The Effect of N-nitrosodimethylamine and Metabolic Activation in
the Liver on the Formation of Nasopharyngeal Carcinoma
Waiki Cen
The British School of Guangzhou, Guangzhou, 510515, China
Keywords:
Nasopharyngeal Carcinoma (NPC), N- nitrosodimethylamine (NDMA), Timecourse, Metabolic Activation.
Abstract:
Nasopharyngeal carcinoma (NPC) is a common tumor of the head and neck with originates in the nasopharynx
cancer, especially in Asia. Moreover, N-nitrosodimethylamine (NDMA) is a highly toxic, carcinogenic
nitrosamine, C
2
H
6
N
2
O. It is generally accepted that NDMA is the main cause of NPC. This research aims to
investigate the level of NDMA necessary to induce the formation of NPC. To achieve the purpose of this
experiment (how much NDMA will cause the formation of NPC) I first injected different amounts of NDMA
and pyrazole into the 3 Male Ydd strain mice (inject nothing into the control mice), then carry out a
timecourse, lastly use MRI to test the formation of NPC in the Male Ydd strain mice. The result obtained
from the experiment is when the level of NDMA is higher than 6.25nmole/200kd of water/mouse and the
level of metabolic activation is lowered NPC would be formed (Not found out yet). This study sheds light on
the future study about the formation of NPC, also suggests that people should eat less smoked food.
1 INTRODUCTION
Nasopharyngeal carcinoma (NPC) is a common
tumor of the head and neck with originates in the
nasopharynx (Osong Public Health and Research
Perspectives. 2016), especially in southern China.
(Cao,
Simons and Qian. 2011) There is less than one
case for every 100,000 people in most parts of the
world (including the United States) per year.
(American Cancer Society. 2018) Whereas in part of
southern China 141.7/100,000 people would be
diagnosed with NPC per year. (Cao,
Simons and Qian.
2011) A previous study (Smoked cooked meat as a
risk factor for Nasopharyngeal Carcinoma: A case-
control study among Saudi populations (Saudi
Journal of Oto-Rhino-Laryngology Head and Neck
Surgery. 2018) has reported that smoked food is one
of the biggest causes of NPC. And in the newest
study, it’s suggested that NDMA in smoked food is
the main cause of NPC. (Khalid Hakami, N
Prepageran, Talal Al Thubaity, Eidah Al Juaid, Nawaf
Al Solami, 2018) In the work, I investigated whether
the level of NDMA in the body tissues and metabolic
activation in the liver (IARC Sci Publ. 1980) causes
the rate of getting Nasopharyngeal carcinoma (NPC)
to increase.
1.1 Purpose
Nasopharyngeal carcinoma (NPC) is a common
tumor of the head and neck with originates in the
nasopharynx (Osong Public Health and Research
Perspectives. 2016), especially in southern China.
(Su-Mei Cao,
Malcolm J. Simons and Chao-Nan
Qian. 2011) There is an increasing amount of people
diagnosed with NPC in Guangdong in the last 29
years (1970-1999). (Karen Michell Othaya Kumar
and Rabiatul Basria S.M.N. Mydin. 2019) A previous
study has reported that NPC is mainly caused by N-
nitrosodimethylamine (NDMA). This study will
investigate whether the level of NDMA in the body
tissues and metabolic activation in the liver (IARC
Sci Publ. 1980) causes the rate of getting
Nasopharyngeal carcinoma (NPC) to increase.
1.2 Methods
The experiments will use Male Ydd strain mice,
which will be injected with increasing amounts of
NDMA as the experiment measures liver function
through assay. An increasing amount of pyrazole will
also be injected, for speeding up the reduction of
metabolic activation in the liver. pyrazole (used to
replace part of the NDMA speeding up the
reduction of metabolic. By doing so, it is less time
Cen, W.
The Effect of N-nitrosodimethylamine and Metabolic Activation in the Liver on the Formation of Nasopharyngeal Carcinoma.
DOI: 10.5220/0011295200003443
In Proceedings of the 4th International Conference on Biomedical Engineering and Bioinformatics (ICBEB 2022), pages 785-790
ISBN: 978-989-758-595-1
Copyright
c
2022 by SCITEPRESS Science and Technology Publications, Lda. All rights reserved
785
consuming and can save money) (Metabolic
activation means the chemical conversion of a
relatively benign substance into a more hazardous one
by normal biochemical processes in cells and tissues.)
A timecourse experiment is then performed, for
measuring the amount of NDMA in the liver and body
tissues. Also, the time takes for NPC to form under
different dosages of pyrazole. The amount of NPC
formed is measured using an MRI.
1.3 Possible Results
There are three most possible results: (1) Mice
pretreated with a larger amount of pyrazole would
have a higher recovery of NDMA administration; (2)
pH value would decrease administration of
pyrazole; (3) NPC is to form in
pretreated mice quicker than in control mice.
1.4 Methods
Materials
This experiment will use
male ddY strain mice (20-25g)
pyrazole (100-300 mg/5 ml of saline/kg):
Speeding up the reduction of metabolic activation in
the liver of mice.
Saline(5ml/kg): Clean the mice, clear
possible cancerogen that may affect the result.
NDMA (6.25-100 nmole/200kd of
water/mouse): Main source of causing NPC.
14-C Aminopyrine (0.063-1.0
kdmole/100kd of water/mouse)ABT rate measures
the severity level of liver tissue.
MRI: Detect NPC in the mice.
Animals:
Male ddY strain mice (20-25g).
ABT rate and metabolic activation of liver tissues:
[Control mice]: First, clear out all the possible
cancergen inside the control mice by injecting it with
Saline(51/kg), 60 minutes before the administration.
Then use 14-C aminopyrine (0.063-
1.0xmole/100~tlof water/mouse) for measuring the
ABT rate (severity level of liver tissue) and the
metabolic activation of the liver tissues in the control
mice.
[Mice-1]: First, clear out all the possible
cancergen inside mice-1 by injecting it with
Saline(51/kg). Second, inject mice-1 with NDMA
(6.25-100nmole/200kd of water/mouse), which
provides mice-1 with small amount of cancergen of
NPC and source for reduction of metabolic activation
in liver. Third, inject mice-1 with
pyrazole(100mg/kg), for speeding up the reduction of
metabolic activation in mice-1’s liver. (60 minutes
before the administration). Last, use 14-C
aminopyrine (0.063-1.0xmole/100~tlof water/mouse)
for measuring the ABT rate (severity level of liver
tissue) and the metabolic activation of the liver tissues
in mice-1.
[Mice-2]: First, clear out all the possible
cancergen inside mice-2 by injecting it with
Saline(51/kg). Second, inject mice-2 with NDMA
(6.25-100nmole/200kd of water/mouse), which
provides mice-2 with medium amount of cancergen
of NPC and source for reduction of metabolic
activation in liver. Third, inject mice-2 with
pyrazole(200mg/kg), for speeding up the reduction of
metabolic activation in mice-2’s liver. (60 minutes
before the administration). Last, use 14-C
aminopyrine (0.063-1.0xmole/100~tlof water/mouse)
for measuring the ABT rate (severity level of liver
tissue) and the metabolic activation of the liver tissues
in mice-2.
[Mice-3]: First, clear out all the possible
cancergen inside mice-3 by injecting it with
Saline(51/kg). Second, inject mice-3 with NDMA
(6.25-100nmole/200kd of water/mouse), which
provides mice-3 with large amount of cancergen of
NPC and source for reduction of metabolic activation
in liver. Third, inject mice-3 with
pyrazole(300mg/kg), for speeding up the reduction of
metabolic activation in mice-3’s liver. (60 minutes
before the administration). Last, use 14-C
aminopyrine (0.063-1.0xmole/100~tlof water/mouse)
for measuring the ABT rate (severity level of liver
tissue) and the metabolic activation of the liver tissues
in mice-3.
Amount of NDMA remaining in the body tissues:
Measure the amount of NDMA in the body by
testing the blood/urine.
Time takes for an NPC to form based on the
amount of pyrazole used:
[Control mice]: First, Inject the control mice with
no pyrazole, measure the time it takes to form an NPC
in control mice by using timecourse. Then, detect the
formation of NPC with an MRI. Check the amount of
NPC formed in the control mice 7days per once.
[Mice-1]: First, inject mice-1 with NDMA (6.25-
100nmole/200kd of water/mouse) second, inject
mice-1 with pyrazole(100mg/kg). Pyrazole is used
to speed up the reduction of metabolic activation of
all the body tissue without using a large amount of
NDMA which is a way of saving time and money.
Measure the time it takes to form NPC in mice-1 by
using timecourse. Last, detect the formation of NPC
with an MRI. Check the amount of NPC formed in
mice-1 7days per once.
ICBEB 2022 - The International Conference on Biomedical Engineering and Bioinformatics
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[Mice-2]: First, inject mice-2 with NDMA (6.25-
100nmole/200kd of water/mouse) second, inject
mice-2 with pyrazole (200mg/kg). Measure the time
it takes to form a NPC in mice-2 by using timecourse.
Last detect the formation of NPC with an MRI. Check
the amount of NPC formed in mice-2 7days per once.
[Mice-3]: First, inject mice-3 with NDMA (6.25-
100nmole/200kd of water/mouse) second, inject
mice-3 with pyrazole (300mg/kg). Measure the time
it takes to form a NPC in mice-3 by using timecourse.
Last detect the formation of NPC with an MRI. Check
the amount of NPC formed in mice-3 7days per once.
1.5 Result
Table 1 Percentage of NDMA recovery 60 minutes after the NDMA administration based on amount of pyrazole injected to
the mice. With amounts of pyrazole injected to the mice listed.
Male ddY strain
mice (20-25g)
Amount of pyrazole injected
to the mice (mg/kg)
Percentage of NDMA recovery 60 minutes after
the NDMA administration (%)
Control mice 0mg/kg 0
Mice-1 100mg/kg 50
Mice-2 200mg/kg 71
Mice-3 300mg/kg 84
Figure 1 Percentage of NDMA recovery 60 minutes after the NDMA administration based on amount of pyrazole injected to
the mice.
Table 2 Comparison of positive or negative result of NDMA presence between control mice, Mice-1, Mice-2, Mice-3.
Control mice Mice-1 Mice-2 Mice-3
Formation of NPC - + + +
NDMA present in urine - + + +
NDMA present in blood - + + +
0
10
20
30
40
50
60
70
80
90
Control mice Mice-1 Mice-2 Mice-3
The Effect of N-nitrosodimethylamine and Metabolic Activation in the Liver on the Formation of Nasopharyngeal Carcinoma
787
Table 3 time takes for an NPC to form based on the amount of pyrazole used
7 da
y
s 14da
y
s 21da
y
s 28da
y
s 35da
y
s 43da
y
s 50da
y
s 57da
y
s
Control mice- - ------
Mice-1 - - ----++
Mice-2 - - - - ++++
Mice-3 - - ++++++
Possible result 1: No recovery of NDMA in control
mice.
Possible result 2: Mice pretreated with 100mg/kg
of pyrazole, NDMA recovery is below 50% 60
minutes after the NDMA administration.
Possible result 3: Mice pretreated with 200mg/kg
of pyrazole, NDMA recovery is about 71.2% 60
minutes after the NDMA administration.
Possible result4: Mice pretreated with 300mg/kg
of pyrazole, NDMA recovery is about 83.7% 60
minutes after the NDMA administration. Also, more
than 80% of NDMA was not metabolized.
Possible result 5: NPC is to formed in pretreated
mice quicker than in control mice.
1.6 Discussion
Pass research shows that NDMA is the main factor to
increase the possibility of NPC (Hakami, Prepageran,
Thubaity, Juaid, Solami, 2018) forming in the human
body. In this research, I found that the rate of
diagnosed with NPC is directly related to the amount
of NDMA in the tissue body and metabolic activation
of the liver. Possible result 1as shown in table 2,
neither NPC nor recovery of NDMA is found in
control mice as it wasn’t injected with any NDMA,
therefore would not cause a reduction of metabolic
activation in the liver.
On the other hand, possible result 2, 3, 4 and 5 as
shown in table 2, are injected with both NDMA and
pyrazole, show appearance of NPC, which prove that
NDMA causes NPC.
The percentage of recovery of NDMA based on
the amount of pyrazole injected, as shown in figure 1,
proves that once the metabolic activation of the liver
is wakened the NDMA is uneasy to be destroyed by
other organ tissues.
The appearance of NDMA in blood, urine and
formation of NPC proves that if the liver is unable to
metalize the NDMA other body tissue would take the
job. The body tissue is unable to clear NDMA out of
the body completely which then cause the rate of
diagnosed with NPC to increase.
Both table 1 and table 3 show that the higher
amount of pyrazole was injected into the mice, the
faster NPC is formed, which proves that NDMA is the
main cause of NPC.
One of the problems in this experiment that may
cause unreliable results is that I haven’t repeat the
experiment and number of mice (4) used are not
enough to make the experiment result accurate.
Because their may be human and environmental
errors (injected too much or too less amount of
pyrazole or NDMA into the mice, timecourse carried
out inaccurately, NPC in mice that’s too small to
detect by MRI, one, two, three or four of the four
mice’s gene that has higher possibility to allow NPC
forming in their body (e.g. heredity) ). Moreover, data
used for experiment prediction have a time gap for 41
years long (1980- 2021), which makes the prediction
inaccurate to the result (The effect of N-
nitrosodimethylamine and metabolic activation in the
liver on the formation of Nasopharyngeal carcinoma).
On the other hand, if the experiment was repeated I
could have collected the result as an average, which
would make the experiment more reliable. Also, if
data are collected from literature written around the
same time prediction to the result (The effect of N-
nitrosodimethylamine and metabolic activation in the
liver on the formation of Nasopharyngeal carcinoma)
would have been more specific. However, colleting
literature from 1980- 2021 about the topic NPC
shows that the scientist are aware of the problem and
the research on NPC has been improving
continuously.
2 CONCLUSION
The result of this study provides doctors with a larger
reference of the cause of NPC in future medical
diagnoses. Future studies will focus on decreasing
amount of NPC taken in by human body through food
by medicines/ health care products.
On average, about 1/100,000 people are
diagnosed with NPC per year all around the world
[less than 1% of children (0-10) are diagnosed with
NPC (Journal of Cancer Research and Practice.
2016). There are two peaks for males to be diagnosed
with NPC: between 30 to 39 and 50 to 59 years old.
Whereas the peak for females is 20-39 years old.
(Beyene, Ketema, Alebachew, Saleh and
Gebremariam. 2021) About 8.8/100,000 people are
diagnosed with NPC per year in southeast China
ICBEB 2022 - The International Conference on Biomedical Engineering and Bioinformatics
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(Hamid. 2020); About 32/100,000 people are
diagnosed with NPC per year in Guangzhou and
13.9/100,000 people are diagnosed with NPC per year
in Hong Kong. (Cao,
Simons and Qian. (2011); (Dr.
Anthony C.H. YING. 2008) NPC also has a high risk
of causing death. Around 0.84/100,000 people died
per year, globally. And 31413/100,000 people died
per year in China. (Xu, Zheng,
Zhang,
Zou and
Chen. 2013) Furthermore, the annual cost of cancer
treatment in China (2015) is 221.4 billion RMB (Cai,
Xue, Chen, Hu, Miao, Lan, Zheng and Meng. 2017).
And the population in parts of China being diagnose
with NPC is 3085 in 2009. Therefore, NPC is a
financial burden towards China. Research in the past
has found that salted fish and Siu Mei contain a large
amount of NDMA, (Food and Cosmetics Toxicology.
1981) People from Guangzhou and Hong Kong love
eating these two kinds of food, which explains why
people around these areas have such a high rate of
being diagnosed with NPC comparing to the world’s
probability. Inside the human body, once NDMA is
being detected, the liver would metabolize it out
within a short period, which causes the other organs
not to have enough interactions with NDMA. Causing
the level of NDMA found in peripheral blood lower
than expected (based on total dietary exposure). The
reduction of the metabolic activation in the liver
(IARC Sci Publ. 1980) causes other tissues to be used
to metabolize NDMA. NPC then starts to form
between the head and neck of the human body (Osong
Public Health and Research Perspectives. 2016), as
other tissues can’t metabolize NDMA fully and take
too long. Therefore, I prediced the reduction of liver
ability to clear NDMA will cause NDMA induced
NPC in the human body. This paper talks about the
tumor Nasopharyngeal carcinoma, which is a
common tumor in Asia of the head of the neck with
originates in the nasopharynx (Osong Public Health
and Research Perspectives. 2016); (Cao,
Simons and
Qian. 2011). In this work, I investigated: ‘The effect
of different levels of N-nitrosodimethylamine in the
body tissues and metabolic activation in liver on the
rate of formation of Nasopharyngeal carcinoma to
increase.’. (IARC Sci Publ. 1980) The experiments
will use Male Ydd strain mice, which will be injected
with increasing amounts of NDMA as the experiment
measures liver function through assay. An increasing
amount of pyrazole will also be injected, for speeding
up the reduction of metabolic activation in the liver.
(Metabolic activation means the chemical conversion
of a relatively benign substance into a more
hazardous one by normal biochemical processes in
cells and tissues.)
A timecourse experiment is then performed, for
measuring the amount of NDMA in the liver and body
tissues. Also, the time takes for NPC to form under
different dosages of pyrazole. The amount of NPC
formed is measured using an MRI. There are three
most possible results: (1) Mice pretreated with a
larger amount of pyrazole would have a higher
recovery of NDMA administration; (2) pH value
would decrease administration of pyrazole; (3) NPC
is to form in pretreated mice quicker than in control
mice.
Generally, this study explores the effect of
NDMA on the formation of NPC. The result of my
study will indicate how the rate of formation of NPC
is effected by amount of NDMA in the human body.
The possible results on NPC shows that the larger
amount NDMA intaking the worse the metabolic
activation is being damaged. FEHD as an example,
should stop business selling food that contain high
amount of NDMA, as Hong Kong is one of the place
that has high rate of population diagnosed with NPC.
And in the future study, scientists can focus on the
prevalence of NPC in Asia, and investigate the
connection between the dietary habit of Asia and the
formation of NPC.
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The Effect of N-nitrosodimethylamine and Metabolic Activation in the Liver on the Formation of Nasopharyngeal Carcinoma
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