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Dendrophthoe pentandra (L.) Miq extract effectively inhibits inflammation, proliferation and induces p53 expression on colitis-associated colon cancer

View Article: PubMed Central - PubMed

ABSTRACT

Background: Indonesian mistletoe grows on various trees. Mango Mistletoes (Dendrophthoe pentandra) is one type of mistletoe that grown on mango tree (.benalu mangga in bahasa Indonesia). Our study used mistletoe as a parasitic plant that has been used for traditional medicine. It has been known that Dendrophtoe pentandra extract (DPE) anti-inflammatory and anticancer. Furthermore, it is necessary to follow-up study in vivo to evaluate the response to treatment of new cancer therapeutic agents. This research aimed to determine the levels of IL-22, myeloperoxide (MPO), proliferation and wild-type p53 expression after the administration of DPE to murine models of CAC.

Methods: Mouse colitis associated colon cancer (CAC) was induced firstly by azoxymethane (AOM) and followed by administration of drinking water containing 5 % dextran sodium sulfate (DSS) in a cycle protocol, each cycle consisted of seven days of 5 % DSS in the drinking water and followed by seven days of regular water. This study consists of five treatment groups: I was treated water only (control), II was administrated by (DSS only, without DPE), (III-V) were administrated by DPE (125 mg/kg BW, 250 mg/kg BW and 500 mg/kg BW) respectively. The administrated of DPE were started from the 8th weeks, were continued until 21 weeks. At the end of 21 weeks of the experiment, mice were sacrificed, colon tissue was removed, and then subjected to ELISA, flow cytometry, real-time PCR and histology examination.

Results: Administration of DPE 250 mg/kgBW significantly reduce the levels of IL-22 and MPO compared with DSS only group (p < 0.001; p < 0.001). Colonic epithelial cells proliferation of group IV (DPE 250 mg/kgBW) were significantly lower than III and V groups. There was no significant change in the S phase in mice were treated DPE 125 mg/kg BW and 500 mg/kg BW, while administration of DPE 250 mg/kg BW was able to increase the percentage of cells in S phase. The expression of mRNA p53 was up regulated in mice received DPE 125 mg/kg BW.

Conclusion: These findings indicate that the DPE could inhibit colonic epithelial cells proliferation through p53 pathway independently. This study also showed that DPE could be potential sources of new therapy.

No MeSH data available.


DPE decreased IL-22 levels in CAC murine models. IL-22 levels were measured from supernatants of colon organ culture by enzyme linked immunosorbent assay. Each group consisted of at least four mice. Results shown are mean + SD, with n = 4 replicates in each group. Results are mean ± SD. *, p < 0.05. **, p < 0.001
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Fig2: DPE decreased IL-22 levels in CAC murine models. IL-22 levels were measured from supernatants of colon organ culture by enzyme linked immunosorbent assay. Each group consisted of at least four mice. Results shown are mean + SD, with n = 4 replicates in each group. Results are mean ± SD. *, p < 0.05. **, p < 0.001

Mentions: AOM and DSS administration increase IL-22 levels in supernatant colon culture significantly (p = 0.000). The administration of DPE at all doses in group lll (doses (125 mg/kg), p = 0.000; group lV (250 mg /kg), p = 0.000, group V (500 mg/kg) p = 0.010) decreased the levels of IL-22 significantly compared with DPE (−) group (Fig. 2). The greatest decrease was a dose of DPE (250 mg/kg).Fig. 2


Dendrophthoe pentandra (L.) Miq extract effectively inhibits inflammation, proliferation and induces p53 expression on colitis-associated colon cancer
DPE decreased IL-22 levels in CAC murine models. IL-22 levels were measured from supernatants of colon organ culture by enzyme linked immunosorbent assay. Each group consisted of at least four mice. Results shown are mean + SD, with n = 4 replicates in each group. Results are mean ± SD. *, p < 0.05. **, p < 0.001
© Copyright Policy - OpenAccess
Related In: Results  -  Collection

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getmorefigures.php?uid=PMC5037598&req=5

Fig2: DPE decreased IL-22 levels in CAC murine models. IL-22 levels were measured from supernatants of colon organ culture by enzyme linked immunosorbent assay. Each group consisted of at least four mice. Results shown are mean + SD, with n = 4 replicates in each group. Results are mean ± SD. *, p < 0.05. **, p < 0.001
Mentions: AOM and DSS administration increase IL-22 levels in supernatant colon culture significantly (p = 0.000). The administration of DPE at all doses in group lll (doses (125 mg/kg), p = 0.000; group lV (250 mg /kg), p = 0.000, group V (500 mg/kg) p = 0.010) decreased the levels of IL-22 significantly compared with DPE (−) group (Fig. 2). The greatest decrease was a dose of DPE (250 mg/kg).Fig. 2

View Article: PubMed Central - PubMed

ABSTRACT

Background: Indonesian mistletoe grows on various trees. Mango Mistletoes (Dendrophthoe pentandra) is one type of mistletoe that grown on mango tree (.benalu mangga in bahasa Indonesia). Our study used mistletoe as a parasitic plant that has been used for traditional medicine. It has been known that Dendrophtoe pentandra extract (DPE) anti-inflammatory and anticancer. Furthermore, it is necessary to follow-up study in vivo to evaluate the response to treatment of new cancer therapeutic agents. This research aimed to determine the levels of IL-22, myeloperoxide (MPO), proliferation and wild-type p53 expression after the administration of DPE to murine models of CAC.

Methods: Mouse colitis associated colon cancer (CAC) was induced firstly by azoxymethane (AOM) and followed by administration of drinking water containing 5&nbsp;% dextran sodium sulfate (DSS) in a cycle protocol, each cycle consisted of seven days of 5&nbsp;% DSS in the drinking water and followed by seven days of regular water. This study consists of five treatment groups: I was treated water only (control), II was administrated by (DSS only, without DPE), (III-V) were administrated by DPE (125&nbsp;mg/kg BW, 250&nbsp;mg/kg BW and 500&nbsp;mg/kg BW) respectively. The administrated of DPE were started from the 8th weeks, were continued until 21&nbsp;weeks. At the end of 21&nbsp;weeks of the experiment, mice were sacrificed, colon tissue was removed, and then subjected to ELISA, flow cytometry, real-time PCR and histology examination.

Results: Administration of DPE 250&nbsp;mg/kgBW significantly reduce the levels of IL-22 and MPO compared with DSS only group (p&thinsp;&lt;&thinsp;0.001; p&thinsp;&lt;&thinsp;0.001). Colonic epithelial cells proliferation of group IV (DPE 250&nbsp;mg/kgBW) were significantly lower than III and V groups. There was no significant change in the S phase in mice were treated DPE 125&nbsp;mg/kg BW and 500&nbsp;mg/kg BW, while administration of DPE 250&nbsp;mg/kg BW was able to increase the percentage of cells in S phase. The expression of mRNA p53 was up regulated in mice received DPE 125&nbsp;mg/kg BW.

Conclusion: These findings indicate that the DPE could inhibit colonic epithelial cells proliferation through p53 pathway independently. This study also showed that DPE could be potential sources of new therapy.

No MeSH data available.