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Reasoning as an Attack Surface: Adaptive Evolutionary CoT Jailbreaks for LLMs
ProActor: Timing-Aware Reinforcement Learning for Proactive Task Scheduling Agents
CODESKILL: Learning Self-Evolving Skills for Coding Agents
STREAM: A Data-Centric Framework for Mining High-Value Task-Oriented Dialogues from Streaming Media
NPSolver: Neural Poisson Solver with Iterative Physics Supervision
OASIS: Observation-Action Space Alignment via SE(3) Trajectory Prediction for Robotic Manipulation
Voting with the Graph: Stable RLAIF via Topological Consistency Maximization
PathMem: Toward Cognition-Aligned Memory Transformation for Pathology MLLMs
Topology-Driven Transferability Estimation of Medical Foundation Models for Segmentation
Cooperative Memory Paging with Keyword Bookmarks for Long-Horizon LLM Conversations
Depth Registers Unlock W4A4 on SwiGLU: A Reader/Generator Decomposition
Copy-as-Decode: Grammar-Constrained Parallel Prefill for LLM Editing
Committed SAE-Feature Traces for Audited-Session Substitution Detection in Hosted LLMs
Chain of Evidence: Pixel-Level Visual Attribution for Iterative Retrieval-Augmented Generation
Exploring the prognostic role of senescence-related genes in gastric cancer through multi-omics integration and machine learning
Hum Genomics. 2026 May 9. doi: 10.1186/s40246-026-00979-y. Online ahead of print.
ABSTRACT
Cellular senescence plays a context-dependent role in gastric cancer (GC), functioning both through tumor-suppressive arrest and the tumor-promoting senescence-associated secretory phenotype. However, its systematic integration into prognostic models remains limited. Here, we develop a novel interpretable framework to identify and validate a robust senescence-related gene signature for GC prognosis. We first introduce a dual-model interpretable feature selection strategy that integrates a biologically informed Kolmogorov-Arnold Network with a tabular foundation model to identify cancer-associated senescence genes. From the initial candidates, an ensemble of ten machine learning algorithms distills a core 4-gene signature to construct a Senescence Risk Score (SRS). The SRS proves to be a powerful and independent prognostic indicator, effectively stratifies patients into high- and low-risk groups with distinct overall survival across multiple cohorts. High-risk patients exhibit an "immune-hot" but potentially dysfunctional tumor microenvironment, characterized by enriched immune cell infiltration, elevated checkpoint expression, and distinct metabolic reprogramming favoring pathways such as angiogenesis and epithelial-mesenchymal transition (EMT). Furthermore, the SRS correlates with differential somatic mutation profiles and suggests potential sensitivity to specific chemotherapeutic agents. In vitro functional assays confirmed the oncogenic role of SERPINE1, a top-ranked core gene, in promoting GC cell proliferation. Regulatory network analysis revealed potential upstream transcription factors and miRNAs governing the signature. Collectively, we present a validated senescence-related prognostic signature that enables effective risk stratification of patients with gastric cancer.
PMID:42106891 | DOI:10.1186/s40246-026-00979-y
XPO1 inhibitor KPT-330 disrupts the core transcriptional regulatory circuitry of dedifferentiated liposarcoma by modulating the translation process
Oncogene, Published online: 16 April 2026; doi:10.1038/s41388-026-03794-w
XPO1 inhibitor KPT-330 disrupts the core transcriptional regulatory circuitry of dedifferentiated liposarcoma by modulating the translation process