Skip to main content

Updates on clinical studies of selenium supplementation in radiotherapy

Abstract

To establish guidelines for the selenium supplementation in radiotherapy we assessed the benefits and risks of selenium supplementation in radiotherapy. Clinical studies on the use of selenium in radiotherapy were searched in the PubMed electronic database in January 2013. Sixteen clinical studies were identified among the 167 articles selected in the initial search. Ten articles were observational studies, and the other 6 articles reported studies on the effects of selenium supplementation in patients with cancer who underwent radiotherapy. The studies were conducted worldwide including European, American and Asian countries between 1987 and 2012. Plasma, serum or whole blood selenium levels were common parameters used to assess the effects of radiotherapy and the selenium supplementation status. Selenium supplementation improved the general conditions of the patients, improved their quality of life and reduced the side effects of radiotherapy. At the dose of selenium used in these studies (200–500 μg/day), selenium supplementation did not reduce the effectiveness of radiotherapy, and no toxicities were reported. Selenium supplementation may offer specific benefits for several types of cancer patients who undergo radiotherapy. Because high-dose selenium and long-term supplementation may be unsafe due to selenium toxicity, more evidence-based information and additional research are needed to ensure the therapeutic benefits of selenium supplementation.

Introduction

Radiotherapy is one of the most common and effective treatments for cancer [1]. Radiation damages cancer cells by direct ionization of DNA and by indirect effects caused by reactive oxygen species (ROS) [2]. Ionizing radiation consists of electromagnetic radiations, including X-rays and gamma rays, and particulate radiation such as electrons, protons and neutrons [2]. Exposure to ionizing radiation produces ROS in the tissue environment; including hydroxyl radicals (the most damaging), superoxide anion radicals and other oxidants such as hydrogen peroxide [2]. Although radiotherapy is effective in killing cancer cells, ROS produced in radiotherapy may threaten the integrity and survival of the surrounding normal cells and may cause late side effects of radiotherapy [13]. The administration of radioprotective agents, which are supposed to scavenge radiation-induced radicals and reduce the effects of radiation at an early stage, has been suggested as one approach for prophylaxis of radiation effects in normal tissues [4, 5].

Selenium, a trace element, is an essential nutrient of fundamental importance in human biology [6] and as a preventive approach to ROS detoxification, which activates and stimulates the endogenous system [4, 7, 8]. Some of the most fundamental cellular processes, such as DNA synthesis, depend on the presence of selenium within the catalytic site of thioredoxin reductases (TrxR) [9, 10]. A moderate deficiency of selenium has been linked to many conditions, such as an increased risk of cancer, infections and male infertility; a decrease in immune and thyroid function; and several neurological conditions [6, 9]. A review paper reported that in prospective studies published in the 1980s and early 1990s involving 8,000 to 11,000 individuals, low selenium status was associated with significantly increased risks of cancer incidence and mortality [6].

A number of mechanisms have been suggested to explain the anti-cancer effects of selenium [11]. Selenium in selenoproteins can reduce oxidative damage and can limit DNA damage, both of which are linked to cancer risk [11]. Other cellular processes and molecular pathways that may be involved in the anti-cancer effects of selenium are the induction of phase II conjugating enzymes that detoxify carcinogens, enhancement of the immune response, an increase in tumor-suppressor protein p53, inactivation of protein kinase C (PKC), alterations in DNA methylation, blockage of the cell cycle to allow DNA repair, induction of apoptosis in cancer cells and inhibition of angiogenesis [11]. In survey studies, selenium has been reported as a complementary alternative medicine (CAM) used in lung and prostate cancer patients undergoing radiotherapy [12, 13].

However, there are no guidelines on selenium supplementation in radiotherapy which should consist of inclusion and exclusion criteria for selenium supplementation, applicable cancer types, dose of supplementation, chemical form of selenium, duration of supplementation and the possible side effects of supplementation in radiotherapy. First, however, the benefits and risks of selenium use in radiotherapy should be clarified, as such information is still insufficient. Tabassum et al. [14] summarized the protective effect of selenium against prostate cancer and Fritz et al. [15] reviewed the relationship between selenium and lung cancer, suggesting positive effects of selenium in radiotherapy. Dennert and Horneber reviewed two clinical trials published in 2006 as a Cochrane database systematic review, and the review was revised in 2011 with the addition of one trial [16]. The subjects in the Cochrane database systematic reviews were limited to those included in randomized controlled trials; therefore, only 3 studies were reviewed, yielding no clear evidence that selenium supplements improve the side effects of cancer therapy [16]. In this paper, we summarized the clinical studies on selenium and radiotherapy to provide evidence-based information on the benefits and risks of selenium supplementation to aid in the establishment of guidelines for selenium supplementation in radiotherapy.

Methodology

The flowchart of our literature search is shown in Figure 1. Briefly, a PubMed electronic database search using medical subject headings (MeSH) terms and the keywords “selenium”, “radiation” and “therapy” in January 2013 yielded 167 articles, 16 of which were clinical studies on selenium and radiotherapy. The detailed keyword search was as follows: “selenium” [MeSH Terms] OR “selenium” [All Fields]) AND (“radiotherapy” [Subheading] OR “radiotherapy” [All Fields] OR (“radiation” [All Fields] AND “therapy” [All Fields]) OR “radiation therapy” [All Fields] OR “radiotherapy” [MeSH Terms] OR (“radiation” [All Fields] AND “therapy” [All Fields]) OR “radiation therapy” [All Fields]).

Figure 1
figure 1

Flowchart of the literature search.

Clinical studies on selenium and radiotherapy

Table 1 lists the 16 articles on selenium and radiotherapy in clinical studies. The studies were conducted worldwide, including European, American and Asian countries, between 1987 and 2012. A total of 1303 patients undergoing radiotherapy participated in the studies. Of the 16 articles, 10 articles were observational studies investigating patients’ selenium levels before, during and/or after radiotherapy, while the other 6 articles investigated the effects of selenium supplementation studies on cancer patients who underwent radiotherapy. The cancer types investigated were upper gastrointestinal, breast, lung, larynx, head and neck, non-Hodgkin lymphoma, brain, oral, prostate and gynecological cancers.

Table 1 Clinical studies on selenium and radiotherapy between 1987 and 2012

Among the 16 articles, only 7 articles mentioned the types of radiotherapy delivered to the patients, and in most cases, electromagnetic radiations was used.

Observational studies

Table 2 presents the observational studies investigating the selenium levels in patients who underwent radiotherapy without selenium supplementation. In addition to the 10 observational studies, 2 studies assessed selenium levels in patients who did not received selenium supplementation, who served as a placebo group and control group in the selenium supplementation studies. Thus, a total of 12 studies measured the selenium levels in patients who underwent radiotherapy without selenium supplementation.

Table 2 Observational studies investigating the selenium levels in patients who underwent radiotherapy without selenium supplementation
Selenium levels

Selenium levels were determined in the plasma, serum or whole blood using atomic absorption spectrometry (AAS) in 9 studies, inductively coupled plasma mass spectrometry (ICP-MS) in 2 studies and a fluorometric method in 1 study. The measurements were performed before radiotherapy, during radiotherapy, at the end of therapy and at specific time points (2 weeks, 6 weeks, 8 weeks or 1 year) after therapy completion.

Effect of radiotherapy on selenium levels

The results of selenium levels in patients who underwent radiotherapy without supplementation demonstrated that selenium levels had a tendency to decrease after radiotherapy. In 7 studies (study No. 2, 4, 5, 7, 10, 12, and 15), the selenium levels were not significantly different before and after therapy, but in 3 studies (study No. 1, 8, and 9), the selenium levels after therapy were significantly lower than those before therapy.

Effect of selenium supplementation on selenium levels

Table 3 shows the selenium levels in the patients who underwent radiotherapy with selenium supplementation. The selenium levels in patients who received selenium supplementation had a tendency to increase after radiotherapy. However, the selenium levels decreased again at 8 weeks (study No.12) and 6 weeks (study No.15) after the completion of radiotherapy without selenium supplementation.

Table 3 Selenium levels in patients who underwent radiotherapy with selenium supplementation

Selenium supplementation studies

Table 4 provides a summary of selenium supplementation studies. The selenium supplementation studies in patients who underwent radiotherapy were conducted from 1998 to 2010. Different types of studies were conducted, including a randomized double-blind placebo-controlled study (study No. 12), a multicenter phase 3 trial (study No. 15), and a randomized phase 2 study (study No.16).

Table 4 Selenium supplementation studies in patients who underwent radiotherapy
Therapeutic form of selenium, dose and administration

All of the studies of selenium supplementation in patients who underwent radiotherapy used sodium selenite as the form of selenium for supplementation. Sodium selenite was administered orally in most studies (study No. 12–16) and in physiological saline in another report. The dose of supplementation by oral administration ranged from 200 to 500 μg daily, or 1,000 μg daily by infusion in physiological saline.

Parameters observed or measured

To assess the effectiveness of selenium supplementation in radiotherapy, the parameters measured or observed in the studies were selenium levels in the serum, plasma or whole blood; mineral elements in the blood and other blood parameters (aspartate amino transferase (AST), alanine amino transferase (ALT), gamma glutamyl transpeptidase (γ-GTP) and erythrocyte sedimentation rate (ESR)) [27]; immune function [28]; quality of life [29]; enzymatic and non-enzymatic antioxidants [30]; and side effects [31, 32].

Effects of selenium supplementation on therapy

Most of the studies revealed positive effects of selenium supplementation on the general condition of the patients and their quality of life. The effects of supplementation were different depending on cancer type. No reduction in effectiveness of radiotherapy [31] and no selenium toxicities or complications were reported in any of the supplementation studies.

Pakdaman (study No.11) reported that treatment with sodium selenite in patients with brain tumors was well tolerated by all patients and increased blood selenium levels [27]. A significant diminution of symptoms of intracranial pressure was achieved in 76% of patients after sodium selenite treatment [27].

In the study by Kiremidjian-Schumacher et al. (study No. 12), sodium selenite treatment was shown to significantly enhance cell-mediated immune responsiveness in head and neck cancer patients [28]. This outcome related to the ability of selenium to enhance the expression of both the α- (p55) and β- (p70/75) subunits of the interleukin-2 receptor (IL2-R), which resulted in a greater number of high-affinity IL2-R/cells and enhanced proliferation and differentiation in cytotoxic effector cells [28, 34, 35].

Micke et al. (study No. 13) demonstrated, using the visual analogue scale, that the self-assessment of the quality of life of patients suffering from head and neck cancer with lymphedema significantly improved after selenium supplementation [29].

Elango et al. (study No. 14) found that supplementation with selenium in oral cancer patients for 6 months may help to increase the enzymatic (superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), Glutathione reductase (GRx), Glucose-6-phosphate dehydrogenase (G6PDH)) and non-enzymatic (glutathione (GSH), vitamin E, vitamin C, vitamin A and ceruloplasmin) defense systems. The mechanism of the increase in the activity of the enzymatic defense system is due to increased GPx synthesis as a result of the enhanced de novo synthesis of this enzyme in the erythroid precursors of red blood cells [30].

Muecke et al. (study No. 15) reported that selenium supplementation in cervical and uterine cancer patients yielded significant prevention of diarrhea and thus improved the quality of life [31]. The increased activity of the protective intestinal GPx isoenzymes may be responsible for these effects due to the enhanced neutralization of radiation-induced hydroperoxides and free radicals in the small intestinal mucosa included in the radiation volume [31].

In the study by Büntzel et al. (study No.16) selenium supplementation reduced the radiation-associated side-effects of dysphagia developments in patients with head and neck cancer patients [32].

Parameters used to assess the effect of radiotherapy on selenium status

We found that the plasma, serum or whole blood selenium levels were common parameters used to assess the effect of radiotherapy on selenium status and the effectiveness of selenium supplementation. Selenium levels had a tendency to decrease after radiotherapy and to increase with selenium supplementation. The mechanism of this decrease is still unclear [24, 25]. Pothier et al. suggested that poor dietary intake due to anorexia, nausea, and obstruction, compounded by selenium loss from vomiting, diarrhea, and malabsorption, probably played a role in the decrease [17]. Radiotherapy and chemotherapy, combined with the suboptimal nutrition of cancer patients, may further aggravate the selenium deficiency [24, 31]. Muecke et al. highlighted that patients with higher blood selenium levels had a better radiation tolerance, without any effect on the survival data [31]. Therefore, Muecke et al. and Franca et al. strongly recommended that physicians take the selenium status into account before prescribing any anticancer therapy to their patients or consider additional supplementation before therapy when the current selenium status appears insufficient [24, 31].

Sodium selenite supplementation

In the studies reviewed, sodium selenite was the only form of selenium used for supplementation. In nature, selenium exists in many forms. The most well studied forms are selenomethionine (SeMet), sodium selenite, selenium methylselenocysteine, 1,4,-phenylenebis (methylene) selenocyanate (p-XSC), and methylseleninic acid (MSA) [15]. Selenomethionine and selenocysteine (SeCys) are found predominantly in foods such as bread, cereals, nuts, meat, fish, and other seafood [36]. In human antioxidant systems, selenium participates in the form of SeCys incorporated into the various selenoproteins [11, 15]. There are at least 25 known selenoproteins, including GPx, TrxR, iodothyroninedeiodinase, and the selenoproteins P, W and R [37]. The most abundant selenoproteins in the blood are selenoprotein P, which accounts for approximately 50% of plasma selenium [36, 38, 39], and GPx, which accounts for 10–30% of plasma selenium [36, 39].

Sodium selenite, an inorganic form of selenium, was used for supplementation because it can primarily improve the expression of selenoproteins after specific incorporation as SeCys [31]. Sodium selenite also has high biological activity and availability in the body [28] and is known to easily pass the blood–brain barrier [27]. It does not raise the concentrations of nonspecific selenium-containing proteins (e.g., selenium-albumin), which is in contrast to other widely used organic selenium supplements (e.g., selenomethionine) [31].

Selenium toxicity

The Food and Nutrition Board, Institute of Medicine, suggested a recommended dietary allowance (RDA) of selenium for both men and women of 55 μg (0.7 μmol)/day [40]. The tolerable upper intake level (UL) of selenium in adults is set at 400 μg (5.1 μmol)/day based on the adverse effect of selenosis [40]. The results of our review of supplementation studies revealed that selenium supplementation doses ranging from 200–500 μg/day by oral administration was well tolerated by all patients, and no toxicities were reported. Selenium supplementation increased the blood selenium level, improved the general condition of patients, improved quality of life and prevented or reduced the side effects of radiotherapy. Muecke et al. [31] also implied that supplementation with selenium neither interferes with the biological effects of ionizing radiation nor protects tumor cells.

The Nutritional Prevention of Cancer (NPC) trial reported that selenium supplementation in subjects, with histories of non-melanoma skin cancers significantly decreased the incidence of lung cancer in patients with low baseline selenium concentrations, but supplementation did not significantly decrease this incidence among individuals in the overall population [41]. Therefore, selenium supplementation may have benefits if the selenium is administered to patients with low selenium levels.

High-dose selenium and long-term supplementation may be ineffective and unsafe because selenium can be toxic at high concentrations. The NPC trial also reported an association between long-term selenium supplementation and an increased risk of diabetes [42]. A review paper in 2006 [43] revealed that serum selenium levels ranging from 400–30,000 μg/l were associated with acute toxicity and that levels ranging from 500–1,400 μg/l were associated with chronic toxicity (mean normal serum selenium level is 125 μg/l [44]).

Another high-dose selenium case consisting of the use of a liquid dietary supplement containing 200 times the labeled concentration of selenium was reported in the United States [44]. Of the 201 cases identified in 10 states, 1 person was hospitalized. The median estimated dose of selenium consumed was 41,749 μg/day. The frequently reported symptoms included diarrhea (78%), fatigue (75%), hair loss (72%), joint pain (70%), nail discoloration (61%) and nausea (58%). The symptoms persisting 90 days or longer included fingernail discoloration and loss (52%), fatigue (35%), and hair loss (29%) [44].

Conclusion

This paper summarized 16 clinical studies on selenium and radiotherapy conducted from 1987 to 2012. The studies included 1303 cancer patients. To assess the selenium status in patients before and after radiotherapy, the plasma, serum or whole blood selenium level was a common parameter used to assess the effect of radiotherapy on selenium status and the effectiveness of selenium supplementation. Selenium supplementation increased the blood selenium level, improved the general condition of patients, improved quality of life, prevented or reduced the side effects of radiotherapy and did not reduce the effectiveness of radiotherapy or cause any toxicity.

The results of our summary suggest that selenium supplementation in the form of sodium selenite at doses ranging from 200–500 μg daily by oral administration may offer benefits for head and neck cancer; head and neck cancer with lymphedema; and oral, cervical and uterine cancer patients who undergo radiotherapy and have low selenium levels. In the future, further research and additional evidence of the benefits of selenium supplementation in patients during radiotherapy are required to clarify optimal dosing strategies in specific types of cancer and the associated risks, to ensure therapeutic efficacy before it can be recommended for broad clinical use.

Abbreviations

ROS:

Reactive oxygen species

TrxR:

Thioredoxin reductases

PKC:

Protein kinase C

CAM:

Complementary alternative medicine

MeSH:

Medical subject headings

AAS:

Absorption spectrometry

ICP-MS:

Inductively coupled plasma mass spectrometry

AST:

Aspartate amino transferase

ALT:

Alanine amino transferase

γ-GTP:

Gamma glutamyl transpeptidase

ESR:

Erythrocyte sedimentation rate

IL2-R:

Interleukin-2 receptor

SOD:

Superoxide dismutase

CAT:

Catalase

GPx:

Glutathione peroxidase

GRx:

Glutathione reductase

G6PDH:

Glucose-6-phosphate dehydrogenase

GSH:

Glutathione

SeMet:

Selenomethionine

p-XSC:

1,4,-phenylenebis (methylene) selenocyanate

MSA:

Methylseleninic acid

SeCys:

Selenocysteine

RDA:

Recommended dietary allowance

UL:

Upper intake level

NPC:

Nutritional prevention of cancer.

References

  1. Shirazi A, Ghobadi G, Ghazi-Khansari M: A radiobiological review on melatonin: a novel radioprotector. J Radiat Res 2007, 48: 263-272. 10.1269/jrr.06070

    Article  CAS  PubMed  Google Scholar 

  2. Borek C: Antioxidants and radiation therapy. J Nutr 2004, 134: 3207S-3209S.

    CAS  PubMed  Google Scholar 

  3. Bentzen SM: Preventing or reducing late side effects of radiation therapy: radiobiology meets molecular pathology. Nat Rev Cancer 2006, 6: 702-713. 10.1038/nrc1950

    Article  CAS  PubMed  Google Scholar 

  4. Dörr W: Effects of selenium on radiation responses of tumor cells and tissue. Strahlenther Onkol 2006, 182: 693-695. 10.1007/s00066-006-1595-8

    Article  PubMed  Google Scholar 

  5. Weiss JF, Landauer MR: Radioprotection by antioxidants. Ann N Y Acad Sci 2000, 899: 44-60.

    Article  CAS  PubMed  Google Scholar 

  6. Rayman MP: The importance of selenium to human health. Lancet 2000, 356: 233-241. 10.1016/S0140-6736(00)02490-9

    Article  CAS  PubMed  Google Scholar 

  7. Breccia A, Badiello R, Trenta A, Mattii M: On the chemical radioprotection by organic selenium compounds in vivo. Radiat Res 1969, 38: 483-492. 10.2307/3572608

    Article  CAS  PubMed  Google Scholar 

  8. Weiss JF, Srinivasan V, Kumar KS, Landauer MR: Radioprotection by metals: selenium. Adv Space Res 1992, 12: 223-231.

    Article  CAS  PubMed  Google Scholar 

  9. Papp LV, Lu J, Holmgren A, Khanna KK: From selenium to selenoproteins: synthesis, identity, and their role in human health. Antioxid Redox Signal 2007, 9: 775-806. 10.1089/ars.2007.1528

    Article  CAS  PubMed  Google Scholar 

  10. Arner ES, Holmgren A: Physiological functions of thioredoxin and thioredoxin reductase. Eur J Biochem 2000, 267: 6102-6109. 10.1046/j.1432-1327.2000.01701.x

    Article  CAS  PubMed  Google Scholar 

  11. Rayman MP: Selenium in cancer prevention: a review of the evidence and mechanism of action. Proc Nutr Soc 2005, 64: 527-542. 10.1079/PNS2005467

    Article  CAS  PubMed  Google Scholar 

  12. Ponholzer A, Struhal G, Madersbacher S: Frequent use of complementary medicine by prostate cancer patients. Eur Urol 2003, 43: 604-608. 10.1016/S0302-2838(03)00155-6

    Article  PubMed  Google Scholar 

  13. Micke O, Buntzel J, Kisters K, Schafer U, Micke P, Mucke R: Complementary and alternative medicine in lung cancer patients: a neglected phenomenon? Front Radiat Ther Oncol 2010, 42: 198-205.

    Article  CAS  PubMed  Google Scholar 

  14. Tabassum A, Bristow RG, Venkateswaran V: Ingestion of selenium and other antioxidants during prostate cancer radiotherapy: a good thing? Cancer Treat Rev 2010, 36: 230-234. 10.1016/j.ctrv.2009.12.008

    Article  CAS  PubMed  Google Scholar 

  15. Fritz H, Kennedy D, Fergusson D, Fernandes R, Cooley K, Seely A, Sagar S, Wong R, Seely D: Selenium and lung cancer: a systematic review and meta analysis. PLoS One 2011, 6: e26259. 10.1371/journal.pone.0026259

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  16. Dennert G, Horneber M: Selenium for alleviating the side effects of chemotherapy, radiotherapy and surgery in cancer patients. Cochrane Database Syst Rev 2006, 3: CD005037.

    PubMed  Google Scholar 

  17. Pothier L, Lane WW, Bhargava A, Michielson C, Douglass HO Jr: Plasma selenium levels in patients with advanced upper gastrointestinal cancer. Cancer 1987, 60: 2251-2260. 10.1002/1097-0142(19871101)60:9<2251::AID-CNCR2820600925>3.0.CO;2-T

    Article  CAS  PubMed  Google Scholar 

  18. Antila HM, Salo MS, Nanto V, Nikkanen V, Kirvela O: The effect of postoperative radiotherapy on leukocyte zinc, serum trace elements and nutritional status of breast cancer patients. Acta Oncol 1992, 31: 569-572. 10.3109/02841869209088308

    Article  CAS  PubMed  Google Scholar 

  19. Piccinini L, Borella P, Bargellini A, Medici CI, Zoboli A: A case–control study on selenium, zinc, and copper in plasma and hair of subjects affected by breast and lung cancer. Biol Trace Elem Res 1996, 51: 23-30. 10.1007/BF02790144

    Article  CAS  PubMed  Google Scholar 

  20. Rostkowska-Nadolska B, Pospiech L, Bochnia M: Content of trace elements in serum of patients with carcinoma of the larynx. Arch Immunol Ther Exp (Warsz) 1999, 47: 321-325.

    CAS  Google Scholar 

  21. Yadav SP, Gera A, Singh I, Chanda R: Serum selenium levels in patients with head and neck cancer. J Otolaryngol 2002, 31: 216-219. 10.2310/7070.2002.21096

    Article  CAS  PubMed  Google Scholar 

  22. Last KW, Cornelius V, Delves T, Sieniawska C, Fitzgibbon J, Norton A, Amess J, Wilson A, Rohatiner AZ, Lister TA: Presentation serum selenium predicts for overall survival, dose delivery, and first treatment response in aggressive non-Hodgkin’s lymphoma. J Clin Oncol 2003, 21: 2335-2341. 10.1200/JCO.2003.06.145

    Article  PubMed  Google Scholar 

  23. Fraunholz I, Eberlein K, Schopohl B, Bottcher HD, Rodel C: Selenium levels during the course of radiotherapy. No influence of irradiation on blood selenium concentration. Strahlenther Onkol 2008, 184: 411-415. 10.1007/s00066-008-1867-6

    Article  PubMed  Google Scholar 

  24. Franca CA, Nogueira CR, Ramalho A, Carvalho AC, Vieira SL, Penna AB: Serum levels of selenium in patients with breast cancer before and after treatment of external beam radiotherapy. Ann Oncol 2011, 22: 1109-1112. 10.1093/annonc/mdq547

    Article  CAS  PubMed  Google Scholar 

  25. Zeng YC, Xue M, Chi F, Xu ZG, Fan GL, Fan YC, Zheng MH, Zhong WZ, Wang SL, Zhang ZY, Chen XD, Wu LN, Jin XY, Chen W, Li Q, Zhang XY, Xiao YP, Wu R, Guo QY: Serum levels of selenium in patients with brain metastases from non-small cell lung cancer before and after radiotherapy. Cancer Radiother 2012, 3: 179-182.

    Article  Google Scholar 

  26. Eroglu C, Unal D, Cetin A, Orhan O, Sivgin S, Ozturk A: Effect of serum selenium levels on radiotherapy-related toxicity in patients undergoing radiotherapy for head and neck cancer. Anticancer Res 2012, 32: 3587-3590.

    PubMed  Google Scholar 

  27. Pakdaman A: Symptomatic treatment of brain tumor patients with sodium selenite, oxygen, and other supportive measures. Biol Trace Elem Res 1998, 62: 1-6. 10.1007/BF02820015

    Article  CAS  PubMed  Google Scholar 

  28. Kiremidjian-Schumacher L, Roy M, Glickman R, Schneider K, Rothstein S, Cooper J, Hochster H, Kim M, Newman R: Selenium and immunocompetence in patients with head and neck cancer. Biol Trace Elem Res 2000, 73: 97-111. 10.1385/BTER:73:2:97

    Article  CAS  PubMed  Google Scholar 

  29. Micke O, Bruns F, Mücke R, Schäfer U, Glatzel M, DeVries AF, Schönekaes K, Kisters K, Büntzel J: Selenium in the treatment of radiation-associated secondary lymphedema. Int J Radiat Oncol Biol Phys 2003, 56: 40-49. 10.1016/S0360-3016(02)04390-0

    Article  CAS  PubMed  Google Scholar 

  30. Elango N, Samuel S, Chinnakkannu P: Enzymatic and non-enzymatic antioxidant status in stage (III) human oral squamous cell carcinoma and treated with radical radio therapy: influence of selenium supplementation. Clin Chim Acta 2006, 373: 92-98. 10.1016/j.cca.2006.05.021

    Article  CAS  PubMed  Google Scholar 

  31. Muecke R, Schomburg L, Glatzel M, Berndt-Skorka R, Baaske D, Reichl B, Buentzel J, Kundt G, Prott FJ, Devries A, Stoll G, Kisters K, Bruns F, Schaefer U, Willich N, Micke O: Oncology-AKTE GWGTEaEi. Multicenter, phase 3 trial comparing selenium supplementation with observation in gynecologic radiation oncology. Int J Radiat Oncol Biol Phys 2010, 78: 828-835. 10.1016/j.ijrobp.2009.08.013

    Article  CAS  PubMed  Google Scholar 

  32. Büntzel J, Riesenbeck D, Glatzel M, Berndt-Skorka R, Riedel T, Mücke R, Kisters K, Schönekaes KG, Schäfer U, Bruns F, Micke O: Limited effects of selenium substitution in the prevention of radiation-associated toxicities. results of a randomized study in head and neck cancer patients. Anticancer Res 2010, 30: 1829-1832.

    PubMed  Google Scholar 

  33. AMA Manual of Style: A Guide for Authors and Editors. 10th edition. New York: Oxford University Press; 2007.

    Google Scholar 

  34. Kiremidjian-Schumacher L, Roy M, Wishe HI, Cohen MW, Stotzky G: Regulation of cellular immune responses by selenium. Biol Trace Elem Res 1992, 33: 23-35. 10.1007/BF02783989

    Article  CAS  PubMed  Google Scholar 

  35. Roy M, Kiremidjian-Schumacher L, Wishe HI, Cohen MW, Stotzky G: Effect of selenium on the expression of high affinity interleukin 2 receptors. Proc Soc Exp Biol Med 1992, 200: 36-43. 10.3181/00379727-200-43391

    Article  CAS  PubMed  Google Scholar 

  36. Ashton K, Hooper L, Harvey LJ, Hurst R, Casgrain A, Fairweather-Tait SJ: Methods of assessment of selenium status in humans: a systematic review. Am J Clin Nutr 2009, 89: 2025S-2039S. 10.3945/ajcn.2009.27230F

    Article  CAS  PubMed  Google Scholar 

  37. Abdulah R, Miyazaki K, Nakazawa M, Koyama H: Chemical forms of selenium for cancer prevention. J Trace Elem Med Biol 2005, 19: 141-150. 10.1016/j.jtemb.2005.09.003

    Article  CAS  PubMed  Google Scholar 

  38. Akesson B, Bellew T, Burk RF: Purification of selenoprotein P from human plasma. Biochim Biophys Acta 1994, 1204: 243-249. 10.1016/0167-4838(94)90014-0

    Article  CAS  PubMed  Google Scholar 

  39. Deagen JT, Butler JA, Zachara BA, Whanger PD: Determination of the distribution of selenium between glutathione peroxidase, selenoprotein P, and albumin in plasma. Anal Biochem 1993, 208: 176-181. 10.1006/abio.1993.1025

    Article  CAS  PubMed  Google Scholar 

  40. Panel on Dietary Antioxidants and Related Compounds, Subcommittees on Upper Reference Levels of Nutrients and Interpretation and Uses of DRIs, Standing Committee on the Scientific Evaluation of Dietary Reference Intakes, Food and Nutrition Board, Institute of Medicine: DRI Dietary Referece Intakes for Vitamin C, Vitamin E, Selenium, and Carotenoids. Washington D.C: National Academy Press; 2000.

    Google Scholar 

  41. Reid ME, Duffield-Lillico AJ, Garland L, Turnbull BW, Clark LC, Marshall JR: Selenium supplementation and lung cancer incidence: an update of the nutritional prevention of cancer trial. Cancer Epidemiol Biomarkers Prev 2002, 11: 1285-1291.

    CAS  PubMed  Google Scholar 

  42. Stranges S, Marshall JR, Natarajan R, Donahue RP, Trevisan M, Combs GF, Cappuccio FP, Ceriello A, Reid ME: Effects of long-term selenium supplementation on the incidence of type 2 diabetes: a randomized trial. Ann Intern Med 2007, 147: 217-223. 10.7326/0003-4819-147-4-200708210-00175

    Article  PubMed  Google Scholar 

  43. Nuttall KL: Evaluating selenium poisoning. Ann Clin Lab Sci 2006, 36: 409-420.

    CAS  PubMed  Google Scholar 

  44. MacFarquhar JK, Broussard DL, Melstrom P, Hutchinson R, Wolkin A, Martin C, Burk RF, Dunn JR, Green AL, Hammond R, Schaffner W, Jones TF: Acute selenium toxicity associated with a dietary supplement. Arch Intern Med 2010, 170: 256-261. 10.1001/archinternmed.2009.495

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hiroshi Koyama.

Additional information

Competing interests

The authors have no competing interests to declare.

Authors’ contributions

IMP, TN and HK were responsible for the study design. IMP, RA, CY and SK were responsible for articles collections and analysis. TN and HK were responsible for supervising the study. All authors participated in the drafting and revising of the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( https://creativecommons.org/publicdomain/zero/1.0/ ) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Puspitasari, I.M., Abdulah, R., Yamazaki, C. et al. Updates on clinical studies of selenium supplementation in radiotherapy. Radiat Oncol 9, 125 (2014). https://doi.org/10.1186/1748-717X-9-125

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1748-717X-9-125

Keywords