Gulhane Pooja, Singh Shailza
Department of Pathogenesis and Cellular Response, Computational and Systems Biology Lab, National Centre for Cell Science, SP Pune University Campus, Pune, India.
J Cell Biochem. 2022 Nov;123(11):1827-1840. doi: 10.1002/jcb.30319. Epub 2022 Aug 17.
Increasing research suggests that sphingolipid metabolism is essential for the progression and metastasis of cancer. The underlying mechanistic insight into the dysregulation of sphingolipid metabolism affecting pathways is poorly investigated. As a result, the goal of the current study was to glean knowledge from the systems biology approach to investigate how the sphingolipid metabolism affects the signal transduction network in non-small cell lung cancer (NSCLC), the most common type of cancer in terms of occurrence and death globally. Our paper includes system-level models representing the diseased and healthy states elucidating that sphingolipids and its enzymes mediate PI3K/AKT pathway. Notably, its activation of downstream signaling mediators has led to cancer growth. Considering the critical role of sphingolipids in NSCLC, our study advocates the target CERS6 which can be potentially inhibited using hsa-miR-520c-3p to combat NSCLC for future precision medicine.
越来越多的研究表明,鞘脂代谢对于癌症的进展和转移至关重要。然而,对于影响相关通路的鞘脂代谢失调的潜在机制研究甚少。因此,本研究的目的是从系统生物学方法中获取知识,以研究鞘脂代谢如何影响非小细胞肺癌(NSCLC)中的信号转导网络,NSCLC是全球发病率和死亡率最高的常见癌症类型。我们的论文包括代表疾病和健康状态的系统水平模型,阐明了鞘脂及其酶介导PI3K/AKT通路。值得注意的是,其对下游信号介质的激活导致了癌症生长。鉴于鞘脂在NSCLC中的关键作用,我们的研究主张以CERS6为靶点,未来可使用hsa-miR-520c-3p对其进行潜在抑制,以对抗NSCLC,实现精准医疗。