CCR5 and CXCL12 allelic variants: Possible association with childhood neuroblastoma susceptibility?

Neuroblastoma (NB) is a heterogeneous and particularly malignant childhood neoplasm in its higher stages, prone to form metastasis in selected organs and for which there is still no efficient treatment available beyond surgery. Evidence indicates that chemokines and their receptors present involveme...

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Veröffentlicht in:Journal of neuroimmunology 2020-05, Vol.342, p.577193-577193, Article 577193
Hauptverfasser: Vieira-Filho, Daniel Rubens Marques, Amarante, Marla Karine, Ishibashi, Cyntia Mayumi, Ariza, Carolina Batista, Vitiello, Glauco Akelinghton Freire, de Oliveira, Karen Brajão, Guembarovski, Roberta Losi, Watanabe, Maria Angelica Ehara
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Sprache:eng
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Zusammenfassung:Neuroblastoma (NB) is a heterogeneous and particularly malignant childhood neoplasm in its higher stages, prone to form metastasis in selected organs and for which there is still no efficient treatment available beyond surgery. Evidence indicates that chemokines and their receptors present involvement as mediators of neuroinflammation and have a neurophysiological role. In the present study, we aimed to verify if CCR5 (rs333) and CXCL12 (rs1801157) allelic variants were associated with NB. For CCR5 (rs333) D32 carriers (OR: 5.96, IC: 2.21–16.06) and for CXCL12 genotype 3′A/3′A (OR:26.18, IC:6.15–111.4) there were statistically significant differences as well to allelic frequency (OR:4.20, IC: 2.19–8.03). Although no correlation was verified regarding prognostic parameters for both CCR5 and CXCL12 polymorphic variants, these polymorphisms may be associated with NB susceptibility which deserve attention for future investigations. [Display omitted] •Neuroblastoma (NB) is a heterogeneous, and malignant childhood neoplasm.•Chemokines and their receptors present involvement as mediators of neuroinflammation.•The CCR5 (rs333) and CXCL12 (rs1801157) allelic variants were associated with NB.•No correlation was verified regarding prognostic parameters for CCR5 and CXCL12.
ISSN:0165-5728
1872-8421
DOI:10.1016/j.jneuroim.2020.577193