ABCC Gene Variants and Their Effects on Non-Response and Relapse in Pediatric Patients with Central Nervous System Tumors: A Cohort Study
Luz María Torres-Espíndola, Juan Carlos Pérez-De Marcos, Manuel de Jesús Castillejos-López, Arnoldo Aquino-Gálvez, Liliana Velasco-Hidalgo, Rocío Cárdenas-Cardós, Armando De Uña-Flores, Marta Zapata-Tarrés, Anjartah Higuera-Iglesias

TL;DR
This study finds that specific genetic variants in ABCC1 and ABCC2 genes are linked to poor treatment response and higher relapse risk in children with brain tumors.
Contribution
The study identifies novel associations between ABCC1 and ABCC2 gene variants and clinical outcomes in pediatric CNS tumor patients.
Findings
ABCC1 r.5540 G>C variant is significantly associated with non-response and relapse in pediatric CNS tumor patients.
ABCC2 c.3972 C>T variant is significantly linked to relapse in a recessive model.
Multivariate analysis confirms the predictive value of these SNVs after adjusting for age and sex.
Abstract
The variability in outcomes among individuals is caused by multiple factors, including genetic variations in drug transporter genes known as ABCs. This study investigates the clinical effect of single-nucleotide variants (SNVs) in the ABCC1/MRP1, ABCC2/MRP2, and ABCC4/MRP4 genes on the clinical response and relapse of pediatric patients with central nervous system tumors. In a cohort-based association study involving 111 cancer patients, genotyping of ABCC1/MRP1, ABCC2/MRP2, and ABCC4/MRP4 was conducted using real-time PCR with TaqMan probes. Treatment response was evaluated using the Response Assessment in Neuro-Oncology (RANO) criteria. Univariate and multivariate analyses were conducted using the Cox proportional hazards (adjusted) model. Multivariate analysis adjusted for sex and age showed a significant association between ABCC1 r.5540out G>C; rs12921623 in the gene and…
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Taxonomy
TopicsDrug Transport and Resistance Mechanisms · Glioma Diagnosis and Treatment · Ferroptosis and cancer prognosis
