Lymphoma Translational Group, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain.
Laboratory of Immunopharmacology and Molecular Biology, Sao Francisco University Medical School, Braganca Paulista 01246-100, São Paulo, Brazil.
Cells. 2023 Jan 28;12(3):433. doi: 10.3390/cells12030433.
Primarily identified as an important regulator of cytoskeletal dynamics, the small GTPase Ras homolog gene family member A (RHOA) has been implicated in the transduction of signals regulating a broad range of cellular functions such as cell survival, migration, adhesion and proliferation. Deregulated activity of RHOA has been linked to the growth, progression and metastasis of various cancer types. Recent cancer genome-wide sequencing studies have unveiled both gain and loss-of-function mutations in primary leukemia/lymphoma, suggesting that this GTPase may exert tumor-promoting or tumor-suppressive functions depending on the cellular context. Based on these observations, RHOA signaling represents an attractive therapeutic target for the development of selective anticancer strategies. In this review, we will summarize the molecular mechanisms underlying RHOA GTPase functions in immune regulation and in the development of hematological neoplasms and will discuss the current strategies aimed at modulating RHOA functions in these diseases.
主要被鉴定为细胞骨架动力学的重要调节因子,Ras 同源基因家族成员 A(RHOA)小 GTPase 已被牵涉到调节广泛的细胞功能的信号转导中,如细胞存活、迁移、黏附和增殖。RHOA 的活性失调与各种癌症类型的生长、进展和转移有关。最近的癌症全基因组测序研究揭示了原发性白血病/淋巴瘤中获得和丧失功能的突变,表明这种 GTPase 可能根据细胞环境发挥促进肿瘤或抑制肿瘤的功能。基于这些观察结果,RHOA 信号转导代表了开发选择性抗癌策略的有吸引力的治疗靶点。在这篇综述中,我们将总结 RHOA GTPase 功能在免疫调节和血液系统肿瘤发生中的分子机制,并讨论目前旨在调节这些疾病中 RHOA 功能的策略。