Research context: This article summarizes findings reported in the linked sources. Much of the research described here uses cell models, animals or isolated Spirulina compounds; it does not establish that eating Spirulina prevents or treats cancer in people. SPRU is a food, not a substitute for cancer screening, diagnosis or care.
Research has explored Spirulina and isolated compounds in cancer models. Much of this work is preclinical and cannot establish prevention or treatment effects in people.
The anti-cancer research has been conducted on pure (dried) Spirulina biomass as well as on 1) polysaccharides isolated from Spirulina; 2) hot water extracts of (dried)Β SpirulinaΒ biomass that has not been specifically isolated for a single active constituent; and quite notable and extensiveΒ research on 3) the blue pigment found only in SpirulinaΒ and other species of blue-green microalgae calledΒ βphycocyanin.β
This research has examined a variety of cancers in an assortment ofΒ different organs.
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CARCINOMA,Β MELANOMA AND FIBROSARCOMA
Polysaccharide cancer research began inΒ 1998 on Calcium Spirulan with a study examining itsΒ effects on three different types of cancers - carcinoma,Β melanoma and fibrosarcoma. Calcium Spirulan significantly inhibited the invasion of each of these tumor cells.
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CHEMO-PROTECTIVE AND RADIO-PROTECTIVE CAPABILITY
Further research conducted on stem cell systemsΒ has also shown potential for Spirulina-derived polysaccharides. One such study from 2001 concluded, βThe polysaccharide of Spirulina platensis has chemo-protective and radio-protective capability, and may be a potential adjunct to cancer therapyβ.
A later study in theΒ same area found that the polysaccharide extract from spirulina significantly increased the levels of interleukins 1 and 3 and tumorΒ necrosis factor alpha.
Water extracts from spirulina contain the water solubleΒ pigment C-phycocyanin. There are several recent studiesΒ over the last few years that show cancer related benefitsΒ to both unrefined water extracts of spirulina as well as isolated C-phycocyanin.
ORAL CANCER
TwoΒ studies have shown an effect again on oral cancer and a third demonstrated an enhancement of antitumor naturalΒ killer cells through consumption of the extract.
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ENHANCED TUMORICIDALΒ NK ACTIVATIONΒ
The thirdΒ study is of particular interest - conclusions drawn foundΒ that orally administered spirulina enhanced tumoricidalΒ NK activation and inferred a potential for antitumorΒ immunotherapy.
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LEUKEMIA
Research has been conducted in the last six years on phycocyaninβs antitumoral effect. The results have provenΒ very promising:
β’ 49% decrease in the proliferation of leukemia cellΒ lines
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LIVER CANCER
β’ 50% decrease in the proliferation of hepatocellularΒ carcinoma (liver cancer) cell lines
β’ significant decrease in HeLa cells in vitro compared toΒ control cellsΒ (HeLa cells are an immortal cancerous cell line extracted from cervical cancer cells inΒ 1951)
β’ inducement of apoptotic features including cell shrinkage in these same HeLa cells
β’ impedance of the reproduction of HeLa cells
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MELANOMA AND BREAST CANCER
β’ in conjunction with selenium, phycocyanin was foundΒ to be a potent antiproliferative agent against humanΒ melanoma cells and human breast adenocarcinomaΒ MCF-7 cells.
Many researchers find phycocyanin to be a truly excitingΒ compound - described as a non-toxic fluorescent proteinΒ pigment with potent antioxidant, anti-inflammatory andΒ anti-cancer properties.Β This pigment is onlyΒ found in spirulina and other species of blue green algae.
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COLON CANCER
An interesting study compared the activity of spirulinaΒ with two other nutritional compounds - Vitamin E andΒ germanium-132 - in pre-cancerous crypts in the colon.
While the researchers found that all three compounds hadΒ some inhibitory effects, they pointed out that when testedΒ after 9, 13 and 16 weeks, the number of aberrant cryptsΒ was significantly less in the spirulina group as comparedΒ to the control group.
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SKIN AND STOMACH TUMORS
Another study on pure spirulina biomass measured theΒ inhibition of tumors in skin and stomach. At spirulinaΒ usage levels in rodents of 250 mg and 500 mg/kg bodyΒ weight, inhibition of tumors was found in both the skinΒ and stomach regions. The skin tumors in the SpirulinaΒ group reduced from 4.86 to 1.20% at the lower dose andΒ from 4.86 to 1.15% in the higher dose group. In stomach tumors, the low dose group found a reduction fromΒ 3.73 to 2.05% and the high dose group found a reduction from 3.73 to 1.73%.
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