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LR24ES15: Laboratory of Clinical and Molecular Biology


LR24ES15

 
BioCliMol
Laboratory of Clinical and Molecular Biology
Code: LR24ES15
Director: Prof. Salima Ferchichi
 
 
Name of the laboratory  Clinical and Molecular Biology
Acronym  BioCliMol
LR Code  LR24ES15
Director of the laboratory  Pr. Salima Ferchichi
Discipline  Biochemistry
 
 
Who are we?
 
The Laboratory of Clinical and Molecular Biology – LR24ES15, directed by Professor Salima Ferchichi, was created in 2024, following the evolution of the research unit UR17ES29 founded in 2017. This laboratory brings together a multidisciplinary team composed of clinicians, researchers, engineers and bioinformaticians, working together to explore the complex biological mechanisms related to various human pathologies. Anchored in an integrated approach, the laboratory combines expertise in molecular biology, genomics, epigenetics and artificial intelligence. The research carried out focuses on five complementary areas: the study of lysosomal storage diseases in Tunisia, with a focus on specific mutations and metabolic abnormalities; personalized therapy for metastatic colorectal cancer, integrating molecular biomarkers, monoclonal antibodies and antagomiRs; the identification of epigenetic factors and predictive biomarkers associated with autism spectrum disorder; the analysis of epigenetic modifications and non-coding RNAs in recurrent spontaneous abortions; and the use of bioinformatics approaches for the analysis of genetic variants and the prediction of their functional impacts on protein stability and molecular interactions. This collaborative and thematic dynamic gives the laboratory a strong identity in the service of innovative and relevant biomedical research.
 
Research Areas
Topic I: Frequency, metabolic abnormalities and specific mutations of lysosomal storage diseases in Tunisia
Topic II: Personalized therapy for metastatic colorectal cancer: AI approach integrating molecular biomarkers, monoclonal antibodies, and antagomiR
Topic III: Epigenetic factors and molecular biomarkers predictive of autism spectrum disorder
Topic IV: Impact of epigenetic modifications and non-coding RNAs in the etiopathogenesis of recurrent spontaneous abortions
Topic V: Bioinformatic approaches for the analysis of genetic variants and the prediction of functional impacts on protein stability and molecular interactions.
 
 
Topic 1: Frequency, metabolic abnormalities and specific mutations of lysosomal storage diseases in Tunisia
•Axis 1.1. : Frequency and distribution of lysosomal storage diseases in Tunisia: Study the incidence of these diseases at the national level and their geographical distribution, in relation to genetic and environmental factors.
• Axis 1.2: Metabolic abnormalities associated with mucopolysaccharidoses and oligosaccharidoses: Analyze specific metabolic profiles and underlying mechanisms, with a focus on diagnostic biomarkers and clinical implications.
• Axis 1. 3: Identification and comparison of genetic mutations specific to the Tunisian population: Identify mutations related to lysosomal storage diseases in the Tunisian population and compare them with those observed in other populations, highlighting local particularities.
  Name Rank Email addresses
Project Chief  Salima Ferchichi Professor trimechesaly@yahoo.fr
Involved Researchers Yosra Hasni Professor y.hasni@gmail.com
Amina Bouatay Professor amina bouatayamina@yahoo.fr
Wael Bahia Assistant Professor bahiawael@gmail.com
Nadia Leban Assistant Professor lebannadia@yahoo.fr
Akram Alaya Assistant Professor akram_alaya@yahoo.co.uk
Azza Dendana Post-Doc azzadandana@yahoo.fr
Involved students Nouhé Alimi PhD student Aliminouha12@gmail.com
     
 
 
Topic 2: Personalized therapy for metastatic colorectal cancer: AI approach integrating molecular biomarkers, monoclonal antibodies, and antagomir
Axis I: Identification and validation of molecular biomarkers in metastatic colorectal cancer
Study molecular biomarkers specific to metastatic colorectal cancer, such as genetic mutations, transcriptomic and proteomic alterations, in order to better understand their role in tumor progression and response to treatments. This approach includes the use of techniques like next generation sequencing and mass spectrometry to identify prognostic and theranostic molecular signatures.
 
Axis II: Application of artificial intelligence and design of decision support systems for treatment personalization
Using artificial intelligence (AI) tools, such as neural networks and machine learning algorithms, to analyze complex biomolecular data from metastatic colorectal cancer. This approach allows for the prediction of individual therapeutic responses based on the molecular profiles of tumors. Moreover, the design of decision support systems, based on these analyses, would guide clinicians in choosing the most suitable treatment for each patient, thus optimizing therapeutic effectiveness and reducing the risks of ineffective treatments.
 
 • Axis III: Development of monoclonal antibodies targeting key molecular pathways.
Explore the use of monoclonal antibodies to target specific molecular pathways involved in metastatic colorectal cancer progression, such as those related to growth receptor signaling and immune evasion. This work includes the identification of potential therapeutic targets and the optimization of monoclonal antibodies to improve the efficiency and specificity of treatment.
 
Axis IV: Role of antagomiR in modulating gene expression and controlling tumor progression
Study the use of antagomiRs (microRNAs inhibitors) to target miRNAs involved in the regulation of metastatic progression of colorectal cancer. This therapeutic approach would restore altered genetic regulatory pathways and prevent resistance to treatments, offering a new path for personalized therapy.
 
  Name Rank Email adress
Project Chief  Wael Bahia Assistant Professor  
Involved Researchers Salima Ferchichi Professor trimechesaly@yahoo.fr
Yosra Hasni Professor y.hasni@gmail.com
Henda Chahed Professor hendchahed05@gmail.com
Nadia Leban Assistant Professor lebannadia@yahoo.fr
Akram Alaya Assistant Professor akram_alaya@yahoo.co.uk
Ismael Soltani Post-Doc soltaniismael@yahoo.fr
Azza Dendana Post-Doc azzadandana@yahoo.fr
Involved Students Nouhé Alimi PhD student Aliminouha12@gmail.com
     
 
 
 
 
Topic 3: Epigenetic factors and molecular biomarkers predictive of autism spectrum disorder
 
• Axis 1: Study of epigenetic modifications associated with autism
This axis explores the epigenetic mechanisms, in particular DNA methylation, histone modification and the action of non-coding RNAs, which could influence the expression of genes involved in autism spectrum disorders (ASD). The objective is to identify characteristic epigenetic profiles of patients.
 
• Axis 2: Identification of early molecular biomarkers
It is about looking for detectable biomarkers (RNA, proteins, metabolites) in blood or other biological fluids, allowing early detection of ASD. The challenge is to facilitate diagnosis before the appearance of obvious clinical signs.
 
• Axis 3: Correlation between environmental factors and epigenetic alterations
This axis aims to study how environmental factors (pollutants, diet, prenatal stress) can induce epigenetic changes likely to modulate the risk of developing ASD. It highlights the gene-environment interaction.
 
• Axis 4: Development of predictive bioinformatics models
The objective is to build predictive models using multi-omics data (epigenomic, transcriptomic, proteomic) and artificial intelligence, in order to anticipate the probability of ASD in an individual. This paves the way for personalized medicine.
  Name Rank Email addresses
Project Chief  Nadia Leban Assistant Professor  
Involved Researchers Salima Ferchichi Professor trimechesaly@yahoo.fr
Yosra Hasni Professor y.hasni@gmail.com
Henda Chahed Professor hendchahed05@gmail.com
Wael Bahia Assistant Professor bahiawael@gmail.com
Akram Alaya Assistant Professor akram_alaya@yahoo.co.uk
Ismael Soltani Post-Doc soltaniismael@yahoo.fr
Sinda Slama Post-Doc slama.sinda@gmail.com
Azza Dendana Post-Doc azzadandana@yahoo.fr
Involved Students Malek Dargouthi PhD student malekdargouthi@gmail.com
     
 
 
Theme 4: Impact of epigenetic modifications and non-coding RNAs in the etiopathogenesis of recurrent spontaneous abortions
• Axis 1: Analysis of DNA methylation profiles in endometrial tissues
This axis aims to study alterations in DNA methylation at the level of genes involved in embryonic implantation and immune tolerance. These modifications could disrupt the maternal-fetal dialogue and promote early gestational loss.
 
• Axis 2: Role of microRNAs in the regulation of key pregnancy genes
This component focuses on the identification of microRNAs (miRNAs) that are overexpressed or underexpressed in women with a history of recurrent spontaneous abortions. These small regulatory RNAs can modulate the expression of genes essential for embryonic survival.
 
• Axis 3: Study of long non-coding RNAs in uterine remodeling
This axis explores the function of lncRNAs in processes of decidual transformation, vascularization and embryonic reception. A deregulation of these non-coding RNAs could compromise the preparation of the uterus for implantation.
 
• Axis 4: Influence of epigenetic factors on maternal immunity
This last axis examines how epigenetic modifications influence the differentiation of immune cells (such as uterine NK cells or regulatory T cells), essential for fetal tolerance. An immune imbalance could be the cause of recurrent abortions.
  Name Rank Email addresses
Project Chief  Yosra Hasni Professor y.hasni@gmail.com
Involved Researchers Salima Ferchichi Professor trimechesaly@yahoo.fr
Anis Haddad Professor  
Henda Chahed Professor hendchahed05@gmail.com
Nadia Leban Assistant Professor lebannadia@yahoo.fr
Akram Alaya Assistant Professor akram_alaya@yahoo.co.uk
Wael Bahia Assistant Professor bahiawael@gmail.com
Ismael Soltani Post-Doc soltaniismael@yahoo.fr
Azza Dendana Post-Doc azzadandana@yahoo.fr
Involved Students Oumaima Takrouni PhD student oumaymatakrouni43@gmail.com
     
 
 
Theme 5: Bioinformatic approaches for the analysis of genetic variants and the prediction of functional impacts on protein stability and molecular interactions.
• Axis 1: Detection and functional annotation of genetic variants
This component aims to identify mutations from sequencing data (WES/WGS) and annotate them using bioinformatics tools such as ANNOVAR or VEP. The objective is to distinguish pathogenic variants from benign variants.
 
• Axis 2: Structural modeling of the effects of variants on protein stability
This axis focuses on predicting the impact of non-synonymous mutations on the three-dimensional structure and stability of proteins using software like FoldX, I-Mutant or AlphaFold. This allows understanding potential functional alterations.
 
• Axis 3: Analysis of molecular interactions affected by mutations
The objective here is to evaluate how variants can disrupt protein-protein or protein-DNA interactions. Tools like HADDOCK, ClusPro or PyMOL allow to simulate and visualize the modifications in interaction networks.
 
• Axis 4: Integration of multi-omics data for global functional prediction
This axis proposes to combine genomic, transcriptomic and proteomic data in integrated bioinformatics pipelines. Multi-level analysis allows for a more precise evaluation of the biological consequences of a genetic variant
  Name Rank Email addresses
Project Chief  Wael Bahia Assistant Professor bahiawael@gmail.com
Involved Researchers Salima Ferchichi Professor trimechesaly@yahoo.fr
Yosra Hasni Professor y.hasni@gmail.com
Henda Chahed Professor hendchahed05@gmail.com
Nadia Leban Assistant Professor lebannadia@yahoo.fr
Akram Alaya Assistant Professor akram_alaya@yahoo.co.uk
Ismael Soltani Post-Doc soltaniismael@yahoo.fr
Azza Dendana Post-Doc azzadandana@yahoo.fr
Involved students Nouhé Alimi PhD student Aliminouha12@gmail.com
     
 
 
 
 
Mastered Techniques
 
Molecular Biology Techniques
• DNA, RNA and protein extraction from various biological samples
• PCR, RT-PCR, qPCR (quantitative PCR)
• multiplex PCR and allele-specific PCR
• Sanger sequencing
• Next generation sequencing (NGS): library preparation, targeted panel analysis
• Electrophoresis on agarose and polyacrylamide gel
Genetic and epigenetic analysis techniques
• DNA methylation: bisulfite sequencing, MS-PCR
• Analysis of histonic modifications (ChIP-qPCR, ChIP-seq)
• Profiling of non-coding RNAs (miRNA, lncRNA) by RT-qPCR or NGS
• Variant genotyping by HRM or TaqMan
• Differential gene expression assay
Proteomics and Immunology Techniques
• Western blot
• ELISA
• Immunoprecipitation
• Immunohistochemistry (IHC)
 
Bioinformatics and data analysis
• Sequencing data analysis (NGS): alignment, variant call, annotation (BWA, GATK, ANNOVAR)
• Prediction of the effect of mutations on protein structure and stability (PolyPhen, SIFT, I-Mutant)
• Gene network visualization and annotation tools (Cytoscape, STRING)
• Differential expression analysis (DESeq2, EdgeR)
• AI tools applied to biomarker classification (R, Python, Scikit-learn
 
Equipements
• PCR systems (Thermocyclers)
• qPCR (real-time PCR)
• Gel electrophoresis + UV/LED transilluminator
• Gel documentation system
• Nanodrop / Spectrophotometer for the quantification of nucleic acids
• Refrigerated centrifuges
• Water bath, agitators, vortex
• Optical microscopes
• Freezers -20°C and -80°C
• Complete Western blot system
• ELISA microplate reader
 

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