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Boswellic
acids inhibit glioma growth: a new treatment option?
Winking
M, Sarikaya S, Rahmanian A, Jodicke A, Boker DK
Neurosurgical
Clinic, Justus-Liebig University Giessen, Germany
Conventional
malignant glioma therapy (surgery, radiation therapy and chemotherapy) does not
yield satisfying results.
The prognosis of the glioma patient depends more on the histological grading of
the tumor and patient's age than on the therapy.
Especially the adjuvant chemotherapy failed to date to influence survival time
in glioma patients significantly.
To improve results in malignant glioma therapy additional therapeutic regimes
are necessary.
In an earlier study we were able to show a significant reduction on perifocal
edema by an extract from gum resin (EGR) accompanied with a clinical improvement
in patients with malignant glioma.
Also a decrease of urinary LTE4-excretion as a metabolite of leukotriene
synthesis in brain tumors was observed.
Furthermore we had found a proliferation inhibiting activity of the extract form
EGR, the boswellic acids in cell cultures.
The purpose of this experimental study was to elucidate the effects of the
boswellic acids, which are constituents of an extract from gum resin on tumor
growth in vivo.
Female wistar rats weighing 200-250 g were treated with the drug 14 days after
inoculation of C6 tumor cells into their right caudate nucleus and randomization
into 4 groups.
The treatment groups received different dosages and were compared to a control
group without any additional treatment.
Survival time of the rats in the highest dosage group (3 x 240 mg/kg body
weight) was more than twice as long as in the control group (P < 0.05).
In a second experiment the inhibition of tumor cell proliferation was examined.
The C6 tumor cells were implanted into the caudate nucleus.
Drug treatment was started immediately after implantation and stopped after 14
days.
The animals were sacrificed and the brains were examined microscopically.
Comparing low and high dosage of EGR treatment a significant difference in tumor
volume was detected (P < 0.05).
The proportion of apoptotic tumor cells in animals with high dose treatment was
significantly larger than in the low dose (treatment) group (P < 0.05).
These data demonstrate an influence of EGR in rat glioma growth and might
represent a new therapeutic option on glioma treatment in man in future.
Further
experimental work on human gliomas is needed to definitively answer this
question.
PMID:
10894362 [PubMed - indexed for MEDLINE]
Source:
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=10894362&dopt=Abstract
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