Radiodynamic Therapy with Chlorine-Based Photosensitizer on Pliss Lymphosarcoma Solid Tumor: In Vivo Experiment
- Authors
-
-
D.A. Tzerkovsky
Laboratory of Photodynamic Therapy and Hyperthermia with Chemotherapy Group, N.N. Alexandrov National Cancer Center of Belarus, Lesnoy, Republic of Belarus -
A.N. Mazurenko
Department of Centralized Dilution of Cytostatics, N.N. Alexandrov National Cancer Center of Belarus, Lesnoy, Republic of Belarus -
D.I. Kozlovsky
Radiation Therapy Engineering Department, N.N. Alexandrov National Cancer Center of Belarus, Lesnoy, Republic of Belarus -
F.F. Borychevsky
Neurosurgical Department, Minsk Regional Clinical Hospital, Lesnoy, Republic of Belarus
-
- Keywords:
- Chlorine-based photosensitizer, radiation therapy, radiodynamic therapy, laboratory animals, Pliss lymphosarcoma
- Abstract
-
The aim of this study was to investigate the antitumor efficacy of radiodynamic therapy (RDT) with a chlorin-based photosensitizer (PS) in an in vivo experiment.
Material and Methods: The study was performed in 35 white outbred rats weighing 180±30 g. Subcutaneously transplanted Pliss lymphosarcoma (PLS) was used as tumor model. Chlorin-based PS «Photolon» (RUE «Belmedpreparaty», Republic Belarus) was injected intravenously at a dose of 2.5 mg/kg. The radiation therapy sessions (RT) were carried out once 2.5–3 hours after the administration of the PS by the contact method on the device «microSelectron-HDR V3 Digital» (Elekta, Sweden) using γ-radiation (192Ir) in single focal doses (SFD) 2, 4 and 6 Gy. All laboratory animals were subdivided into 7 groups of 5 animals each: intact control, RT 2 Gy, RT 4 Gy, RT 6 Gy, PS + RT 2 Gy, PS + RT 4 Gy and PS + RT 6 Gy. The antitumor effectiveness of exposure was evaluated according to the indicators characterizing the dynamics of volume changes: Vav. (cm3), the coefficient of absolute tumor growth (K, units) and the coefficient of tumor growth inhibition (TGI, %). The frequency of complete regressions (СR) was estimated 60 days after the performed exposures. In each group, the share of animals (%) with no visual and palpatory signs of tumor growth was evaluated. The differences were considered statistically significant at the significance level of p<0.05.
Results: On the 16th day from the beginning of the experiment Vav. in groups were 39.07±4.19; 23.06±3.25 (р=0.012); 35.04±2.35 (р=0.419); 25.83±3.06 (р=0.027); 28.36±3.45 (0.074); 25.47±1.88 (р=0.013) and 16.56±3.64 cm3 (р=0,002), respectively. The K coefficients in the experimental groups were 1219.94; 657.86; 1296.78; 716.50; 833.12; 669.26 and 590.43 units, respectively. The TGI coefficients in the experimental groups were 40.98%; 10.31%; 33.89%; 27.41%; 34.81% and 57.61%, respectively. The frequency of complete tumor regressions 60 days after the start of the experiment was 0%, 20%, 0%, 0%, 0%, 0% and 40%, respectively.
Conclusion: RDT is a recent extension of conventional photodynamic therapy, in which visible/near infrared light irradiation is replaced by a well-tolerated dose of X-rays. Systemic administration of chlorin-based PS before the RT session increases the antitumor efficacy of RT in animals with PLS transplantable tumors. The data obtained indicate that further studies of the radiosensitizing properties of PS are promising.
- References
-
Takahashi J, Nagasawa S, Ikemoto MJ, et al. Verification of 5-aminolevurinic radiodynamic therapy using a murine melanoma brain metastasis model. Int J Mol Sci 2019; 20: 5155. https://doi.org/10.3390/ijms20205155
Takahashi J, Nagasawa S, Doi M, et al. In vivo study of the efficacy and safety of 5-aminolevulinic radiodynamic therapy for glioblastoma fractionated radiotherapy. Int J Mol Sci 2021; 22: 9762. https://doi.org/10.3390/ijms22189762
Yamamoto J, Ogura S, Shimajiri S, et al. 5-Aminolevulinic acidinduced protoporphyrin IX with multi-dose ionizing irradiation enhances host antitumor response and strongly inhibits tumor growth in experimental glioma in vivo. Mol Med Rep 2015; 11(3): 1813-19. https://doi.org/10.3892/mmr.2014.2991
Luksiene Z, Juzenas P, Moan J. Radiosensitization of tumours by porphyrins. Cancer Lett 2006; 235: 40-7. https://doi.org/10.1016/j.canlet.2005.03.041
Schaffer M, Kulka U, Schaffer P. The role of radical derivatives of high reactivity in the radiosensitizing action of Photofrin II. J Porphyrins Phthalocyanines 2006; 10: 1398-1402. https://doi.org/10.1142/S1088424606000776
Tzerkovsky DA, Protopovich YaL, Kozlovsky DI, Suslova VA. Antitumor efficiency of contact radiotherapy in combination with a chlorin-based photosensitizer in experiment. Biomed Photonics 2021; 10(2): 25-33. https://doi.org/10.24931/2413-9432-2021-10-2-25-33
Algorri JF, Ochoa M, Roldán-Varona P, et al. Photodynamic therapy: a compendium of latest reviews. Cancers (Basel) 2021; 13(17): 4447. https://doi.org/10.3390/cancers13174447
Schaffer M, Schaffer PM, Jori G, et al. Radiation therapy combined with photofrin or 5-ALA: effect on Lewis sarcoma tumor lines implanted in mice. Tumori 2002; 88: 407-10. https://doi.org/10.1177/030089160208800511
Schaffer M, Ertl-Wagner B, Schaffer PM, et al. Porphyrins as radiosensitizing agents for solid neoplasms. Curr Pharm Des 2003; 9(25): 2024-35. https://doi.org/10.2174/1381612033454153
Rutkovskienė L, Plėšnienė L, Sendiulienė D, et al. Sensitization of rat C6 glioma cells to ionizing radiation by porphyrins. Acta Medica Lituanica 2011; 18(2): 56-62. https://doi.org/10.6001/actamedica.v18i2.1816
Schaffer M, Kulka U, Ertl-Wagner B, et al. Effect of Photofrin II as a radio-sensitizing agent in two different oesophageal carcinoma cell lines. J Porphyrins Phthalocyanines 2005; 9: 470-75. https://doi.org/10.1142/S1088424605000587
Tzerkovsky DA. Photosensitizers as radiosensitizing agents in experimental and clinical neurooncology. Biomed Photonics 2017; 6(2): 27-33 (in Russian).
Moradi A, Hashemi B, Hassan Z. In vivo evaluation of photofrin II radiosensitivity for the treatment of adenocarcinoma tumors in balb/C mice using brachytherapy. IFMBE Proceedings 2009; 25(1): 141-43. https://doi.org/10.1007/978-3-642-03474-9_41
Bloznelytė-Plėšnienė L, Rutkovskiene L. Radiosensitized treatment of primary or metastatical malignant brain tumors with hematoporphyrin derivative. Electron Electric Engineer 2006; 4(68): 83-6.
Schaffer M, Еrtl-Wagner В, Schaffer РМ. Feasibility of photofrin II as a radiosensitizing agent in solid tumors – preliminary results. Onkologie 2006; 29: 514-19. https://doi.org/10.1159/000095979
Schaffer М, Hofstetter А, Ertl-Wagner В, et al. Treatment of astrocytoma grade III with Photofrin II as a radiosensitizer. A case report. Strahlenther Onkol 2013; 189(11): 972-76. https://doi.org/10.1007/s00066-013-0430-2
Schaffer Р, Batash R, Ertl-Wagner В, et al. Treatment of cervix carcinoma FIGO IIIb with Photofrin II as a radiosensitizer: a case report. Photochem Photobiol Sci 2019; 18: 1275-79. https://doi.org/10.1039/C8PP00576A
- Downloads
- Published
- 2022-09-28
- Issue
- Vol. 11 (2022)
- Section
- Articles
- License
-

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
Similar Articles
- Atara Isaiah Ntekim, Oluyemisi Folake Folasire, Ayorinde Mobolande Folasire , Prevalence of Malnutrition among Cancer Patients in a Nigerian Institution , Journal of Analytical Oncology: Vol. 6 No. 2 (2017)
- Sally McLaren, Frank Arfuso, Nik Zeps, Arun Dharmarajan, The Role of Secreted Frizzled Related Protein 4 (sFRP-4) in Regulating Oestradiol-Induced Growth of the MCF-7 Breast Cancer Cell Line , Journal of Analytical Oncology: Vol. 3 No. 1 (2014)
- Yu Niu, ZiyanZhao, Gang Jin, Detection of Neuron Specific Enolase (NSE) with the Protein Biosensor Based on Imaging Ellipsometry , Journal of Analytical Oncology: Vol. 1 No. 1 (2012)
- Satoshi Hibi, Yuko Shirokawa, Kengo Nanya, Yuko Kato, Nobuto Ito, Takae Kataoka, Takashi Yoshida, Yoshiaki Marumo, Satoshi Kayukawa, Shu Yuasa, Yoshiteru Tanaka, Kenji Ina, Application of the Plan-Do-Check-Act Cycle for Managing Immune-Related Adverse Events , Journal of Analytical Oncology: Vol. 10 (2021)
- Jing Bai, Duo Guo, Xiangyi Liu, Curcumin Inhibits Retinoblastoma Cell Proliferation by miR-26a Targeting the Tumor Suppressor Gene Rb1 in Y79 Cells , Journal of Analytical Oncology: Vol. 9 (2020)
- Jing Bai, Haishun Liu, Hongfei Wan, Xiangyi Liu, Serum Biomarkers Study and the Establishment of Diagnostic Models for Hepatitids B-Related HCC , Journal of Analytical Oncology: Vol. 9 (2020)
- Abigail Ruiz de Lobera, Aitziber Buqué, Alberto Muñoz, Sergio Carrera, Aintzane Sancho, Itziar Rubio, Eddy I. Gutierrez, Mikel Arruti, Inés Marrodán, Guillermo López-Vivanco, Bevacizumab in Combination with FOLFIRI in the First-Line Treatment of Patients with Advanced Colorectal Cancer: A Single-Institution Experience , Journal of Analytical Oncology: Vol. 3 No. 1 (2014)
- Antonieta Salud, Vicente Alonso, Pilar Escudero, Miguel Burillo, Cristina Martín, Fernando Rivera, Alfonso Yubero, Carlos García-Girón, Alberto Muñoz, Phase II Study of Irinotecan in Combination with Capecitabine on a 3-Weekly Schedule as First-Line Chemotherapy for Patients with Metastatic or Locally Advanced Colorectal Cancer , Journal of Analytical Oncology: Vol. 2 No. 3 (2013)
- B.R. Kiran Kumar, Geeta S. Narayanan, M.S. Ganesh, Amritha Prabha Shankar, Marjolins Ulcer: Clinicopathological Profile and Treatment Patterns , Journal of Analytical Oncology: Vol. 12 (2023)
- Novoa Vargas Arturo, Neoadyuvant Hormonotherpy for Posmenopausics Women with Locallity Advanced Breast Cancer , Journal of Analytical Oncology: Vol. 2 No. 1 (2013)
You may also start an advanced similarity search for this article.
Most read articles by the same author(s)
- T.P. Artsemyeva, D.A. Tzerkovsky, Efficacy of Photodynamic Therapy with Chlorine-Based Photosensitizer in the Treatment of Basal Cell Carcinomas , Journal of Analytical Oncology: Vol. 12 (2023)
- D.A. Tzerkovsky, A.N. Mazurenko, F.F. Borychevsky, D.V. Shashkouski, Radiodynamic Therapy with Photosensitizers: Mini-Review of Experimental and Clinical Studies , Journal of Analytical Oncology: Vol. 11 (2022)
- F.F. Borichevsky, I.S. Lioubichtchev, A.E. Sahun, A.S. Trus, D.A. Tzerkovsky, Magnetotherapy in Experimental and Clinical Neuro-Oncology: A Review , Journal of Analytical Oncology: Vol. 12 (2023)
