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. 2024 Dec 1;109(12):3847-3849.
doi: 10.3324/haematol.2024.286085.

AURKA targeting: a NEAT approach to halt myeloma

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AURKA targeting: a NEAT approach to halt myeloma

Antonio Giovanni Solimando et al. Haematologica. .
No abstract available

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Figures

Figure 1.
Figure 1.
Schematic representation of a novel therapeutic strategy aimed at inhibiting NEAT1 and AURKA to potentially counteract the progression of multiple myeloma. Disruption of the M/G1 checkpoint prevents the proper assembly of chromatids on the mitotic spindle, thereby arresting the division of multiple myeloma (MM) cells. Intervention at the G1/S checkpoint impedes the activation of growth factors and organelle production, curtailing cell growth. The inhibition of AURKA’s function in mitosis compromises spindle assembly and chromosome segregation. Furthermore, perturbation of the G2/M checkpoint impairs DNA damage repair mechanisms, culminating in the apoptosis of MM cells. This dual targeting represents a significant advancement in the treatment of MM, exploiting the pro-survival and pro-oncogenic properties of NEAT14 and AURKA. AURKA: aurora kinase A; TGF-b: transforming growth factor-beta; ATP: adenosine triphosphate; NEAT1: nuclear paraspeckle assembly transcript 1.

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