Heravi Gioia, Jang Hyejeong, Wang Xiaokun, Long Ze, Peng Zheyun, Kim Seongho, Liu Wanqing
Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, United States.
Biostatistics and Bioinformatics Core, Department of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI, United States.
Front Oncol. 2022 Aug 15;12:942798. doi: 10.3389/fonc.2022.942798. eCollection 2022.
Fatty Acid Desaturase-1 (FADS1) or delta 5 desaturase (D5D) is a rate-limiting enzyme involved in the biosynthesis of long-chain polyunsaturated fatty acids (LC-PUFAs), i.e., arachidonic acid (ARA) and eicosapentaenoic (EPA). These LC-PUFAs and their metabolites play essential and broad roles in cancer cell proliferation, metastasis, and tumor microenvironment. However, the role of FADS1 in cancers remains incompletely understood. Utilizing The Cancer Genome Atlas (TCGA) database, we explored the role of FADS1 across different cancer types using multiple bioinformatics and statistical tools. Moreover, we studied the impact of a FADS1 inhibitor (D5D-IN-326) on proliferation of multiple cancer cell lines. We identified that FADS1 gene is a predictor for cancer survival in multiple cancer types. Compared to normal tissue, the mRNA expression of FADS1 is significantly increased in primary tumors while even higher in metastatic and recurrent tumors. Mechanistically, pathway analysis demonstrated that FADS1 is associated with cholesterol biosynthesis and cell cycle control genes. Interestingly, FADS1 expression is higher when TP53 is mutated. Tumors with increased FADS1 expression also demonstrated an increased signatures of fibroblasts and macrophages infiltration among most cancer types. Our assays showed that D5D-IN-326 significantly inhibited cell proliferation of kidney, colon, breast, and lung cancer cell lines in a dose-dependent manner. Lastly, single nucleotide polymorphisms (SNPs) which are well-established expression quantitative trait loci (eQTLs) for FADS1 in normal human tissues are also significantly correlated with FADS1 expression in tumors of multiple tissue types, potentially serving as a marker to stratify cancer patients with high/low FADS1 expression in their tumor tissue. Our study suggests that FADS1 plays multiple roles in cancer biology and is potentially a novel target for precision cancer treatment.
脂肪酸去饱和酶-1(FADS1)或δ5去饱和酶(D5D)是一种参与长链多不饱和脂肪酸(LC-PUFA)生物合成的限速酶,即花生四烯酸(ARA)和二十碳五烯酸(EPA)。这些LC-PUFA及其代谢产物在癌细胞增殖、转移和肿瘤微环境中发挥着重要而广泛的作用。然而,FADS1在癌症中的作用仍未完全明确。利用癌症基因组图谱(TCGA)数据库,我们使用多种生物信息学和统计工具探究了FADS1在不同癌症类型中的作用。此外,我们研究了FADS1抑制剂(D5D-IN-326)对多种癌细胞系增殖的影响。我们发现FADS1基因是多种癌症类型中癌症生存的一个预测指标。与正常组织相比,FADS1的mRNA表达在原发性肿瘤中显著增加,而在转移性和复发性肿瘤中甚至更高。从机制上讲,通路分析表明FADS1与胆固醇生物合成和细胞周期调控基因有关。有趣的是,当TP53发生突变时,FADS1的表达更高。在大多数癌症类型中,FADS1表达增加的肿瘤也表现出成纤维细胞和巨噬细胞浸润的特征增加。我们的实验表明,D5D-IN-326以剂量依赖性方式显著抑制肾、结肠、乳腺和肺癌细胞系的细胞增殖。最后,在正常人体组织中作为FADS1的既定表达数量性状位点(eQTL)的单核苷酸多态性(SNP)也与多种组织类型肿瘤中的FADS1表达显著相关,有可能作为一种标志物来对肿瘤组织中FADS1表达高/低的癌症患者进行分层。我们的研究表明,FADS1在癌症生物学中发挥多种作用,并且可能是精准癌症治疗的一个新靶点。