Comprehensive detection of CRLF2 alterations in acute lymphoblastic leukemia: a rapid and accurate novel approach

被引:5
作者
Gil, Jose Vicente [1 ]
Miralles, Alberto [1 ]
de las Heras, Sandra [1 ]
Such, Esperanza [1 ,2 ,3 ]
Avetisyan, Gayane [1 ]
Diaz-Gonzalez, Alvaro [1 ]
Santiago, Marta [1 ]
Fuentes, Carolina [4 ,5 ]
Fernandez, Jose Maria [4 ,5 ]
Lloret, Pilar [1 ,2 ]
Navarro, Irene [1 ,2 ]
Montesinos, Pau [1 ,2 ]
Llop, Marta [1 ,3 ,6 ]
Barragan, Eva [1 ,3 ,6 ]
机构
[1] Inst Invest Sanitaria La Fe, Accredited Res Grp Hematol, Valencia, Spain
[2] Hosp Univ & Politecn La Fe, Hematol Serv, Valencia, Spain
[3] Inst Salud Carlos III, Ctr Invest Biomed Red Canc, CIBERONC CB16 12 00284, Madrid, Spain
[4] Inst Invest Sanitaria La Fe, Accredited Res Grp Clin & Translat Canc Res, Valencia, Spain
[5] Hosp Univ & Politecn La Fe, Pediat Serv, Oncohematol Unit, Valencia, Spain
[6] Hosp Univ & Politecn La Fe, Clin Anal Serv, Mol Biol Unit, Valencia, Spain
关键词
acute lymphoblastic leukemia; Ph-like ALL; CRLF2; overexpression; variants; JAK2; RT-qPCR-SYBR-HRM; RESIDUAL DISEASE; EXPRESSION; IKZF1; GENE; JAK; MUTATIONS; FUSION;
D O I
10.3389/fmolb.2024.1362081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Acute lymphoblastic leukemia (ALL) is a prevalent childhood cancer with high cure rate, but poses a significant medical challenge in adults and relapsed patients. Philadelphia-like acute lymphoblastic leukemia (Ph-like ALL) is a high-risk subtype, with approximately half of cases characterized by CRLF2 overexpression and frequent concomitant IKZF1 deletions. Methods: To address the need for efficient, rapid, and cost-effective detection of CRLF2 alterations, we developed a novel RT-qPCR technique combining SYBR Green and highresolution melting analysis on a single plate. Results: The method successfully identified CRLF2 expression, P2RY8::CRLF2 fusions, and CRLF2 and JAK2 variants, achieving a 100% sensitivity and specificity. Application of this method across 61 samples revealed that 24.59% exhibited CRLF2 overexpression, predominantly driven by IGH::CRLF2 (73.33%). High Resolution Melting analysis unveiled concurrent CRLF2 or JAK2 variants in 8.19% of samples, as well as a dynamic nature of CRLF2 alterations during disease progression. Discussion: Overall, this approach provides an accurate identification of CRLF2 alterations, enabling improved diagnostic and facilitating therapeutic decision-making.
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