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Lopez-Contreras, A. J.

Publications and source records attributed to Lopez-Contreras, A. J..

3 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↗

Supraphysiological protection from replication stress does not extend mammalian lifespan

Replication Stress (RS) is a type of DNA damage generated at the replication fork, characterized by single-stranded DNA (ssDNA) accumulation, and which can be caused by a variety of factors. Previous studies have reported elevated RS levels in aged cells. In addition, mouse models with a deficient RS response show accelerated aging. However, the relevance of endogenous or physiological RS, compared to other sources of genomic instability, for the normal onset of aging is unknown. We have performed long term survival studies of transgenic mice with extra copies of the Chk1 and/or Rrm2 genes, which we previously showed extend the lifespan of a progeroid ATR-hypomorphic model suffering from high levels of RS. In contrast to their effect in the context of progeria, the lifespan of Chk1, Rrm2 and Chk1/Rrm2 transgenic mice was similar to WT littermates in physiological settings. Most mice studied died due to tumors -mainly lymphomas-irrespective of their genetic background. Interestingly, a slightly higher percentage of transgenic mice developed tumors compared to WT mice. Our results indicate that supraphysiological protection from RS does not extend lifespan, indicating that RS may not be a relevant source of genomic instability on the onset of "normal" aging.

cancer biology↗

ATR expands embryonic stem cell fate potential in response to replication stress

Unrepaired DNA damage during embryonic development can be potentially inherited by a large population of cells. However, the quality control mechanisms that minimize the contribution of damaged cells to developing embryos remain poorly understood. Here, we uncovered an ATR- and CHK1-mediated transcriptional response to replication stress (RS) in ESCs that induces genes expressed in totipotent two-cell (2C) stage embryos and 2C-like cells. This response is mediated by Dux, a multicopy retrogene defining the cleavage-specific transcriptional program in placental mammals. In response to RS, DUX triggers the transcription of 2C-like markers such as murine endogenous retrovirus-like elements (MERVL) and Zscan4. This response can also be elicited by ETAA1-mediated ATR activation in the absence of RS. ATR-mediated activation of DUX requires GSRF1 dependent post-transcriptional regulation of Dux mRNA. Strikingly, activation of ATR expands ESCs fate potential by extending their contribution to both embryonic and extra{-}embryonic tissues. These findings define a novel ATR dependent pathway involved in maintaining genome stability in developing embryos by controlling ESCs fate in response to RS.

cell biology↗