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Alexandros G. Georgakilas

Researcher at National Technical University of Athens

Publications -  172
Citations -  11657

Alexandros G. Georgakilas is an academic researcher from National Technical University of Athens. The author has contributed to research in topics: DNA damage & DNA repair. The author has an hindex of 48, co-authored 156 publications receiving 9260 citations. Previous affiliations of Alexandros G. Georgakilas include University of the East & Brookhaven National Laboratory.

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Immune evasion in cancer: Mechanistic basis and therapeutic strategies

TL;DR: The advances made toward understanding the basis of cancer immune evasion are discussed, the efficacy of various therapeutic measures and targets that have been developed or are being investigated to enhance tumor rejection are summarized and some natural agents and phytochemicals merit further study.
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Role of oxidative stress and DNA damage in human carcinogenesis.

TL;DR: The current status of knowledge and evidence on the mechanisms and involvement of intracellular oxidative stress and DNA damage in human malignancy evolution and possible use of these parameters as cancer biomarkers are presented and controversies related to specific methodologies used for the measurement of oxidatively induced DNA lesions in human cells or tissues are discussed.
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Oxidative stress, DNA methylation and carcinogenesis

TL;DR: Growing evidence supports a role of ROS-induced generation of oxidative stress in these epigenetic processes and as such the authors can hypothesize of potential mode(s) of action) by which oxidative stress modulates epigenetic regulation of gene expression.
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Broad targeting of resistance to apoptosis in cancer.

TL;DR: This review provides a roadmap for the design of successful anti-cancer strategies that overcome resistance to apoptosis for better therapeutic outcome in patients with cancer.
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Sustained proliferation in cancer: Mechanisms and novel therapeutic targets

TL;DR: Natural compounds found to inhibit one or more pathways that contribute to proliferation have been found and will be very important for identifying signaling pathways and molecular targets that may provide early diagnostic markers and/or critical targets for the development of new drugs or drug combinations that block tumor formation and progression.