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急性早幼粒细胞白血病对维甲酸治疗耐药性的预测模型

Predictive modelling of acute Promyelocytic leukaemia resistance to retinoic acid therapy.

作者信息

Sánchez-Villanueva José A, N'Guyen Lia, Poplineau Mathilde, Duprez Estelle, Remy Élisabeth, Thieffry Denis

机构信息

Aix Marseille Université, CNRS, I2M, 163 avenue de Luminy, 13009 Marseille, France.

Integrative molecular biology in hematopoiesis and leukemia, Equipe Labellisée Ligue Contre le Cancer, CRCM, Inserm UMR1068, CNRS UMR7258, Institut Paoli-Calmettes, Aix Marseille Univ, 27 Bd Lei Roure, 13009 Marseille, France.

出版信息

Brief Bioinform. 2024 Nov 22;26(1). doi: 10.1093/bib/bbaf002.

Abstract

Acute Promyelocytic Leukaemia (APL) arises from an aberrant chromosomal translocation involving the Retinoic Acid Receptor Alpha (RARA) gene, predominantly with the Promyelocytic Leukaemia (PML) or Promyelocytic Leukaemia Zinc Finger (PLZF) genes. The resulting oncoproteins block the haematopoietic differentiation program promoting aberrant proliferative promyelocytes. Retinoic Acid (RA) therapy is successful in most of the PML::RARA patients, while PLZF::RARA patients frequently become resistant and relapse. Recent studies pointed to various underlying molecular components, but their precise contributions remain to be deciphered. We developed a logical network model integrating signalling, transcriptional, and epigenetic regulatory mechanisms, which captures key features of the APL cell responses to RA depending on the genetic background. The explicit inclusion of the histone methyltransferase EZH2 allowed the assessment of its role in the resistance mechanism, distinguishing between its canonical and non-canonical activities. The model dynamics was thoroughly analysed using tools integrated in the public software suite maintained by the CoLoMoTo consortium (https://colomoto.github.io/). The model serves as a solid basis to assess the roles of novel regulatory mechanisms, as well as to explore novel therapeutical approaches in silico.

摘要

急性早幼粒细胞白血病(APL)源于涉及维甲酸受体α(RARA)基因的异常染色体易位,主要是与早幼粒细胞白血病(PML)或早幼粒细胞白血病锌指(PLZF)基因发生易位。由此产生的癌蛋白阻断造血分化程序,促进异常增殖的早幼粒细胞生成。维甲酸(RA)疗法对大多数PML::RARA患者有效,而PLZF::RARA患者则经常产生耐药性并复发。最近的研究指出了各种潜在的分子成分,但其确切作用仍有待阐明。我们开发了一个整合信号传导、转录和表观遗传调控机制的逻辑网络模型,该模型根据遗传背景捕捉了APL细胞对RA反应的关键特征。明确纳入组蛋白甲基转移酶EZH2可以评估其在耐药机制中的作用,区分其经典和非经典活性。使用CoLoMoTo联盟维护的公共软件套件(https://colomoto.github.io/)中集成的工具对模型动力学进行了全面分析。该模型为评估新型调控机制的作用以及在计算机上探索新型治疗方法提供了坚实的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dbe/11729720/cddfa5a0cb1d/bbaf002f1.jpg

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