Growth Suppression of Human Laryngeal Squamous Cell Carcinoma by Adenoviral-mediated Interleukin-12

被引:9
|
作者
Tian, L. [1 ]
Chen, X. [2 ]
Sun, Y. [1 ]
Liu, M. [1 ]
Zhu, D. [1 ]
Ren, J. [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 2, Dept Otorhinolaryngol Head & Neck Surg, Harbin, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 3, Dept Oncol, Harbin, Peoples R China
关键词
LARYNGEAL SQUAMOUS CELL CARCINOMA; INTERLEUKIN-12; ADENOVIRAL-MEDIATED-INTERLEUKIN-12; GENE THERAPY; APOPTOSIS; NATURAL-KILLER-CELLS; IL-12; GENE-THERAPY; STIMULATORY FACTOR; HUMAN OSTEOSARCOMA; FAS EXPRESSION; CANCER MODEL; NECK-CANCER; INHIBITION; HEAD; ANGIOGENESIS;
D O I
10.1177/147323001003800326
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This study explored the inhibitory role of the adenoviral-mediated-interleukin (IL)-12 (Ad.mIL-12) gene in the growth of laryngeal squamous cell carcinoma (LSCC). Human epithelial type 2 (Hep-2) cells were transfected with Ad.mIL-12, and IL-12 gene expression of the cells was evaluated. The proliferation and apoptosis of Hep-2 cells in vitro were detected by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay and flow cytometry. Experimental tumours in mice were injected intratumourally with the same recombinant adenoviruses and inhibition of tumour growth observed. Apoptosis in Hep-2 xenotransplants was detected using TUNEL (terminal deoxynucleotidyl transferase dUTP nick-end labelling) assay and transmission electron microscopy. The expression of IL-12 in Ad.mIL-12 transfected Hep-2 cells was significantly increased. In vitro, Ad.mIL-12 decreased the viability of and increased apoptosis in Hep-2 cells. Increased apoptosis was also seen in vivo. The mean weight and volume of tumours in Ad.mIL-12 treated mice were significantly lower than in the control group. It is concluded that Ad.mIL-12 can suppress LSCC growth and induce apoptosis.
引用
收藏
页码:994 / 1004
页数:11
相关论文
共 50 条
  • [21] Phase I study with Interleukin-12 intratumorally in patients with recurrent head and neck squamous cell carcinoma.
    Van Herpen, CML
    Gosse, JA
    Henri, AMM
    De Wilde, P
    Pieter, HMD
    CLINICAL CANCER RESEARCH, 1999, 5 : 3805S - 3805S
  • [22] Adenoviral-mediated p53 tumor suppressor gene therapy of human ovarian carcinoma
    Mujoo, K
    Maneval, DC
    Anderson, SC
    Gutterman, JU
    ONCOGENE, 1996, 12 (08) : 1617 - 1623
  • [23] Local interleukin-2 and interleukin-12 therapy of bovine ocular squamous cell carcinomas
    Stewart, RJE
    Masztalerz, A
    Jacobs, JJL
    Den Otter, W
    VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2005, 106 (3-4) : 277 - 284
  • [25] Expression and significance of intratumoral interleukin-12 and interleukin-18 in human gastric carcinoma
    Ye, Zheng-Bao
    Ma, Tao
    Li, Hao
    Jin, Xiao-Long
    Xu, Hai-Min
    WORLD JOURNAL OF GASTROENTEROLOGY, 2007, 13 (11) : 1747 - 1751
  • [26] Gene therapy of a rat follicular thyroid carcinoma model with adenoviral vectors transducing murine interleukin-12
    Zhang, RS
    DeGroot, LJ
    ENDOCRINOLOGY, 2003, 144 (04) : 1393 - 1398
  • [27] Adenovirus-mediated interleukin-12 gene therapy for metastatic colon carcinoma
    Caruso, M
    PhamNguyen, K
    Kwong, YL
    Xu, BS
    Kosai, KI
    Finegold, M
    Woo, SLC
    Chen, SH
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (21) : 11302 - 11306
  • [28] Combination treatment with interleukin-2 and interleukin-12 for murine renal cell carcinoma
    Onishi T.
    Ohishi Y.
    Goto H.
    Imagawa K.-I.
    Ohmoto Y.
    Wada K.
    International Journal of Clinical Oncology, 1999, 4 (6) : 364 - 371
  • [29] ENHANCEMENT OF HUMAN B-CELL DIFFERENTIATION BY INTERLEUKIN-12
    BRAATEN, JK
    JELINEK, DF
    FASEB JOURNAL, 1994, 8 (04): : A256 - A256