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Anna Skwarska

Researcher at Gdańsk University of Technology

Publications -  21
Citations -  5516

Anna Skwarska is an academic researcher from Gdańsk University of Technology. The author has contributed to research in topics: Programmed cell death & Biology. The author has an hindex of 9, co-authored 16 publications receiving 5031 citations. Previous affiliations of Anna Skwarska include Medical University of Białystok.

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DNA-Damaging Imidazoacridinone C-1311 Induces Autophagy followed by Irreversible Growth Arrest and Senescence in Human Lung Cancer Cells

TL;DR: It is suggested that in NSCLC, a C-1311–induced senescence program is preceded and corroborated but not exclusively determined by the induction of autophagy, and a small interfering RNA–mediated knockdown of theAutophagy-associated Beclin 1 and ATG5 genes attenuated but failed to block development ofsenescence.
Journal Article

Antitumor DNA-Damaging C-1748 is a New Inhibitor of Autophagy that Triggers Apoptosis in Human Pancreatic Cancer Cell Lines

TL;DR: Surprisingly, simultaneous exposure of pancreatic cancer cells to C-1748 in combination with the late-stage autophagy inhibitor, chloroquine, neither significantly increased the cytotoxic activity of C- 1748 nor ameliorated its apoptosis-inducing potential.
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Microporous Polyurethane Thin Layer as a Promising Scaffold for Tissue Engineering.

TL;DR: A successful fabrication of the microporous polyurethane thin layer (MPTL) of 1 mm thick is reported, which was produced using SC/PL technique combined with phase separation (PS), which can be considered a suitable scaffold for tissue engineering purpose, according to the morphology criterion.
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Diminished toxicity of C-1748, 4-methyl-9-hydroxyethylamino-1-nitroacridine, compared with its demethyl analog, C-857, corresponds to its resistance to metabolism in HepG2 cells.

TL;DR: The crucial role of hypoxic conditions and the direct involvement of POR in the metabolism of both compounds were demonstrated and the low reactivity of C-1748 and the stability of its metabolites are postulated to contribute significantly to the diminished toxicity of this compound observed in animals.