Kronik Lenfositik Lösemi Olgularında NOTCH1 Gen Amplifikasyonu

Yıl 2024, Cilt: 46 Sayı: 1, 104 - 109, 16.01.2024

Sevgi Işık , Gülçin Günden , Nur Oguz Davutoglu , Hülya Özen , Ebru Erzurumluoğlu , Oğuz Çilingir , Sevilhan Artan , Eren Gunduz , Beyhan Durak Aras

https://doi.org/10.20515/otd.1329205

Öz

Kronik lenfositik lösemi (KLL) ileri yaş hastalarda en sık gözlenen lösemi türü olup, hem klinik hem de genetik açıdan oldukça heterojen bir hastalıktır. Kronik lenfositik lösemi de tekrarlayan kromozom anomalilerinin prognostik önemleri uzun yıllardır bilinmekte olup, gen mutasyonlarının da klinik önemleri açığa kavuşmaya başlamıştır. NOTCH1 gen mutasyonları KLL’de en sık mutasyon gözlenen gen olup, tedavi direnci ve Richter Sendromuna dönüşüm ile ilişkilendirilmektedir. Son yıllarda yapılan çalışmalarda NOTCH1 gen amplifikasyonları çeşitli kanser tiplerinde raporlanmıştır. Bizim daha önce izole delesyon 13q saptanan KLL vakaları ile yaptığımız bir çalışmada NOTCH1 gen dizisini içeren kopya sayısı artışları mikroarray yöntemi ile saptanmıştır ancak klinik bulgular ile ilişkilendirilmemiştir. Biz de bu çalışmamızda çeşitli kromozomal anomalilere sahip ve daha fazla KLL olgusuna ait periferik kan örneklerinde NOTCH1 gen kopya sayısı artışlarını FISH yöntemi ile incelemeyi ve KLL’nin klinik heterojenitesinde NOTCH1 amplifikasyonunun etkisini araştırmayı amaçladık. Çalışmaya dahil edilen 130 KLL vakasının 4’ünde FISH çalışması başarısızlıkla tamamlanmış olup, geriye kalan 126 olgunun hiçbirinde NOTCH1 gen kopya sayısı değişikliği tespit edilmemiştir. Çalışmamız sonucunda KLL’nin klinik heterojenitesinde NOTCH1 gen amplifikasyonlarının bir etkisi olmadığı sonucuna varılmıştır. Ancak olgu grubumuzun büyük kısmının, iyi prognostik etkiye sahip sitogenetik belirteçlere sahip olması sebebiyle, kötü klinik seyre sahip, daha fazla sayıda KLL vakalarında NOTCH1 gen kopya sayısının araştırılması gerekmektedir.

Anahtar Kelimeler

KLL, FISH, NOTCH1 gen amplifikasyonu

Destekleyen Kurum

Eskişehir Osmangazi Üniversitesi Bilimsel Araştırmalar Projeleri (BAP)

Proje Numarası

TSA-2021-1668

NOTCH1 Gene Amplification in Chronic Lymphocytic Leukemia

Öz

Chronic lymphocytic leukemia (CLL) is the most common type of leukemia observed in elderly patients and is a highly heterogeneous disease both clinically and genetically. The prognostic significance of recurrent chromosomal abnormalities in chronic lymphocytic leukemia has been known for many years, and the clinical significance of gene mutations has begun to emerge. NOTCH1 gene mutations are the most frequently mutated gene in CLL and are associated with treatment resistance and conversion to Richter Syndrome. In recent studies, NOTCH1 gene amplifications have been reported in various cancer types. In a study we conducted with CLL cases with isolated deletion 13q, copy number increases containing the NOTCH1 gene sequence were detected by microarray method, but they were not associated with clinical findings.In this study, we aimed to examine the NOTCH1 gene copy number increases in peripheral blood samples of more CLL cases with various chromosomal anomalies by FISH method and to investigate the effect of NOTCH1 amplification on the clinical heterogeneity of CLL. FISH study was completed unsuccessfully in 4 of 130 CLL cases included in the study, and NOTCH1 gene copy number changes were detected in any of the remaining 126 cases. As a result of our study, it was concluded that NOTCH1 gene amplifications have no effect on the clinical heterogeneity of CLL. However, since most of our case group has cytogenetic markers with good prognostic effect, it is necessary to investigate the NOTCH1 gene copy number in more CLL cases with poor clinical course.

Anahtar Kelimeler

CLL, FISH, NOTCH! gene amplifications

Proje Numarası

TSA-2021-1668

Kaynakça

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