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Biology subjects

del Rio Oliva, M.

Publications and source records attributed to del Rio Oliva, M..

2 recordsLinked to original sources

PROTAC-Driven Protective Therapy increases the therapeutic window of anticancer drugs

Targeted protein degradation is emerging as a powerful anticancer therapy, mostly focused on eliminating oncogenic drivers. In contrast, we propose using PROTACs that exploit E3 ligase defects in cancer cells to selectively protect healthy tissues from the dose-limiting toxicity of anticancer drugs. We term this approach PROTAC-Driven Protective Therapy (PDPT). PDPT consists of a combinatorial treatment of a given anticancer compound with a PROTAC that promotes the degradation of proteins required for the drug-induced toxicity. Potential targets of protective PROTACs include drug uptake transporters, enzymes activating pro-drugs, and the actual drug target in cases that mediates the drug-induced toxicity. Notably, these protective PROTACs must be designed to recruit E3 ligases that are mutated or defective in the cancer cells while remain active in healthy tissues. As a proof of concept of our strategy, we used CRBN-recruiting and VHL-recruiting PROTACs to demonstrate that PARP1 degradation alleviates the cytotoxicity of PARP inhibitors (PARPi) in E3 ligase-proficient cells, while E3 ligase-deficient cancer cells remain fully sensitive. Remarkably, PDPT also protects primary human bone marrow progenitors from PARPi-induced toxicity, which are the most clinically relevant cells affected by PARPi-associated side effects in cancer patients, supporting the clinical relevance of this strategy. We further uncover that TP53-mutant cancers display critically low expression of the E3 ligase MDM2 and show inefficient MDM2-recruiting PROTAC activity. This tumor-intrinsic feature enables PDPT using MDM2-recruiting PROTACs in TP53-mutant cancers. PDPT opens a new direction for targeted protein degradation by improving tolerability and expanding the therapeutic window of both established and future cancer therapies.

cancer biology↗

HMCES corrupts replication fork stability during base excision repair in homologous recombination deficient cells

Apurinic/apyrimidinic (AP) sites and single-strand breaks (SSB) arising from base excision repair (BER) during misincorporation of damaged nucleobases may hinder replication fork stability in homologous recombination-deficient (HRD) cells. At templated AP-sites, HMCES DNA-protein crosslinks (DPC) regulate replication fork speed while avoiding APE1-mediated cytotoxic double-strand breaks (DSB). Whereas the role of HMCES at template DNA strand is well studied, its consequences on nascent DNA are less understood. Here, we provide evidence that HMCES play detrimental roles during removal of 5- hydroxymethyl-2-deoxycytidine (5hmdC)-derived 5-hydroxymethyl-2-deoxyuridine (5hmdU) by BER at replication forks. HRD cells display heightened HMCES chromatin levels, which increase upon 5hmdC exposure, suggesting that HMCES binds both spontaneous and 5hmdC-induced AP-sites. HMCES depletion largely suppresses 5hmdC- mediated Fancd2-/- replication fork defects, chromosomal aberrations and cell lethality, suggesting that HMCES is responsible for the replication fork impairment and lethality observed in HRD cells. Therefore, HMCES-DPCs are a novel source of BER-initiated PRIMPOL-mediated ssDNA gaps, implying endogenous DPCs as a source of DNA damage in HRD tumours. TeaserCovalent binding of HMCES to nascent DNA blocks replication progression and kills homologous recombination deficient cancer cells

molecular biology↗