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Xingcong Ren

Researcher at Penn State Cancer Institute

Publications -  51
Citations -  7660

Xingcong Ren is an academic researcher from Penn State Cancer Institute. The author has contributed to research in topics: Autophagy & Medicine. The author has an hindex of 26, co-authored 41 publications receiving 6914 citations. Previous affiliations of Xingcong Ren include Rutgers University & Penn State Milton S. Hershey Medical Center.

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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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Regulation of autophagy by a beclin 1-targeted microRNA, miR-30a, in cancer cells

TL;DR: It is reported here that microRNAs (miRNAs), a class of endogenous, 22–24 nucleotide noncoding RNA molecules able to affect stability and translation of mRNA, may represent a previously unrecognized mechanism for regulating beclin 1 expression and autophagy.
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Therapeutic Targeting of Autophagy in Disease: Biology and Pharmacology

TL;DR: A better understanding of the biology of Autophagy and the pharmacology of autophagy modulators has the potential for facilitating the development ofAutophagy-based therapeutic interventions for several human diseases.
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eEF-2 Kinase Dictates Cross-Talk between Autophagy and Apoptosis Induced by Akt Inhibition, Thereby Modulating Cytotoxicity of Novel Akt Inhibitor MK-2206

TL;DR: Regulatory mechanisms through which apoptosis and autophagy were modulated in tumor cells subjected to Akt inhibition by MK-2206 are investigated, suggesting that targeting eEF-2 kinase may reinforce the antitumor efficacy of Akt inhibitors such as MK- 2206.
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MK-2206, a Novel Allosteric Inhibitor of Akt, Synergizes with Gefitinib against Malignant Glioma via Modulating Both Autophagy and Apoptosis

TL;DR: It is reported here that MK-2206, a potent allosteric Akt inhibitor currently in phase I trials in patients with solid tumors, could reinforce the cytocidal effect of gefitinib against glioma and the combination of these two drugs may be utilized as a new therapeutic regimen for malignantglioma.