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Paramithiotis, E.

Publications and source records attributed to Paramithiotis, E..

2 recordsLinked to original sources

scACORN: Context-engineered agent orchestration of specialized small language models for single-cell transcriptomic interpretation

Single-cell atlases now exceed 66 million cells, but turning a ranked expression profile and a free-form biological question into a reliable, evidence-grounded answer remains unsolved. Scaling a single model does not resolve this, because single-cell interpretation is a heterogeneous family of tasks whose correct answer depends on tissue, cohort, perturbation and annotation resolution. Here we present scACORN, an agentic alternative to monolithic single-cell language models that combines specialized small language models with context-engineered agent orchestration for their selection and composition at inference time. Each expert is built in two stages: domain-aligned contrastive adaptation fits a pretrained cell-to-text backbone to the transcriptomic geometry of a target dataset, and geometry-preserving specialization learns question-conditioned biological completions without eroding that geometry. A fixed orchestrating language model agent then selects and combines experts under a natural-language playbook that is itself optimized from textual feedback, with no gradient updates to the orchestrator. Across 10 Tabula Sapiens tissues, domain alignment raised transfer macro-F1 from 0.36 to 0.64 and Recall@5 from 0.87 to 0.97; specialized experts reached 0.89 mean exact-match annotation accuracy; and playbook optimization reduced unsupported gene citations from 14.5% to 3.5%. Our findings support specialization and orchestration as complementary responses to the heterogeneity and evidentiary demands of single-cell analysis.

bioinformatics↗

Dysfunction of exocytosis causes catecholamine hypersecretion in patient with pheochromocytoma

Pheochromocytoma (Pheo) is a neuroendocrine tumor that develops from chromaffin cells of the adrenal medulla, and is responsible of an excess of catecholamines secretion leading to severe clinical symptoms such as hypertension, elevated stroke risk and various cardiovascular complications. Surprisingly, hypersecretory activity of Pheo has never been explored at the cellular and molecular levels from individual tumor cells. In the present study, we have combined catecholamine secretion measurement by carbon fiber amperometry on human tumor cells directly cultured from freshly resected Pheo, with the analysis by mass spectrometry of the exocytotic proteins differentially expressed between the tumor and the matched adjacent non-tumor tissue. Catecholamine secretion recordings from individual Pheo cells obtained from most patients reveal a higher number of exocytic events per cell associated with faster kinetic parameters. Accordingly, we unravel significant tumor-associated modifications in the expression of key proteins involved in different steps of the calcium-regulated exocytic pathway. Altogether, our findings indicate that dysfunction of the calcium-regulated exocytosis at the level of individual Pheo cell is a cause of the tumor-associated hypersecretion of catecholamines.

cancer biology↗