Publications by authors named "Pascal Pineau"

The persistent evolution of SARS-CoV-2 highlights the crucial role of genomic surveillance in tracking emerging variants and guiding public health interventions. We performed whole-genome sequencing on 235 SARS-CoV-2-positive samples collected across Morocco between 2021 and 2024 to characterize viral evolution and variant dynamics. Our analysis revealed a temporal shift in variant prevalence that paralleled global trends: initial co-circulation of Alpha and Delta variants, followed by complete replacement by Omicron and its sub-lineages in 2022.

View Article and Find Full Text PDF

Pierre Tiollais, a French physician-biologist, died on August 5, 2024, at 89. He is celebrated for cloning and sequencing the hepatitis B virus (HBV) genome and developing one of the first recombinant HBV vaccines. Professor at the Pasteur Institute and the University Paris VII (now University Paris Cité), Pierre Tiollais has played a key role in the application of molecular biology and genetic engineering in medical research, notably in the fight against HBV and human immunodeficiency virus (HIV).

View Article and Find Full Text PDF

Intrahepatic cholangiocarcinoma (ICA) is a highly aggressive primary liver cancer, which originates from the epithelial cells of the bile ducts. The transcriptional profile of metabolic enzymes was investigated at both bulk and single-cell levels in tumor samples from distinct ICA cohorts. In a training cohort (TCGA consortium), 16 genes encoding for metabolic enzymes were found overexpressed in cases with poor survival.

View Article and Find Full Text PDF

Background And Aims: Genetic factors, including polymorphisms in the TNFRSF13B gene, which regulates humoral immunity, can influence susceptibility to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This study aims to investigate the association between two polymorphisms, rs12603708 and rs3751987, and SARS-CoV-2 susceptibility, disease severity, and humoral immune responses in a Moroccan population.

Materials And Methods: A total of 303 unvaccinated COVID-19 patients (151 severe cases and 152 asymptomatic/moderate cases) and 150 individuals from a SARS-CoV-2-negative group were included in the analysis.

View Article and Find Full Text PDF

Medulloblastoma (MB) is the most common malignant brain tumor in children, typically arising during infancy and childhood. Despite multimodal therapies achieving a response rate of 70% in children older than 3 years, treatment remains challenging. Ferroptosis, a form of regulated cell death, can be induced in medulloblastoma cells in vitro using erastin or RSL3.

View Article and Find Full Text PDF

(1) Background: Hepatoblastoma and medulloblastoma are two types of pediatric tumors with embryonic origins. Both tumor types can exhibit genetic alterations that affect the β-catenin and Wnt pathways; (2) Materials and Methods: This study used bioinformatics and integrative analysis of multi-omics data at both the tumor and single-cell levels to investigate two distinct pediatric tumors: medulloblastoma and hepatoblastoma; (3) Results: The cross-transcriptome analysis revealed a commonly regulated expression signature between hepatoblastoma and medulloblastoma tumors. Among the commonly upregulated genes, the transcription factor LEF1 was significantly expressed in both tumor types.

View Article and Find Full Text PDF

Background: Restriction factors are host cell proteins that limit virus replication and form part of the intrinsic immune response, acting as a first line of defense. Hepatitis B virus (HBV) does not escape this rule and TREX1, a host restriction enzyme, plays a key role in inhibiting HBV replication.

Methods: TREX1-expressing constructs were generated and modified by site-directed mutagenesis.

View Article and Find Full Text PDF

Hepatoblastoma is the most common primary liver malignancy in children, with metabolic reprogramming playing a critical role in its progression due to the liver's intrinsic metabolic functions. Enhanced glycolysis, glutaminolysis, and fatty acid synthesis have been implicated in hepatoblastoma cell proliferation and survival. In this study, we screened for altered overexpression of metabolic enzymes in hepatoblastoma tumors at tissue and single-cell levels, establishing and validating a hepatoblastoma tumor expression metabolic score using machine learning.

View Article and Find Full Text PDF

Background: Hepatoblastoma, the most common pediatric liver malignancy, is characterized by significant molecular heterogeneity and poor prognosis in advanced stages. Recent studies highlight the importance of metabolic reprogramming and epigenetic dysregulation in hepatoblastoma pathogenesis. This review aims to explore the metabolic alterations and epigenetic mechanisms involved in hepatoblastoma and how these processes contribute to tumor progression and survival.

View Article and Find Full Text PDF
Article Synopsis
  • Hepatoblastoma is the most common liver cancer in kids, and poor outcomes are linked to metastases, or spread of the cancer.
  • Researchers used a database to find 41 metabolic enzymes that are overexpressed in hepatoblastoma tumors compared to healthy liver tissue and identified 18 of these enzymes that can predict whether metastasis occurs.
  • A new metabolic score based on two key enzymes was created, showing high sensitivity and specificity in predicting metastasis and confirming its role as an independent adverse predictor in combination with clinical factors.
View Article and Find Full Text PDF
Article Synopsis
  • Cranial neural crest cells play a critical role in the various transcriptional processes during developmental differentiation, particularly affecting facial formation in some animal models.
  • Changes in transcription factors like PAX7 can contribute to facial malformations, suggesting a genetic link to such disorders.
  • The study explores how epigenetic regulation and transcription factors interact in human cranial neural crest development, revealing a dynamic balance in gene regulation based on the growth stage of the neural cells.
View Article and Find Full Text PDF
Article Synopsis
  • The study investigates how genetic variations in the IFIH1 gene relate to COVID-19 susceptibility and severity among Moroccans, highlighting the importance of genetic factors in immune response to the virus.
  • Results showed that the TT genotype of the rs1990760 variant is linked to higher susceptibility to COVID-19, while the CT genotype appears to offer protective benefits against both infection and severe disease.
  • No significant association was found with another variant, rs3747517, indicating that not all genetic factors play a role in COVID-19 outcomes.
View Article and Find Full Text PDF

Background: Nucleotide-binding oligomerization domain 1 (NOD1) and NOD2 are involved in carcinogenic processes by recognizing bacterial cell wall components and triggering inflammation. This study explored the association between genetic variations in NOD1 and NOD2 and susceptibility to hepatocellular carcinoma (HCC) and its progression in a Moroccan population.

Methods: Genotyping of NOD1 rs2075820 (C>T) and NOD2 rs718226 (A>G) was performed using the TaqMan allelic discrimination assay in 467 Moroccan individuals.

View Article and Find Full Text PDF

Background: The risk of SARS-CoV-2 transmission to health care workers in intensive care units (ICU) and the contribution of airborne and fomites to SARS-CoV-2 transmission remain unclear. To assess the rate of air and surface contamination and identify risk factors associated with this contamination in patients admitted to the ICU for acute respiratory failure due to SARS-CoV-2 pneumonia.

Methods: Prospective multicentric non-interventional study conducted from June 2020 to November 2020 in 3 French ICUs.

View Article and Find Full Text PDF

Introduction: Few studies on SARS-CoV-2 seroprevalence in Ivory Coast have been conducted since the first case was reported on March 11, 2020. The main objective of this study was to observe and better understand the circulation of SARS-CoV-2 in Abidjan.

Methodology: This prospective study collected data concerning age, sex, vaccination status, municipality of origin, monthly income, frequency of malaria, and frequency of diarrheal diseases in persons who gave their informed consent.

View Article and Find Full Text PDF

Interleukin-6 (IL-6), a pro-inflammatory cytokine, is an important regulator of the inflammatory immune response. We aimed to assess the association of common single nucleotide polymorphisms (SNPs) in (rs1800795 G > C, rs1800797 A > G) and () (rs2228145 A > C) genes with HIV-1 infection, AIDS progression, and response to treatment. In this case-control study involving 199 individuals living with HIV-1 and 200 HIV-uninfected controls, we conducted genotyping of SNPs using TaqMan real-time PCR assays.

View Article and Find Full Text PDF
Article Synopsis
  • Chronic inflammation caused by hepatitis B (HBV) and C (HCV) increases interleukin 6 (IL-6) levels, which can lead to liver damage and increase the risk of developing hepatocellular carcinoma (HCC).
  • A study with 314 participants, including 157 HCC patients, found significantly higher IL-6 levels in HCC patients compared to controls, especially in those with metabolic liver disease.
  • Despite higher IL-6 levels in HCC patients, genetic variants rs1800795 and rs1800797 of the IL-6 gene did not show a significant association with the risk of developing HCC.
View Article and Find Full Text PDF
Article Synopsis
  • - This study investigates the prevalence of hepatitis B virus (HBV) in French Polynesia, where HBV infection significantly increases the risk of hepatocellular carcinoma (HCC), especially in the Austral archipelago, known for its high detection rates.
  • - Blood samples from nearly 2,000 adults were tested, revealing that 1.0% were carriers of HBV, with higher rates found specifically in certain areas like the Austral and Marquesas archipelagos. Factors such as location, age, and education level influenced HBV carriage.
  • - Although French Polynesia generally shows low HBV endemicity and low risk for hepatitis C and delta infections, the findings highlight a need for improved detection and prevention efforts, especially
View Article and Find Full Text PDF

Background: Liver resection is the mainstay treatment option for patients with hepatocellular carcinoma in the non-cirrhotic liver (NCL-HCC), but almost half of these patients will experience a recurrence within five years of surgery. Therefore, we aimed to develop a rationale-based risk evaluation tool to assist surgeons in recurrence-related treatment planning for NCL-HCC.

Methods: We analyzed single-center data from 263 patients who underwent liver resection for NCL-HCC.

View Article and Find Full Text PDF
Article Synopsis
  • Hepatocellular carcinoma (HCC) is a primary liver cancer, and the study focuses on the role of the PPARGC1A gene in HCC risk among Moroccans.* -
  • Researchers found that individuals with certain genetic variations (GA/AA) of the PPARGC1A gene had a significantly higher risk of developing HCC compared to those with the GG variant.* -
  • While one genetic variant (rs8192678) showed a strong association with HCC risk, another variant (rs12640088) did not, highlighting the potential for using rs8192678 as a marker for liver cancer prognosis.*
View Article and Find Full Text PDF

Genotype I, the penultimate HBV genotype to date, was granted the status of a bona fide genotype only in the XXIst century after some hesitations. The reason for these hesitations was that genotype I is a complex recombinant virus formed with segments from three original genotypes, A, C, and G. It was estimated that genotype I is responsible for only an infinitesimal fraction (<1.

View Article and Find Full Text PDF
Article Synopsis
  • Chronic hepatitis B virus (CHB) infection is a significant public health issue, and the study focuses on whether the PPARGC1A gene variant (Gly482Ser) affects the spontaneous clearance of HBV and chronic disease progression in Moroccan patients.
  • The research involved 292 CHB patients and 181 individuals who cleared the virus, analyzing a specific SNP (rs8192678) to assess its relationship with HBV outcomes.
  • Findings indicate that certain genotypes (CT and TT) in the rs8192678 variant are linked to higher spontaneous clearance rates, while no significant connection was found between this variant and the progression of liver disease in CHB patients.
View Article and Find Full Text PDF
Article Synopsis
  • Hepatitis A virus (HAV) is a major cause of acute hepatitis, especially in developing countries like Morocco, where many are exposed during childhood; studying circulating strains is vital for controlling outbreaks.
  • In a study of 618 suspected cases, 162 tested positive for HAV, and subsequent analyses revealed a 26.2% infection rate and a 45% viraemia rate among those tested further.
  • Phylogenetic analysis showed two circulating subgenotypes of HAV (IA and IB), with IA being the most prevalent at 87%, highlighting the genetic diversity of the virus in Morocco.
View Article and Find Full Text PDF

Hepatocellular carcinoma (HCC) is the fifth most common human malignancy and the fourth most frequent cause of cancer-related deaths worldwide. Toll-like receptors (TLRs), are known to play a key role in hepatocarcinogenesis through induction of inflammation. We aimed to investigate the association between rs3804099, rs4986790, rs4986791, and rs11536889 and 5 rs5744174 and HCC risk in a total of 306 Moroccan subjects, including 152 HCC patient and 154 controls using a TaqMan allelic discrimination assay.

View Article and Find Full Text PDF