Immunobiology · 2021
Upregulation of leukemia-induced non-coding activator RNA (LUNAR1) predicts poor outcome in pediatric T-acute lymphoblastic leukemia.
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El-Khazragy Nashwa, Abdel Aziz Mahfouz A, Hesham Manar, Matbouly Safa, Mostafa Sally Abdallah, Bakkar Ashraf, Abouelnile Mariam, Noufal Yassmin, Mahran Nievin Ahmed, Abd Elkhalek Marwa Ali, Abdelmaksoud Mariam Fathy
Аннотация
T-cell Acute Lymphoblastic Leukemia (T-ALL) accounts for around 10-15% of all lymphoblastic leukemia in children. Previous studies have proven that dysregulation of Leukemia-induced non-coding activator RNA-1 (LUNAR1) expression promotes T-ALL cell growth by enhancing the NOTCH1/IGF-1R signaling pathway. We aimed to investigate the prognostic value of LUNAR1 in pediatric T-ALL, in addition, to find out its association with NOTCH1 and IGF-1R. The LUNAR1, NOTCH1, and IGF-IR gene expression were measured in peripheral blood (PB) samples of l85 children with T-ALL and forty non-leukemic samples as a control group. Cox regression analysis revealed that overexpression of LUNAR1, NOTCH1, and IGF-IR was significantly correlated with poor prognosis, short overall survival, and progression-free survival. We concluded that LUNAR1 could serve as an independent prognostic biomarker for T-ALL in children.
Предметные рубрики MeSH
Antineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCase-Control StudiesChildDisease ManagementDisease SusceptibilityFemaleGene Expression Regulation, LeukemicHumansImmunophenotypingKaplan-Meier EstimateMalePrecursor T-Cell Lymphoblastic Leukemia-LymphomaPrognosisRNA, Long NoncodingTreatment Outcome