4.6 Article

Kinase-Independent Functions of MASTL in Cancer: A New Perspective on MASTL Targeting

Journal

CELLS
Volume 9, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/cells9071624

Keywords

MASTL; actin; contractility; cell cycle; cancer; therapeutic targeting; kinase inhibitor

Categories

Funding

  1. Academy of Finland [325464]
  2. Sigrid Juselius Foundation
  3. Finnish Cancer Organization
  4. Finnish Cultural Foundation
  5. European Union [841973]
  6. Academy of Finland (AKA) [325464, 325464] Funding Source: Academy of Finland (AKA)
  7. Marie Curie Actions (MSCA) [841973] Funding Source: Marie Curie Actions (MSCA)

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Microtubule-associated serine/threonine kinase-like (MASTL; Greatwall) is a well-characterized kinase, whose catalytic role has been extensively studied in relation to cell-cycle acceleration. Importantly, MASTL has been implicated to play a substantial role in cancer progression and subsequent studies have shown that MASTL is a significant regulator of the cellular actomyosin cytoskeleton. Several kinases have non-catalytic properties, which are essential or even sufficient for their functions. Likewise, MASTL functions have been attributed both to kinase-dependent phosphorylation of downstream substrates, but also to kinase-independent regulation of the actomyosin contractile machinery. In this review, we aimed to highlight the catalytic and non-catalytic roles of MASTL in proliferation, migration, and invasion. Further, we discussed the implications of this dual role for therapeutic design.

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