Cell Reports · 45(10), 118145 · 27 October 2026
Publications / Selected bibliography
Evidence behind
the research.
Recent contributions and the earlier work that shaped my research, spanning cancer biology, translation, metabolism and cell regulation.
2025–2026 in focus · MET–ISR, oncogene priming, Janus and invasive growth
Read the scientific context ↗Trends Open · Opinion · Online 14 October 2026 · Corrected proof
Cancer progression as the chronic stabilization of invasive growth
Life Science Alliance · 9(3), e202503523 · March 2026; online 29 December 2025
The Janus framework of the integrated stress response: from homeostasis to maladaptation
The EMBO Journal
The integrated stress response drives MET oncogene overexpression in cancers
Scientific Reports
An mTOR feedback loop mediates the “flare” (“rebound”) response to MET tyrosine kinase inhibition
JCI Insight
Osteopontin promotes age-related adipose tissue remodeling through senescence-associated macrophage dysfunction
Cancers (Basel)
An Observatory for the MET Oncogene: A Guide for Targeted Therapies
International Journal of Molecular Sciences
The PSI Domain of the MET Oncogene Encodes a Functional Disulfide Isomerase Essential for the Maturation of the Receptor Precursor
Life Science Alliance
METΔ14 promotes a ligand-dependent, AKT-driven invasive growth
Circulation
Dysregulated Phenylalanine Catabolism Plays a Key Role in the Trajectory of Cardiac Aging
Cell Systems
Exploring Quantitative Yeast Phenomics with Single-Cell Analysis of DNA Damage Foci
Cell Reports
Rif1 controls DNA replication timing in yeast through the PP1 phosphatase Glc7
PLoS ONE
Differentially expressed androgen-regulated genes in androgen-sensitive tissues reveal potential biomarkers of early prostate cancer
Molecular Endocrinology
Direct cooperation between androgen receptor and E2F1 reveals a common regulation mechanism for androgen-responsive genes in prostate cells
Molecular and Cellular Endocrinology
Cell cycle regulated expression of NCoR might control cyclic expression of androgen responsive genes in an immortalized prostate cell line
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