Khalil Md Imtiaz, Madere Christopher, Ghosh Ishita, Adam Rosalyn M, De Benedetti Arrigo
LSU Health Sciences Center, Department of Biochemistry and Molecular Biology, Shreveport, LA 71103, USA.
Department of Urology, Boston Children's Hospital and Department of Surgery, Harvard Medical School, Boston, MA 02115, USA.
Pathophysiology. 2021 Jul 20;28(3):339-354. doi: 10.3390/pathophysiology28030023.
Prostate cancer (PCa) progression is characterized by the emergence of resistance to androgen deprivation therapy (ADT). AKT/PKB has been directly implicated in PCa progression, often due to the loss of PTEN and activation of PI3K>PDK1>AKT signaling. However, the regulatory network of AKT remains incompletely defined. Here, we describe the functional significance of AKTIP in PCa cell growth. AKTIP, identified in an interactome analysis as a substrate of TLK1B (that itself is elevated following ADT), enhances the association of AKT with PDK1 and its phosphorylation at T308 and S473. The interaction between TLK1 and AKTIP led to AKTIP phosphorylation at T22 and S237. The inactivation of TLK1 led to reduced AKT phosphorylation, which was potentiated with AKTIP knockdown. The TLK1 inhibitor J54 inhibited the growth of the LNCaP cells attributed to reduced AKT activation. However, LNCaP cells that expressed constitutively active, membrane-enriched Myr-AKT (which is expected to be active, even in the absence of AKTIP) were also growth-inhibited with J54. This suggested that other pathways (like TLK1>NEK1>YAP) regulating proliferation are also suppressed and can mediate growth inhibition, despite compensation by Myr-AKT. Nonetheless, further investigation of the potential role of TLK1>AKTIP>AKT in suppressing apoptosis, and conversely its reversal with J54, is warranted.
前列腺癌(PCa)进展的特征是对雄激素剥夺疗法(ADT)产生耐药性。AKT/PKB直接参与PCa进展,这通常是由于PTEN缺失以及PI3K>PDK1>AKT信号通路的激活所致。然而,AKT的调控网络仍未完全明确。在此,我们描述了AKTIP在PCa细胞生长中的功能意义。在相互作用组分析中,AKTIP被鉴定为TLK1B的底物(ADT后TLK1B本身水平升高),它增强了AKT与PDK1的结合及其在T308和S473位点的磷酸化。TLK1与AKTIP之间的相互作用导致AKTIP在T22和S237位点磷酸化。TLK1失活导致AKT磷酸化减少,而AKTIP敲低可增强这种减少。TLK1抑制剂J54抑制LNCaP细胞生长,这归因于AKT激活的减少。然而,表达组成型活性、膜富集的Myr-AKT(预计即使在没有AKTIP的情况下也具有活性)的LNCaP细胞也被J54抑制生长。这表明尽管Myr-AKT有补偿作用,但其他调节增殖的途径(如TLK1>NEK1>YAP)也受到抑制并可介导生长抑制。尽管如此,仍有必要进一步研究TLK1>AKTIP>AKT在抑制细胞凋亡中的潜在作用,以及J54对其的逆转作用。