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Growth Inhibition of Cultured Human Liver Carcinoma Cells by Ki-energy (Life-energy): Scientific Evidence for Ki-effects on Cancer Cells

‘Ki-energy’ (life-energy) is believed to increase the immune activity of its practitioners. It has also been shown to cause neuropsychological effects. We undertook this study to obtain objective and scientific evidence as to whether or not a ‘Ki-effectcould inhibit the growth of cultured cancer cells. Cultured human liver carcinoma cells, HepG2, were used. A Japanese Ki-expert held his fingers toward the cells in culture dishes for 5 or 10 min. After culturing for 24 h, we measured cell numbers, protein concentration per cell, certain mRNA expressions and the synthesis of regucalcin. The results were compared with those for control cells (non-treated cells). We found that the number of cells in the Ki-exposed groups were less than those in the controls by 30.3 and 40.6% with 5 and 10 min Ki-exposure, respectively. The protein content per cell in the Ki-exposed groups (5 and 10 min) was higher than that in the control groups by 38.8 and 62.9%, respectively. These results were statistically significant. Using RT–PCR, we found that the mRNA expression for c-myc, a tumor stimulator gene, was decreased, while that for regucalcin, which suppresses DNA synthesis, was increased. Our molecular biological studies and mathematical model analysis demonstrated that Ki-energy inhibited cancer cell division. The data also indicate that the Ki-effects involve some form of infrared radiation from the human body. This study suggests the possibility that Ki-energy may be beneficial for cancer patients because it suppresses cancer cell growth, and at the same time, it stimulates immune functions of the patients.

Many people believe that ‘Ki-energy’ (life-energy) is a ‘superpsychological’ or ‘supernaturalphenomenon. The aim of this paper is to provide evidence that ‘Ki’ is a ‘natural’ phenomenon. If it is a ‘natural’ phenomenon, it can be studied scientifically. In order to accomplish this goal, we formed a research team consisting of two biophysicists, two molecular biologists and a Japanese Ki-expert, Kozo Nishino (who was once a medical student, then a ballet choreographer and finally became a master of Aikido, a Japanese martial art). Nishino has developed a breathing method of enhancing the level of life-energy or vitality called ‘Ki’ (16). Many of his students experienced improvement in their health in areas such as high blood pressure, osteoporosis, arthritis and heart ailments. A dozen students overcame cancer without surgery (59). A study demonstrated that this breathing method increased the immune activity of the practitioners as judged by the blood level of NK cell activity (10). Nishino developed his Breathing Method independently of the Chinese Qigong practice.

Qigong practice has been known to raise energy levels (called ‘Qi’ in Chinese) and improve health (1118). A group of Japanese scientists made a pioneering observation that the Chinese Qigong practice involved a neuropsychological effect in which the brain wave activities of both a Qigong healer and a volunteer who received his Qi-energy were synchronized (19).

Using human liver carcinoma cells, HepG2, we performed a series of simple, straightforward experiments to test whether the Ki-effect could be studied scientifically. Namely, cells in culture dishes were exposed to 5 or 10 min of Ki-emission from Nishino's fingers. They were subsequently incubated for 24 h to examine whether cell growth was reduced as compared to those in the control dishes to which no Ki was applied.

We searched to see if a specific protein was expressed in Ki-exposed cells, since that might relate to a mechanism of the Ki-effect. We also tested the possibility of whether or not Nishino's Ki-energy might penetrate skin and muscle to reach cancer-afflicted organs and attack cancer cells. From the study of the materials that pass or block the Ki-effect, we also tried to search for the nature of the Ki-energy.

α-Minimum essential medium (α-MEM) and penicillin (5000 U ml−1)–streptomycin (5000 μg ml−1) solution were obtained from Gibco Laboratories (Grand Island, NY, USA). Fetal bovine serum (FBS) was purchased from Sigma-Aldrich (St Louis, MO, USA).

All experiments were performed at the Graduate School of the University of Shizuoka. The cloned human hepatoma cells, HepG2, were maintained for 24–72 h in α-MEM supplemented with 10% FBS, 50 U ml−1 penicillin and 50 μg ml−1 streptomycin in humidified 5% CO2 or 95% air at 37°C. We normally seeded 1 × 105 cells per ml per dish and cultured until the start of the experiment. (When we needed a larger number of dishes for an experiment, the seeded cell number per dish was decreased accordingly.) The cells were settled and attached onto the dishes in ∼3 h and proliferated. We performed the Ki-exposure experiments between 24 and 48 h after seeding, in other words, long after the cells were settled. Before the experiment, we took several dishes and counted the cell numbers of each dish to confirm that the numbers were equal for all dishes. The number was normally ∼2–4 × 105 cells per ml per dish. Under these conditions, the dishes were <20% confluency (in 35 mm diameter culture dishes) (20). Since this was much less than the full confluent condition, the cell doubling time, which was 24 h under our conditions, did not change with the cell number.

Cultured dishes were randomly distributed into the control and Ki-exposure groups. Then, each culture dish was taken out to a sterilized hood and the lid was removed. The dish was exposed to the Ki-energy emitted from Nishino's fingers (Fig. 1A) for 5 or 10 min. His fingers were sterilized with 70% ethanol before each exposure in order to prevent possible bacterial contamination. The control dish was handled similarly without the Ki-exposure. The culture dishes were returned to the incubator and incubated for 24 h. We chose 24 h because the cell doubling time was 24 h. Then, cell counting, protein studies and/or RT–PCR were performed. Since both control and Ki-exposed groups had the same number of cells at the start of the experiment, the difference between these two groups were caused by the Ki-effect.

We also tested the effect of the hands of another person (who had no Ki training and who covered the dish as shown in Fig. 1B) on the Ki inhibition of cell growth. This is a test for evaluating the effect of an intervening human tissue when Ki is emitted aiming at an internal organ afflicted by cancer. Our experiments per day consisted of three sets of 5 min control and 5 min Ki-exposure experiments (n = 3), and one or two sets of 10 min experiments (n = 1 or 2). We limited the amount of Ki-emission for the purpose of maintaining the level of the emitter's Ki-energy. In order to accumulate more data points, we performed 5 min experiments on three different days (total n = 9). Although the exact cell numbers per dish were slightly different in each experiment, by taking the ratio between the control and the Ki-exposed group, and by analyzing it with appropriate statistics we were able to obtain statistically meaningful data.

After trypsinization of the cells in each culture dish using a Ca2+/Mg2+-free phosphate-buffered saline (PBS) containing 0.2% trypsin and 0.02% EDTA for 2 min at 37°C, cells were collected and wash-centrifuged in a PBS solution at 100 g for 5 min. The cells were resuspended in a 0.5 ml PBS solution, and an aliquot was stained with eosin. The cells were counted under a microscope using a hemocytometer plate. For each dish, we took the average of two counts.

After culture, cells were washed three times with PBS, scraped with 0.5 ml of ice-cold 0.25 M sucrose solution containing 1 mM phenylmethylsulfonyl fluoride and 10 μg ml−1 leupeptin, and sonicated for 60 s. Then, the samples were used for protein quantitation by the method of Lowry (21) or for immunoassay of regucalcin by western blot analysis.

In order to investigate the molecular mechanism behind the Ki-effect, we examined the change in tumor-related gene expression in the cloned human hepatoma HepG2 cells exposed to Ki-energy. The cells were exposed to Ki-energy for 5 min, and were cultured for another 24 h. The changes in mRNAs for c-myc [a tumor stimulator gene, (22)], p53 [a tumor suppressor gene, (23)], regucalcin [a protein which suppresses DNA synthesis, (24)] and β-actin (a protein not related to cancer) were analyzed by using RT–PCR. Total RNAs were prepared using the method of Chomczynski and Sacchi (25) from the cloned human hepatoma HepG2 cells. RT–PCR was performed with a Titan™ One Tube RT–PCR Kit (Roche Molecular Biochemicals, Indianapolis, IN, USA) as recommended by the supplier to determine the gene expression of c-myc, p53, regucalcin or β-actin.

The primers were generated based upon the published human sequences. The primers for the amplification of c-myc cDNA were 5′-(692)-CCAGCGAGGATATCTGGAAG-(712)-3′ and 5′-(1239)-CGTCGAGGAGAGCAGAGAAT-(1259)-3′ (22). The primers for p53 cDNA were 5′-(369)-CCAGCTTCGGAACAAGAGAC-(389)-3′ and 5′-(910)-CACAGAGCCAGGCTTTCATC-(930)-3′ (23). The primers for regucalcin were 5′-(316)-GGAGGCTATGTTGCCACCATTGGA-(317)-3′ and 5′-(850)-CCCTCCAAAGCAGCATGAAGTTG-(872)-3′ (26). The primers for β-actin cDNA were 5′-(410)-CCAAGGCCAACCGCGAGAAGATGAC-(434)-3′and 5′-(996)-AGGGTACATGGTGGTGCCGCCAGAC-(996)-3′ (27).

RT–PCR was performed using a reaction mixture (20 μl) containing 1 μg of total RNAs, the RT–PCR buffer supplied, the Titan™ enzyme mix (AMV and Expand™ High Fidelity), 0.2 mM deoxynucleotide triphosphate, 5 mM dithiothreitol, 5 U RNase inhibitor, 2.5 U Taq DNA polymerase and 0.3 μM primers. Samples were incubated at 50°C for 30 min and at 94°C for 2 min, and then amplified for 25 sets under the following conditions; denaturation for 30 s at 94°C, annealing for 30 s at 60°C and extension for 60 s at 68°C. The amplified PCR products were separated using electrophoresis on a 1.5% agarose gel, and visualized by ethidium bromide staining and quantitated using a densitometer.

The homogenate of cultured cell was centrifuged for 10 min at 5500 g at 4°C, and the supernatant was used for western blot analysis (28). An aliquot of protein (10 μg) was subjected to SDSPAGE (12% polyacrylamide gel). After electrophoresis, proteins were transferred onto a polyvinylidene difluoride membrane at 100 mA for 4 h. The membranes were incubated for 1 h with a polyclonal rabbit anti-regucalcin antibody (29), which was diluted 1:2000 with a washing buffer [10 mM TrisHCl, pH 8, containing 150 mM NaCl, 0.1% (w/v) Tween-20] containing 5% (w/v) skim milk. The membrane was then washed four times with the washing buffer and, subsequently, the membrane was incubated for 1 h with horseradish peroxidase-linked anti-rabbit IgG, which was diluted 1:5000 with the washing buffer containing 5% (w/v) skim milk. After washing the membrane, protein bands were detected and quantitated using an enhanced chemiluminescent kit (Biosciences, Piscataway, NJ, USA) following the manufacture's instruction. The molecular size of the detecting protein was determined by running the standard proteins with known sizes in parallel.

This was done using StatView™ software. Data were expressed as the mean ± SEM. For the data shown in Fig. 2, the significance of the differences between the control and the Ki-exposed groups was determined by the Student's t-test for comparison of two groups, and by analysis of variance with the Fisher's PLSD test for comparison of multiple groups. For the data shown in Table 1, data were collected from tests performed on different days. Therefore, we first expressed the Ki-effect by the percent change in each set, which consisted of a control dish and a Ki-exposed dish. Then, we analyzed them using the Mann–Whitney test (because of the non-parametric nature of the data) to determine the significance of the differences. These data expressed in terms of ratios were used for the mathematical model analysis. In all experiments, the difference was considered statistically significant when P < 0.05.

First, we performed an experiment with 5 min of Ki-exposure. Figure 2A and B show typical data. In this experiment, the decrease in cell numbers as counted 24 h later was 30.5% (P < 0.01), and the increase in the protein content per cell was 33.6% (P < 0.01). When a person who had not practiced Nishino's method imitated the action of Nishino, no effect was observed (data not shown).

All experiments gave statistically significant results. The results for one group are shown in Fig. 2A and B and for the second group in Fig. 2C. The results for the third experiment were similar (data not shown). For the 5 min experiments, we had nine sets. For each set, we expressed the effect of Ki-exposure by a percent change. We then analyzed the effect of Ki statistically using a non-parametric Mann–Whitney test. As shown in Table 1 (A), the differences in both cell numbers and protein contents between the control and the Ki-exposed groups were statistically significant (n = 9). For 10 min Ki-experiments, we performed altogether five sets of the control and Ki-exposure experiments. We analyzed them in the same fashion. As shown in Table 1 (B), the results were also statistically significant (n = 5).

Figure 2C shows that the emission of Ki through the hand of another person still inhibited the growth (P < 0.05), although the degree of inhibition was somewhat less. The figure also shows that the shielding hands alone did not reduce the number of cells.

We examined the validity of our data using a simple cell division model. Suppose we start with 100 cells. When cell division is finished in 24 h, the number will be 200. If the number is reduced by Ki-energy by a%, then the number is 200 (1 − a/100). If we assume that the protein content per undivided cell and that per divided cell are 2 and 1, respectively, then the total protein amount is (100 − a) × 2 + 2a × 1 = 200 (this simple model assumes that all undivided cells reach the protein content of 2 in 24 h. This may overestimate the protein content per cell because the value for some cells would be <2). Then, the protein content per cell is 1/(1 − a/100). The percent increase in protein content per cell is expressed by a/(100 − a) × 100 (%). Figure 3 shows the relationship between the growth inhibition (a%) and the protein content increase (%). As shown in the figure, the actual values for growth inhibition and protein content increase for 5 and 10 min of Ki-exposure (taken from Table 1) are situated relatively close to this theoretical curve.

With this model, we can also estimate the percentage of cells that have finished cell division. Let that percentage be b, then b = 100 − 2a. Therefore, with 5 and 10 min of Ki-exposure, 39.4 and 18.8% of the cells underwent cell division in 24 h, respectively. With no Ki-exposure, a = 0 and thus, b = 100%. This result supports our notion that the mechanism of Ki-inhibition is to slow down cell division in cancer cells.

As shown in Fig. 4, the expression of c-myc mRNA was significantly suppressed (P < 0.01), while the expression of regucalcin mRNA was significantly increased (P < 0.01). The expressions of p53 and β-actin mRNAs were not altered with the Ki-exposure.

Besides its mRNA level, we also determined the protein level of regucalcin in the hepatoma cells by the western blot analysis. The level in the Ki-exposed cells was 125.1 ± 2.5% of the control (mean ± SEM; n = 4) (Fig. 5). It was statistically significant (P < 0.05). The increase in the regucalcin protein level must have resulted from the enhancement of regucalcin mRNA induced by the Ki-energy.

We also studied the effects of materials that could interfere with the Ki-effects. As shown in Table 2, when the culture dish was covered with aluminum foil (0.05 mm thick), the Ki-effect was completely blocked. Table 2 also shows the experiments to test the effects of plastics. Both culture dish and lid are made of transparent polystyrene (thickness 0.6 mm). Normally, we exposed culture dishes to Ki-energy without the lid. For this test, we left the lid closed and the Ki-energy was applied. As shown in this table, leaving the lid closed did not interfere with the Ki-effect. However, when we placed two plates made of black acrylic (1.6 mm thick; one on top and the other under the culture dishes) while the Ki-energy was being applied, the Ki-effect was completely blocked.

We have conducted simple and straightforward experiments to investigate the effects of Ki-energy using cultured human carcinoma cells. The results for the measurement of both cell numbers and protein contents were statistically significant with n = 9 for 5 min Ki-exposure and n = 5 for 10 min Ki-exposure (Table 1). In separate experiments where only the cell numbers were counted, the results were also statistically significant with n = 7 (Table 2). The total number of our experiments is still small. We have to increase the number and should adopt a blind test procedure. These are goals of our future investigation.

It is interesting to note that the protein content of Ki-exposed cells was remarkably higher than that of the controls. It is well known that the content of a cell increases when the cell is preparing for cell division, and that the amount is almost doubled right before cell division. Therefore, the observed increase in the protein content of Ki-exposed cells suggests that cell division was delayed by Ki-energy. The mathematical model analysis supported this conclusion (Fig. 3).

Regucalcin, a regulatory protein in the intracellular signaling system (30), exerts a suppressive effect on proliferation of cloned rat hepatoma cells (26). Regucalcin is present in the nucleus of rat liver (31). Moreover, regucalcin suppresses the expression of c-myc and Ha-ras mRNAs in cloned rat hepatoma cells (32). Presumably, the Ki-energy suppressed proliferation of human hepatoma cells by influencing gene expression in the nucleus.

Our data indicated that the level of p53 did not change with the Ki-exposure, but the levels of c-myc and regucalcin were changed. Both hyperthermia therapy (42°C) and X-ray radiation are known to increase the p53 level in nude mice bearing human tumor cells, and consequently, these therapies inhibit the growth of the tumor (33,34). Our result implies that the observed Ki-effect is different from that caused by high temperature treatment or high energy emission. This raises the interesting possibility of using Ki-energy in cancer therapy. If the Ki-therapy is combined with hyperthermia and/or X-ray radiation, it may produce synergistic effects to inhibit tumor growth more effectively. Indeed, a Chinese medical study reported that the combination of the Qigong therapy and modern medical treatment produced beneficial effects (12). Several other scientific studies also demonstrated that Qi-energy has detectable biological and physiological effects (13,3537).

What is the nature of observed Ki-energy? It passes through a clear plastic plate, but was blocked by aluminum foil. This suggests that it may be a form of electromagnetic wave. In this regards, it is interesting to note that Kawano et al. (19) found that a form of energy was transmitted through the air from a Chinese Qigong practitioner to another person who was sitting in front of him.

Then, a question to be asked is ‘What is the frequency?’ Since the Ki-energy goes through a clear plastic plate it cannot be a UV radiation, because plastics generally absorb ultraviolet. The fact that black acrylic plates effectively block the Ki-energy indicates that it may be a form of infrared radiation, because if this is in a radio or TV frequency range, it can go through a black plastic plate. A human body radiates infrared by virtue of its temperature. In 1978, Chinese scientists published the finding of infrared radiation from the hand of a Qigong practitioner (38). Since then, several investigators reported that the Ki-energy may involve infrared radiation (3944).

In our experiments, if the infrared radiation was blocked, then the Ki-effect of inhibiting cell growth was lost. In other words, there was a direct linkage between the two. If the Ki-energy is a form of infrared radiation it could penetrate human tissue, therefore explaining Ki-energy's ability to inhibit cell growth through human hands (Fig. 2C).

The level of p53 was known to increase by a high temperature treatment (42°C) or by X-ray radiation (33,34). However, since the level did not change in our case (Fig. 5), the intensity of infrared radiation must be very low. We still do not know the mechanism of how such a small amount of energy from the human body could cause a tangible change in the cells.

In conclusion, we have shown evidence that the effects of Ki-energy can be analyzed scientifically using an established cell culture model. Our experiments using cultured cancer cells demonstrated that cell growth was delayed by exposure to Ki-energy for 5–10 min. The mechanism seems to be related to a decrease in mRNA expression for c-myc, a tumor stimulator gene, and to an increase of that for regucalcin, which suppresses DNA synthesis. Our data suggest that infrared radiation may be involved in the observed Ki-effects.