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Serum Levels of Trace Elements in Patients with Testicular Cancers

Abstract

Introduction:

Trace elements are primary components of biological structures; however, they can be toxic when their concentrations are higher than those needed for biological functions.

Materials and Methods:

In the present study serum levels of trace elements were measured in 30 patients (mean age was 26.9±11.2 years) newly diagnosed with germ cell testicular cancer and 32 healthy volunteers (mean age: 27.4±10.8) by using furnace atomic absorption spectrophotometer. Serum samples were stored at-20°C until assays.

Results:

In patients with germ cell testicular cancer, the diagnosis was seminoma in 15, mix germ cell tumor in 7, embryonal carcinoma in 4, yolk sac tumor in 2 and teratoma in 2 patients. There was stage I testicular tumor in 19 patients (63.3%) while stage II in 6 patients (20.0%), stage IIIA in 4 patients (13.3%) and stage IIIC in one patient (3.4%). It was found that serum Co, Cu, Mg and Pb levels were increased (p<0.05), whereas Fe, Mn, and Zn levels were decreased in patients with testicular cancer (p<0.05).

Conclusions:

These alterations may be important in the pathogenesis of testicular cancers; however, further prospective studies are needed to identify the relationship between testicular cancer and trace elements.

Testicular Neoplasms; Trace Elements; Tumor Markers; Biological


INTRODUCTION

Testicular cancers are the most commonly seen cancers in men aged 15-40 years (11. Chia VM, Quraishi SM, Devesa SS, Purdue MP, Cook MB, McGlynn KA. International trends in the incidence of testicular cancer, 1973-2002. Cancer Epidemiol Biomarkers Prev. 2010; 19:1151-9.). They comprise 1% of all cancers in men. Germ cell tumors comprise 90-95% of all primary testicular tumors. In the past, overall survival rate was approximately 10%, while it increased up to 90% by advances in tumor markers and imaging techniques, and cisplatin-based chemotherapy regimens. The incidence of testicular cancer varies according to race and socioeconomic status. The likelihood of incident testicular cancer is higher in Scandinavian countries, while it is lower in Asian countries (22. Greenlee RT, Hill-Harmon MB, Murray T, Thun M. Cancer statistics, 2001. CA Cancer J Clin. 2001; 51:15-36. Erratum in: CA Cancer J Clin 2001; 51:144.).

The trace elements are primary components of biological structures; however, they can exert toxic effect when their concentrations are higher than those needed for biological functions. Moreover, the toxicity can also be true for other non-essential elements which have very similar atomic properties and ability to mimic the reactivity of trace elements. Thus, this above-mentioned toxicity/duality leads biological system to develop ability of recognizing and delivering the metal to its target without enabling it to involve in toxic reactions (33. Gecit I, Kavak S, Demir H, Gunes M, Pirincci N, Cetin C, et al. Serum trace element levels in patients with bladder cancer. Asian Pac J Cancer Prev. 2011; 12:3409-13., 44. Sayir F, Kavak S, Meral I, Demir H, Cengiz N, Cobanoğlu U. Effects of crush and axotomy on oxidative stress and some trace element levels in phrenic nerve of rats. Brain Res Bull. 2013; 92:84-8.). Proteins are the primary compounds involved in this recognition and transport. The majority of the associations between a trace element and other biological molecules result in undesirable chemical modifications in these molecules.

In living organisms, biological mechanisms have been developed in order to use vital trace elements including zinc and copper and to minimize toxic effects of heavy metals such as cadmium, mercury and lead (55. Solioz M, Odermatt A, Krapf R. Copper pumping ATPases: common concepts in bacteria and man. FEBS Lett. 1994; 346:44-7.). Oxidative processes are most intensive in a background where an imbalance is present in trace elements involved in the structure of enzymes accounted for antioxidant defense (66. Hoekstra WG, Suttie JW, Ganther HG, Mentz W. Trace elements metabolism in animals, University Park Press, Baltimore. 1974;2:61.). Alterations in the ion content of trace elements including iron, copper and zinc can affect activity of antioxidants (77. Yelinova V, Glazachev Y, Khramtsov V, Kudryashova L, Rykova V, Salganik R. Studies of human and rat blood under oxidative stress: changes in plasma thiol level, antioxidant enzyme activity, protein carbonyl content, and fluidity of erythrocyte membrane. Biochem Biophys Res Commun. 1996; 221:300-3.). In several cancers, it has been reported that significant differences occur in the normal distribution of iron, copper and zinc (88. Spartz L, Bloom AD. Biological consequences of oxidative stress: implications for cardiovascular disease and carcinogenesis. Oxford University Press, New York, 1992; pp. 138-61.). In some trials, serum Cu/Zn ratio was employed as chemoprophylaxis (99. Li Y, Xue Q, Chen L, Chen H, Chai C, Shi B, et al. Research on relationships of gastric cancer with serum trace elements, Helicobacter pylori and COX-2 in gastric tissue. Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2004; 21:107-10.). Moreover, it has been also used to evaluate and assess the prognosis in patients with cancer (1010. Shukla VK, Adukia TK, Singh SP, Mishra CP, Mishra RN. Micronutrients, antioxidants, and carcinoma of the gallbladder. J Surg Oncol. 2003; 84:31-5., 1111. Mazdak H, Yazdekhasti F, Movahedian A, Mirkheshti N, Shafieian M. The comparative study of serum iron, copper, and zinc levels between bladder câncer patients and a control group. Int Urol Nephrol. 2010; 42:89-93.).

In the present study, serum levels of trace elements were measured and it was found that Mn, Co, Cu, Mg, Fe and Zn concentrations were altered in sera of the patients with testicular cancer in comparison to healthy subjects.

MATERIALS AND METHODS

The study included 30 men with germ cell testicular cancer. Mean age was 26.9±11.2 years. All patients were lifetime non-smokers and had no history of alcohol addiction, drug abuse, antioxidant use and metabolic diseases. No comorbid disease was present in any of the patients. All patients had newly diagnosed testicular cancer and preoperative blood samples were taken. Thirty two healthy male subjects (mean age: 27.4±10.8) were randomly selected as controls among volunteers who had no history of smoking, alcohol consumption, drug or antioxidant use, and known comorbid disease. The patient and control groups had similar socioeconomic status.

According to 2009 TNM tumor staging system, there was stage I testicular tumor in 19 patients (63.3%) while stage II in 6 patients (20.0%), stage IIIA in 4 patients (13.3%) and stage IIIC in one patient (3.4%). The study was conducted in accordance to Helsinki Declaration, 1989 Revision. All participants gave written informed consent before participation in the study.

Blood Samples

Blood samples were drawn at morning after 12 hours fasting and stored on ice at 4°C. Then, sera were separated by centrifugation at 3000 rpm for 10 minutes. Serum samples were stored at −20°C until assays.

Measurements of Mineral-Heavy Metal Levels

Two milliliters of HNO3/H2O2 mixture (2:1) were added to 0.7 g of the serum samples. The mixture was placed into the water bath at 70°C for 30 min and stirred occasionally. Then, one mL of the same acid mixture was added, and the mixture was transferred into a Teflon vessel bomb for the microwave oven. The bomb was closed, and the solution was placed inside the microwave oven. Radiation was applied for 3 min at 450 W. After addition of 0.5mL of the same acid mixture, radiation was repeated for 3 min. After cooling for 5 min, 2.0mL of 0.1mol/L HNO3 was added, and the solution was transferred to a Pyrex tube. After centrifugation, the clear solution was used to determine Mn, Cd, Cu, Pb, Fe, Mg, Co and Zn levels. They were measured by using atomic absorption spectrophotometer technique with a UNICAM-929 spectrophotometer (Unicam Ltd, York Street, Cambridge, UK).

Statistical Analysis

All data were analyzed by using SPSS for Windows version 13.0. Descriptive statistics of the traits evaluated were expressed as mean, standard deviation, minimum and maximum values. Mann-Whitney U test was used for intergroup comparisons. P<0.05 was considered as significant.

RESULTS

There was seminoma in 15, mix germ cell tumor in 7, embryonal carcinoma in 4, yolk sac tumor in 2 and teratoma in 2 patients. The demographic characteristics are presented Table-1. Trace elements levels are presented in Table-2. No statistical difference was detected between patients with testicular cancer and controls regarding age and body mass index (BMI).

Table 1
Demographic characteristics.
Table 2
Descriptive Statistics and Comparison Results According to the Groups for specifications.

Trace element levels were compared between groups. It was found that Co, Cu, Mg and Pb levels were significantly higher in the patient group compared to the controls. It was also found that Zn, Fe and Mn levels were significantly lower in the patient group compared to controls. Cd levels were found to be higher in patients with testicular tumors compared to controls, but this didn't reach statistical significance.

DISCUSSION

Traces elements are accepted as essential components of biological structures, which play complex roles in the cancer development or inhibition. There are many questions regarding their essential and toxic effects on human health above the concentrations needed for their biological functions. In this context, there are conflicting results in the literature (1212. 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., 1313. Zowczak M, Iskra M, Torliński L, Cofta S. Analysis of serum copper and zinc concentrations in cancer patients. Biol Trace Elem Res. 2001; 82:1-8.).

Mn is an essential element which is required for several enzyme activities. It has a major role in the antioxidant defense system and comprises part of SOD enzyme (1414. Johnson S. The possible crucial role of iron accumulation combined with low tryptophan, zinc and manganese in carcinogenesis. Med Hypotheses. 2001; 57:539-43.). Therefore, it can be suggested that decreased serum Mn concentrations with disturbance of antioxidant mechanism can make target organs sensitive to carcinogens. Decreased serum Mn concentrations were reported in patients with bladder and renal cancers (1515. Gecit İ, Kavak S, Meral I, Pirinçci N, Güneş M, Demir H, et al. Effects of shock waves on oxidative stress, antioxidant enzyme and element levels in kidney of rats. Biol Trace Elem Res. 2011; 144:1069-76., 1616. Pirincci N, Gecit I, Gunes M, Kaba M, Tanik S, Yuksel MB, et al. Levels of serum trace elements in renal cell carcinoma cases. Asian Pac J Cancer Prev. 2013; 14:499502.). Our study showed that serum Mn concentrations were lower in patients with testicular cancer compared to controls. According to our hypothesis, Mn can result in oxidant/antioxidant imbalance in patients with testicular cancer, as being a trace element affecting oxidation status.

Zinc plays an anti-carcinogenic role through structural stabilization of deoxyribonucleic acid (DNA), ribonucleic acid (RNA), and ribosome. Zinc is also important in the functions of several transcription factors and proteins that are involved in the recognition of specific DNA sequences and regulation of gene transcription. Zinc has a protective effect against free-radical injury (1717. Wu T, Sempos CT, Freudenheim JL, Muti P, Smit E. Serum iron, copper and zinc concentrations and risk of cancer mortality in US adults. Ann Epidemiol. 2004; 14:195-201.). In previous studies, it has been reported that serum Zn concentrations were decreased in patients with ovarian, cervical, bladder and renal cancer (1515. Gecit İ, Kavak S, Meral I, Pirinçci N, Güneş M, Demir H, et al. Effects of shock waves on oxidative stress, antioxidant enzyme and element levels in kidney of rats. Biol Trace Elem Res. 2011; 144:1069-76.1919. Yaman M, Kaya G, Simsek M. Comparison of trace element concentrations in cancerous and noncancerous human endometrial and ovary tissues. Int J Gynecol Cancer. 2007; 17:220-8.). It seems that it is necessary to determine serum zinc levels in patients with ovarian cancer in comparison with healthy controls in order to fully elucidate the relationship between serum Zn levels and ovarian cancer. In addition, in a previous study, there were normal or elevated zinc concentrations only in the sera of the cases with primary liver cancer in contrast to decreased serum zinc levels in remaining cases, suggesting a differential sign favoring transformation from hepatocirrhosis to cancer (2020. Karlinskiĭ VM, Bogomolova GG. Change in zinc metabolism in malignant neoplasms. Vopr Onkol. 1985; 31:25-9.). Our study demonstrated decreased Zn concentrations in patients with testicular cancer compared to controls.

Fe is a trace element which is physiologically essential but dangerous in biochemical aspect. Either excess or deficiency of Fe can lead to oxidative DNA damage, although it is an important nutritional element (2121. Ames BN. DNA damage from micronutrient deficiencies is likely to be a major cause of cancer. Mutat Res. 2001; 475:7-20.). Moreover, it was proposed that low iron levels may have a role in the prevention of infection and cancer (2222. Weinberg ED. Cellular iron metabolism in health and disease. Drug Metab Rev. 1990; 22:531-79.).

There is substantial evidence supporting the hypothesis of a relationship between testicular cancer and disruption of iron metabolism and that testicular cancer may be a clinical manifestation of iron-induced testicular damage, presumably through an underlying free-radical mechanism (2323. Crawford RD. Proposed role for a combination of citric acid and ascorbic acid in the production of dietary iron overload: a fundamental cause of disease. Biochem Mol Med. 1995; 54:1-11.). In our study, results indicated that there was a significant difference in serum Fe levels between patient and control groups.

Physiological Cd doses lead to an increased endothelial permeability through inhibition of endothelial proliferation and induction of cell death mediated by DNA damage, which is also inhibited by zinc (2424. Messner B, Knoflach M, Seubert A, Ritsch A, Pfaller K, Henderson B, et al. Cadmium is a novel and independent risk factor for early atherosclerosis mechanisms and in vivo relevance. Arterioscler Thromb Vasc Biol. 2009; 29:1392-8.). It has been reported that doubling of soil cadmium is associated with an increased risk for lung cancer by 57% (2525. Nawrot TS, Thijs L, Den Hond EM, Roels HA, Staessen JA. An epidemiological re-appraisal of the association between blood pressure and blood lead: a meta-analysis. J Hum Hypertens. 2002; 16:123-31.). It was also shown that serum Cd levels were increased in patients with bladder cancer (33. Gecit I, Kavak S, Demir H, Gunes M, Pirincci N, Cetin C, et al. Serum trace element levels in patients with bladder cancer. Asian Pac J Cancer Prev. 2011; 12:3409-13.). In cadmium carcinogenicity, proto-oncogene activation, tumor suppressor gene inactivation, disrupted cell adhesion and inhibition of DNA repair are the implied cellular and molecular mechanisms (2626. Waalkes MP. Cadmium carcinogenesis. Mutat Res. 2003; 533:107-20., 2727. Waisberg M, Joseph P, Hale B, Beyersmann D. Molecular and cellular mechanisms of cadmium carcinogenesis. Toxicology. 2003; 192:95-117.). In addition, it has been reported that elevated Cd concentration may result in prostate, kidney and lung cancers (2828. Drasch G, Schöpfer J, Schrauzer GN. Selenium/cadmium ratios in human prostates: indicators of prostate cancer risk of smokers and nonsmokers, and relevance to the cancer protective effects of selenium. Biol Trace Elem Res. 2005; 103:103-7.). In the past decade, it has been reported that the injection of cadmium metal powder and various cadmium compounds induce sarcoma in local and interstitial cell testicular tumor in a systemic manner (2929. World Health Organization Regional Office for Europe. Air quality guidelines, 2nd edn. World Health Organization, Copenhagen, Denmark. 2000.). In our study, Cd levels were found to be higher in patients with testicular cancer compared to controls. However, the difference didn't reach statistical significance.

In our study, it was also demonstrated that serum levels of Pb, Co, Cu and Mg were increased when compared to controls. It is well-known that Pb and Cd are toxic and carcinogenic metals (2525. Nawrot TS, Thijs L, Den Hond EM, Roels HA, Staessen JA. An epidemiological re-appraisal of the association between blood pressure and blood lead: a meta-analysis. J Hum Hypertens. 2002; 16:123-31.). It has been suggested that Pb has a predisposing role in the carcinogenesis with inhibition of DNA synthesis and repair, oxidative injury and interaction with DNA-binding proteins and tumor suppressor proteins (3030. Inskip PD, Linet MS, Heineman EF. Etiology of brain tumors in adults. Epidemiol Rev. 1995; 17:382-414., 3131. Van Wijngaarden E, Dosemeci M. Brain cancer mortality and potential occupational exposure to lead: findings from the National Longitudinal Mortality Study, 1979-1989. Int J Cancer. 2006; 119:1136-44. Erratum in: Int J Cancer. 2007; 121:698.). Exposure to inorganic lead at early life induces teratoma and pre-neoplasm of renal and urinary bladder (3232. Moulin JJ, Wild P, Romazini S, Lasfargues G, Peltier A, Bozec C, et al. Lung cancer risk in hard-metal workers. Am J Epidemiol. 1998; 148:241-8.). Recent research indicated negative health consequences of lower level of lead exposure, including impaired functions of renal tubular cells, inhibition of sperm formation, fetal damage, decelerated velocity of motor nerves, and central nervous system dysfunction as well as hypertension and other cardiovascular diseases (3333. Landrigan PJ. Toxicity of lead at low dose. Br J Ind Med. 1989; 46:593-6., 3434. Møller L, Kristensen TS. Blood lead as a cardiovascular risk factor. Am J Epidemiol. 1992; 136:1091-100.). It was also shown that Pb levels were significantly increased in patients with malignant glioma compared to controls (3535. Arslan M, Demir H, Arslan H, Gokalp AS, Demir C. Trace elements, heavy metals and other biochemical parameters in malignant glioma patients. Asian Pac J Câncer Prev. 2011; 12:447-51.). In our study, Pb levels were found to be significantly higher in the patient group compared to controls.

Co is a constituent of vitamin B12 in humans. In human studies, evidence is inconclusive regarding relationship between inhalational exposure to cobalt and cancer. In the only available study on oral exposure to cobalt, no correlation was reported between cobalt and cancer deaths. In a study on workers refining and processing cobalt and sodium, it was shown that there was an increase in deaths from lung cancer in workers exposed to cobalt. Effects of exposure to cobalt salts were investigated in only one study. Preliminary results indicated an increased risk for lung cancer in those working at cobalt production, but follow-up didn't show any increase in the risk for cancer (3636. Tokar EJ, Diwan BA, Waalkes M P. Early life inorganic lead exposure induces testicular teratoma and renal and urinary bladder preneoplasia in adult metallothionein-knockout mice but not in wild type mice. Toxicology. 2010;276:5-10.). However, that study was limited by the small number of workers who developed cancer. In our study, Co levels were found to be significantly higher in the patient group compared to controls.

Cu plays a role in the production of hemoglobin, myelin, collagen and melanin as an essential nutrient (44. Sayir F, Kavak S, Meral I, Demir H, Cengiz N, Cobanoğlu U. Effects of crush and axotomy on oxidative stress and some trace element levels in phrenic nerve of rats. Brain Res Bull. 2013; 92:84-8.). In recent studies, it was shown that normal immune function requires adequate Cu intake (33. Gecit I, Kavak S, Demir H, Gunes M, Pirincci N, Cetin C, et al. Serum trace element levels in patients with bladder cancer. Asian Pac J Cancer Prev. 2011; 12:3409-13., 44. Sayir F, Kavak S, Meral I, Demir H, Cengiz N, Cobanoğlu U. Effects of crush and axotomy on oxidative stress and some trace element levels in phrenic nerve of rats. Brain Res Bull. 2013; 92:84-8.). It is well-known that serum Cu levels increase in several malignancies such as osteosarcoma, gastrointestinal tumors and lung cancer (3737. Turecký L, Kalina P, Uhlíková E, Námerová S, Krizko J. Serum ceruloplasmin and copper levels in patients with primary brain tumors. Klin Wochenschr. 1984; 62:187-9.). In some studies, it was shown that there was an increase in Cu levels within tumor cells or lung epithelial lining fluid of patients with lung cancer (3838. Dìez M, Cerdàn FJ, Arroyo M, Balibrea JL. Use of the copper/zinc ratio in the diagnosis of lung cancer. Cancer. 1989; 63:726-30., 3939. Mahabir S, Spitz MR, Barrera SL, Beaver SH, Etzel C, Forman MR. Dietary zinc, copper and selenium, and risk of lung cancer. Int J Cancer. 2007; 120:1108-15.). In our study, serum Cu levels were found to be significantly higher in the patient group compared to controls.

The observed effects of magnesium on either tumor transplant-or chemical-induced cancers depended on the duration of Mg supplementation or deficiency (4040. Collery P, Anghileri LJ, Coudoux P, et al. Magnesium and cancer: clinical data. Magnesium Bull. 1981; 3: 11-20.). Optimal Mg supplementation may have prophylactic effects against some neoplasms, but Mg alone isn't recommended for therapeutic purposes as cancer cells have also high metabolic requirements (4040. Collery P, Anghileri LJ, Coudoux P, et al. Magnesium and cancer: clinical data. Magnesium Bull. 1981; 3: 11-20.). Recently, in rats, it was shown that Mg supplementation inhibited increased DNA synthesis at colon epithelium. In that study, it was suggested that the finding might be related to suppression of oncogene-induced bowel carcinogenesis by Mg (4141. Mori H, Morishita Y, Mori Y, Yoshimi N, Sugie S, Tanaka T. Effect of magnesium hydroxide on methylazoxymethanol acetate-induced epithelial proliferation in the large bowels of rats. Cancer Lett. 1992;62:43-8.). In our study, serum Mg levels were found to be significantly higher in patients with testicular cancer compared to controls.

In our study, serum levels of trace elements were assessed in germ cell testicular cancer. Serum levels of trace elements can differ in different germ cell testicular cancer as in serum levels of tumor markers. Further studies are needed to evaluate this issue. Germ cell testicular cancers (other than choriocarcinoma) initially spread to retroperitoneal lymph nodes. Retrospective studies with larger series which compare early stage, non-metastatic and metastatic tumors are necessary in order to investigate effects of metastasis on alterations in serum trace element levels.

In conclusion, an association was observed between testicular cancer and trace elements in the present study. We also think that increases in Co, Cu, Mg and Pb levels and decreases in Zn, Mn and Fe levels can play important roles in the induction of testicular cancers. However, future prospective studies on the reasons of alteration in the serum concentrations of trace elements in patients with testicular cancer seem to be well grounded. Further prospective studies are needed to clarify the relationship between various stages of testicular cancer and serum levels of trace elements.

REFERENCES

  • 1
    Chia VM, Quraishi SM, Devesa SS, Purdue MP, Cook MB, McGlynn KA. International trends in the incidence of testicular cancer, 1973-2002. Cancer Epidemiol Biomarkers Prev. 2010; 19:1151-9.
  • 2
    Greenlee RT, Hill-Harmon MB, Murray T, Thun M. Cancer statistics, 2001. CA Cancer J Clin. 2001; 51:15-36. Erratum in: CA Cancer J Clin 2001; 51:144.
  • 3
    Gecit I, Kavak S, Demir H, Gunes M, Pirincci N, Cetin C, et al. Serum trace element levels in patients with bladder cancer. Asian Pac J Cancer Prev. 2011; 12:3409-13.
  • 4
    Sayir F, Kavak S, Meral I, Demir H, Cengiz N, Cobanoğlu U. Effects of crush and axotomy on oxidative stress and some trace element levels in phrenic nerve of rats. Brain Res Bull. 2013; 92:84-8.
  • 5
    Solioz M, Odermatt A, Krapf R. Copper pumping ATPases: common concepts in bacteria and man. FEBS Lett. 1994; 346:44-7.
  • 6
    Hoekstra WG, Suttie JW, Ganther HG, Mentz W. Trace elements metabolism in animals, University Park Press, Baltimore. 1974;2:61.
  • 7
    Yelinova V, Glazachev Y, Khramtsov V, Kudryashova L, Rykova V, Salganik R. Studies of human and rat blood under oxidative stress: changes in plasma thiol level, antioxidant enzyme activity, protein carbonyl content, and fluidity of erythrocyte membrane. Biochem Biophys Res Commun. 1996; 221:300-3.
  • 8
    Spartz L, Bloom AD. Biological consequences of oxidative stress: implications for cardiovascular disease and carcinogenesis. Oxford University Press, New York, 1992; pp. 138-61.
  • 9
    Li Y, Xue Q, Chen L, Chen H, Chai C, Shi B, et al. Research on relationships of gastric cancer with serum trace elements, Helicobacter pylori and COX-2 in gastric tissue. Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2004; 21:107-10.
  • 10
    Shukla VK, Adukia TK, Singh SP, Mishra CP, Mishra RN. Micronutrients, antioxidants, and carcinoma of the gallbladder. J Surg Oncol. 2003; 84:31-5.
  • 11
    Mazdak H, Yazdekhasti F, Movahedian A, Mirkheshti N, Shafieian M. The comparative study of serum iron, copper, and zinc levels between bladder câncer patients and a control group. Int Urol Nephrol. 2010; 42:89-93.
  • 12
    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.
  • 13
    Zowczak M, Iskra M, Torliński L, Cofta S. Analysis of serum copper and zinc concentrations in cancer patients. Biol Trace Elem Res. 2001; 82:1-8.
  • 14
    Johnson S. The possible crucial role of iron accumulation combined with low tryptophan, zinc and manganese in carcinogenesis. Med Hypotheses. 2001; 57:539-43.
  • 15
    Gecit İ, Kavak S, Meral I, Pirinçci N, Güneş M, Demir H, et al. Effects of shock waves on oxidative stress, antioxidant enzyme and element levels in kidney of rats. Biol Trace Elem Res. 2011; 144:1069-76.
  • 16
    Pirincci N, Gecit I, Gunes M, Kaba M, Tanik S, Yuksel MB, et al. Levels of serum trace elements in renal cell carcinoma cases. Asian Pac J Cancer Prev. 2013; 14:499502.
  • 17
    Wu T, Sempos CT, Freudenheim JL, Muti P, Smit E. Serum iron, copper and zinc concentrations and risk of cancer mortality in US adults. Ann Epidemiol. 2004; 14:195-201.
  • 18
    Cunzhi H, Jiexian J, Xianwen Z, Jingang G, Shumin Z, Lili D. Serum and tissue levels of six trace elements and copper/zinc ratio in patients with cervical cancer and uterine myoma. Biol Trace Elem Res. 2003; 94:113-22.
  • 19
    Yaman M, Kaya G, Simsek M. Comparison of trace element concentrations in cancerous and noncancerous human endometrial and ovary tissues. Int J Gynecol Cancer. 2007; 17:220-8.
  • 20
    Karlinskiĭ VM, Bogomolova GG. Change in zinc metabolism in malignant neoplasms. Vopr Onkol. 1985; 31:25-9.
  • 21
    Ames BN. DNA damage from micronutrient deficiencies is likely to be a major cause of cancer. Mutat Res. 2001; 475:7-20.
  • 22
    Weinberg ED. Cellular iron metabolism in health and disease. Drug Metab Rev. 1990; 22:531-79.
  • 23
    Crawford RD. Proposed role for a combination of citric acid and ascorbic acid in the production of dietary iron overload: a fundamental cause of disease. Biochem Mol Med. 1995; 54:1-11.
  • 24
    Messner B, Knoflach M, Seubert A, Ritsch A, Pfaller K, Henderson B, et al. Cadmium is a novel and independent risk factor for early atherosclerosis mechanisms and in vivo relevance. Arterioscler Thromb Vasc Biol. 2009; 29:1392-8.
  • 25
    Nawrot TS, Thijs L, Den Hond EM, Roels HA, Staessen JA. An epidemiological re-appraisal of the association between blood pressure and blood lead: a meta-analysis. J Hum Hypertens. 2002; 16:123-31.
  • 26
    Waalkes MP. Cadmium carcinogenesis. Mutat Res. 2003; 533:107-20.
  • 27
    Waisberg M, Joseph P, Hale B, Beyersmann D. Molecular and cellular mechanisms of cadmium carcinogenesis. Toxicology. 2003; 192:95-117.
  • 28
    Drasch G, Schöpfer J, Schrauzer GN. Selenium/cadmium ratios in human prostates: indicators of prostate cancer risk of smokers and nonsmokers, and relevance to the cancer protective effects of selenium. Biol Trace Elem Res. 2005; 103:103-7.
  • 29
    World Health Organization Regional Office for Europe. Air quality guidelines, 2nd edn. World Health Organization, Copenhagen, Denmark. 2000.
  • 30
    Inskip PD, Linet MS, Heineman EF. Etiology of brain tumors in adults. Epidemiol Rev. 1995; 17:382-414.
  • 31
    Van Wijngaarden E, Dosemeci M. Brain cancer mortality and potential occupational exposure to lead: findings from the National Longitudinal Mortality Study, 1979-1989. Int J Cancer. 2006; 119:1136-44. Erratum in: Int J Cancer. 2007; 121:698.
  • 32
    Moulin JJ, Wild P, Romazini S, Lasfargues G, Peltier A, Bozec C, et al. Lung cancer risk in hard-metal workers. Am J Epidemiol. 1998; 148:241-8.
  • 33
    Landrigan PJ. Toxicity of lead at low dose. Br J Ind Med. 1989; 46:593-6.
  • 34
    Møller L, Kristensen TS. Blood lead as a cardiovascular risk factor. Am J Epidemiol. 1992; 136:1091-100.
  • 35
    Arslan M, Demir H, Arslan H, Gokalp AS, Demir C. Trace elements, heavy metals and other biochemical parameters in malignant glioma patients. Asian Pac J Câncer Prev. 2011; 12:447-51.
  • 36
    Tokar EJ, Diwan BA, Waalkes M P. Early life inorganic lead exposure induces testicular teratoma and renal and urinary bladder preneoplasia in adult metallothionein-knockout mice but not in wild type mice. Toxicology. 2010;276:5-10.
  • 37
    Turecký L, Kalina P, Uhlíková E, Námerová S, Krizko J. Serum ceruloplasmin and copper levels in patients with primary brain tumors. Klin Wochenschr. 1984; 62:187-9.
  • 38
    Dìez M, Cerdàn FJ, Arroyo M, Balibrea JL. Use of the copper/zinc ratio in the diagnosis of lung cancer. Cancer. 1989; 63:726-30.
  • 39
    Mahabir S, Spitz MR, Barrera SL, Beaver SH, Etzel C, Forman MR. Dietary zinc, copper and selenium, and risk of lung cancer. Int J Cancer. 2007; 120:1108-15.
  • 40
    Collery P, Anghileri LJ, Coudoux P, et al. Magnesium and cancer: clinical data. Magnesium Bull. 1981; 3: 11-20.
  • 41
    Mori H, Morishita Y, Mori Y, Yoshimi N, Sugie S, Tanaka T. Effect of magnesium hydroxide on methylazoxymethanol acetate-induced epithelial proliferation in the large bowels of rats. Cancer Lett. 1992;62:43-8.

Publication Dates

  • Publication in this collection
    Nov-Dec 2015

History

  • Received
    15 Sept 2014
  • Accepted
    10 June 2015
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