TP53 gene chronic lymphocytic leukemia clinical biomarkers hematological parameters polymorphism 72

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2023
Historique:
received: 04 08 2023
accepted: 30 09 2023
medline: 1 11 2023
pubmed: 1 11 2023
entrez: 1 11 2023
Statut: epublish

Résumé

Genetic variations in A case-control study was conducted in Tunisia from February 2019 to November 2021, 160 Pro variant was associated with higher susceptibility to CLL than Arg variant (p= 0.023). A significant association was found between Pro variant and prognostic classification of Binet stage C (p= 0.001), low hemoglobin level (p= 0.003) and low platelet count (p= 0.016). We suggest that Pro variant may increase the risk of developing CLL in our population and could be associated with the severity of the disease.

Sections du résumé

Background UNASSIGNED
Genetic variations in
Materials and methods UNASSIGNED
A case-control study was conducted in Tunisia from February 2019 to November 2021, 160
Results UNASSIGNED
Pro variant was associated with higher susceptibility to CLL than Arg variant (p= 0.023). A significant association was found between Pro variant and prognostic classification of Binet stage C (p= 0.001), low hemoglobin level (p= 0.003) and low platelet count (p= 0.016).
Conclusion UNASSIGNED
We suggest that Pro variant may increase the risk of developing CLL in our population and could be associated with the severity of the disease.

Identifiants

pubmed: 37909012
doi: 10.3389/fonc.2023.1272876
pmc: PMC10613635
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1272876

Informations de copyright

Copyright © 2023 Ounalli, Moumni, Mechaal, Chakroun, Barmat, Rhim, Menif and Safra.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Asma Ounalli (A)

Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, University of Tunis El Manar, Tunis, Tunisia.
Faculty of Mathematics, Physics and Natural Sciences of Tunis, University of Tunis El Manar, Tunis, Tunisia.

Imen Moumni (I)

Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, University of Tunis El Manar, Tunis, Tunisia.

Amal Mechaal (A)

Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, University of Tunis El Manar, Tunis, Tunisia.
Department of Hematopoietic Biology and Malignancy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Aya Chakroun (A)

Laboratory of Hematology, Rabta Hospital, Tunis, Tunisia.

Mbarka Barmat (M)

Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, University of Tunis El Manar, Tunis, Tunisia.

Rim El Elj Rhim (REE)

Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, University of Tunis El Manar, Tunis, Tunisia.

Samia Menif (S)

Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, University of Tunis El Manar, Tunis, Tunisia.

Ines Safra (I)

Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, University of Tunis El Manar, Tunis, Tunisia.

Classifications MeSH