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Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models

  • Authors:
    • Ming Zhao
    • Qian Ma
    • Jinhui Xu
    • Shaozhi Fu
    • Lanlan Chen
    • Biqiong Wang
    • Jingbo Wu
    • Linglin Yang
  • View Affiliations / Copyright

    Affiliations: Department of Oncology, Affliated Hospital of Luzhou Medical College, Luzhou, Sichuan 646000, P.R. China
    Copyright: © Zhao et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 768-772
    |
    Published online on: May 27, 2015
       https://doi.org/10.3892/ol.2015.3281
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Abstract

Radiotherapy is an important treatment method for cervical cancer, but the efficacy requires improvement. Therefore, novel methods of treatment are required. Previous data have demonstrated that the CXC chemokine ligand 10 (CXCL10) inhibits angiogenesis, induces apoptosis and causes avoidance of the S phase of the cell cycle in cervical cancer cells. The aim of the present study was to evaluate the anti‑tumor effect of radiotherapy combined with CXCL10 gene therapy. Mouse models of cervical carcinoma were created by inoculation with HeLa cells, and were treated by combining intravenously administered plasmid‑encoding CXCL10, administered 5 times (days 12, 15, 18, 21 and 24 following inoculation), with direct radiation (20 Gy/5 fractions) administered on 5 consecutive days (~day 27 after inoculation). The vessel density and tumor cell proliferation were observed by immunostaining, and apoptosis was determined using a TUNEL assay. The results revealed a significant increase in the inhibition of tumor growth, reduced vessel density, decreased cell proliferation and increased apoptosis in the tumor cells of the combination therapy group. Overall, these findings resulted in the conclusion that CXCL10 gene therapy in combination with radiotherapy is a novel effective therapeutic strategy for cervical cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Zhao M, Ma Q, Xu J, Fu S, Chen L, Wang B, Wu J and Yang L: Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models. Oncol Lett 10: 768-772, 2015.
APA
Zhao, M., Ma, Q., Xu, J., Fu, S., Chen, L., Wang, B. ... Yang, L. (2015). Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models. Oncology Letters, 10, 768-772. https://doi.org/10.3892/ol.2015.3281
MLA
Zhao, M., Ma, Q., Xu, J., Fu, S., Chen, L., Wang, B., Wu, J., Yang, L."Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models". Oncology Letters 10.2 (2015): 768-772.
Chicago
Zhao, M., Ma, Q., Xu, J., Fu, S., Chen, L., Wang, B., Wu, J., Yang, L."Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models". Oncology Letters 10, no. 2 (2015): 768-772. https://doi.org/10.3892/ol.2015.3281
Copy and paste a formatted citation
x
Spandidos Publications style
Zhao M, Ma Q, Xu J, Fu S, Chen L, Wang B, Wu J and Yang L: Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models. Oncol Lett 10: 768-772, 2015.
APA
Zhao, M., Ma, Q., Xu, J., Fu, S., Chen, L., Wang, B. ... Yang, L. (2015). Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models. Oncology Letters, 10, 768-772. https://doi.org/10.3892/ol.2015.3281
MLA
Zhao, M., Ma, Q., Xu, J., Fu, S., Chen, L., Wang, B., Wu, J., Yang, L."Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models". Oncology Letters 10.2 (2015): 768-772.
Chicago
Zhao, M., Ma, Q., Xu, J., Fu, S., Chen, L., Wang, B., Wu, J., Yang, L."Combining CXCL10 gene therapy and radiotherapy improved therapeutic efficacy in cervical cancer HeLa cell xenograft tumor models". Oncology Letters 10, no. 2 (2015): 768-772. https://doi.org/10.3892/ol.2015.3281
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