Selected Papers

Identification of PLK1 as a therapeutic target in BRCA1-deficient cancers (2019)

In this work we developed a flow-cytometry-based co-culture screening technology for drug discovery, and we used to explore a public kinase inhibitor set.

Bioprospecting South American flora for synthetic lethal lead compounds (2020)

In this work we used our flow-cytometry-based co-culture screening technology to screen a collection of 50 plants species from South America in a wide dose-response scheme.

Screening of regulatory partners of ZEB1 to inhibit its pro-metastatic properties (2019)

In this work we performed In Silico screenings to identifty phosphor regulatory sites of the EMT factor ZEB1 and validated PKCα as a novel partner capable of modulating its premetastatic properties.

Repurposing of breast cancer transcriptomic signature for pan-cancer applications (2020)

In this work we perform studies of correlations of drug sensitivity of a cell line database with transcriptomic classes of cancer cells derived from a commercial breast cancer signature.

Identification of PLK1 as a therapeutic target in BRCA1-deficient cancers (2019)

In this work we developed a flow-cytometry-based co-culture screening technology for drug discovery, and we used to explore a public kinase inhibitor set.

Bioprospecting South American flora for synthetic lethal lead compounds (2020)

In this work we used our flow-cytometry-based co-culture screening technology to screen a collection of 50 plants species from South America in a wide dose-response scheme.

Screening of regulatory partners of ZEB1 to inhibit its pro-metastatic properties (2019)

In this work we performed In Silico screenings to identifty phosphor regulatory sites of the EMT factor ZEB1 and validated PKCα as a novel partner capable of modulating its premetastatic properties.

Repurposing of breast cancer transcriptomic signature for pan-cancer applications (2020)

In this work we perform studies of correlations of drug sensitivity of a cell line database with transcriptomic classes of cancer cells derived from a commercial breast cancer signature.

Publications