Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, 110025, India.
Translational Research Lab, Department of Biotechnology, Faculty of Natural Sciences, Jamia Millia Islamia, New Delhi, 110025, India.
Funct Integr Genomics. 2023 Jul 6;23(3):223. doi: 10.1007/s10142-023-01144-7.
The anillin actin-binding protein (ANLN) is immensely overexpressed in cancers, including lung cancer (LC). Phytocompounds have gained interest due to their broader potential and reduced unwanted effects. Screening numerous compounds presents a challenge, but in silico molecular docking is pragmatic. The present study aims to identify the role of ANLN in lung adenocarcinoma (LUAD), along with identification and interaction analysis of anticancer and ANLN inhibitory phytocompounds followed by molecular dynamics (MD) simulation. Using a systematic approach, we found that ANLN is significantly overexpressed in LUAD and mutated with a frequency of 3.73%. It is linked with advanced stages, clinicopathological parameters, worsening of relapse-free survival (RFS), and overall survival (OS), pinpointing its oncogenic and prognostic potential. High-throughput screening and molecular docking of phytocompounds revealed that kaempferol (flavonoid aglycone) interacts strongly with the active site of ANLN protein via hydrogen bonds, Vander Waals interactions, and acts as a potent inhibitor. Furthermore, we discovered that ANLN expression was found to be significantly higher (p) in LC cells compared to normal cells. This is a propitious and first study to demonstrate ANLN and kaempferol interactions, which might eventually lead to removal of rout from cell cycle regulation posed by ANLN overexpression and allow it to resume normal processes of proliferation. Overall, this approach suggested a plausible biomarker role of ANLN and the combination of molecular docking subsequently led to the identification of contemporary phytocompounds, bearing symbolic anticancer effects. The findings would be advantageous for pharmaceutics but require validation using in vitro and in vivo methods. HIGHLIGHTS: • ANLN is significantly overexpressed in LUAD. • ANLN is implicated in the infiltration of TAMs and altering plasticity of TME. • Kaempferol (potential ANLN inhibitor) shows important interactions with ANLN which could remove the alterations in cell cycle regulation, imposed by ANLN overexpression eventually leading to normal process of cell proliferation.
肌动蛋白结合蛋白(ANLN)在癌症中高度过表达,包括肺癌(LC)。由于其更广泛的潜力和减少不必要的副作用,植物化合物引起了人们的兴趣。筛选大量化合物是一个挑战,但在计算机分子对接是务实的。本研究旨在确定 ANLN 在肺腺癌(LUAD)中的作用,以及鉴定和分析抗癌和 ANLN 抑制性植物化合物的相互作用,然后进行分子动力学(MD)模拟。使用系统的方法,我们发现 ANLN 在 LUAD 中显著过表达,并且突变频率为 3.73%。它与晚期、临床病理参数、无复发生存(RFS)和总生存(OS)恶化相关,指出其致癌和预后潜力。高通量筛选和植物化合物的分子对接表明,山柰酚(类黄酮糖苷)通过氢键、范德华相互作用与 ANLN 蛋白的活性位点强烈相互作用,并作为一种有效的抑制剂。此外,我们发现 LC 细胞中的 ANLN 表达明显高于正常细胞(p)。这是一项有利的和首次研究,证明了 ANLN 和山奈酚的相互作用,这最终可能导致 ANLN 过表达引起的细胞周期调节被消除,并使其恢复正常的增殖过程。总的来说,这种方法表明 ANLN 是一个有前途的生物标志物,随后的分子对接导致了具有象征意义的抗癌作用的现代植物化合物的鉴定。这些发现将对制药学有利,但需要使用体外和体内方法进行验证。要点: • ANLN 在 LUAD 中显著过表达。 • ANLN 参与 TAMs 的浸润和改变 TME 的可塑性。 • 山奈酚(潜在的 ANLN 抑制剂)与 ANLN 显示出重要的相互作用,这些相互作用可以消除由 ANLN 过表达引起的细胞周期调节的改变,最终导致细胞增殖的正常过程。