shandong, Peoples R ChinaShandong First Med Univ, Hosp Shandong Acad Med Sci, Dept Gynaecol & Obstet, Affiliated Hosp 3, Jinan 750031, Shandong, Peoples R China
Li, Kun
Zhou, Min
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Jinan Seventh Peoples Hosp, Dept Gynaecol & Obstet, Jinan 250101, Shandong, Peoples R ChinaShandong First Med Univ, Hosp Shandong Acad Med Sci, Dept Gynaecol & Obstet, Affiliated Hosp 3, Jinan 750031, Shandong, Peoples R China
Zhou, Min
Zhang, Yan
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Shandong First Med Univ, Hosp Shandong Acad Med Sci, Dept Gynaecol & Obstet, Affiliated Hosp 3, Jinan 750031, Shandong, Peoples R ChinaShandong First Med Univ, Hosp Shandong Acad Med Sci, Dept Gynaecol & Obstet, Affiliated Hosp 3, Jinan 750031, Shandong, Peoples R China
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Sojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, JapanSojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Beppu, Takuro
Nishi, Koji
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Sojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Sojo Univ, DDS Res Inst, Nishi Ku, Kumamoto 8600082, JapanSojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Nishi, Koji
Imoto, Shuhei
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Sojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Sojo Univ, DDS Res Inst, Nishi Ku, Kumamoto 8600082, JapanSojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Imoto, Shuhei
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Araki, Waka
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Setoguchi, Itaru
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Ueda, Ayaka
Suetsugi, Naho
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Sojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, JapanSojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Suetsugi, Naho
Ishima, Yu
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Tokushima Univ, Inst Biomed Sci, Dept Pharmacokinet & Biopharmaceut, Tokushima 7708505, JapanSojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Ishima, Yu
Ikeda, Tokunori
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Sojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, JapanSojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Ikeda, Tokunori
Otagiri, Masaki
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Sojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Sojo Univ, DDS Res Inst, Nishi Ku, Kumamoto 8600082, JapanSojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Otagiri, Masaki
Yamasaki, Keishi
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Sojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan
Sojo Univ, DDS Res Inst, Nishi Ku, Kumamoto 8600082, JapanSojo Univ, Fac Pharmaceut Sci, Nishi Ku, 4-22-1 Ikeda, Kumamoto 8600082, Japan