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Conventional cytotoxic therapies for synovial sarcoma provide limited benefit, and no drugs specifically targeting its driving SS18-SSX fusion oncoprotein are currently available. Patients remain at high risk for early and late metastasis. A high-throughput drug screen consisting of over 900 tool compounds and epigenetic modifiers, representing over 100 drug classes, was undertaken in a panel of synovial sarcoma cell lines to uncover novel sensitizing agents and targetable pathways. Top scoring drug categories were found to be HDAC inhibitors and proteasomal targeting agents. We find that the HDAC inhibitor quisinostat disrupts the SS18-SSX driving protein complex, thereby reestablishing expression of EGR1 and CDKN2A tumor suppressors. In combination with proteasome inhibition, HDAC inhibitors synergize to decrease cell viability and elicit apoptosis. Quisinostat inhibits aggresome formation in response to proteasome inhibition, and combination treatment leads to elevated endoplasmic reticulum stress, activation of pro-apoptotic effector proteins BIM and BIK, phosphorylation of BCL-2, increased levels of reactive oxygen species, and suppression of tumor growth in a murine model of synovial sarcoma. This study identifies and provides mechanistic support for a particular susceptibility of synovial sarcoma to the combination of quisinostat and proteasome inhibition.

The strength of interactions among species in a network tends to be highly asymmetric. We evaluate the hypothesis that this asymmetry results from the distribution of abundance among species, so that species interactions occur randomly among individuals. We used a database on mutualistic and antagonistic bipartite quantitative interaction networks. We show that across all types of networks asymmetry was correlated with abundance, so that rare species were asymmetrically affected by their abundant partners, while pairs of interacting abundant species tended to exhibit more symmetric, reciprocally strong effects. A null model shows that abundance provides a sufficient explanation of the asymmetry structure in some networks, but suggests the role of additional factors in others. Although not universal, our hypothesis holds for a substantial fraction of networks analyzed here, and should be considered as a null model in all studies aimed at evaluating the ecological and evolutionary consequences of species interactions.

The strength of interactions among species in a network tends to be highly asymmetric. We evaluate the hypothesis that this asymmetry results from the distribution of abundance among species, so that species interactions occur randomly among individuals. We used a database on mutualistic and antagonistic bipartite quantitative interaction networks. We show that across all types of networks asymmetry was correlated with abundance, so that rare species were asymmetrically affected by their abundant partners, while pairs of interacting abundant species tended to exhibit more symmetric, reciprocally strong effects. A null model shows that abundance provides a sufficient explanation of the asymmetry structure in some networks, but suggests the role of additional factors in others. Although not universal, our hypothesis holds for a substantial fraction of networks analyzed here, and should be considered as a null model in all studies aimed at evaluating the ecological and evolutionary consequences of species interactions.

Reviews A wealth of research has documented that various aspects of family relationships are predictably related to the quality of children's interactions and relationships with peers... This volume advances the field by discussing several mechanisms that may account for continuities across family and peer relationships. A variety of theoretical perspectives are represented in the book. Family Therapy