Antitumor effect of photodynamic therapy with a novel targeted photosensitizer on cervical carcinoma

  • Authors:
    • Peng-Xi Li
    • Jiang-Hong Mu
    • Hua-Lang Xiao
    • Dong-Hong Li
  • View Affiliations

  • Published online on: November 7, 2014     https://doi.org/10.3892/or.2014.3593
  • Pages: 125-132
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Abstract

The antitumor effect of photodynamic therapy (PDT) mediated by a novel photosensitizer I (Ps I; {γ-[N-poly(ethyleneglycol)]folic acid}-5,10,15-tris(3-hydroxyphenyl)-20-(4-carboxyphenyl)chlorin), in which chlorin was used as a photoactive unit, folic acid as a tumor‑targeting warhead, and polyethylene glycol as a linker, on cervical carcinoma was studied in vitro and in vivo. Ps I exhibited a considerably higher cellular uptake by HeLa cells than folic acid-free analogue Ps A (tert-butyl N-poly(ethyleneglycol)ethylcarbamate-5,10,15-tris(3-hydroxyphenyl)-20-(4-carboxyphenyl)chlorin), and the cellular uptake by HeLa cells of Ps I could be competitively inhibited by excess folic acid. Moreover, at different time points after the intravenous (i.v.) injection of Ps I and A, Ps I produced a >2-fold higher tumor to normal tissue ratio in tumor-bearing nude mice as compared to Ps A. MTT assay indicated that the HeLa cell proliferation inhibition ratio was increased 34% after Ps I-PDT compared with Ps A-PDT with a photosensitizer concentration of 15.2 µmol/l. Administration of Ps I (7 mg/kg, i.v.) followed by light exposure (80 J/cm2) markedly suppressed the growth of xenograft tumors, and the tumor volume was 10-fold smaller than that of the control group. Tumor growth inhibition in vitro and in vivo had an obvious dependency on the Ps I concentration and irradiation dose. The mode of cell death post-Ps I-PDT was analyzed by flow cytometry, confocal laser scanning microscopy, and electron microscope, and the results suggested that apoptosis was the primary mode of HeLa cell death induced by Ps I-PDT. The results also demonstrated that tumor targeting of Ps I was clearly improved because of the endocytosis mediated by the folate receptor. As a result, Ps I-PDT exhibited higher antitumor activity than Ps A-PDT and has potential as an alternative treatment modality for cervical cancer.
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January-2015
Volume 33 Issue 1

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Spandidos Publications style
Li P, Mu J, Xiao H and Li D: Antitumor effect of photodynamic therapy with a novel targeted photosensitizer on cervical carcinoma. Oncol Rep 33: 125-132, 2015
APA
Li, P., Mu, J., Xiao, H., & Li, D. (2015). Antitumor effect of photodynamic therapy with a novel targeted photosensitizer on cervical carcinoma. Oncology Reports, 33, 125-132. https://doi.org/10.3892/or.2014.3593
MLA
Li, P., Mu, J., Xiao, H., Li, D."Antitumor effect of photodynamic therapy with a novel targeted photosensitizer on cervical carcinoma". Oncology Reports 33.1 (2015): 125-132.
Chicago
Li, P., Mu, J., Xiao, H., Li, D."Antitumor effect of photodynamic therapy with a novel targeted photosensitizer on cervical carcinoma". Oncology Reports 33, no. 1 (2015): 125-132. https://doi.org/10.3892/or.2014.3593