Functional variants of TIM-3/HAVCR2 3'UTR in lymphoblastoid cell lines
- PMID: 29796301
- PMCID: PMC5961449
- DOI: 10.4155/fsoa-2017-0121
Functional variants of TIM-3/HAVCR2 3'UTR in lymphoblastoid cell lines
Abstract
Aim: Variants of TIM-3/HAVCR2 3'UTR miRNA binding sites are significantly associated with cancer; however, roles in post-transcriptional regulation have not been elucidated.
Methods: The regulatory and coding region single nucleotide polymorphisms (SNPs) of TIM-3/HAVCR2 were identified using an online database. Single nucleotide polymorphism Function Prediction was used to predict potential functional relevance of miRNA binding sites.
Results: The analysis indicated rs9313439, rs4704846, rs3087616 and rs1036199 affect possible miRNA binding sites in TIM-3/HAVCR2 3'UTR. We used additional data on genotypes and limited minor allele frequency >5% in the HapMap populations. Only rs3087616 and rs4704846 were significantly associated with TIM-3/HAVCR2.
Conclusion: Both rs3087616 and rs4704846 could be putative variants mediating post-transcriptional regulation of the TIM-3/HAVCR2. Deeper understanding of how 3'UTR variants influence the activity by TIM-3/HAVCR2 for therapy against cancer.
Keywords: TIM-3/HAVCR2; genetic; miRNA; polymorphism; variant.
Conflict of interest statement
Financial & competing interests disclosure This work is supported by Grants from the Clinical Medical Research Project of Wuhan (number WX17Q38) and the Funded Research Project of Wuhan No.1 Hospital, Wuhan Integrated TCM & Western Medicine Hospital (number 2017Y01). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. No writing assistance was utilized in the production of this manuscript.
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