Clouvel, A. | bioRxiv Science

bioRxiv2024

Targeting FEN1 to enhance efficacy of PARP inhibition in triple-negative breast cancer

Patients with triple-negative breast cancer (TNBC) have limited targeted therapeutic options. PARP inhibitors (PARPi) have demonstrated an important role for BRCA-mutant patients with early TNBC. Combination approaches with PARPi can broaden the use of PARPi to a larger cohort of TNBC patients. We selected six genes from our previously identified 63-gene signature that was associated with PARPi response. siFEN1 increased cells in G2/M arrest, DNA damage and particularly apoptosis. Targeting FEN1 with a chemical inhibitor enhanced the efficacy of PARPi in 7/10 cell lines, and synergy was demonstrated mainly in PARPi-resistant TNBC cell lines. A BRCA2-mutant cell line with acquired resistance to olaparib (HCC1395-OlaR) was strongly synergistic, with a combination index value of 0.20. The combination of PARPi and FEN1 inhibition also showed synergy in a PARPi-resistant xenograft-derived organoid model. Two mechanisms which explain the underlying efficacy are rapid progression in DNA replication fork speed and enhancement of DNA damage. The combination induced the highest fork speed (47% difference in comparison to control, P<0.0001) when FEN1 inhibition and PARPi equally increased fork speed individually in a cell line with a pre-existing increase in replication stress. The combination also increased DNA damage at lower drug concentrations, driving response in most of the synergistic cell lines. Gene expression analysis suggested that the sensitizing role of FEN1 inhibition in PARPi-resistant cell lines may be due to downregulation of pathways including mismatch repair. Therefore, targeting FEN1 shows great therapeutic potential as a targeted combination approach, particularly in the context of PARPi-resistant TNBC.

cancer biology↗

bioRxiv2022

MAP4K4 regulates biomechanical forces at adherens junctions and focal adhesions to promote collective cell migration

Collective cell migration is important for normal development and tissue homeostasis, but can also promote cancer metastasis. To migrate collectively, cells need to coordinate their protrusion formation, rear retraction, adhesion sites dynamics, as well as forces generation and transmission. Nevertheless, the regulatory mechanisms coordinating these processes remain elusive. Using the A431 carcinoma cell line, we identify the kinase MAP4K4 as a central regulator of collective migration. We show that MAP4K4 inactivation blocks the migration of clusters while its overexpression decreases cluster cohesion. MAP4K4 regulates protrusion and retraction dynamics, remodels the actomyosin cytoskeleton, and controls the stability of both cell-cell and cell substrate adhesion. MAP4K4 promotes focal adhesion disassembly through the phosphorylation of Moesin, an actin and plasma membrane cross-linker, but disassembles adherens junctions through a Moesin-independent mechanism. By analyzing traction and intercellular forces, we found that the stabilization of adhesion sites in MAP4K4 loss of function leads to a tensional disequilibrium throughout the cell cluster, increasing the traction forces exerted onto the substrate and the tension loading at the cell-cell adhesions. Together, our results indicates that MAP4K4 activity is a key regulator of biomechanical forces at adhesion sites, promoting collective migration.

cell biology↗