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The study on the
Inhibition Effects of FRC001 (China No. 1 Tian Xian Sarcoma
Liquid)
on Transplantation S180 and Hepatocarcinoma
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Introduction of Authors •
Abstract • Background
• Materials and Methods
• Results and Discussions
The study on the Inhibition Effects of
FRC001 (China No. 1 Tian Xian Sarcoma Liquid)
INTRODUCTION OF AUTHORS
Kexiang Ding
Vice President of Cancer Society, China
Director/Professor of Anti-aging Research Center, Guangzhou, China
Consultant of FRC Free Radical Research Center, Taipei
Chung Wan, Su
Ph.D. of Clinical Biochemistry, Cleveland University, USA.
FRC Free Radical Research Center, Taipei
Robert W. Bradford
Professor of Capital University, Washington, US
Founder & President of Bradford Research Institute
Honored Superintendent of Bradford Integrative Treatment Center,
Taipei
ABSTRACT :
The transplantation sarcoma S180 and hepatic carcinoma of mouse
are the most popular and important models in the screening of antineoplastic
drugs. This paper studied the inhibition effects of FRC001 on these
two models. The results showed that on FRC001 had inhibition effects,
to some extent, sarcoma S180 and hepatic carcinoma. Among then,
the inhibition rate of high, middle and low dose of FRC001 on S180
were 59.73%, 52.57%, 41.33% respectively which showed obvious dose-dependent
effects; FRC001 also had some effects on hepatic carcinoma foci,
and the inhibition rate was 47.81%; after the treatment of FRC001,
the average weight decreased and the carcinoma foci shrinked apparently
compared with the control group (P<0.05 or P<0.01). FRC001
is an antineoplastic using traditional Chinese medicine as the main
ingredient.
Key Words : FRC001; Transplantation tumor; Sarcoma S180; Inhibition
effect on hepatic carcinoma.
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BACKGROUND
Malignant tumor is a series of commonly encountered diseases which
harm the human. The treatment of it is a difficult problem of today’s
world medical science. Besides operation, radiotherapy, chemotherapy,
the roles of TCM and the combination of Chinese and Western medicine
are widely noted by medical circles. FC001 is prepared mainly using
traditional Chinese drugs which can eliminate the pathogenic factor
and support healthy energy. The supporting healthy energy includes
invigorating Qi and enriching the blood, warming Yang and nourishing
Yin; the eliminating the pathogenic factor includes promoting blood
circulation to remove stasis, clearing away heat and toxic material
and softening and resolving hard mass. These methods have better
inhibition effect on tumors.
This paper studies the effects of FRC001 on transplantation carcinoma
S180 and hepatic carcinoma of mice.
MATERIALS AND METHODS
1. Materials
1.1 Test Drug : FRC001 (liquid extract of Chinese drugs).
1.2 Experimental Animal : mouse pure Kunming bred C57, 18~22g, healthy
2-3 months, male and female provided by Experimental Animal Center
of Jiangsu Tumor Prophylactico-therapeutic Research Institution.
1.3 Test Tumor Strain : (1) Sarcoma S180 strain; (2) Hepatic carcinoma
strain, provided by Medicine Research Department of Jiangsu Tumor
Prophylactico-therapeutic Research Institution.
2. Methods of Preparing Animal Pattern
2.1 Sarcoma S180
Ascites S180 sarcoma were drawn from mice in which S180 had been
inoculated 7-9 days ago, diluted by normal saline to be 1 X108 /ml
sarcoma cell solution. The next day, mice were inoculated the sarcoma
cell solution 0.2 ml subcutaneously in their right forefeet by aseptic
manipulation; then were randomly grouped and put into experiment.
The mice were endogastrictly given drugs such as FRC001, etc, one
time daily for successive 12 days, and dissected to get sarcoma
on the 13th day. The sarcoma were weighted precisely (g), and calculate
the inhibition rates of drugs on sarcoma by following formula.
A% = ((X-Y)/X) X 100%
A -- Inhibition rate of FRC001 on sarcoma S180
X – The average S180 weight of control group (g)
Y – The average S180 weight of experimental group.
2.2 Hepatic Carcinoma :
Hepatic carcinoma strain was diluted to 1 X 108 /ml carcinoma cell
suspension solution by normal saline. The mice were inoculated above
carcinoma solution 0.2 ml in their right forefeet by aseptic manipulation.
The next day, they were randomly grouped and given drug such as
FRC001, etc/one time daily for successive 8 days, and dissected
on the 9th day. The body weight and hepatocarcinoma weight were
got accurately. To calculate the inhibition rates of drugs on hepatic
carcinoma by following formula.
C% = (1- (W/Z)) X 100%
C% - Inhibition rate of drug on hepatic carcinoma
W – Average hepatocarcinoma weight of experimental group (g)
Z – Average hepatocarcinoma weight of control group (g)
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RESULTS AND DISCUSSION
1. The inhibition effect of FRC001 on transplantation Sarcoma S180
of mice :
To explore the dose-effect of FRC001 on S180 and find the optimal
dose, we tested three doses, i.e. high dose (6.0 ml/kg.bw), middle
dose (3.0ml/kg.bw) and low dose(1.5ml/kg.bw) of FRC001 on transplantation
sarcoma S180 of mice (results showed in Table 1 and Figure 1,2)
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(n)
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(ml/kg.bw)
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Days (d)
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of S180
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(X±D)
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Rate (%)
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Group
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Dose
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Dose
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Dose
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Compared to control group, *P > 0.05; **P<0.05; ***P<0.01;
****P<0.001
Table 1. The effects of FRC001 on Transplantation Sarcoma S180
of Mice.

Figure 1. Dose-effect Curve of FRC001 on S180.
Figure 2. Inhibition rates of Different Doses of FRC001 on S180
According to Table 1, three doses of FRC001 had different inhibition
effects on transplantation Sarcoma S180 of mouse. The average weights
of S180 of the three doses were significantly smaller than that
of control group (P<0.05 or P<0.01). These findings showed
that FRC001 had some inhibition effect on sarcoma S180.
According to Figure 1, the inhibition of FRC001 on transplantation
sarcoma S180 of mouse were dose-dependent, i.e. as the increasing
of the dose of FRC001, the inhibition effects on S180 enhanced,
the weight of sarcoma decreased and the foci shrinked.
On the basis of the dose-effect research, high dose of FRC001 (6.0
ml/kg.bw) was chosen to test and its effects on the body weight,
carcinoma weight of experimental animal of hepatic carcinoma and
the inhibition rate were investigated (showed in Table 2 and Figure
3,4).
According to Table 2, these drugs had some inhibition effects on
hepatic carcinoma foci of experimental animals which showed in the
decrease of carcinoma weights. The average carcinoma weights of
drug I – VI were 1.41g, 1.09g, 1.26g, 1.49g, 1.02g, 0.71g,
respectively, decreased 0.65g, 0.97g, 0.80g, 0.59g, 1.04g, 1.35g,
respectively compared with control group. Compared to the control
group, the effects of drug I, Iv were not significant statistically
(P>0.05), whereas drug II, III, V, VI had significant effects
(P<0.01 or P<0.001).
Figure 3 showed that the carcinoma weight of control group was
the biggest, the carcinoma weights of drug I – VI decreased
to some extent, but there were carcinoma foci in all drug groups.
The orders of carcinoma weights of all experimental groups : Control
> drug IV > drug I > drug III > drug II > drug V
> drug VI.
Figure 4 showed these drugs had some inhibition effects on carcinoma
foci. According to the anti-neoplastic screening procedures and
standards that the inhibition rate must be up to 30 %, except for
drug IV (27.67%), all drugs had good inhibition effects. The orders
of inhibition rates of drug I -VI:drug VI>drug V>drug II>drug
III>drug I>drug IV. Drug VI is 5-Fu which is one of the chemotherapeutic
drugs having good anti-neoplastic effect. Drug V is a new complex
preparation of Chinese and Western drugs which is being screened
by author. Drug II is a marketing anti-neoplastic and its effect
is weaker than drug VI and drug V.
These results showed that, as a antineoplastic, FRC001 had some
effects on sarcoma S180 and hepatocarcinoma. The mechanisms may
be : (1) FRC001 is a complex preparation of Chinese and Western
drugs, can promote blood circulation to remove stasis, clear away
heat and toxic material, soften and resolve hard mass, invigorate
Qi, enrich the blood, warm Yang and nourish Yin, so it can help
body to eliminate the pathogenic factor and support healthy energy,
clear away toxic material and resist tumors; (2) The components
in Edfrann maybe have the function of invigorating QI, spleen, resolving
dampness, soothing the liver and regulating the circulation of Qi,
digestant, regulating absorption, eliminating disturbance of substance
metabolism, enhancing circulation, hemopoiesis, immunity, and can
regulate the function of nerve, endocrine, electrolyte, cyclic nucleoside,
etc; (3) FRC001 can inhibit the growth of tumor by regulating immunologic
function, enhancing the phagocytic function of reticuloendothelial
system; (4) FRC001 maybe has the function of inhibiting the metabolism
of RNA and DNA of carcinoma cell so as to kill the carcinoma cell
or inhibit the growth of carcinoma cell; (5) FRC001 maybe has the
function of eliminating free radicals, as the free radicals play
an important role in mutagenesis and carcinogenesis. FRC001 contains
macromolecule and micromolecule radical scavenge. Of course, the
growth, development or inhibition is a complicated biologic course,
the effects and accurate mechanism of FRC001 on tumor are awaited
to further study.
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