본문으로 건너뛰기
← 뒤로

Status of IKZF1 Deletions in Diagnose and Relapsed Pediatric B-ALL Patients.

1/5 보강
Biochemical genetics 📖 저널 OA 14.2% 2026 Vol.64(1) p. 152-167
Retraction 확인
출처

Erbilgin Y, Firtina S, Kirat E, Khodzhaev K, Karakas Z, Ünüvar A, Ocak S, Celkan TT, Zengin E, Aylan Gelen S, Yildirmak ZY, Toluk O, Hatirnaz Ng O, Ozbek U, Sayitoglu M

📝 환자 설명용 한 줄

IKZF1 deletions (ΔIKZF1) are common in precursor B-cell acute lymphoblastic leukemia (B-ALL) and are assumed to have a prognostic impact.

이 논문을 인용하기

↓ .bib ↓ .ris
APA Erbilgin Y, Firtina S, et al. (2026). Status of IKZF1 Deletions in Diagnose and Relapsed Pediatric B-ALL Patients.. Biochemical genetics, 64(1), 152-167. https://doi.org/10.1007/s10528-024-11018-7
MLA Erbilgin Y, et al.. "Status of IKZF1 Deletions in Diagnose and Relapsed Pediatric B-ALL Patients.." Biochemical genetics, vol. 64, no. 1, 2026, pp. 152-167.
PMID 39786526

Abstract

IKZF1 deletions (ΔIKZF1) are common in precursor B-cell acute lymphoblastic leukemia (B-ALL) and are assumed to have a prognostic impact. We aimed to determine the prognostic implications of ΔIKZF1 and CRLF2 overexpression in pediatric B-ALL. Furthermore, we sought to compare the multiplex polymerase chain reaction (PCR) assay with standard multiplex ligand-dependent probe amplification (MLPA) methods to ascertain IKZF1 status in a clinical context. Seventy-nine diagnoses and 43 relapse B-ALL samples were evaluated for deletions of IKZF1 Δ2-7, Δ4-7, and Δ4-8 by conventional PCR and then sequenced by targeted sequencing. Subsequently, MLPA analysis was performed for ΔIKZF1 detection, and CRLF2 expression was evaluated in 42 diagnose time B-ALL patients by QRT-PCR. ΔIKZF1 was detected in 10 out of 79 diagnose samples (12.66%) and eight of the 43 first relapsed materials (18.60%). Our results revealed no association between survival outcomes with ΔIKZF1 or CRLF2 overexpression status in pediatric B-ALL patients. However, we found ΔIKZF1 was more frequent among relapsed samples, and the deletions showed consistency between diagnose-first/second relapse pairs of samples. These results suggest that ΔIKZF1 may contribute to the development of treatment failure in B-ALL. Furthermore, we demonstrated methodological adjustments in conventional PCR and MLPA for selected alterations in ΔIKZF1.

🏷️ 키워드 / MeSH