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Inhibition of STAT3 signaling as critical molecular event in resveratrol-suppressed ovarian cancer cells

Overview of attention for article published in Journal of Ovarian Research, April 2015
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Title
Inhibition of STAT3 signaling as critical molecular event in resveratrol-suppressed ovarian cancer cells
Published in
Journal of Ovarian Research, April 2015
DOI 10.1186/s13048-015-0152-4
Pubmed ID
Authors

Li-Xia Zhong, Hong Li, Mo-Li Wu, Xiao-Yu Liu, Ming-Jun Zhong, Xiao-Yan Chen, Jia Liu, Yang Zhang

Abstract

Resveratrol exerts inhibitory effects on ovarian cancer cells, while its underlying mechanism and critical molecular target(s) have been lesser known. Activations of Wnt, Notch and STAT3 signaling are frequent in ovarian cancers/OCs and supposed to be important for OC formation and progression, while the impacts of resveratrol on these signaling pathways in OC cells remain obscure. In this study, two human ovarian cancer cell lines, OVCAR-3 and CAOV-3, were treated by 120 μM resveratrol and their responses to the treatment and the statuses of Wnt, Notch and STAT3 signaling in them were analyzed by multiple experimental approaches. Selective inhibitors of Wnt, Notch or STAT3 signaling were employed to treat OVCAR-3 and CAOV-3 cells to elucidate the significance of individual signaling pathways for ovarian cancers. The results demonstrated distinct inhibitory effects of resveratrol on human ovarian cancer cells in terms of remarkable G1 phase accumulation, increased apoptosis fraction and concurrent suppression of Wnt, Notch and STAT3 signaling as well as their downstream cancer-related gene expression. Treatments with Wnt, Notch or STAT3 selective inhibitor revealed that only AG490, a JAK-specific inhibitor, inhibits OVCAR-3 and CAOV-3 cells in the extent as similar as that of resveratrol. Our results suggest the significance of STAT3 activation in the maintenance and survival of ovarian cancer cells. The activated STAT3 signaling is the critical molecular target of resveratrol. Resveratrol would be a promising candidate in the management of ovarian cancers, especially the ones with resistance to conventional therapeutic agents.

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The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 29 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 29 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 21%
Other 4 14%
Student > Ph. D. Student 4 14%
Student > Postgraduate 3 10%
Student > Master 3 10%
Other 4 14%
Unknown 5 17%
Readers by discipline Count As %
Medicine and Dentistry 7 24%
Agricultural and Biological Sciences 4 14%
Chemistry 4 14%
Pharmacology, Toxicology and Pharmaceutical Science 3 10%
Biochemistry, Genetics and Molecular Biology 3 10%
Other 3 10%
Unknown 5 17%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 27 August 2016.
All research outputs
#20,269,439
of 22,800,560 outputs
Outputs from Journal of Ovarian Research
#427
of 585 outputs
Outputs of similar age
#224,054
of 265,536 outputs
Outputs of similar age from Journal of Ovarian Research
#11
of 12 outputs
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So far Altmetric has tracked 585 research outputs from this source. They receive a mean Attention Score of 3.2. This one is in the 1st percentile – i.e., 1% of its peers scored the same or lower than it.
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We're also able to compare this research output to 12 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.