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Polyyne-Enriched Extract from Oplopanax elatus Significantly Ameliorates the Progression of Colon Carcinogenesis in ApcMin/+ Mice.


ABSTRACT: Colorectal cancer (CRC) is the third most common cancer in the world. Oplopanax elatus is widely used in traditional medicine. However, little is known about its pharmacological effects and bioactive compounds. We evaluated the effects of the polyyne-enriched extract from O. elatus (PEO) on the progression of colon carcinogenesis in ApcMin/+ mice. In addition, these effects were also investigated in HCT116 and SW480 cells. After PEO oral administration (0.2% diet) for 12 weeks, PEO significantly improved body weight changes and reduced the tumor burden and tumor multiplicity compared with the untreated mice. Meanwhile, western blot and immunohistochemistry results showed PEO significantly reduced the expression of ?-catenin and cyclinD1 in both small intestine and the colon tissues compared with the untreated mice. In addition, PEO treatment significant decreased the cell viability in both HCT116 and SW480 cell lines. It also decreased the levels of ?-catenin, cyclinD1, c-myc and p-GSK-3? in HCT116 and SW480 cells at 25 ?M. These results indicate that PEO may have potential value in prevention of colon cancer by down-regulating Wnt-related protein.

SUBMITTER: Qiao X 

PROVIDER: S-EPMC6151504 | biostudies-literature | 2017 Sep

REPOSITORIES: biostudies-literature

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Polyyne-Enriched Extract from Oplopanax elatus Significantly Ameliorates the Progression of Colon Carcinogenesis in Apc<sup>Min/+</sup> Mice.

Qiao Xin X   Sun Wei W   Wang Chongzhi C   Zhang Li L   Li Ping P   Wen Xiaodong X   Yang Jie J   Yuan Chunsu C  

Molecules (Basel, Switzerland) 20170922 10


Colorectal cancer (CRC) is the third most common cancer in the world. <i>Oplopanax elatus</i> is widely used in traditional medicine. However, little is known about its pharmacological effects and bioactive compounds. We evaluated the effects of the polyyne-enriched extract from <i>O. elatus</i> (PEO) on the progression of colon carcinogenesis in <i>Apc</i><sup>Min/+</sup> mice. In addition, these effects were also investigated in HCT116 and SW480 cells. After PEO oral administration (0.2% diet)  ...[more]

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