Skip to main content
Log in

Evaluation of ecological and in vitro effects of boron on prostate cancer risk (United States)

  • Original Paper
  • Published:
Cancer Causes & Control Aims and scope Submit manuscript

An Erratum to this article was published on 01 March 2007

Abstract

Objective

To determine: (1) the correlation of prostate cancer incidence and mortality with groundwater boron and selenium concentrations; and (2) the impact of boron on prostate cancer cell proliferation during co-treatment with alternative chemo-preventative agents, along with boron pre-treatment effects on cell sensitivity to ionizing radiation.

Methods

For regression analysis, data on prostate cancer incidence and mortality were obtained from the Texas Cancer Registry, while groundwater boron and selenium concentrations were derived from the Texas Water Development Board. Cultured DU-145 prostate cancer cells were used to assess the impact of boric acid on cell proliferation when applied in combination with selenomethionine and genistein, or preceding radiation exposure.

Results

Groundwater boron levels correlated with a decrease in prostate cancer incidence (R = 0.6) and mortality (R = 0.6) in state planning regions, whereas selenium did not (R = 0.1; R = 0.2). Growth inhibition was greater during combined treatments of boric acid and selenomethionine, or boric acid and genistein, versus singular treatments. 8-day boric acid pre-exposure enhanced the toxicity of ionizing radiation treatment, while dose-dependently decreasing the expression of anti-apoptotic protein Bcl-2.

Conclusions

Increased groundwater boron concentrations, across the state of Texas, correlate with reduced risk of prostate cancer incidence and mortality. Also, boric acid improves the anti-proliferative effectiveness of chemo-preventative agents, selenomethionine and genistein, while enhancing ionizing radiation cell kill.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Jemal A, Murray T, Ward E, et al (2005). Cancer statistics. CA Cancer J Clin 55(1):10–30

    Article  PubMed  Google Scholar 

  2. Willis MS, Wians FH (2004) The role of nutrition in preventing prostate cancer: a review of the proposed mechanism of action of various dietary substances. Clinica Chimica Acta 330: 57–83

    Article  CAS  Google Scholar 

  3. Djavan B, Zlotta A, Schulman C, et al (2004) Chemotherapeutic prevention studies of prostate cancer. J Urol 171(2 Pt 2): S10–S13

    Article  PubMed  Google Scholar 

  4. Klein EA, Thompson IM, Lippman SM, et al (2001) SELECT: the next prostate cancer prevention trial. Selenium and Vitamin E Cancer Prevention Trial. J Urol 166(4): 1311–1315

    Article  PubMed  CAS  Google Scholar 

  5. http://www.clinicaltrials.gov

  6. Cui Y, Winton MI, Zhang ZF, et al (2004) Dietary boron intake and prostate cancer risk. Oncol Rep 11(4): 887–892

    PubMed  CAS  Google Scholar 

  7. Gallardo-Williams MT, Chapin RE, King PE, et al (2004) Boron supplementation inhibits the growth and local expression of IGF-1 in human prostate adenocarcinoma (LNCaP) tumors in nude mice. Toxicol Pathol 32: 73–78

    Article  PubMed  CAS  Google Scholar 

  8. Gallardo-Williams MT, Maronpot RR, Wine RN, Brunssen SH, Chapin RE (2003) Inhibition of the enzymatic activity of prostate specific antigen by BA and 3-nitrophenyl boronic acid. Prostate 54: 44–49

    Article  PubMed  CAS  Google Scholar 

  9. Barranco WT, Eckhert CD (2004) BA inhibits human prostate cancer cell proliferation. Cancer Lett 216(1): 21–9

    Article  PubMed  CAS  Google Scholar 

  10. Kobayashi M, Matoh T, Azuma J (1996) Two chains of rhamnogalacturonan II are cross-linked by borate-diol ester bonds in higher plant cell walls. Plant Physiol 110(3): 1017–1020

    PubMed  CAS  Google Scholar 

  11. O’Neill MA, Warrenfeltz D, Kates K, et al (1997) Rhamnogalacturonan-II, a pectic polysaccharide in the walls of growing plant cell, forms a dimer that is covalently cross-linked by a borate ester. In vitro conditions for the formation and hydrolysis of the dimer. J Biol Chem 271(37): 22923–22930

    Google Scholar 

  12. Takano J, Noguchi K, Yasumori M, et al (2002) Arabidopsis boron transporter for xylem loading. Nature 420(6913): 337–340

    Article  PubMed  CAS  Google Scholar 

  13. Anderson DL, Cunningham WC, Lindstrom TR (1994) Concentrations and intakes of H, B, S, K Na, Cl, and NaCl in foods. J Food Comp Anal 7: 59–82

    Article  CAS  Google Scholar 

  14. Dietary reference intakes for vitamin A, vitamin K, arsenic, boron, chromium, copper, iodine, iron, manganese, molybdenum, nickel, silicon, vanadium, and zinc. A report of the panel on micronutrients, subcommittees on upper reference levels of nutrients and of interpretation and use of dietary reference intakes, and the standing committee on the scientific Evaluation of dietary reference Intakes. (2001) Food and Nutrition Board, Institute of Medicine, National Academy Press, Washington, D.C., p C-13

  15. Hudak PF (2004) Boron and selenium contamination in south Texas groundwater. J Environ Sci Health A Tox Hazard Subst Environ Eng 39(11–12):2827–2834

    Article  PubMed  CAS  Google Scholar 

  16. Hem JD (1985) Study and interpretation of the chemical characteristics of natural water. U.S. Geological Survey Water Supply Paper 2254

  17. http://www.tcc.state.tx.us/tcplan/goal2/goal2_obje_frames.html

  18. http://www.dshs.state.tx.us/tcr, accessed May 31, 2005

  19. http://www.twdb.state.tx.us, accessed May 31, 2005

  20. Panel on Dietary Reference Intakes for Electrolytes and Water (2004) Dietary reference intakes for water, potassium, sodium, chloride, and sulfate. National Academies Press, Washington, D.C., p 494.

  21. Dietary reference intakes for vitamin C, vitamin E, selenium, and carotenoids (2000) Selenium. National Academies Press, Washington, D.C., p. 284.

  22. Clark LC, Dalkin B, Krongrad A, et al (1998) Decreased incidence of prostate cancer with selenium supplementation: results of a double-blind cancer prevention trial. Br J Urol 81: 730–734

    PubMed  CAS  Google Scholar 

  23. Eckhert CD, Lockwood MK, Shen B (1993) Influence of selenium on the microvascular circulation of the retina. Microvas Res 45: 74–82

    Article  CAS  Google Scholar 

  24. Thornber JM, Eckhert CD (1984) Protection against sucrose induced retinal capillary damage in the Wistar rat. J Nutr 114:1070−1075

    PubMed  CAS  Google Scholar 

  25. Bischof M, Abdollahi A, Gong P, et al (2004) Triple combination of irradiation, chemotherapy (pemetrexed), and VEGFR inhibition (SU5416) in human endothelial and tumor cells. Int J Radiat Oncol Biol Phys 60(4):1220–1232

    Article  PubMed  CAS  Google Scholar 

  26. Yan SX, Ejima Y, Sasaki R, et al (2004) Combination of genistein with ionizing radiation on androgen-independent prostate cancer cells. Asian J Androl 6(4): 285–290

    PubMed  CAS  Google Scholar 

  27. Husbeck B, Peehl DM, Knox SJ (2005) Redox modulation of human prostate carcinoma cells by selenite increases radiation-induced cell killing. Free Radic Biol Med 38(1):50–57

    Article  PubMed  CAS  Google Scholar 

  28. Bendel P (2005) Biomedical applications of 10B and 11B NMR. NMR Biomed 18(2): 74–82

    Article  PubMed  CAS  Google Scholar 

  29. Rudner J, Jendrossek V, Belka C (2002) New insights in the role of Bcl-2 Bcl-2 and the endoplasmic reticulum. Apoptosis 7(5): 441–447

    Article  PubMed  CAS  Google Scholar 

  30. Rosser CJ, Reyes AO, Vakar-Lopez F et al (2003) Bcl-2 is significantly overexpressed in localized radio-recurrent prostate carcinoma, compared with localized radio-naive prostate carcinoma. Int J Radiat Oncol Biol Phys 56(1): 1–6

    Article  PubMed  CAS  Google Scholar 

  31. Chendil D, Ranga RS, Meigooni D, Sathishkumar S, Ahmed MM (2004) Curcumin confers radiosensitizing effect in prostate cancer cell line PC-3. Oncogene 23(8): 1599–1607

    Article  PubMed  CAS  Google Scholar 

  32. Campbell MJ, Dawson M, Koeffler HP (1998) Growth inhibition of DU-145 prostate cancer cells by a Bcl-2 antisense oligonucleotide is enhanced by N-(2-hydroxyphenyl) all-trans retinamide. Br J Cancer 77(5): 739–744

    PubMed  CAS  Google Scholar 

  33. Raffo A, Lai JC, Stein CA, et al (2004) Antisense RNA down-regulation of bcl-2 expression in DU145 prostate cancer cells does not diminish the cytostatic effects of G3139 (Oblimersen). Clin Cancer Res May 10(9): 3195–3206

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We thank Dr. Allan Pantuck and Randy Kallilew for their expertise concerning the culturing of prostate cancer cells, along with Kurt Hafer and Cecelia Chan for aiding in the administration of ionizing radiation. Funding for this research was provided by: DOD prostate idea grant DAMD17–03-1-0067 (CD Eckhert) and UC TRS&TP (WT Barranco). In the spirit of full disclosure, we declare that since 1997 the National Institutes of Health has without exception declined funding of all grant applications submitted by CE on the role of boron in biology or cancer with recent applications triaged prior to full review.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Curtis D. Eckhert.

Additional information

An erratum to this article is available at http://dx.doi.org/10.1007/s10552-007-9023-7.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Barranco, W.T., Hudak, P.F. & Eckhert, C.D. Evaluation of ecological and in vitro effects of boron on prostate cancer risk (United States). Cancer Causes Control 18, 71–77 (2007). https://doi.org/10.1007/s10552-006-0077-8

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10552-006-0077-8

Keywords

Navigation