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Hypoxia targeted bifunctional suicide gene expression enhances radiotherapy in vitro and in vivo.


ABSTRACT:

Purpose

To investigate whether hypoxia targeted bifunctional suicide gene expression-cytosine deaminase (CD) and uracil phosphoribosyltransferase (UPRT) with 5-FC treatments can enhance radiotherapy.

Materials and methods

Stable transfectants of R3327-AT cells were established which express a triple-fusion-gene: CD, UPRT and monomoric DsRed (mDsRed) controlled by a hypoxia inducible promoter. Hypoxia-induced expression/function of CDUPRTmDsRed was verified by western blot, flow cytometry, fluorescent microscopy, and cytotoxicity assay of 5-FU and 5-FC. Tumor-bearing mice were treated with 5-FC and local radiation. Tumor volume was monitored and compared with those treated with 5-FC or radiation alone. In addition, the CDUPRTmDsRed distribution in hypoxic regions of tumor sections was visualized with fluorescent microscopy.

Results

Hypoxic induction of CDUPRTmDsRed protein correlated with increased sensitivity to 5-FC and 5-FU. Significant radiosensitization effects were detected after 5-FC treatments under hypoxic conditions. In the tumor xenografts, the distribution of CDUPRTmDsRed expression visualized with fluorescence microscopy was co-localized with the hypoxia marker pimonidazole positive staining cells. Furthermore, administration of 5-FC to mice in combination with local irradiation resulted in significant tumor regression, as in comparison with 5-FC or radiation treatments alone.

Conclusions

Our data suggest that the hypoxia-inducible CDUPRT/5-FC gene therapy strategy has the ability to specifically target hypoxic cancer cells and significantly improve the tumor control in combination with radiotherapy.

SUBMITTER: Sun X 

PROVIDER: S-EPMC3747309 | biostudies-literature | 2012 Oct

REPOSITORIES: biostudies-literature

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Publications

Hypoxia targeted bifunctional suicide gene expression enhances radiotherapy in vitro and in vivo.

Sun Xiaorong X   Xing Ligang L   Deng Xuelong X   Hsiao Hung Tsung HT   Manami Akiko A   Koutcher Jason A JA   Clifton Ling C C   Li Gloria C GC  

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 20120829 1


<h4>Purpose</h4>To investigate whether hypoxia targeted bifunctional suicide gene expression-cytosine deaminase (CD) and uracil phosphoribosyltransferase (UPRT) with 5-FC treatments can enhance radiotherapy.<h4>Materials and methods</h4>Stable transfectants of R3327-AT cells were established which express a triple-fusion-gene: CD, UPRT and monomoric DsRed (mDsRed) controlled by a hypoxia inducible promoter. Hypoxia-induced expression/function of CDUPRTmDsRed was verified by western blot, flow cy  ...[more]

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