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Research & Publications

Overview

 Please Note: LCS101 is the research name for Protectival, LCS102 is the research name for Tonix-R

 

LCS101 (Protectival) is a formula of 14 highly concentrated bio-active botanicals, which were tested in over 1000 modern scientific studies for their active components, safety, and the action of the individual ingredients in cancer care.

LCS101 was developed and researched for over 15 years in collaboration with oncologists, biologists and scientists from 7 Medical Centers and University Cancer Laboratories  in Israel, US and in Europe including:

  • MD Anderson – Collaboration with integrative cancer lab (US)
  • Harvard Medical School – Prof. Rosenthal (US)
  • Bar-Ilan University – Cancer Research Center (Israel)
  • Sheba Hospital – Tal center integrative Oncology Research Center (Israel)
  • Ichilov Hospital – Biology laboratories (Israel)
  • Jagiellonian University – molecular biology –  (Poland)
  • Miami Children Hospital – Pathology Laboratories (US)
  • Refuot Integrative Medical Center (IsraelL)

The research included:

These findings were published in peer-reviewed medical journals and have been presented to the medical community of the World Health Organization(WHO), UNESCO, the American Society for Integrative Oncology and others.

The scientific evidence and healing effect of LCS101. Presented at the Traditional Medicine Forum Sponsored by the WHO

This website is an educational resource on the botanical formula LCS101 and the research conducted on the formula.

Research

 

LCS101 protection from Chemotherapy side effects

The protective properties of LCS101 were tested in a randomized, controlled, double blind clinical trial that was conducted on breast cancer patients at the Sourasky (Ichilov) Medical Center, in Tel-Aviv, Israel. All patients had been diagnosed with localized tumors and referred to chemotherapy before they were included in the study.

The patients were randomized to receive either chemotherapy with LCS101 or chemotherapy with a placebo.

The interventions (LCS101 or Placebo) were started two weeks prior to the first chemotherapy dose and continued until the last dose. Neither the patients nor the medical staff were aware of who was on the placebo and who was on LCS101, following the double-blind protocol.

This study focused on the rates of anemia and leukopenia, and showed that 82% of patients who took LCS101 did not suffer from a decrease of white blood cells (WBC) or red blood cells (RBC) counts.

Publisher:  The Oncologist Journal
Click here for the full publication. 

An additional clinical trial tested the effect of LCS101 on chemotherapy side-effects in breast cancer patients.

89% of the patients reported LCS101 improved their quality of life and helped reduce their symptoms such as fatigue, weakness, pain, nausea, vomiting and decreased appetite.

Publisher: Integrative Medicine Insights Journal
Click here for the full publication. 

 


LCS101 Anti-Cancer effect

The selective killing effect of LCS101 was tested in pre-clinical trials (in vitro).

The aim of the study was to examine the selectivity of the effects of the compound, alone and in conjunction with conventional chemotherapy agents, on cancer cells.

The study demonstrated that the formula actively destroys breast, colon and prostate cancer cell lines. The formula was also shown to protect normal cells from the damages associated with chemotherapy, and potentiating the cancer cells to the treatment.

Publisher: International Journal of Oncology
Click here for the full publication. 


LCS101 Immunological effect

The effect of LCS101 on various components of the immune system was evaluated in a pre-clinical trial. The study focused on the potential role of LCS101 in immune system stimulation.

The results suggest that LCS101 has an immune-modulating capacity – as evidenced by improvement in both adaptive and innate immunity.

Publisher: OncoTargets and Therapy
Click here for the full publication. 


LCS101 interaction with chemotherapy

The research included pre-clinical studies conducted with a chemotherapy testing dose and time dependent interaction with on over 10 different type of cancers and 10 different types of chemotherapy.

The findings of the study showed that the botanical formula LCS101 does not reduce the cytotoxic effects of multiple chemotherapy agents. Instead, the addition of LCS101 led to increased death of cancer cells from the chemotherapy agents.

Publisher: Journal of Cancer Science & Therapy
Click here for the full publication. 


LCS101 effect on anti cancer effect of Radiation therapy

This pre-clinical study examined the interaction between LCS101 and radiation therapy on cancer cell lines where incremental doses of LCS101 were added to 5 types of cell lines 4 hours after single-dose of radiation.

The addition of the botanical formula LCS101 to irradiated cancer cells results in an apparent additive effect, most likely through a ROS-mediated mechanism. These findings support the use of LCS101 by patients undergoing radiation therapy, for both its clinical as well as anti-cancer effects.

Publisher: Journal of Cancer Research and Clinical Oncology
Click here for the full publication. 

Botanicals

A table of the 14 botanical ingredients  of the formula LCS101 with scientific references for their effect:

 

Botanical NameAnti-Cancer (in vitro, in vivo)Immune SystemChemo Side Effects, Protection
Astragalus membranaceus
Huang Qi
Glioma[1]
Myeloid tumors [2]
T cells [3-5]; Macrophages [2, 6-8]
B cells [5, 6, 9]
LAK cells [10, 11]
Anti-inflammatory [12, 13] General [6, 9, 14]
Immune system [5, 6, 15, 16] Heart [17-19]
Liver [20]
Renal [21]
Anti-mutagenic [22]
Atractylodes macrocephala
Bai Zhu
Leukemia & lymphoma [23]Anti-allergic [24]
Citrus reticulata
Chen Pi
Colon [25]
Gastric [26]
Anti-inflammatory [27-29]Cell protection [30]
Glehnia littoralis
Bei Sha Shen
Anti-inflammatory [32, 33]
Ligustrum lucidum
Nu Zhen Zi
Glioma [34]T cells [4]
Anti-inflammatory [35] Macrophages [7]
Anti-mutagenic [22]
Lycium chinense
Gou Qi Zi
Liver [36, 37]
Bone marrow [38]
Milletia reticulata
Ji Xue Teng
Anti-inflammatory [39]
Oldenlandia diffusa
Bai Hua She She Cao
Melanoma [40]
Renal cell carcinoma [41]
T cells [42]
Anti-inflammatory [43]
Macrophages [41, 44]
General [9]
Anti-mutagenic [22, 45, 46]
Ophiopogon japonicus
Mai Men Dong
Anti-inflammatory [48]Adaptogens: Strength, Stamina [49]
Paeonia lactiflora
Bai Shao
Bladder cancer in vivo [51]
Poria cocos
Fu Ling
Anti-inflammatory [52, 53]
Immuno-stimulatory [54]
Prunella vulgaris
Xia Ku Cao
NSCLC [55, 56]
Melanoma
(lung metastasis) [57]
Anti-inflammatory [58, 59]
Macrophages [60]
Scutellaria barbata
Ban Zhi Lian
Breast cancer [61-63]Prostate cancer prevention [64]
Renal cell carcinoma [41]
Macrophages [41]Anti-mutagenic [22, 45, 46]

References

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23. Huang HL, Chen CC, Yeh CY, Huang RL: Reactive oxygen species mediation of baizhu-induced apoptosis in human leukemia cells. J Ethnopharmacol 2005, 97(1):21-29.
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25. Kang SA, Park HJ, Kim MJ, Lee SY, Han SW, Leem KH: Citri Reticulatae Viride Pericarpium extract induced apoptosis in SNU-C4, human colon cancer cells. J Ethnopharmacol 2005, 97(2):231-235.
26. Kim MJ, Park HJ, Hong MS, Park HJ, Kim MS, Leem KH, Kim JB, Kim YJ, Kim HK: Citrus Reticulata blanco induces apoptosis in human gastric cancer cells SNU-668. Nutr Cancer 2005, 51(1):78-82.
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29. Zhou XM, Huang MM, He CC, Li JX: Inhibitory effects of citrus extracts on the experimental pulmonary fibrosis. J Ethnopharmacol 2009, 126(1):143-148.
30. Xu GH, Chen JC, Liu DH, Zhang YH, Jiang P, Ye XQ: Minerals, phenolic compounds, and antioxidant capacity of citrus peel extract by hot water. J Food Sci 2008, 73(1):C11-18.
31. Xu RH, Peng XE, Chen GZ, Chen GL: Effects of cordyceps sinensis on natural killer activity and colony formation of B16 melanoma. Chin Med J (Engl) 1992, 105(2):97-101.
32. Yoon T, Cheon MS, Lee AY, Lee do Y, Moon BC, Chun JM, Choo BK, Kim HK: Anti-inflammatory activity of methylene chloride fraction from Glehnia littoralis extract via suppression of NF-kappa B and mitogen-activated protein kinase activity. J Pharmacol Sci 2010, 112(1):46-55.
33. Yoon T, Lee do Y, Lee AY, Choi G, Choo BK, Kim HK: Anti-inflammatory effects of Glehnia littoralis extract in acute and chronic cutaneous inflammation. Immunopharmacol Immunotoxicol 2010, 32(4):663-670.
34. Jeong JC, Kim JW, Kwon CH, Kim TH, Kim YK: Fructus ligustri lucidi extracts induce human glioma cell death through regulation of Akt/mTOR pathway in vitro and reduce glioma tumor growth in U87MG xenograft mouse model. Phytother Res 2011, 25(3):429-434.
35. An HJ, Jeong HJ, Um JY, Park YJ, Park RK, Kim EC, Na HJ, Shin TY, Kim HM, Hong SH: Fructus Ligustrum lucidi inhibits inflammatory mediator release through inhibition of nuclear factor-kappaB in mouse peritoneal macrophages. J Pharm Pharmacol 2007, 59(9):1279-1285.
36. Ha KT, Yoon SJ, Choi DY, Kim DW, Kim JK, Kim CH: Protective effect of Lycium chinense fruit on carbon tetrachloride-induced hepatotoxicity. J Ethnopharmacol 2005, 96(3):529-535.
37. Zhang R, Kang KA, Piao MJ, Kim KC, Kim AD, Chae S, Park JS, Youn UJ, Hyun JW: Cytoprotective effect of the fruits of Lycium chinense Miller against oxidative stress-induced hepatotoxicity. J Ethnopharmacol 2010, 130(2):299-306.
38. Hsu HY, Yang JJ, Ho YH, Lin CC: Difference in the effects of radioprotection between aerial and root parts of Lycium chinense. J Ethnopharmacol 1999, 64(2):101-108.
39. Hsu CC, Hsu CL, Tsai SE, Fu TY, Yen GC: Protective effect of Millettia reticulata Benth against CCl(4)-induced hepatic damage and inflammatory action in rats. J Med Food 2009, 12(4):821-828.
40. Gupta S, Zhang D, Yi J, Shao J: Anticancer activities of Oldenlandia diffusa. J Herb Pharmacother 2004, 4(1):21-33.
41. Wong BY, Lau BH, Jia TY, Wan CP: Oldenlandia diffusa and Scutellaria barbata augment macrophage oxidative burst and inhibit tumor growth. Cancer Biother Radiopharm 1996, 11(1):51-56.
42. Shan BE, Yoshida Y, Sugiura T, Yamashita U: Stimulating activity of Chinese medicinal herbs on human lymphocytes in vitro. Int J Immunopharmacol 1999, 21(3):149-159.
43. Kim SJ, Chung WS, Kim SS, Ko SG, Um JY: Antiinflammatory effect of Oldenlandia diffusa and its constituent, hentriacontane, through suppression of caspase-1 activation in mouse peritoneal macrophages. Phytother Res 2011, 25(10):1537-1546.
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45. Wong BY, Lau BH, Teel RW: Chinese medicinal herbs modulate mutagenesis, DNA binding and metabolism of benzo[a]pyrene 7,8-dihydrodiol and benzo[a]pyrene 7,8-dihydrodiol-9,10-epoxide. Cancer Lett 1992, 62(2):123-131.
46. Wong BY, Lau BH, Yamasaki T, Teel RW: Inhibition of dexamethasone-induced cytochrome P4-mediated mutagenicity and metabolism of aflatoxin B1 by Chinese medicinal herbs. Eur J Cancer Prev 1993, 2(4):351-356.
47. Song YH, Jeong SJ, Kwon HY, Kim B, Kim SH, Yoo DY: Ursolic acid from Oldenlandia diffusa induces apoptosis via activation of caspases and phosphorylation of glycogen synthase kinase 3 beta in SK-OV-3 ovarian cancer cells. Biol Pharm Bull, 35(7):1022-1028.
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51. Ou TT, Wu CH, Hsu JD, Chyau CC, Lee HJ, Wang CJ: Paeonia lactiflora Pall inhibits bladder cancer growth involving phosphorylation of Chk2 in vitro and in vivo. J Ethnopharmacol 2011, 135(1):162-172.
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61. Fong S, Shoemaker M, Cadaoas J, Lo A, Liao W, Tagliaferri M, Cohen I, Shtivelman E: Molecular mechanisms underlying selective cytotoxic activity of BZL101, an extract of Scutellaria barbata, towards breast cancer cells. Cancer Biol Ther 2008, 7(4):577-586.
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* These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

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