Evolutionary analysis of LMP-1 genetic diversity in EBV-associated nasopharyngeal carcinoma: Bioinformatic insights into oncogenic potential

被引:1
|
作者
Alanazi, Abdullah E. [1 ]
Alhumaidy, Aroob Abdullah [2 ]
Almutairi, Hatim [2 ]
Awadalla, Maaweya E. [3 ]
Alkathiri, Abdulrahman [4 ]
Alarjani, Modhi [3 ]
Aldawsari, Mesfer Abdullah [5 ]
Maniah, Khalid [6 ]
Alahmadi, Reham M. [4 ]
Alanazi, Bader S. [3 ]
Eifan, Saleh [4 ]
Alosaimi, Bandar [3 ]
机构
[1] King Fahad Med City, Comprehens Canc Ctr, Riyadh Hlth Cluster 2, Riyadh 11525, Saudi Arabia
[2] Publ Hlth Author, Publ Hlth Labs, Riyadh 13351, Saudi Arabia
[3] King Fahad Med City, Res Ctr, Riyadh Heath Cluster 2, Riyadh 11525, Saudi Arabia
[4] King Saud Univ, Coll Sci, Bot & Microbiol Dept, Riyadh 11451, Saudi Arabia
[5] Alyamamah Hosp, Dept Hlth Educ, Riyadh Heath Cluster 2, Riyadh 11525, Saudi Arabia
[6] King Khalid Mil Acad, Dept Biol, Riyadh 22140, Saudi Arabia
关键词
LMP-1; Bioinformatics; Evolution; Genetic diversity; EBV; NPC; Mutation; Variants; EPSTEIN-BARR-VIRUS; LATENT MEMBRANE PROTEIN-1; VARIANTS; SEQUENCE; METASTASIS; ACTIVATION; INDUCTION;
D O I
10.1016/j.meegid.2024.105586
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
EBV latent membrane protein 1 (LMP-1) is an important oncogene involved in the induction and maintenance of EBV infection and the activation of several cell survival and proliferative pathways. The genetic diversity of LMP1 has an important role in immunogenicity and tumorigenicity allowing escape from host cell immunity and more metastatic potential of LMP-1 variants. This study explored the evolutionary of LMP-1 in EBV-infected patients at an advanced stage of nasopharyngeal carcinoma (NPC). Detection of genetic variability in LMP-1 genes was carried out using Sanger sequencing. Bioinformatic analysis was conducted for translation and nucleotide alignment. Phylogenetic analysis was used to construct a Bayesian tree for a deeper understanding of the genetic relationships, evolutionary connections, and variations between sequences. Genetic characterization of LMP-1 in NPC patients revealed the detection of polymorphism in LMP-1 Sequences. Motifs were identified within three critical LMP-1 domains, such as PQQAT within CTAR1 and YYD within CTAR2. The presence of the JACK3 region at specific sites within CTAR3, as well as repeat regions at positions (122-132) and (133-143) within CTAR3, was also annotated. Additionally, several mutations were detected including 30 and 69 bp deletions, 33 bp repeats, and 15 bp insertion. Although LMP-1 strains appear to be genetically diverse, they are closely related to 3 reference strains: prototype B95.8, Med- 30 bp deletion, and Med + 30 bp deletion. In our study, one of the strains harboring the 30 bp deletion had both bone and bone marrow metastasis which could be attributed to the fact that LMP-1 is involved in tumor metastasis, evasion and migration of NPC cells. This study provided valuable insights into genetic variability in LMP-1 sequences of EBV in NPC patients. Further functional studies would provide a more comprehensive understanding of the molecular characteristics, epidemiology, and clinical implications of LMP-1 polymorphisms in EBV-related malignancies.
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页数:8
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