Publications by authors named "P Rouyer"

Article Synopsis
  • Richter syndrome (RS) represents the transformation of chronic lymphocytic leukemia (CLL) into an aggressive form of lymphoma, primarily diffuse large B-cell lymphoma (DLBCL).
  • Researchers analyzed 58 primary RS samples using DNA methylation and transcriptome profiling, leading to the identification of epigenetic patterns and a method to assess CLL-RS clonal relationships without the original CLL tumor DNA.
  • The study developed classifiers based on DNA and transcriptomic data, revealing a poor-prognosis subset of DLBCL that shares similarities with RS, highlighting the potential to improve prognosis assessment and treatment strategies for affected patients.
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Meningiomas are the most common primary tumors of the central nervous system. Based on the 2021 WHO classification, they are classified into three grades reflecting recurrence risk and aggressiveness. However, the WHO's histopathological criteria defining these grades are somewhat subjective.

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Background: epi-cblC is a recently discovered inherited disorder of intracellular vitamin B metabolism associating hematological, neurological, and cardiometabolic outcomes. It is produced by an epimutation at the promoter common to CCDC163P and MMACHC, which results from an aberrant antisense transcription due to splicing mutations in the antisense PRDX1 gene neighboring MMACHC. We studied whether the aberrant transcription produced a second epimutation by encompassing the CpG island of the TESK2 gene neighboring CCDC163P.

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Background: Although radiation therapy represents a core cancer treatment modality, its efficacy is hampered by radioresistance. The effect of ionizing radiations (IRs) is well known regarding their ability to induce genetic alterations; however, their impact on the epigenome landscape in cancer, notably at the CpG dinucleotide resolution, remains to be further deciphered. In addition, no evidence is available regarding the effect of IRs on the DNA methylome profile according to the methionine dependency phenotype, which represents a hallmark of metabolic adaptation in cancer.

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Article Synopsis
  • A study identified 14 low-frequency genetic variants linked to body mass index (BMI) in a large group of mostly European individuals.
  • The research aimed to evaluate how two genetic scores (GS) related to obesity risk, BMI changes before and after lifestyle interventions, and outcomes after bariatric surgery.
  • Findings showed that while the risk GS didn't correlate with severe obesity or pre-intervention BMI, BMI-decreasing variants were less common in obese individuals; however, the protective GS led to more significant BMI decreases after bariatric surgery and influenced the likelihood of weight regain.
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