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Catherine Andreadi

Researcher at University of Leicester

Publications -  16
Citations -  6239

Catherine Andreadi is an academic researcher from University of Leicester. The author has contributed to research in topics: Kinase & Autophagy. The author has an hindex of 13, co-authored 14 publications receiving 5685 citations. Previous affiliations of Catherine Andreadi include Leicester Royal Infirmary.

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Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Involvement of Nrf2, p38, B-Raf, and Nuclear Factor-κB, but Not Phosphatidylinositol 3-Kinase, in Induction of Hemeoxygenase-1 by Dietary Polyphenols

TL;DR: Induction of HO-1 by curcumin, EGCG, or low concentrations of helenalin did not protect MDA-MB468 breast cells or B-lymphoblasts from apoptosis, suggesting that signaling through p38 mitogen-activated protein kinase, NF-κB, and Nrf2 as well as other unidentified molecules is involved in HO- 1 induction by hemin and both polyphenols, but cell-specific factors also play a role.
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Sulfate Metabolites Provide an Intracellular Pool for Resveratrol Generation and Induce Autophagy with Senescence

TL;DR: The findings suggest that resveratrol is delivered to target tissues in a stable sulfate-conjugated form and that the parent compound is gradually regenerated in selected cells and may give rise to the beneficial effects in vivo.
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Predicting the physiological relevance of in vitro cancer preventive activities of phytochemicals.

TL;DR: This review considers the physiologically achievable doses for a few of the best studied agents and summarizes the data derived from studies using these low concentrations in cell culture to conclude that each of the compounds shows an encouraging range of activities in vitro at concentrations which are likely to be physiologically relevant.