Kotecha Nikesh, Flores Nikki J, Irish Jonathan M, Simonds Erin F, Sakai Debbie S, Archambeault Sophie, Diaz-Flores Ernesto, Coram Marc, Shannon Kevin M, Nolan Garry P, Loh Mignon L
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Cancer Cell. 2008 Oct 7;14(4):335-43. doi: 10.1016/j.ccr.2008.08.014.
Progress in understanding the molecular pathogenesis of human myeloproliferative disorders (MPDs) has led to guidelines incorporating genetic assays with histopathology during diagnosis. Advances in flow cytometry have made it possible to simultaneously measure cell type and signaling abnormalities arising as a consequence of genetic pathologies. Using flow cytometry, we observed a specific evoked STAT5 signaling signature in a subset of samples from patients suspected of having juvenile myelomonocytic leukemia (JMML), an aggressive MPD with a challenging clinical presentation during active disease. This signature was a specific feature involving JAK-STAT signaling, suggesting a critical role of this pathway in the biological mechanism of this disorder and indicating potential targets for future therapies.
在理解人类骨髓增殖性疾病(MPD)分子发病机制方面取得的进展,已促使在诊断过程中将基因检测与组织病理学相结合形成指南。流式细胞术的进步使得同时测量因基因病变而产生的细胞类型和信号异常成为可能。通过流式细胞术,我们在疑似患有青少年粒单核细胞白血病(JMML)的患者样本子集中观察到一种特定的诱发STAT5信号特征,JMML是一种侵袭性MPD,在疾病活跃期临床表现具有挑战性。这种特征是涉及JAK-STAT信号传导的一个特定特点,表明该通路在这种疾病的生物学机制中起关键作用,并为未来治疗指明了潜在靶点。