Alessandro Vindigni, PhD

Medical School Department Pathology and Immunology
Alessandro Vindigni

Researcher Background

Primary Academic Title

Professor of Medicine, Pathology and Immunology , WashU Medicine

Training

  • 1995 - 1999: Postdoctoral Fellow, WashU Medicine, St. Louis, MO

Education

  • 1995: PhD, Biochemistry and Molecular Biophysics, University of Padua, Padua, Italy

Research & Selected Publications

Research Interest

Aberrant DNA replication is one of the leading causes of mutations and chromosome rearrangements associated with several cancer related pathologies. At the same time, agents that stall or damage DNA replication forks are widely used for chemotherapy, in the attempt to selectively target highly proliferating cancer cells. Our group studies the mechanisms that operate in eukaryotic cells to maintain replication fork integrity upon chemical treatment with cancer chemotherapeutics.

MRN-CtIP, EXO1, and DNA2-WRN/BLM act bidirectionally to process DNA gaps in PARPi-treated cells without strand cleavage.
Authors:

Seppa IM, Ceppi I, Tennakoon M, one or more additional authors omitted Vindigni A

Journal & Year:

Genes Dev • 2025

Genetic buffering mechanisms in SNF2-family translocases.
Authors:

Agashe S, Vindigni A

Journal & Year:

Trends Genet • 2025

A RAD18-UBC13-PALB2-RNF168 axis mediates replication fork recovery in BRCA1-deficient cancer cells.
Authors:

Cybulla E, Wallace S, Meroni A, one or more additional authors omitted Vindigni A

Journal & Year:

Nucleic Acids Res • 2024

Nucleolytic processing of abasic sites underlies PARP inhibitor hypersensitivity in ALC1-deficient BRCA mutant cancer cells.
Authors:

Ramakrishnan N, Weaver TM, Aubuchon LN, one or more additional authors omitted Vindigni A, one or more additional authors omitted Verma P

Journal & Year:

Nat Commun • 2024

DNA combing versus DNA spreading and the separation of sister chromatids.
Authors:

Meroni A, Wells SE, Fonseca C, one or more additional authors omitted Vindigni A

Journal & Year:

J Cell Biol • 2024