Our research on cancer tissue indicates that the following abnormal parameters coexist:

1) marked increase in Oncogene C-fos Ab2; 2) marked increase in Integrin α5β1; 3) marked increase in Hg; 4) marked decrease in Acetylcholine; 5) marked increase in viral infection; 6) marked decrease in NO (change is similar and proportional to the change in Acetylcholine); 7) increase in Glucose (maximum about 2 times the blood glucose level); 8) increase in Telomere (amount of increase in cancer cell is about 2 to 4 times the normal cell of the same organ); 9) increase in Cycline E; and 10) increase in KI 67. For non-invasive screening of cancer, the author used either 60ng of Oncogene C-fos Ab2 or 60ng of Integrin α5β1 as reference control substance. Since 1990, for non-invasive quick laser beam screening of the cancer, the author only used 4 extremities, but since 2001, the following 6 locations are routinely used for the initial basic cancer screening which require 2-3 minutes: 1) right hand palm; 2) Suprasternal Notch corresponding to acupuncture point CV22, tian tu; 3) left hand palm; 4) Umbilicus; 5) right upper thigh; 6) left upper thigh. Red spectrum laser beam with wavelength of 560-670nm with 1-5mW output is projected from the hand of the intermediary to these 6 locations one-by-one to find whether there is strong resonance or not; for example, with 60ng Integrin α5β1. If CV22 is cancer positive, to rule out cancer in the brain, R- & L-ear lobules should also be examined. If the umbilicus or upper thigh is cancer positive, anus, the back of the upper thigh, and vertebrae LI & L5 areas will be examined by projecting laser beam. If any area shows a cancer-positive response using the same or similar red spectrum laser line, the whole body is scanned using X- Axis Laser Line Scanning and Y-Axis Laser Line Scanning, and a red line is drawn on the positive area. The crossing points of the X-axis and Y-axis Integrin α5β1 strong positive area is often the center of the cancer. Once the center of the cancer positive areas are localized, the actual boundary of each cancer is mapped using a metal electrode by detecting resonance using 60ng Integrin α5β1. Once the exact location & outline of the cancer is identified, the cell type of each cancer can be identified non-invasively using microscope slide of different cancers, and then laboratory confirmation for sensitive cancer markers for specific cancer will be ordered along with standard imaging studies using most suitable method among with X-ray, CT Scan, MRI, or Ultrasonic imaging techniques. For cancer markers, the author made a convenient chart of a list of about 45 sensitive cancer markers for different kinds of cancers. Once cancer is identified, either standard cancer therapy (such as surgery, chemotherapy, radiation therapy) or the following more safe & natural alternative methods of treatment, or a modified standard treatment combined with our safe alternative method, are used after the patient obtains a 2nd or 3rd opinion and discusses treatment with their regular physician. Regardless of the treatment method, if any medication is used, the degree of potential beneficial effects of each medication as well as compatibility, drug ineffectiveness or toxicity, and drug interactions with other medications can be detected using the Bi-Digital O-Ring Test before giving multiple medications to a specific cancer patient. The author found that many patients are taking many substances well known to be effective for cancer but, often, no anti-cancer effect exists due to the canceling effect of drug interactions among multiple effective medications, and the cancer spreads more quickly than if the patient were taking just one effective anti-cancer drug.

If the number of the tumors is few and the location of the tumor is clearly identifiable, the Selective Drug Uptake Enhancement Method (which was originally discovered by this author in 1990 after successfully mapping the accurate organ representation areas on the hands and other different parts of the body) is used to deliver effective medication selectively to the pathological area while markedly reducing drug uptake to normal parts of the body by stimulating accurate organ representation areas on the hands or other parts of the body, including feet and ears. However, when there are multiple metastases and the number of the cancer positive areas are more than 15 or 20, the Selective Drug Uptake Enhancement Method requires full-time attention because each organ representation area requires 15-20 minutes stimulation every 4-6 hours to maintain drug uptake. Our non-toxic, safe, natural approach to cancer treatment uses, for the average adult, a gelatin capsule of 180 mg EPA with 120 mg DHA as a safe and effective antiviral agent, and 100 mg of Cilantro compound, the effect of which was discovered in 1995 by the author, to remove localized excessive deposits of Hg in cancer cells as well as other abnormally deposited metals such as Al and Pb in non-cancerous tissue. If the drug uptake is maintained continuously and effectively, often the cancer shrinks. As a result, one can co-exist with cancer, but often with this method cancer cells are not completely destroyed. When the Selective Drug Uptake Enhancement Method is used in the presence of 2 or 3 cancer positive areas, it is possible to manage by spending 15-20 min. stimulating the organ representation areas corresponding to each cancer positive area after taking medication for cancer treatment. In the presence of multiple cancer metastases (more than 15-20 metastases), it is not possible to stimulate each one of the organ representation areas. However, in 1998, the author succeeded in lowering the cancer telomere while increasing the normal cell telomere. The cancer cell telomere can be decreased and the normal cell telomere can be increased by giving acupuncture at True St. 36, which is located next to the Tibial Tuberosity, and it usually has a round shape with a diameter 8-13mm, depending on the individual. The Traditional St. 36 is located on the extension of the same Tibial Tuberosity, laterally beyond the location of the True St.36. However, since 1984, using the Bi-Digital O-Ring Test Resonance Phenomena between 2 identical substances, it became possible to localize the exact location of an acupuncture point and the 12 major meridians. According to this study, in the location described in Traditional St.36, there is no acupuncture point. The medial boundary of True St.36 is touching the Anterior Tibial Crest at the borderline of the Tibial Tuberosity of the same leg. In some individuals there are 2 Tibial Tuberosities on the same tibial bone, but usually the one nearest to the knee is the correct one. The exact location and outline of True St.36 can be accurately localized using a microscope slide of stomach tissue by detecting the boundary between strong resonance and no resonance. This method has been taught to MDs & DDSs taken in accredited Acupuncture courses organized by the International College of Acupuncture & Electro-Therapeutics and co-sponsored by the New York Academy of Medicine.

Since 2000, the author has refined the technique by semi-permanently inserting a tiny press needle (about 2 mm in length) attached to a small band-aid that is precut in a round or rectangular shape. When the press needle that is inserted on True St.36 was stimulated by the thumb or index finger, the author succeeded in lowering the cancer cell telomere of 1000 - 1,400 ng to less than Ing (often anywhere between 10picograms and lattogram, where an attogram is 10¹⁸ g). Since the lowest amount of telomere found in living humans according to our study is 100ng, with rare exceptions, when the telomere becomes less than 100ng, cancer cell may not be able to divide and under certain conditions may end up apoptotic. Therefore, the lowering of the telomere to less than Ing most likely inhibits cell division of the cancer cell. Our study indicates that as long as one can maintain stimulation after taking EPA & DHA and Cilantro 4 times each day, abnormal cancer cell parameters can be reduced to close to 0 (almost normal). In addition, the author also found that not only does cancer cell telomere go down, but also ail of the anti-cancer medication selectively enters all the metastatic cancer tissue while drug uptake to normal tissue markedly diminishes. As a result, this method becomes a highly efficient treatment for improving or prolonging the life of the terminal cancer patient with multiple metastases as shown by our clinical examples. With this method, concerning the time duration required for stimulation, originally the author used himself as a cancer subject for his adenocarcinoma of the colon and squameous cell carcinoma of the lung. In 2001, the author stimulated a small press needle semi-permanently inserted at True St.36 for 15-20 minutes as often as he could everyday for more than a few weeks, and the cancer parameters were reduced to almost zero, but new skin cancer appeared in the elbow as the result of excessive increase of normal cell telomere of about 300ng to over 2000ng-2500ng and excessive exposure of skin to strong sunlight (The extremity was exposed to strong sun at Phoenix, AZ). To avoid excessive stimulation and maintain safety, we now limit the total amount of stimulation to anywhere between 2-4 minutes after taking each dose of medication, depending on the patient. For cancer of the chest, neck, oral cavity, face, and head, stimulation of the press needle inserted on the True LI.4 of the hands can induce a similar effect as True St.36. However, it is more difficult to keep the press needle in True LI.4 for a long time, as the hand not only moves often but also is often wet when washing the hand or face, but it is possible to keep small press needle with a band-aid on True St.36 for 1 month or even longer. Stimulation of a semi-permanently inserted press needle at True St.36 or True LI.4 is often very effective for treatment of various bacterial or viral infections that cause intractable pain or muscle paralysis. In order to maintain effective drug uptake with the Selective Drug Uptake Enhancement Method, Bi-Digital O-Ring Test negative underwear contacting skin above the pathological area must be replaced by positive underwear, otherwise drug uptake will be markedly inhibited. Similarly, negative watches, metal necklaces, metal bracelets, metal earrings, credit cards, etc., should not be worn close to the skin of the cancer patient.

In addition, the author has been evaluating the reason why cancer is almost non-existent in the heart and small intestine. To explain this, the author proposed the hypothesis that these organs may be secreting anti-cancer substances, particularly the small intestine (jejunum and ileum). This idea was first evaluated by the author himself as the cancer subject. Stimulation of the accurate organ representation areas of the small intestine on both hands each time markedly reduced all the cancer parameters. If this hypothesis is correct, then there is a possibility that stimulation of the accurate organ representation area of the small intestine may reduce existing cancer parameters of cancerous tissue in any organ. Therefore, the technique was repeated with other cancer patients, and a similar result was obtained. While repeating this study with the author himself, it was found that occasionally stimulation of the small intestine representation areas of both hands could not produce maximum reduction of cancer parameters. However, additional stimulation of the accurate organ representation area of the gall bladder on the hand produced significant reduction of cancer parameters. When both the accurate small intestine representation area and the gall bladder representation area are stimulated at the same time, reduction of cancer parameters toward normal was maximum. Usually stimulation of the small intestine representation area on the side ipsilateral to the cancer-positive area produced the strongest cancer parameter-reducing effect. In addition, stimulation of the organ representation area on the hands (or feet, tongue or ears) corresponding to the cancer-positive area enhanced drug uptake to the cancer tissue very significantly, as an application of the Selective Drug Uptake Enhancement Method. These findings may have very important clinical implications. Also the nature & role of Integrin α5β1 rich blood vessels supplying blood for the growth of cancer as well as factors inhibiting blood vessel growth to the cancer tissue are being evaluated. The detail of these studies will be presented in future meetings.