Using Prostatic Fluid Levels of Zinc to Bromine Concentration Ratio in Non-Invasive and Highly Accurate Screening for Prostate Cancer

The prostate gland is subject to various disorders and of them prostate cancer (PCa) is one of the prostate’s most important medical, scientific and public health problems. Worldwide, PCa is the second most commonly diagnosed cancer and the fifth leading cause of cancer deaths in men ¹. PCa is especially prevalent in industrialized countries including North America, Northern and Western Europe and Australia ². The American Cancer Society declares PCa, with a lifetime prevalence of one in six men, is the most common cancer in males and the second leading cause of cancer death ³. Moreover, PCa is the leading cancer in terms of incidence and mortality in men from Africa, Oceania, and the Caribbean ^{1, 2}. PCa in China has also become a major public health concern ⁴.

The survival rate is proportional to the stage reached at diagnosis, hence early-stage diagnosis using effective diagnostic tools is a key to reducing mortality due to PCa ⁵. It is widely acknowledged that screening and early diagnosis of PCa are of vital importance for improving the likelihood of recovery. Current screening relies on prostate-specific antigen (PSA) testing in blood serum and a PSA level of 4 ng/mL is used as the highest level compatible with for non-malignant conditions. However, PSA screening of PCa has some significant disadvantages.

Firstly, PSA is not a cancer-specific biomarker. So there can be an elevated serum concentration (above 4 ng/mL) among patients with benign prostate hyperplasia (BPH) and urogenital infections, including chronic prostatitis (CP). Reliance on PSA testing can result in significant over-detection of alleged PCa and hence inappropriate treatment of non-malignant disease ⁶. Nearly 70-75% of prostate biopsies fail to detect PCa in men who undergo prostate biopsy procedures due to elevated PSA levels discovered after blood serum-test screening ^{5, 7}. In other words, it has been confirmed that only 25-30% of patients with a PSA value ≥ 4 ng/mL were finally diagnosed with PCa, leading to the overtreatment of lowrisk patients, unnecessary biopsies and nonessential radical prostatectomies ⁸. Thus, the level of PSA test specificity (selectivity) can be estimated as about 25-30%.

Secondly, the PSA test misses some aggressive tumors. For example, as was found by Thompson et al. (2004) that 20–25% men diagnosed with PCa including those with a poorly differentiated form (Gleason Score ≥8) have PSA levels below 4 ng/mL ^{6, 9}. Data from other research shows that only 40% of patients with PCa have an abnormal PSA level ¹⁰. Thus, the PSA test’s sensitivity can be estimated as somewhere between 40-75%.

The limitations and potential harm associated with PSA screening stimulate investigation of novel biomarkers with superior ability to detect PCa, compared with traditional PSA tests, so decreasing unnecessary biopsies. Much attention is now turning to fluid-based biomarkers, because obtaining fluid samples is in effect is a minimally invasive liquid biopsy. Other relevant factors of great significance for any novel method of PCa detection include cost-effectiveness, capacity to generate real-time results, “simplicity-of-use”, robustness, and functionality without excessive prior-processing of samples ¹¹.

In our previous studies the significant involvement of Zn, Ca, Mg, Rb and some other trace elements (TEs) in the function of the prostate was studied. (12-22). One of the main functions of the prostate gland is the production of prostatic fluid ²³. It contains a high concentration of Zn and elevated levels of Ca, Mg, Rb, and some other TEs, in comparison with levels in serum and other human body fluids.

The first finding of remarkably high levels of Zn in human expressed prostatic fluid (EPF) was reported in the early 1960s ²⁴. After analyzing EPF expressed from the prostates of 8 apparently healthy men, aged 25-55 years, it was found that Zn concentrations varied from 300 to 730 mg/L. After this finding several investigators suggested that the measurement of Zn levels in EPF may be useful as a marker of abnormal prostate secretory function ^{25, 26}. This suggestion promoted more detailed studies of the Zn concentrations in the EPF of healthy subjects and in those with different prostatic diseases, including PCa ^{26, 27}. A detailed review of these studies, reflecting the contradictions within accumulated data, was given in our earlier publication ²⁷. Moreover, the method and apparatus for micro analysis of Zn and some other TEs in the EPF samples using energy dispersive X-ray fluorescence (EDXRF) activated by radiation from the radionuclide source ¹⁰⁹Cd (¹⁰⁹Cd EDXRF) was developed by us ²⁸. We reasoned that apart from total amounts of TEs the ratios of Zn to some other TE content in EPF are likely to reflect a disturbance of prostate function. It was found that data on changes of TE content and Zn/TE concentration ratios in EPF of patients with PCa are very important, because these significant changes increase our knowledge and recognition of PCa pathogenesis and may prove useful as PCa diagnostic markers ^{29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39}.

The present study had three aims. The main objective was to obtain reliable results about the Br and Zn concentrations in the EPF of healthy men as well as in the EPF of patients with CP, BPH and PCa using the ¹⁰⁹Cd EDXRF method. The second aim was to calculate Zn/Br concentration ratio and to compare the levels of all EPF parameters investigated for normal, inflamed, hyperplastic, and cancerous prostates. The final aim was to select the optimal PCa biomarker among the TEs’ concentrations and Zn/Br concentration ratio by evaluating appropriate characteristics of each potential diagnostic test, with regard to its sensitivity, specificity, and accuracy.

All studies were approved by the Ethical Committees of the Medical Radiological Research Centre, Obninsk. All the procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments, or with comparable ethical standards.

To determine concentration of the TEs by comparison with known standards, aliquots of solutions of commercial, chemically pure compounds were used for calibration ⁴⁰. The standard samples for calibration were prepared in the same way as the samples of prostate fluid. Because there were no available liquid Certified Reference Materials (CRMs), ten sub-samples of the powdered CRM IAEA H-4 (animal muscle) were analyzed to estimate the precision and accuracy of results. Every CRM sub-sample weighing about 3 mg was applied to the piece of adhesive tape serving as an adhesive fixing backing. An acrylic stencil made in the form of a thin-walled cylinder with 11.3 mm inner diameter was used to apply the sub-sample to the adhesive tape. The polished-end acrylic pestle, which is a constituent of the stencil set, was used for uniform distribution of the sub-sample upon the adhesive tape surface restricted by the stencil’s inner cylindrical surface. After the sub-sample was lightly pressed onto the adhesive tape carrier, the stencil was removed. Then the sub-sample was covered with 4 μm gage Dacron film. Before the sample was applied, pieces of adhesive tape and Dacron film were weighed using an analytical balance. They were reweighed after the sample had been placed inside to determine precisely the sub-sample mass.

The facility for the radionuclide-induced EDXRF included an annular ¹⁰⁹Cd source with an activity of 2.56 GBq, A Si(Li) detector with an electric cooling system and a portable multi-channel analyzer based on a personal computer, comprised the detection system. Its resolution was 270 eV at the 6.4 keV line. The facility functioned as follows. Photons with energy 22.1 keV from the ¹⁰⁹Cd source arrived at the surface of the specimen inducing fluorescent K_α X-rays from the TE. The fluorescence reached the detector after passing through a 10 mm diameter collimator. Then the X-ray’s arrival was recorded. The duration of the measurements of Br and Zn concentrations was 60 min for each sample. The intensity of the K_α-line of Br and Zn for EPF samples and standards was estimated from a calculation of the total area under the corresponding photopeaks in the spectra.

(Table 1 and Table 2) depict some statistical characteristics of the parameters investigated and relevant to a normal distribution (M, SD, and SEM) (Table 1) and appropriate for a distribution that may not necessarily be normal (Median, Range) (Table 2).

The ratios of means/medians and the difference between mean/median values of all investigated parameters (Br, Zn, Zn/Br) in EPF samples of normal, inflamed, benign hyperplastic and cancerous prostates determined by the parametric Student's t-test and non-parametric Wilcoxon-Mann-Whitney U-test are presented in Table 3 and Table 4, respectively.

(Table 5) contains important parameters (“Specificity” and “Accuracy”), which reflect the possibilities that Zn concentration and Zn/Br ratio in prostate fluid can aid the diagnosis of PCa (an estimation is made for “PCa or normal, CP, and BPH”), if the level of “Sensitivity” was chosen as 100%.

(Table 6) also contains important parameters (“Sensitivity” and “Accuracy”), which reflect the possibilities that Zn concentration and Zn/Br ratio in prostate fluid can aid the diagnosis of PCa (an estimation is made for “PCa or normal, CP, and BPH”), if the level of “Specificity” was chosen as 100%.

(Table 7) presents optimal (“Sensitivity” is not below 80%) levels of “Sensitivity”, “Specificity” and “Accuracy” when Zn concentration and Zn/Br ratio in prostate fluid are used for the diagnosis of PCa (an estimation is made for “PCa or normal, CP, and BPH”).

Individual data sets for the Br and Zn concentration and also for Zn/Br concentration ratio investigated in EPF samples of normal, inflamed, benign hyperplastic and cancerous prostates are shown in Figure 1.

Figure 1.Individual data sets for Br and Zn concentrations (mg/L), and for Zn/Br concentration ratio in prostate fluid of normal (1), inflamed (2), benign hyperplastic (3) and cancerous prostate (4).

As was shown by us ^{27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39} results from the use of CRM IAEA H-4 as certified reference materials for the analysis of samples of EPF is acceptable. Good agreement of the Br and Zn contents, analyzed by the ¹⁰⁹Cd EDXRF method, with the certified data of reference materials indicates an acceptable accuracy for the results obtained in the study of two TEs of the EPF presented in Table 1, Table 2, Table 3, Table 4, Table 4, Table 5, Table 6, Table 7.

From Table 3 and Table 4, it is observed that in the EPF of inflamed prostates the mean/median values for the Br do not differ significantly from normal levels, while the values of Zn and Zn/Br are significantly lower.

In the EPF from hyperplastic prostates the mean/median values for Br and Zn/Br are not significantly different from normal levels, while the values of Zn is significantly lower (Table 3 and Table 4).

In the EPF of cancerous prostates the mean/median values for the Br do not differ significantly from normal levels, but the values of Zn and Zn/Br are significantly lower. Moreover, these differences also exist when EPFs of cancerous prostates are compared with EPFs of inflamed or hyperplastic prostates (Table 3 and Table 4).

Thus, from Table 3 and Table 4, as well as from individual data sets (Figure 1), it is observed that measurements of the Zn concentration and Zn/Br concentration ratios in EPF could become a powerful diagnostic tool when seeking PCa. To a large extent, continuation of the search for new methods for early diagnosis of PCa was due to experience gained after a critical assessment of the limitations of the current PSA blood serum tests ^{5, 6, 7, 8, 9, 10, 11}. In addition to the PSA test and morphological study of needle-biopsy cores of the prostate, the development of highly precise less invasive testing methods will clearly be very useful. The proportion of subjects with of normal, inflamed, benign hyperplastic and cancerous prostates in the present study represented the Urological Department’s usual patient proportions in the MRRC. Thus, our data allow us to evaluate adequately the importance of Zn concentration and Zn/Br concentration ratio in EPF for the diagnosis of PCa. As is evident from Table 3 and Table 4, as well as from individual data sets (Figure 1), the Zn/Br concentration ratio in EPF is potentially the most informative parameter for a differential diagnosis of PCa.

For example, if “Sensitivity” of a new method of PCa diagnosis is set equal to 100% the resulting values for “Specificity/Selectivity” and “Accuracy” are presented in Table 5. If “Specificity/Selectivity” of a new method of PCa diagnosis is set equal to 100% the resulting values for “Sensitivity” and “Accuracy” are presented in Table 6. The data for “Sensitivity”, “Specificity/Selectivity” and “Accuracy” can be more balanced if a level of ≥ 80% for “Sensitivity” is acceptable (Table 7). It should be noted that the number of people (samples) examined was taken into account for calculation of confidence intervals of data presented in Table 5, Table 6, Table 7⁴¹.

From data in Table 5, Table 6, Table 7 it follows, after comparison, that levels of “Sensitivity”, “Specificity/Selectivity” and “Accuracy” for the Zn and Zn/Br in EPF used as PCa biomarkers are better than results from the PSA level blood serum test. Among them the most informative tumor marker is the Zn/Br ratio. In other words, if level of Zn/Br ratio in EPF sample is lower than 24, one could diagnose a malignant tumor with an accuracy 95±2%. Thus, using the level of Zn/Br in an EPF sample as a tumor marker makes it possible to diagnose cancer in the 80±13% of cases (sensitivity) with specificity/selectivity 97±2%. The high level of specificity/selectivity, 97±2%, means that this test results in a significant decrease in the number of unnecessary biopsies, because on average only 3% (100%-97% = 3%) of prostate biopsies fail to detect PCa (i.e. are false negative) in men who have prostate cancer. Thus, using the proposed test will reduce the number of true negatives after biopsy.

The Zn/Br concentration ratio in EPF as the marker of prostatic malignancy showed higher values for “Specificity/Selectivity” and “Accuracy” than Zn concentration (Table 7). Moreover, EDXRF analysis offers other important advantage for Zn/Br ratio measurement in EPF in comparison with using the Zn concentration as PCa biomarker. Measurement the Zn concentration imposes the necessity of an accurate aliquot volume of EPF, thereby introducing potential errors and variables. The results of direct EDXRF assay of Zn/Br ratio in an EPF drop do not depend from the drop volume and eliminate these variables.

Characteristically, elevated or deficient levels of TEs and electrolytes observed in the EPF of cancerous prostates are discussed in terms of their potential role in the initiation, promotion, or inhibition of prostate cancer. In our opinion, abnormal levels of TE contents and Zn/TE ratios in the EPF of cancerous prostates could be the consequences of malignant transformation. Compared to other fluids of the human body, the prostate’s secretion contains higher level of Zn and some other TEs. These data suggest that these elements could be involved in prostatic function. The suppressed prostatic function can be both a cause and a consequence of CP or BPH. Malignant transformation is accompanied by a drastic loss of tissue-specific functional features, which leads to a significant reduction in the content of some elements associated with functional characteristics of the human EPF, including such TE as Zn.

It is necessary to keep in mind that biochemical, or in other words functional, changes in prostatic cells are present from the earliest development of malignancy, which precedes any histopathological indication of malignancy, and these biochemical changes persist during progression of the malignancy and remain present in advanced prostate cancer. Thus, Zn depletion is an early step in the cancer proliferation process and Zn depletion in EPF precedes the morphological transformation of cells from being histopathologically normal to cancerous.

In our study the portable device we used for EDXRF analysis, with its ¹⁰⁹Cd source for the excitation of X-ray fluorescence in the EPF sample, was developed by ourselves. More powerful devices for EDXRF analysis with X-ray tubes, including “the total reflection” version (TRXRF) of the method, allow reliable determinations of the Br, Zn and many other TE concentrations in a drop of a human body fluid within 10 min ⁴³. EDXRF is a fully instrumental and non-destructive method because a drop of EPF is investigated without requiring any sample pretreatment or its consumption. Moreover, it is well known that among the most modern analytical technologies, EDXRF is one of the simplest, fastest, most reliable and efficient of the available techniques for TE determination ⁴³. There are many different kinds of EDXRF and TRXRF device on the market and technical improvements are frequently announced.

The routine screening for PCa has generally included invasive (by a venipuncture) testing of PSA level in blood serum. The method presented here for PCa screening is a noninvasive and safe procedure because only requires a drop of EPF. This is obtained during a digital rectal examination using prostate gland massage. Many urologists have successfully and easily obtained EPF this way, so it seems likely that others will be able to do likewise for most of their patients.

All of these advantages, including the elimination of CP and BPH as confounding conditions when screening for PCa, along with its “Sensitivity”, “Specificity” and “Accuracy” for PCa identification all exceeding 80-90%, favor the EDXRF of TEs and their ratio in EPF over the use of PSA levels for this purpose. Also these results suggest a strong possibility that it can replace the PSA level determination in screening for PCa. In our opinion, obtaining the levels of TEs and their ratio in a drop of EPF, using EDXRF, is a fast, reliable, and non-invasive diagnostic tool that can be successfully used by physicians, who are not urologists, at the point-of-care for highly effective PCa screening and as an additional test before prostate gland biopsy. Its advantages have been outlined above. Further we believe it is superior to the PSA level determination for this purpose.

There is a critical need for a highly reliable, accurate, simplified biomarker and procedure for the screening for prostate cancer, or as an adjunct for the PSA test during the urological examination of patients as candidates for prostate biopsy. In the present work, Br and Zn concentration measurements were carried out in the EPF samples from normal, inflamed, hyperplastic, and malignant prostates using the non-destructive, instrumental ¹⁰⁹Cd EDXRF micro method developed by us. It was shown that this method is an adequate analytical tool for the non-destructive determination of Br and Zn concentrations as well as for calculation of Zn/Br concentration ratio in the EPF samples of human prostate in normal and some pathological conditions. It was observed that in the EPF of cancerous prostates, levels of Zn and Zn/Br were significantly lower in a comparison with those in the EPF of normal, inflamed, and hyperplastic prostates. It was shown that “Sensitivity”, “Specificity” and “Accuracy” of PCa identification using the Zn and Zn/Br levels in the EPF samples was significantly higher than that using PSA levels in blood serum. It was concluded that study of the Br and Zn levels and their ratio in an EPF drop, obtained by using EDXRF, is a fast, reliable, and non-invasive diagnostic tool that can be successfully used by physicians at the point-of-care for highly effective PCa screening and as an additional test before a the prostate gland biopsy.

The authors are grateful to Dr Tatyana Sviridova, Medical Radiological Research Center, Obninsk for supplying EPF samples. The authors are also extremely grateful to Dr. Sinclair Wynchank for a very valuable and detailed discussion of the results of this work and his help in English.

1. 1.H E Taitt. (2018) Global trends and prostate cancer: A review of incidence, detection, and mortality as influenced by race, ethnicity, and geographic location.Am JMensHealth. 12(6), 1807-1823.
   Search at Google Scholar

1. 2.Dasgupta P, P D Baade, J F Aitken, Ralph N, S K Chambers et al. (2019) . Geographical Variations in Prostate Cancer Outcomes: A Systematic Review of International Evidence.Front Oncol. 9, 238. doi: 10.3389/fonc.2019.00238. eCollection .
   View article·Search at Google Scholar

1. 3.R L Siegel, K D Miller, Jemal A. (2017) Cancer Statistics. , CA Cancer J Clin 67(1), 7-30.
   Search at Google Scholar

1. 4.Qi D, Wu C, Liu F, Gu K, Shi Z et al. (2015) Trends of prostate cancer incidence and mortality in Shanghai. to , China from, Prostate 75, 1662-1668.
   Search at Google Scholar

1. 5.Tkac J, Gajdosova V, Hroncekova S, Bertok T, Hires M. (2019) Prostate-specific antigen glycoprofiling as diagnostic and prognostic biomarker of prostate cancer.Interface. Focus. 9(2): 20180077. doi: 10.1098/rsfs.2018.0077. Epub .
   View article·Search at Google Scholar

1. 6.Zapała P, Dybowski B, Poletajew S, andRadziszewskiP. (2018) What can be expected from prostate cancer biomarkers A Clinical Perspective.UrolInt.100(1). 1-12.
   Search at Google Scholar

1. 7.Sorokin I, B M Mian. (2015) Risk calculators and updated tools to select and plan a repeat biopsy for prostate cancer detection.Asian JAndrol. 17(6), 864-869.
   Search at Google Scholar

1. 8.Qu M, S C Ren, Y H andSun. (2014) Current early diagnostic biomarkers of prostate cancer.Asian JAndrol. 16(4), 549-554.
   Search at Google Scholar

1. 9.I M Thompson, D K Pauler, P J Goodman, C M Tangen, M S Lucia. (2004) Prevalence of prostate cancer among men with a prostate-specific antigen level < or=4.0 ng per milliliter. , N Engl J Med 350, 2239-2246.
   PubMed·View article·Search at Google Scholar

1. 10.Alotaibi. (2019) Incidence of prostate cancer among patients with prostate-related urinary symptoms: A single institution series in 10 years.UrolAnn. 11(2), 135-138.
   PubMed·View article·Search at Google Scholar

1. 11.Hayes B, Murphy C, Crawley A, andO'Kennedy R. (2018) Developments in point-of-care diagnostic technology for cancer detection.Diagnostics (Basel). 8(39), 1-18.
   View article·ScienceDirect·Search at Google Scholar

1. 12.Zaichick V. (2004) INAA and EDXRF applications in the age dynamics assessment of Zn content and distribution in the normal human prostate. , J Radioanal Nucl Chem 262, 229-234.
   Search at Google Scholar

1. 13.Zaichick V, Zaichick S. (2013) The effect of age on Br, Ca, Cl, K, Mg, Mn, and Na mass fraction in pediatric and young adult prostate glands investigated by neutron activation analysis. , Appl Radiat Isot 82, 145-151.
   Search at Google Scholar

1. 14.Zaichick V, Zaichick S. (2013) INAA application in the assessment of Ag. , Co, Cr, Fe, Hg, Rb, Sb, Sc, Se, and, J Radioanal Nucl Chem 298(3), 1559-1566.
   Search at Google Scholar

1. 15.Zaichick V, Zaichick S. (2013) NAA-SLR and ICP-AES Application in the assessment of mass fraction of 19 chemical elements in pediatric and young adult prostate glands. Biol Trace Element Res. 156(1), 357-366.
   Search at Google Scholar

1. 16.Zaichick V, Zaichick S. (2013) Use of neutron activation analysis and inductively coupled plasma mass spectrometry for the determination of trace elements in pediatric and young adult prostate. , Am J Analyt Chem 4, 696-706.
   Search at Google Scholar

1. 17.Zaichick V, Zaichick S. (2014) Relations of bromine, iron, rubidium, strontium, and zinc content to morphometric parameters in pediatric and nonhyperplastic young adult prostate glands. Biol Trace Element Res. 157(3), 195-204.
   Search at Google Scholar

1. 18.Zaichick V, Zaichick S. (2014) Relations of the neutron activation analysis data to morphometric parameters in pediatric and nonhyperplastic young adult prostate glands. Advances in Biomedical Science and Engineering 1(1), 26-42.
   Search at Google Scholar

1. 19.Zaichick V, Zaichick S. (2014) Relations of the Al,B,Ba, Br, Ca, Cl, Cu, Fe, K, Li, Mg, Mn, Na, P, S, Si, Sr, and Zn,mass fractions to morphometric parameters in pediatric and nonhyperplastic young adult prostate glands. , BioMetals 27(2), 333-348.
   Search at Google Scholar

1. 20.Zaichick V, Zaichick S. (2014) The distribution of 54 trace elements including zinc in pediatric and nonhyperplastic young adult prostate gland tissues. , Journal of Clinical and Laboratory Investigation Updates 2(1), 1-15.
   Search at Google Scholar

1. 21.Zaichick V, Zaichick S. (2014) Androgen-dependent chemical elements of prostate gland. , Androl Gynecol: Curr Res 2, 2.
   Search at Google Scholar

1. 22.Zaichick V, Zaichick S. (2015) Differences and relationships between morphometric parameters and zinc content in nonhyperplastic and hyperplastic prostate glands. , BJMMR 8(8), 692-706.
   Search at Google Scholar

1. 23.Zaichick V. (2014) The prostatic urethra as a Venturi effect urine-jet pump to drain prostatic fluid. Med Hypotheses. 83, 65-68.
   Search at Google Scholar

1. 24.A R Mackenzie, Hall T, Whitmore W F Jr. (1962) Zinc content of expressed human prostate fluid. , Nature (London) 193(4810), 72-73.
   Search at Google Scholar

1. 25.J L Marmar, Katz S, D E Praiss, Benedictis T J De. (1980) Values for zinc in whole semen, fraction of split ejaculate and expressed prostatic fluid. , Urology 16(5), 478-480.
   Search at Google Scholar

1. 26.Zaichick V, Tsyb A, V N Dunchik, T V Sviridova. (1981) Method for diagnostics of prostate diseases. Certificate of invention No 997281(30.03.1981). , Russia
   Search at Google Scholar

1. 27.Zaichick V, Sviridova T, Zaichick S. (1996) Zinc concentration in human prostatic fluid: normal, chronic prostatitis, adenoma, and cancer. , Int Urol Nephrol 28(5), 687-694.
   Search at Google Scholar

1. 28.Zaichick V, Zaichick S, Davydov G. (2016) Method and portable facility for measurement of trace element concentration in prostate fluid samples using radionuclide-induced energy-dispersive X-ray fluorescent analysis. , Nucl Sci Tech 27(6), 1-8.
   Search at Google Scholar

1. 29.Zaichick V, Zaichick S. (2018) Effect of age on the Br, Fe, Rb, Sr, and Zn concentrations in human prostatic fluid investigated by energy-dispersive X-ray fluorescent microanalysis. , MicroMed 6(2), 94-104.
   Search at Google Scholar

1. 30.Zaichick V, Zaichick S. (2018) Trace element concentrations in the expressed prostatic secretion of normal and hyperplastic prostate. , J Urol Neph St 1(3), 1-7.
   Search at Google Scholar

1. 31.Zaichick V, Zaichick S. (2018) Trace elements of expressed prostatic secretions as a source for biomarkers of prostatic cancer. , J Clin Res Oncol 1(1), 1-7.
   Search at Google Scholar

1. 32.Zaichick V, Zaichick S. (2018) Br, Fe, Rb, Sr, and Zn levels in the prostatic secretion of patients with chronic prostatitis. , Int Arch Urol Complic 4(46), 1-6.
   Search at Google Scholar

1. 33.Zaichick V, Zaichick S. (2019) Significance of trace element quantities in the prostatic secretion of patients with chronic prostatitis and prostate cancer. , JBRR 2(1), 56-61.
   Search at Google Scholar

1. 34.Zaichick V, Zaichick S. (2019) Ratio of zinc to bromine, iron, rubidium, and strontium concentration in the prostatic fluid of patients with benign prostatic hyperplasia. Acta Scientific Medical Sciences. 3(6), 49-56.
   Search at Google Scholar

1. 35.Zaichick V, Zaichick S. (2019) Ratio of zinc to bromine, iron, rubidium, and strontium concentration in expressed prostatic secretions as a source for biomarkers of prostatic cancer. , American Journal of Research.5-6 140-150.
   Search at Google Scholar

1. 36.Zaichick V, Zaichick S. (2019) Some trace element contents and ratios in prostatic fluids as ancillary diagnostic tools in distinguishing between the benign prostatic hyperplasia and chronic prostatitis. , Archives of Urology 2(1), 12-20.
   Search at Google Scholar

1. 37.Zaichick V, Zaichick S. (2019) Ratio of zinc to bromine, iron, rubidium, and strontium concentration in the prostatic fluid of patients with chronic prostatitis. , Global Journal of Medical Research (F) 41, 9-15.
   Search at Google Scholar

1. 38.Zaichick V, Zaichick S.(2019)Significance of trace element quantities in the prostatic secretion of patients with benign prostatic hyperplasia and prostate cancer. , J Cancer MetastasisTreat 5(48), 1-9.
   Search at Google Scholar

1. 39.Zaichick V, Zaichick S. (2019) Some trace element contents and ratios in prostatic fluids as ancillary diagnostic tools in distinguishing between the chronic prostatitis and prostate cancer. Medical Research and Clinical Case Reports. 3(1), 1-10.
   Search at Google Scholar

1. 40.Zaichick V. (1995) Applications of synthetic reference materials in the medical Radiological Research Centre. , Fresenius J Anal Chem 352, 219-223.
   Search at Google Scholar

1. 41.V S Genes. (1967) Simple methods for cybernetic data treatment of diagnostic and physiological studies. , Nauka, Moscow
   Search at Google Scholar

1. 42.Hjertholm P, Fenger-Gron M, Vestergaard M, M B Christensen, Borre M. (2015) Variation in general practice prostate-specific antigen testing and prostate cancer outcomes: An ecological study. , Int J Cancer 136, 435-442.
   Search at Google Scholar

1. 43.Rossmann M, Zaichick S, Zaichick V. (2016) Determination of key chemical elements by energy dispersive X-Ray fluorescence analysis in commercially available infant and toddler formulas consumed in UK. Nutr Food TechnolOpen Access. 2(4), 1-7.
   Search at Google Scholar

1. 1.Zaichick Vladimir, 2019, A systematic review of the main electrolytes concentrations in the prostate fluid of normal gland, Journal of Analytical & Pharmaceutical Research, 8(6), 214, 10.15406/japlr.2019.08.00341

1. 2.Zaichick Vladimir, 2020, Using Prostatic Fluid Levels of Some Trace Elements and Their Combinations in Non-Invasive and Highly Accurate Screening for Prostate Cancer, Journal of Cancer Therapy, 11(01), 1, 10.4236/jct.2020.111001