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Int. J. Life. Sci. Scienti. Res., 3(4): 1158-1161 JULY 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1158
Altered Level of Serum Magnesium in Patients
with Esophageal and Lung Carcinoma
Gajanand Joshi1
*, R. K. Vyas2
, Ghanshyam Gahlot1
, Yogita Soni3
1
Biochemist, Department of Biochemistry, S. P. Medical College, Bikaner, Rajasthan University of Health & Science,
Bikaner, Rajasthan, India
2
Sr. Professor, Department of Biochemistry, S. P. Medical College, Bikaner, Rajasthan University of Health & Science,
Bikaner, Rajasthan, India
3
Professor, Department of Biochemistry, S. P. Medical College, Bikaner, Rajasthan University of Health & Science,
Bikaner, Rajasthan, India
*
Address for Correspondence: Dr. Gajanand Joshi, Biochemist, Department of Biochemistry, S. P. Medical College,
Bikaner, Rajasthan University of Health & Science, Bikaner, Rajasthan, India
Received: 05 March 2017/Revised: 08 April 2017/Accepted: 03 June 2017
ABSTRACT- Background: Esophageal and Lung carcinoma are the leading cause of years of life lost because of
cancer and is associated with the highest economic burden relative to other tumor types. Epidemiological studies identify
magnesium deficiency as a risk factor for these types of human cancers. The present studies were performed to concerning
the contribution of magnesium to tumorigenesis and investigate the concentration of magnesium in esophageal and lung
carcinoma.
Aims and Objective: The aim of this study was to compare the serum magnesium levels of patients with carcinoma of
lung and esophagus patients and apparently healthy people.
Material and methods: Study group consisted of 50 clinically diagnosed subjects (Biopsy confirmed 25 cases with
Esophageal carcinoma and 25 cases with Lung carcinoma). The control group consisted of 50 healthy subjects were
included in the study. Venous blood samples of each lung and esophagus cancer were obtained and serum magnesium
level was measured by Atomic Absorption Spectrophotometer measurements.
Results: In the study group, we were found mean concentration of serum magnesium was decreased in esophageal
(1.40±0.13 mg %) and lung carcinoma (1.23±0.12 mg %) in comparison to controls (2.08 ± 0.45 mg %).
Conclusions: Serum magnesium was found statistically significantly lower in study group when compared with control
(P<0.0001).
Key-words- Lung and Esophagus Carcinoma, Magnesium, Atomic absorption spectrophotometer
INTRODUCTION
Lung Cancer is the second most common cancer in women
after breast cancer and is also the second leading cause of
cancer-related deaths in women worldwide.1
Uncontrolled
cell growth in tissues of the lung, may lead to metastasis,
which is the invasion of adjacent tissue and infiltration
beyond the lungs. The vast majority of primary lung
cancers are carcinoma of the lung, derived from epithelial
cells. Esophageal cancer is the eighth most common cancer
and sixth leading cause of cancer deaths in the world, with
the majority of cases occurring in developing countries. [1]
Access this article online
Quick Response Code Website:
www.ijlssr.com
DOI: 10.21276/ijlssr.2017.3.4.10
About 90% of esophageal cancers worldwide are
Squamous Cell Carcinomas (SCC), mostly occurring in
defined high-incidence areas of low and middle-resource
countries. Historically, the highest incidences are reported
in regions of Central Asia. One such region is Kashmir
Valley in Northern India.
Some minerals and Trace-heavy elements play significant
role in human health and disease. Trace elements at
optimum levels are required for numerous metabolic and
physiological processes in the human body.[2]
Studies have
shown that 46% of all critically ill cancer patients admitted
to an ICU (intensive care unit) in a tertiary cancer centre
presented with hypomagnesemia and they concluded that
the incidence of hypomagnesemia in critically ill cancer
patients is high.[3]
The incidence rises to 60 to 65% in all
patients admitted into the intensive care units in which
nutrition, diuretics, hypoalbuminemia, and amino
glycosides may play important roles.[4]
Normal
magnesium levels in humans 1.5-2.5 mg/dl and maintained
ARTICLERESEARCH
Int. J. Life. Sci. Scienti. Res., 3(4) JULY 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1159
at a fairly constant level of serum magnesium to label
Hypomagnesaemia is below (1.56 mg/dl).
Over 300 enzymes systems that influence the metabolism
of carbohydrate, amino acids, nucleic acid, protein and ion
transport, require magnesium.[5]
The role of magnesium in
fatty acid and phospholipid metabolism, that affect
permeability and stability of membrane, were elucidated.[6]
It has been proposed that magnesium is central in the cell
cycle, and that its deficiency is an important condition in
pre-cancerous cell transformation.[7]
Magnesium deficiency
would therefore lead to physiological decline in cells
setting the stage for cancer. It is known that carcinogenesis
induces magnesium distribution disturbance, which causes
magnesium mobilization through blood cells and
magnesium depletion in Non-neoplastic tissue.
Magnesium deficiency seems to be carcinogenic and in
case of solid tumours a high level of supplemented
magnesium inhibits carcinogenesis.[8]
Alouane L. et al. [9]
found that patients with lung cancer had serum magnesium
levels lower than in normal controls. It suggested the
hypothesis stipulating an increased magnesium uptake by
the tumor cells. Ahmad et al studied that the concentrations
of zinc and magnesium in blood were significantly
decreased in esophageal cancer patients. This suggested
that these might play some role in carcinogenesis.[10]
However, role of serum level of magnesium in causing
such types of carcinoma has not been studied to great
extent. Therefore, the present study was undertaken to
estimate the serum levels of magnesium & their role in
causing lung and esophageal carcinoma patients with
apparently healthy controls.
MATERIALS AND METHODS
The study was carried out in the Department of
Biochemistry in collaboration with the Department of
Acharya Tulsi Regional Cancer Treatment and Research
Institute in PBM Hospital, affiliated to Sardar Patel
Medical College, Bikaner during 2013. The study was
approved by ethics committee and informed consent was
taken from all the patients. The study group consisted of 50
clinically diagnosed subjects (25 cases with Lung
carcinoma and 25 cases with Esophageal carcinoma). The
control group consisted of 50 Healthy subjects. Both study
and control group were same socio-economic status with
similar diet habits.
Inclusion Criteria
The criteria for the selection of patients were
(i) Biopsy proved cases of Lung carcinoma and Esophageal
carcinoma
(ii)Who had not undergone any treatment i.e.
chemotherapy or radio-therapy
(iii) Who has not taken long course of any mineral
supplement during last six months
Exclusion Criteria
The criteria for the selection of controls
(i) Who were not suffering from any cancerous lesions
(ii) Who has not taken any course of mineral supplement
Sample Collection and Storage
Blood samples were obtained by vein puncture and
collected in a clean dry centrifuge tube. Standard
precautions for trace element determination were taken,
haemolysed samples were discarded. The blood was
centrifuged at 3000rpm for 10 minutes and serum was
stored at - 40
C until the day of the test.
Biochemical Assessments
Serum magnesium concentration was determined by direct
measurement method using Atomic absorption
spectroscopy.[11]
Analytical reagent grade chemicals,
standards were used. Water used for washing laboratory
apparatus and for preparing solutions and standards was
purified by deionization of redistilled water.
STATISTICALANALYSIS
The results were expressed as the mean ± standard error
(SE). One-way ANOVA was used for the comparison of
mean values of the groups. Then, Student-t test was used to
determine the difference between groups. In addition,
Pearson’s correlation analysis was carried out to determine
the relationships among the variables.
RESULTS
The results as presented in the Table (1-2) show that the
mean serum level of Serum Magnesium was altered in
subjects having Esophageal (1.40 ± 0.13) and Lung
carcinoma (1.23 ± 0.12). A statistically significantly lower
(p<0.0001) in serum magnesium levels was observed in
patients with Esophageal and Lung carcinoma group than
the healthy control group (Fig 1-2).
Table 1: Serum Magnesium Concentration (mg %)
Comparison between Esophageal Carcinoma Patients
(Case Group) with Normal Healthy Persons (Control
Group)
Values
Normal Healthy
Persons
(Control Group)
(n=50)
Esophageal Carcinoma
Patients (Case Group)
(n=25)
Mean 2.08 1.408
Range 1.31-3.00 1.18-1.66
SD 0.450 0.134
SE 0.063 0.026
t 7.335
p value 0.0001***
*** Highly significant
Int. J. Life. Sci. Scienti. Res., 3(4) JULY 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1160
Table 2: Serum Magnesium Concentration (mg %)
Comparison between Lung Carcinoma Patients (Case
Group) with Normal Healthy Persons (Control Group)
Values
Normal
Healthy Persons
(Control
Group)
(n=50)
Lung Carcinoma
Patients
(Study Group)
(n=25)
Mean 2.08 1.23
Range 1.31-3.00 1.06-1.53
SD 0.450 0.124
SE 0.063 0.024
t 9.252
p value 0.0001***
*** Highly significant
Fig: 1 Serum Magnesium Concentration (mg %)
Comparison between Esophageal Carcinoma patients
(Case Group) with Normal Healthy Persons (Control
Group)
Fig: 2 Serum Magnesium Concentration (mg %)
Comparison between Lung Carcinoma Patients (Case
Group) with Normal Healthy Persons (Control Group)
DISCUSSION
Trace elements and metals are known to play a vital role in
metabolism. Magnesium is important for maintaining the
integrity of DNA. Mg cations bind to DNA and reduce the
negative charge density, thereby stabilizing the structure of
DNA. It has been proposed that magnesium is central in the
cell cycle, and that its deficiency is an important
conditioner in precancerous cell transformation. In
addition, immune competence (that eliminates transformed
cells) is Mg dependent. Mg supplementation or deficiency
was induced, relative to exposure to oncogens. Optimal Mg
intake may be prophylactic against initiation of some
neoplasm.
The finding of the present study indicates statistically
significant decrease in serum Magnesium was recorded in
Lung and Esophageal Carcinoma as compared to that of
control subjects. It might be possible that due to general
additional mechanisms by which magnesium might have
protected against Cancer. Wolf et al reported that the
decrease concentration level of serum magnesium was
statistically significant in Lung carcinoma as compared to
that of normal subjects was conducted a study and observed
that the low magnesium induced immune-inflammatory
response, which triggers cytokine production, oxidative
stress and endothelial dysfunction which all participate to
low magnesium related effects.[12]
. Gurreo-Romero et al
supported the hypothesis that serum magnesium in Lung
carcinoma patients has very important role in maintain
genoming stability and proposed several additional
mechanisms by which magnesium might have protected
against lung cancer.[13]
As reported by siems et al the statistically significant decrease
in serum magnesium level in Esophageal carcinoma might be
due to low magnesium level induced to oxidative stress is
at present the best candidate for triggering such an
anti-proliferative signal, hormone, different pathways may
be involved depend on whether the cells are diploid,
immortalized or transformed.[14]
Zhi-Gang Sun et al.
observed that the content of magnesium in esophagus
cancerous tissues was significantly lower than that in the
normal tissues (p<0.01).[15]
Although, the mechanism
underlying the deviation of serum magnesium in
malignancy is not clear but however the decrease in serum
magnesium level might be due to stress induced by the
malignancy.
CONCLUSIONS
The serum magnesium concentration was found to be
decreased significantly in esophageal and lung carcinoma
as compared to that of control group might be due to low
magnesium level induced to oxidative stress. So,
magnesium deficiency can lead directly to cancer.
Magnesium deficiency is carcinogenic, and in the case of
solid tumors, a high level of supplemented magnesium
inhibits carcinogenesis. Both carcinogenesis and
magnesium deficiency increase the plasma membrane
permeability and fluidity and modifications of cell
Int. J. Life. Sci. Scienti. Res., 3(4) JULY 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1161
membranes are principal triggering factors in cell
transformation leading to cancer. Using cells from induced
cancers, they found that there is much less magnesium
binding to membrane phospholipids of cancer cells
compared to normal cell membranes. It has been suggested
that magnesium deficiency may trigger carcinogenesis
by increasing membrane permeability. The membranes of
magnesium-deficient cells seem to have a smoother surface
than normal and decreased membrane viscosity, analogous
to changes in human leukaemia cells. The result may be
significant in understanding the possible contribution of
serum magnesium in the patho-physiological process of
developing cancer and may help in developing the
strategies for prevention and early diagnosis.
ACKNOWLEDGMENT
The research was supported by Principal, S. P. Medical
College and Controller of attached hospitals, Bikaner and
all indoor and outdoor patients making it possible for us to
conduct this work in this institution. We are extremely
grateful to Principal, Controller, & our Departmental staff.
REFERENCES
[1] Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer
statistics. 2002, CA Cancer J Clin, 2005; 55: 74-108.
[2] Mertz W. The essential trace elements. Science. 1981;
213:1332-1338.
[3] Dchenzelin D, Negra EM, Tucci MR, saleu MZ, da cruz
VM, Oliveira RM, Nishimoto IN, Hoelz C. Hypomagnesenia
in critically ill cancer patients; A prospective study of
predictive factors. Braz J. Med. Bio Res. 2000; 33(12):
1443–1448.
[4] Ryzen E. Magnesium homeostasis in critically ill patients.
Magnesium. 1989; 8:201-212.
[5] Aikawa JR. Magnesium & Its Biologic significance CRC
press. Boca Raton, FL. 1981; 21-38.
[6] Gventher T, Avendulk R. Membrane of magnesium
deficiency induced neoplastic cells. Magnesium Bull. 1985;
7:146–151.
[7] Walker GM. Magnesium as the fundamental regulator of the
cell cycle. Magnesium 1982; 2:1-160.
[8] Blondell JW. The anti cancer effect of magnesium. Medical
Hypothesis. 1980; 6:863-871.
[9] Alouane L, Alguemi C, Cherif F, Hedhili A, MaalejM Nagati
K. Serum magnesium, zinc and copper in lung cancer. Cur.
Res. in Magnes. Ed. By MJ Halpern & J. Durlach, Chapt.
1996; 22: 87–89.
[10]Ahmad B, Ghani H, Azam S, Bashir S, Begum N. The status
of trace elements in lymphoma and esophageal cancer
patients: A case study. African Journal of Biotechnology.
2011; 10(84):19645-19649.
[11]Tsalev DL, Slaveykova VI, Mandjukov PB. Spectrochim
Varian instruments AA at Work. Acta Rev.1990; 93: 225.
[12]Wolf Fedrica I, Valentina Trapani, Achille Cittadini.
Magnesium and the control of cell proliferation: looking for
a needle in a haysack. Inst. of pathology journal. Magnesium
research.2008; 21(2):83-91.
[13]Guerro-Romero F, Rodriguez-Moran M. Hypomagnesemia,
oxidative stress, inflammation and metabolic syndrome.
Diabetes Metabolism Res. Rev. 2006; 22:471-476.
[14]Siemes, C., Visser, L., Coebergh, J., Splinter, T., Witteman,
J., Uitterlinden, A., Hofman, A., Pols, H. and Stricker, B.
C-reactive protein levels, variation in the C-reactive protein
gene, and cancer risk: The Rotterdam Study. J Clin Oncol.
2006; 24:5216-5222.
[15]Zhi-Gang Sun, Guang-Min Song, Min Zhang, Zhou Wang,
Zhi-Hong Ni. Clinical study on magnesium, copper and
chrome levels in patients with oesophageal squamous cell
carcinoma. Wspolczesna Onkol. 2011; 15(5): 257–260.
International Journal of Life-Sciences Scientific Research (IJLSSR) Open Access
Policy
Authors/Contributors are responsible for originality, contents, correct
references, and ethical issues.
IJLSSR publishes all articles under Creative Commons Attribution- Non-Commercial
4.0 International License (CC BY-NC).
https://creativecommons.org/licenses/by-nc/4.0/legalcode
How to cite this article:
Joshi G, Vyas RK, Gahlot G, Soni Y: Altered Level of Serum Magnesium in Patients with Esophageal and Lung Carcinoma.
Int. J. Life. Sci. Scienti. Res., 2017; 3(4): 1158-1161. DOI:10.21276/ijlssr.2017.3.4.10
Source of Financial Support: Nil, Conflict of interest: Nil

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Serum magnesium level in esophageal and lung carcinoma patients

  • 1. Int. J. Life. Sci. Scienti. Res., 3(4): 1158-1161 JULY 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1158 Altered Level of Serum Magnesium in Patients with Esophageal and Lung Carcinoma Gajanand Joshi1 *, R. K. Vyas2 , Ghanshyam Gahlot1 , Yogita Soni3 1 Biochemist, Department of Biochemistry, S. P. Medical College, Bikaner, Rajasthan University of Health & Science, Bikaner, Rajasthan, India 2 Sr. Professor, Department of Biochemistry, S. P. Medical College, Bikaner, Rajasthan University of Health & Science, Bikaner, Rajasthan, India 3 Professor, Department of Biochemistry, S. P. Medical College, Bikaner, Rajasthan University of Health & Science, Bikaner, Rajasthan, India * Address for Correspondence: Dr. Gajanand Joshi, Biochemist, Department of Biochemistry, S. P. Medical College, Bikaner, Rajasthan University of Health & Science, Bikaner, Rajasthan, India Received: 05 March 2017/Revised: 08 April 2017/Accepted: 03 June 2017 ABSTRACT- Background: Esophageal and Lung carcinoma are the leading cause of years of life lost because of cancer and is associated with the highest economic burden relative to other tumor types. Epidemiological studies identify magnesium deficiency as a risk factor for these types of human cancers. The present studies were performed to concerning the contribution of magnesium to tumorigenesis and investigate the concentration of magnesium in esophageal and lung carcinoma. Aims and Objective: The aim of this study was to compare the serum magnesium levels of patients with carcinoma of lung and esophagus patients and apparently healthy people. Material and methods: Study group consisted of 50 clinically diagnosed subjects (Biopsy confirmed 25 cases with Esophageal carcinoma and 25 cases with Lung carcinoma). The control group consisted of 50 healthy subjects were included in the study. Venous blood samples of each lung and esophagus cancer were obtained and serum magnesium level was measured by Atomic Absorption Spectrophotometer measurements. Results: In the study group, we were found mean concentration of serum magnesium was decreased in esophageal (1.40±0.13 mg %) and lung carcinoma (1.23±0.12 mg %) in comparison to controls (2.08 ± 0.45 mg %). Conclusions: Serum magnesium was found statistically significantly lower in study group when compared with control (P<0.0001). Key-words- Lung and Esophagus Carcinoma, Magnesium, Atomic absorption spectrophotometer INTRODUCTION Lung Cancer is the second most common cancer in women after breast cancer and is also the second leading cause of cancer-related deaths in women worldwide.1 Uncontrolled cell growth in tissues of the lung, may lead to metastasis, which is the invasion of adjacent tissue and infiltration beyond the lungs. The vast majority of primary lung cancers are carcinoma of the lung, derived from epithelial cells. Esophageal cancer is the eighth most common cancer and sixth leading cause of cancer deaths in the world, with the majority of cases occurring in developing countries. [1] Access this article online Quick Response Code Website: www.ijlssr.com DOI: 10.21276/ijlssr.2017.3.4.10 About 90% of esophageal cancers worldwide are Squamous Cell Carcinomas (SCC), mostly occurring in defined high-incidence areas of low and middle-resource countries. Historically, the highest incidences are reported in regions of Central Asia. One such region is Kashmir Valley in Northern India. Some minerals and Trace-heavy elements play significant role in human health and disease. Trace elements at optimum levels are required for numerous metabolic and physiological processes in the human body.[2] Studies have shown that 46% of all critically ill cancer patients admitted to an ICU (intensive care unit) in a tertiary cancer centre presented with hypomagnesemia and they concluded that the incidence of hypomagnesemia in critically ill cancer patients is high.[3] The incidence rises to 60 to 65% in all patients admitted into the intensive care units in which nutrition, diuretics, hypoalbuminemia, and amino glycosides may play important roles.[4] Normal magnesium levels in humans 1.5-2.5 mg/dl and maintained ARTICLERESEARCH
  • 2. Int. J. Life. Sci. Scienti. Res., 3(4) JULY 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1159 at a fairly constant level of serum magnesium to label Hypomagnesaemia is below (1.56 mg/dl). Over 300 enzymes systems that influence the metabolism of carbohydrate, amino acids, nucleic acid, protein and ion transport, require magnesium.[5] The role of magnesium in fatty acid and phospholipid metabolism, that affect permeability and stability of membrane, were elucidated.[6] It has been proposed that magnesium is central in the cell cycle, and that its deficiency is an important condition in pre-cancerous cell transformation.[7] Magnesium deficiency would therefore lead to physiological decline in cells setting the stage for cancer. It is known that carcinogenesis induces magnesium distribution disturbance, which causes magnesium mobilization through blood cells and magnesium depletion in Non-neoplastic tissue. Magnesium deficiency seems to be carcinogenic and in case of solid tumours a high level of supplemented magnesium inhibits carcinogenesis.[8] Alouane L. et al. [9] found that patients with lung cancer had serum magnesium levels lower than in normal controls. It suggested the hypothesis stipulating an increased magnesium uptake by the tumor cells. Ahmad et al studied that the concentrations of zinc and magnesium in blood were significantly decreased in esophageal cancer patients. This suggested that these might play some role in carcinogenesis.[10] However, role of serum level of magnesium in causing such types of carcinoma has not been studied to great extent. Therefore, the present study was undertaken to estimate the serum levels of magnesium & their role in causing lung and esophageal carcinoma patients with apparently healthy controls. MATERIALS AND METHODS The study was carried out in the Department of Biochemistry in collaboration with the Department of Acharya Tulsi Regional Cancer Treatment and Research Institute in PBM Hospital, affiliated to Sardar Patel Medical College, Bikaner during 2013. The study was approved by ethics committee and informed consent was taken from all the patients. The study group consisted of 50 clinically diagnosed subjects (25 cases with Lung carcinoma and 25 cases with Esophageal carcinoma). The control group consisted of 50 Healthy subjects. Both study and control group were same socio-economic status with similar diet habits. Inclusion Criteria The criteria for the selection of patients were (i) Biopsy proved cases of Lung carcinoma and Esophageal carcinoma (ii)Who had not undergone any treatment i.e. chemotherapy or radio-therapy (iii) Who has not taken long course of any mineral supplement during last six months Exclusion Criteria The criteria for the selection of controls (i) Who were not suffering from any cancerous lesions (ii) Who has not taken any course of mineral supplement Sample Collection and Storage Blood samples were obtained by vein puncture and collected in a clean dry centrifuge tube. Standard precautions for trace element determination were taken, haemolysed samples were discarded. The blood was centrifuged at 3000rpm for 10 minutes and serum was stored at - 40 C until the day of the test. Biochemical Assessments Serum magnesium concentration was determined by direct measurement method using Atomic absorption spectroscopy.[11] Analytical reagent grade chemicals, standards were used. Water used for washing laboratory apparatus and for preparing solutions and standards was purified by deionization of redistilled water. STATISTICALANALYSIS The results were expressed as the mean ± standard error (SE). One-way ANOVA was used for the comparison of mean values of the groups. Then, Student-t test was used to determine the difference between groups. In addition, Pearson’s correlation analysis was carried out to determine the relationships among the variables. RESULTS The results as presented in the Table (1-2) show that the mean serum level of Serum Magnesium was altered in subjects having Esophageal (1.40 ± 0.13) and Lung carcinoma (1.23 ± 0.12). A statistically significantly lower (p<0.0001) in serum magnesium levels was observed in patients with Esophageal and Lung carcinoma group than the healthy control group (Fig 1-2). Table 1: Serum Magnesium Concentration (mg %) Comparison between Esophageal Carcinoma Patients (Case Group) with Normal Healthy Persons (Control Group) Values Normal Healthy Persons (Control Group) (n=50) Esophageal Carcinoma Patients (Case Group) (n=25) Mean 2.08 1.408 Range 1.31-3.00 1.18-1.66 SD 0.450 0.134 SE 0.063 0.026 t 7.335 p value 0.0001*** *** Highly significant
  • 3. Int. J. Life. Sci. Scienti. Res., 3(4) JULY 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1160 Table 2: Serum Magnesium Concentration (mg %) Comparison between Lung Carcinoma Patients (Case Group) with Normal Healthy Persons (Control Group) Values Normal Healthy Persons (Control Group) (n=50) Lung Carcinoma Patients (Study Group) (n=25) Mean 2.08 1.23 Range 1.31-3.00 1.06-1.53 SD 0.450 0.124 SE 0.063 0.024 t 9.252 p value 0.0001*** *** Highly significant Fig: 1 Serum Magnesium Concentration (mg %) Comparison between Esophageal Carcinoma patients (Case Group) with Normal Healthy Persons (Control Group) Fig: 2 Serum Magnesium Concentration (mg %) Comparison between Lung Carcinoma Patients (Case Group) with Normal Healthy Persons (Control Group) DISCUSSION Trace elements and metals are known to play a vital role in metabolism. Magnesium is important for maintaining the integrity of DNA. Mg cations bind to DNA and reduce the negative charge density, thereby stabilizing the structure of DNA. It has been proposed that magnesium is central in the cell cycle, and that its deficiency is an important conditioner in precancerous cell transformation. In addition, immune competence (that eliminates transformed cells) is Mg dependent. Mg supplementation or deficiency was induced, relative to exposure to oncogens. Optimal Mg intake may be prophylactic against initiation of some neoplasm. The finding of the present study indicates statistically significant decrease in serum Magnesium was recorded in Lung and Esophageal Carcinoma as compared to that of control subjects. It might be possible that due to general additional mechanisms by which magnesium might have protected against Cancer. Wolf et al reported that the decrease concentration level of serum magnesium was statistically significant in Lung carcinoma as compared to that of normal subjects was conducted a study and observed that the low magnesium induced immune-inflammatory response, which triggers cytokine production, oxidative stress and endothelial dysfunction which all participate to low magnesium related effects.[12] . Gurreo-Romero et al supported the hypothesis that serum magnesium in Lung carcinoma patients has very important role in maintain genoming stability and proposed several additional mechanisms by which magnesium might have protected against lung cancer.[13] As reported by siems et al the statistically significant decrease in serum magnesium level in Esophageal carcinoma might be due to low magnesium level induced to oxidative stress is at present the best candidate for triggering such an anti-proliferative signal, hormone, different pathways may be involved depend on whether the cells are diploid, immortalized or transformed.[14] Zhi-Gang Sun et al. observed that the content of magnesium in esophagus cancerous tissues was significantly lower than that in the normal tissues (p<0.01).[15] Although, the mechanism underlying the deviation of serum magnesium in malignancy is not clear but however the decrease in serum magnesium level might be due to stress induced by the malignancy. CONCLUSIONS The serum magnesium concentration was found to be decreased significantly in esophageal and lung carcinoma as compared to that of control group might be due to low magnesium level induced to oxidative stress. So, magnesium deficiency can lead directly to cancer. Magnesium deficiency is carcinogenic, and in the case of solid tumors, a high level of supplemented magnesium inhibits carcinogenesis. Both carcinogenesis and magnesium deficiency increase the plasma membrane permeability and fluidity and modifications of cell
  • 4. Int. J. Life. Sci. Scienti. Res., 3(4) JULY 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1161 membranes are principal triggering factors in cell transformation leading to cancer. Using cells from induced cancers, they found that there is much less magnesium binding to membrane phospholipids of cancer cells compared to normal cell membranes. It has been suggested that magnesium deficiency may trigger carcinogenesis by increasing membrane permeability. The membranes of magnesium-deficient cells seem to have a smoother surface than normal and decreased membrane viscosity, analogous to changes in human leukaemia cells. The result may be significant in understanding the possible contribution of serum magnesium in the patho-physiological process of developing cancer and may help in developing the strategies for prevention and early diagnosis. ACKNOWLEDGMENT The research was supported by Principal, S. P. Medical College and Controller of attached hospitals, Bikaner and all indoor and outdoor patients making it possible for us to conduct this work in this institution. We are extremely grateful to Principal, Controller, & our Departmental staff. REFERENCES [1] Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer statistics. 2002, CA Cancer J Clin, 2005; 55: 74-108. [2] Mertz W. The essential trace elements. Science. 1981; 213:1332-1338. [3] Dchenzelin D, Negra EM, Tucci MR, saleu MZ, da cruz VM, Oliveira RM, Nishimoto IN, Hoelz C. Hypomagnesenia in critically ill cancer patients; A prospective study of predictive factors. Braz J. Med. Bio Res. 2000; 33(12): 1443–1448. [4] Ryzen E. Magnesium homeostasis in critically ill patients. Magnesium. 1989; 8:201-212. [5] Aikawa JR. Magnesium & Its Biologic significance CRC press. Boca Raton, FL. 1981; 21-38. [6] Gventher T, Avendulk R. Membrane of magnesium deficiency induced neoplastic cells. Magnesium Bull. 1985; 7:146–151. [7] Walker GM. Magnesium as the fundamental regulator of the cell cycle. Magnesium 1982; 2:1-160. [8] Blondell JW. The anti cancer effect of magnesium. Medical Hypothesis. 1980; 6:863-871. [9] Alouane L, Alguemi C, Cherif F, Hedhili A, MaalejM Nagati K. Serum magnesium, zinc and copper in lung cancer. Cur. Res. in Magnes. Ed. By MJ Halpern & J. Durlach, Chapt. 1996; 22: 87–89. [10]Ahmad B, Ghani H, Azam S, Bashir S, Begum N. The status of trace elements in lymphoma and esophageal cancer patients: A case study. African Journal of Biotechnology. 2011; 10(84):19645-19649. [11]Tsalev DL, Slaveykova VI, Mandjukov PB. Spectrochim Varian instruments AA at Work. Acta Rev.1990; 93: 225. [12]Wolf Fedrica I, Valentina Trapani, Achille Cittadini. Magnesium and the control of cell proliferation: looking for a needle in a haysack. Inst. of pathology journal. Magnesium research.2008; 21(2):83-91. [13]Guerro-Romero F, Rodriguez-Moran M. Hypomagnesemia, oxidative stress, inflammation and metabolic syndrome. Diabetes Metabolism Res. Rev. 2006; 22:471-476. [14]Siemes, C., Visser, L., Coebergh, J., Splinter, T., Witteman, J., Uitterlinden, A., Hofman, A., Pols, H. and Stricker, B. C-reactive protein levels, variation in the C-reactive protein gene, and cancer risk: The Rotterdam Study. J Clin Oncol. 2006; 24:5216-5222. [15]Zhi-Gang Sun, Guang-Min Song, Min Zhang, Zhou Wang, Zhi-Hong Ni. Clinical study on magnesium, copper and chrome levels in patients with oesophageal squamous cell carcinoma. Wspolczesna Onkol. 2011; 15(5): 257–260. International Journal of Life-Sciences Scientific Research (IJLSSR) Open Access Policy Authors/Contributors are responsible for originality, contents, correct references, and ethical issues. IJLSSR publishes all articles under Creative Commons Attribution- Non-Commercial 4.0 International License (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/legalcode How to cite this article: Joshi G, Vyas RK, Gahlot G, Soni Y: Altered Level of Serum Magnesium in Patients with Esophageal and Lung Carcinoma. Int. J. Life. Sci. Scienti. Res., 2017; 3(4): 1158-1161. DOI:10.21276/ijlssr.2017.3.4.10 Source of Financial Support: Nil, Conflict of interest: Nil