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Lonnie P. Swift

Researcher at University of Oxford

Publications -  16
Citations -  761

Lonnie P. Swift is an academic researcher from University of Oxford. The author has contributed to research in topics: DNA & DNA damage. The author has an hindex of 11, co-authored 15 publications receiving 674 citations. Previous affiliations of Lonnie P. Swift include La Trobe University & John Radcliffe Hospital.

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Doxorubicin-DNA Adducts Induce a Non-Topoisomerase II–Mediated Form of Cell Death

TL;DR: It is shown that doxorubicin-DNA adducts induce a more cytotoxic response in HL-60 cells than doxorbicin as a single agent, and that theseAdducts are more cytOToxic than topoisomerase II-mediated lesions.
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Human SNM1A and XPF–ERCC1 collaborate to initiate DNA interstrand cross-link repair

TL;DR: It is shown that purified human SNM1A (hSNM 1A), which exhibits a 5'-3' exonuclease activity, can load from a single DNA nick and digest past an ICL on its substrate strand.
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Activation of DNA damage response pathways as a consequence of anthracycline-DNA adduct formation.

TL;DR: Analysis of protein kinases with respect to cell cycle progression indicates that ATR is required for G(2)/M checkpoint responses while ATM appears to function in G(1) mediated responses to anthracycline adducts, which may be potential drug targets to achieve synergistic cytotoxic responses to doxorubicin-DNA adduct forming therapies.
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Sequence specificity of adriamycin-DNA adducts in human tumor cells.

TL;DR: It is shown that when Adriamycin is used in conjunction with the formaldehyde-releasing prodrug AN-9 in IMR-32 tumor cells, this allows the formation of sufficiently high levels of adducts in genomic DNA to enable detection of their DNA sequence specificity for the first time.
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Activation of Adriamycin by the pH-dependent Formaldehyde-releasing Prodrug Hexamethylenetetramine

TL;DR: HMTA has some potential for localized activation of Adriamycin in solid tumors because it is known to hydrolyze under cellular conditions and release six molecules of formaldehyde in a pH-dependent manner.