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Xanthohumol suppresses oestrogen-signalling in breast cancer through the inhibition of BIG3-PHB2 interactions.


ABSTRACT: Xanthohumol (XN) is a natural anticancer compound that inhibits the proliferation of oestrogen receptor-? (ER?)-positive breast cancer cells. However, the precise mechanism of the antitumour effects of XN on oestrogen (E2)-dependent cell growth, and especially its direct target molecule(s), remain(s) largely unknown. Here, we focus on whether XN directly binds to the tumour suppressor protein prohibitin 2 (PHB2), forming a novel natural antitumour compound targeting the BIG3-PHB2 complex and acting as a pivotal modulator of E2/ER? signalling in breast cancer cells. XN treatment effectively prevented the BIG3-PHB2 interaction, thereby releasing PHB2 to directly bind to both nuclear- and cytoplasmic ER?. This event led to the complete suppression of the E2-signalling pathways and ER?-positive breast cancer cell growth both in vitro and in vivo, but did not suppress the growth of normal mammary epithelial cells. Our findings suggest that XN may be a promising natural compound to suppress the growth of luminal-type breast cancer.

SUBMITTER: Yoshimaru T 

PROVIDER: S-EPMC4258681 | biostudies-literature | 2014 Dec

REPOSITORIES: biostudies-literature

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Xanthohumol suppresses oestrogen-signalling in breast cancer through the inhibition of BIG3-PHB2 interactions.

Yoshimaru Tetsuro T   Komatsu Masato M   Tashiro Etsu E   Imoto Masaya M   Osada Hiroyuki H   Miyoshi Yasuo Y   Honda Junko J   Sasa Mitsunori M   Katagiri Toyomasa T  

Scientific reports 20141208


Xanthohumol (XN) is a natural anticancer compound that inhibits the proliferation of oestrogen receptor-α (ERα)-positive breast cancer cells. However, the precise mechanism of the antitumour effects of XN on oestrogen (E2)-dependent cell growth, and especially its direct target molecule(s), remain(s) largely unknown. Here, we focus on whether XN directly binds to the tumour suppressor protein prohibitin 2 (PHB2), forming a novel natural antitumour compound targeting the BIG3-PHB2 complex and act  ...[more]

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