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Ana M. Mendes-Pereira

Researcher at Institute of Cancer Research

Publications -  11
Citations -  1359

Ana M. Mendes-Pereira is an academic researcher from Institute of Cancer Research. The author has contributed to research in topics: PTEN & Tensin. The author has an hindex of 7, co-authored 9 publications receiving 1262 citations. Previous affiliations of Ana M. Mendes-Pereira include The Breast Cancer Research Foundation.

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Synthetic lethal targeting of PTEN mutant cells with PARP inhibitors

TL;DR: The data presented here now suggests that the clinical assessment of PARP inhibitors should be extended beyond those with BRCA mutations to a larger group of patients with PTEN mutant tumours.
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PTEN Deficiency in Endometrioid Endometrial Adenocarcinomas Predicts Sensitivity to PARP Inhibitors

TL;DR: The authors demonstrate that endometrial cancer cell lines that lack the tumor suppressor protein PTEN show defects in the repair of DNA damage and are consequently very sensitive to drugs that block poly(ADP) ribose polymerase (PARP), an enzyme critical for DNA repair.
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Functional viability profiles of breast cancer

TL;DR: A functional genetic screen in >30 commonly used models of breast cancer to identify genes critical to the growth of specific breast cancer subtypes is carried out and potential new therapeutic targets for PTEN-mutated cancers and for estrogen receptor-positive breast cancers are described.
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High-throughput RNA interference screening using pooled shRNA libraries and next generation sequencing

TL;DR: This work describes complete experimental protocols and novel open source computational methodologies, shALIGN and shRNAseq, that allow RNAi screens to be rapidly deconvoluted using next generation sequencing.
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Genome-wide functional screen identifies a compendium of genes affecting sensitivity to tamoxifen

TL;DR: Combining whole-genome shRNA screening with massively parallel sequencing, this work has profiled the impact of more than 56,670 RNA interference reagents targeting 16,487 genes on the cellular response to tamoxifen.