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Perdichizzi, B.

Publications and source records attributed to Perdichizzi, B..

3 recordsLinked to original sources

Subthreshold perturbation of DNA replication induces a secretory response and a bystander effect in naïve human fibroblasts

Replication stress is a hallmark of cancer, where it drives DNA damage and genome instability. Yet subtle, subthreshold perturbations of DNA synthesis likely occur routinely in normal proliferating tissues, and their consequences for cell homeostasis are unknown. Using primary human fibroblasts, we show that doses of the DNA polymerase inhibitor aphidicolin, too low to engage the replication checkpoint, or produce detectable DNA breaks, nonetheless elicit low-level, ATM-dependent {gamma}H2AX phosphorylation uncoupled from overt damage. This near-silent perturbation reprograms gene expression, inducing replication-associated genes together with a discrete secretory programme dominated by matrix-remodelling proteases and matricellular factors. This output is not a senescence-associated secretory phenotype: the NF-{kappa}B/IL-1/IL-6 axis is co-ordinately repressed rather than induced, p53 target genes including CDKN1A are unchanged, and cells remain proliferative and non-senescent. Conditioned medium from exposed cells reproduces ATM-{gamma}H2AX activation in naive fibroblasts without DNA damage, defining a "perturbed-replication bystander effect" (PeRBE). PeRBE is ROS-independent and mediated by heat-labile, proteinaceous factors, and in recipient cells it induces an extracellular-matrix programme that culminates in increased collagen production, without loss of proliferative capacity. A perturbation invisible to every standard replication-stress assay therefore generates a transmissible, protein-borne signal that instructs fibrogenic matrix remodelling in cells that never experienced it.

cell biology↗

HPV16 recruitment of SMARCAL1 to viral and host replication forks is required for the viral life cycle

High-risk human papillomaviruses (HR HPVs) are responsible for around 5% of the worlds cancer burden. Activation and interaction with the host DNA damage response (DDR) promotes the HPV16 life cycle. This study demonstrates a crucial interaction between HPV16 and SMARCAL1, a protein involved in the stabilization of stalled DNA replication forks. SMARCAL1 can complex with E2, is recruited to E1-E2 replicating DNA, and SMARCAL1 knockdown reduces the fidelity of E1-E2 mediated DNA replication in C33a cells but does not alter replication levels. SMARCAL1 is recruited to the HPV16 genome in HPV16-immortalized foreskin keratinocytes (HFK+HPV16), and in situ protein interaction with nascent DNA replication forks (SIRF) assays demonstrated that SMARCAL1 is hyper-recruited to host replication forks in HFK+HPV16 cells. Using COMET, DNA fiber, and cell growth assays it was determined that knockdown of SMARCAL1 increased DNA damage and impaired replication fork progression in HFK+HPV16 cells, ultimately resulting in growth arrest. The viral genome integrates following SMARCAL1 knockdown in HFK+HPV16 cells. Therefore, SMARCAL1 facilitates host and viral DNA replication in HFK+HPV16 cells. Overall, the results demonstrate that HPV16 promotes SMARCAL1 recruitment to viral and host replication forks and is an essential factor for the HPV16 life cycle. The results expand our understanding of DDR proteins that regulate the HPV16 life cycle, and suggest that inhibition of SMARCAL1 function represents a novel anti-viral strategy for the treatment and prevention of HPV infections. ImportanceHPV16 is responsible for the majority of HPV+ cancers, contributing to 54% of cervical cancers and [~]90% of HPV+HNSCC. Integration of viral genomes into host DNA can promote cervical cancer progression and correlates with poor prognosis in HPV-associated HNSCC, where around 70% of HPV+ cancers contain episomal viral genomes. Developing effective antiviral therapies requires a deeper understanding of the interplay between viral replication and host DNA damage response (DDR) pathways. This report demonstrates that SMARCAL1 is essential for HPV16 replication and keratinocyte proliferation and that its depletion leads to replication stress, DNA damage, and viral genome integration. This work underscores the delicate balance between viral exploitation of the host DDR and the risk of genome instability. These insights contribute to the broader understanding of HPV pathogenesis and may inform the development of therapeutic strategies targeting viral replication to prevent disease progression and improve clinical outcomes in HPV-associated cancers.

microbiology↗

Functional correlation between WRN and SAMHD1 in end-resection

Double-strand breaks (DSBs) can cause chromosome rearrangements, leading to cancer and some genetic diseases. WRN and SAMHD1 are proteins implicated in DSB processing and form a complex. Our study shows that SAMHD1 influences the nuclear recruitment of WRN in response to CPT-induced DSBs. Silencing SAMHD1 restores single-stranded DNA formation in WRN-deficient cells. However, DSB accumulation from CPT treatment is not recovered in WRN S1133A or WS cells when SAMHD1 is silenced. This suggests SAMHD1 cooperates with WRN in DNA damage repair and may have additional protective roles when WRN function in DSBs processing is impaired.

cell biology↗