Chi Hoang Thanh, Ly Bui Thi Kim, Vu Hoang Anh, Sato Yuko, Dung Phu Chi, Xinh Phan Thi
Department of Molecular Cytogenetics, Blood Transfusion and Hematology Hospital Ho Chi Minh City, Ho Chi Minh City 711512, Vietnam.
Department of Medical Genome Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo 108‑8639, Japan.
Mol Med Rep. 2015 May;11(5):3969-75. doi: 10.3892/mmr.2015.3203. Epub 2015 Jan 15.
Acute myeloid leukemia (AML) is a heterogeneous disease. Numerous molecular abnormalities have been identified in AML and, amongst these, FMS‑like tyrosine kinase 3 (FLT3) mutations are one of the most common somatic alterations detected. In the present study, an in vitro investigation was performed to evaluate the effects of all‑trans retinoic acid (ATRA) and PKC412, alone and in combination, in FLT3‑mutated AML cell lines. Trypan blue exclusion test, as well as morphological, western blot and isobologram analyses were conducted. The results indicated that the combined ATRA and PKC412 treatment exhibited additive or synergistic effects in FLT3‑mutated AML cell lines. These results provided in vitro evidence for the future clinical trials evaluating the effects of a combination treatment using PKC412 and ATRA on AML patients with FLT3‑mutations.
急性髓系白血病(AML)是一种异质性疾病。在AML中已鉴定出众多分子异常,其中FMS样酪氨酸激酶3(FLT3)突变是检测到的最常见的体细胞改变之一。在本研究中,进行了一项体外研究,以评估全反式维甲酸(ATRA)和PKC412单独及联合使用对FLT3突变的AML细胞系的影响。进行了台盼蓝排斥试验以及形态学、蛋白质印迹和等效线图分析。结果表明,ATRA和PKC412联合治疗在FLT3突变的AML细胞系中表现出相加或协同作用。这些结果为未来评估PKC412和ATRA联合治疗对FLT3突变的AML患者疗效的临床试验提供了体外证据。