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Influence of Ionizing Radiation on Ovarian Carcinoma SKOV-3 Xenografts in Nude Mice under Hypoxic Conditions

  • Zhang, Yong-Chun (Oncology Department, the Affiliated Hospital of Qingdao University) ;
  • Jiang, Gang (Oncology Department, the Affiliated Hospital of Qingdao University) ;
  • Gao, Han (Pathology Department, Qingdao municipal hospital) ;
  • Liu, Hua-Min (Oncology Department, the Affiliated Hospital of Qingdao University) ;
  • Liang, Jun (Oncology Department, the Affiliated Hospital of Qingdao University)
  • Published : 2014.03.01

Abstract

Purpose: We aimed to detect the expression of HIF-1${\alpha}$, VEGF, HPSE-1 and CD31 in SKOV3 xenografts in nude mice treated with different doses of ionizing radiation, trying to explore the possible mechanism of hypoxia and radioresistance. Methods: Nude mice bearing SKOV3 xenografts were randomly divided into 4 groups: Group A (control group, no ionizing radiation), Group B (treated with low dose of ionizing radiation: 50cGy), Group C (treated with high dose of ionizing radiation: 300cGy), Group D ( combined ionizing radiation, treated with ionizing radiation from low dose to high dose : 50cGy first and 300cGy after 6h interval). The mRNA levels of HIF-1 and VEGF in each group were detected by real time polymerase chain reaction, while HPSE-1 expression was measured by ELISA. The microvessel density (MVD) and hypoxic cells were determined through immunohistochemical (IHC) staining of CD31 and HIF-1a. Results: Significant differences of HIF-1${\alpha}$ mRNA level could be found among the 4 groups (F=74.164, P<0.001): Group C>Group A>Group D> Group B. The mRNA level of VEGF in Group C was significantly higher than in the other three groups (t=-5.267, P=0.000), while no significant difference was observed among Group A, B and D (t=1.528, 1.588; P=0.205, 0.222). In addition, the MVD was shown to be the highest in Group C (t=6.253, P=0.000), whereas the HPSE-1 level in Group A was lower than in Group B (t=14.066, P=0.000) and higher than in Group C (t=-21.919, P=0.000), and similar with Group D (t=-2.066, P=0.058). Through IHC staining of HIF-1a, the expression of hypoxic cells in Group A was (++), Group B was (+), Group C was (+++) and Group D was (+). Conclusion: Ionizing radiation with lowerdoses might improve tumor hypoxia through inhibiting the expression of HIF-1 and HPSE-1, whereas higherdoses worsen tumor hypoxic conditions by up-regulating HIF-1${\alpha}$, HPSE-1, VEGF and CD31 levels. A protocol of low-dose ionizing radiation followed by a high-dose irradiation might at least partly improve tumor hypoxia and enhance radiosensitivity.

Keywords

References

  1. Bernaudin M, Nedelec AS, Divoux D, et al (2002). Normobaric hypoxia induces tolerance to focal permanent cerebral ischemia in association with an increased expression of hypoxia-inducible factor-1 and its target genes, erythropoietin and VEGF, in the adult mouse brain. J Cereb Blood Flow Metab, 22, 393-403.
  2. Brown JM (2007). Tumor hypoxia in cancer therapy. Methods Enzymol, 435, 297-321.
  3. Cascio S, D'Andrea A, Ferla R, et al (2010). miR-20b modulates VEGF expression by targeting HIF-1 alpha and STAT3 in MCF-7 breast cancer cells. J Cell Physiol, 224, 242-9.
  4. Greenberg DA, Jin K (2005). Fromangiogenesis to neuropathology. Nature, 438, 954-9. https://doi.org/10.1038/nature04481
  5. Gupta VK, Jaskowiak NT, Beckett MA, et al (2002). Vascular endothelial growth factor enhances endothelial cell survival and tumor radioresistance. Cancer J, 8, 47- 54. https://doi.org/10.1097/00130404-200201000-00009
  6. Harada H (2011). How Can We Overcome Tumor Hypoxia in Radiation Therapy? J Radiat Res, 52, 545-56. https://doi.org/10.1269/jrr.11056
  7. Levy AP, LevyNS, Wegner S, Goldberg MA (1995). Transcriptional regulation of the rat vascular endothelial growth factor gene by hypoxia. J Biol Chem, 270, 13333- 40. https://doi.org/10.1074/jbc.270.22.13333
  8. Li DW, Dong P, Wang F et al (2013). Hypoxia induced multidrug resistance of laryngeal cancer cells via hypoxia-inducible factor-$1\alpha$. Asian Pac J Cancer Prev, 14, 4853-8. https://doi.org/10.7314/APJCP.2013.14.8.4853
  9. Li JM, Li JP, Zhang X, et al (2012). Expression of heparanase in vascular cells and astrocytes of the mouse brain after focal cerebral ischemia. Brain Res, 1433, 137-44. https://doi.org/10.1016/j.brainres.2011.11.032
  10. Liang J, Qian Y, Xu D, et al (2013). Serum tumor markers, hypoxia-inducible factor-$1\alpha$ HIF-$1\alpha$ and vascular endothelial growth factor, in patients with non- small cell lung cancer before and after intervention. Asian Pac J Cancer Prev, 14, 3851-4. https://doi.org/10.7314/APJCP.2013.14.6.3851
  11. Loncaster JA, Copper RA, Logue JP, et al (2000). Vascular endothelial growth factor (VEGF) expression is a prognostic factor for radiotherapy outcome in advanced carcinoma of the cervix. Br J Cancer, 83, 620- 5. https://doi.org/10.1054/bjoc.2000.1319
  12. Lund EL, HOg A, Olsen MW, et al (2004). Differential Regulation of VEGF, H1F1 and angiopoietin-1,-2 and -4 by hypoxia and ionizing radiation in human glioblastoma. Int J Cancer, 108, 833- 8. https://doi.org/10.1002/ijc.11662
  13. Ping W, Jiang WY, Chen WS, et al (2013). Expression and significance of hypoxia inducible factor-$1\alpha$ and lysyl oxidase in non-small cell lung cancer. Asian Pac J Cancer Prev, 14, 3613-8. https://doi.org/10.7314/APJCP.2013.14.6.3613
  14. Seubwai W, Kraiklang R, Wongkham C, Wongkham S (2012). Hypoxia enhances aggressiveness of cholangiocarcinoma cells. Asian Pac J Cancer Prev, 13, 53-8.
  15. Shweiki D, Neeman M, Itin A, Keshet E (1995). Induction of vascular endothelial growth factor expression by hypoxia and by glucose deficiency in multicell spheroids: implications for tumor angiogenesis. Proc Natl Acad Sci USA, 92, 768- 72. https://doi.org/10.1073/pnas.92.3.768
  16. Takahashi S (2011). Vascular endothelial growth factor (VEGF), VEGF receptors and their inhibitors for antiangiogenic tumor therapy. Biol Pharm Bull, 34, 1785-8. https://doi.org/10.1248/bpb.34.1785
  17. Vlodavsky l, Elkin M, llan N (2011). Impact of heparanase and the tumor microenvironment on cancer metastasis and angiogenesis: basic aspects and clinical applications. Rambam Maimonides Med J, 2, e0019.
  18. Yu HS, Liu ZM, Yu XY, et al (2013). Low-dose radiation induces antitumor effects and erythrocyte system hormesis. Asian Pac J Cancer Prev, 14, 4121-6. https://doi.org/10.7314/APJCP.2013.14.7.4121
  19. Zhang ZG, Zhang QN, Wang XH, Tian JH (2013). Hypoxiainducible factor 1 alpha (HIF-$1\alpha$) as a prognostic indicator in patients with gastric tumors: a meta-analysis. Asian Pac J Cancer Prev, 14, 4195-8. https://doi.org/10.7314/APJCP.2013.14.7.4195

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