作者
Yu-Ting Dai,Fan Zhang,Hai Fang,Jinfu Li,Gang Lu,Lu Jiang,Bing Chen,Dong-Dong Mao,Yuan-Fang Liu,Jin Wang,Li-Jun Peng,Chong Feng,Hai-Feng Chen,Jun-Xi Mu,Qun-Ling Zhang,Hao Wang,Hany Ariffin,Tan Ah Moy,Jing-Han Wang,Yinjun Lou,Su-Ning Chen,Qian Wang,Hong Liu,Zhe Shan,Itaru Matsumura,Yasushi Miyazaki,Takahiko Yasuda,Li-Ping Dou,Xiao-Jing Yan,Jin-Song Yan,Allen Eng-Juh Yeoh,Depei Wu,Hitoshi Kiyoi,Fumihiko Hayakawa,Jie Jin,Sheng-Yue Wang,Xiao-Jian Sun,Jian-Qing Mi,Jin-Yan Huang,Sai Juan Chen
摘要
Significance We provide transcriptomic insights into differences between pediatric and adult T cell acute lymphoblastic leukemia (T-ALL) patients through an international collaborative effort integrating RNA-sequencing data of 707 patients. Ten subtypes were identified, each characterized by distinct gene mutation profiles and dysregulated expression signatures of leukemogenic factors, and associated with T cell development stages. Adult T-ALL tends to have characteristics of early T cell precursor ALL, mostly corresponding to the mixed phenotype acute leukemia, whereas pediatric T-ALL shows a wide spectrum of aberrant molecular features, from early T cell precursor to mature T cell compartments. Our findings have important implications for disease mechanism of T-ALL that differs between pediatric and adult patients, facilitating further refined targeted therapy.