Dual inhibition of EZH1/2 induces cell cycle arrest of B cell acute lymphoblastic leukemia cells through upregulation of CDKN1C and TP53INP1

• Published in: International journal of hematology 2023, Vol.117 (1), p.78-89
• Main Authors: Ito, Jumpei, Yamagata, Kazutsune, Shinohara, Haruka, Shima, Yutaka, Katsumoto, Takuo, Aikawa, Yukiko, Kitabayashi, Issay
• Format: Article
• Language: English
• Subjects: Acute lymphoblastic leukemia; Animals; Anticancer properties; Antitumor activity; Apoptosis; Burkitt Lymphoma; Carrier Proteins - genetics; Cell cycle; Cell Cycle Checkpoints - genetics; Chemotherapy; Cyclin-Dependent Kinase Inhibitor p57 - genetics; Cyclin-Dependent Kinase Inhibitor p57 - metabolism; Enhancer of Zeste Homolog 2 Protein; Enzyme Inhibitors - pharmacology; Health risks; Heat-Shock Proteins - genetics; Heat-Shock Proteins - metabolism; Hematology; Humans; Inhibitors; Leukemia; Lymphatic leukemia; Lymphoma, B-Cell; Malignancy; Medicine; Medicine & Public Health; Mice; Oncology; Original Article; Polycomb Repressive Complex 2; Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy; Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics; Up-Regulation; Xenotransplantation
• ISSN: 0925-5710; 1865-3774
• DOI: 10.1007/s12185-022-03469-8

Disease-risk stratification and development of intensified chemotherapy protocols have substantially improved the outcome of acute lymphoblastic leukemia (ALL). However, outcomes of relapsed or refractory cases remain poor. Previous studies have discussed the oncogenic role of enhancer of zeste homolog 1 and 2 (EZH1/2), and the efficacy of dual inhibition of EZH1/2 as a treatment for hematological malignancy. Here, we investigated whether an EZH1/2 dual inhibitor, DS-3201 (valemetostat), has antitumor effects on B cell ALL (B-ALL). DS-3201 inhibited growth of B-ALL cell lines more significantly and strongly than the EZH2-specific inhibitor EPZ-6438, and induced cell cycle arrest and apoptosis in vitro. RNA-seq analysis to determine the effect of DS-3201 on cell cycle arrest-related genes expressed by B-ALL cell lines showed that DS-3201 upregulated CDKN1C and TP53INP1. CRIPSR/Cas9 knockout confirmed that CDKN1C and TP53INP1 are direct targets of EZH1/2 and are responsible for the antitumor effects of DS-3201 against B-ALL. Furthermore, a patient-derived xenograft (PDX) mouse model showed that DS-3201 inhibited the growth of B-ALL harboring MLL-AF4 significantly. Thus, DS-3201 provides another option for treatment of B-ALL.