Chen Hao, Han Tao, Zhao Yi, Feng Liang
Department of Breast Surgery of the First Affiliated Hospital of China Medical University, Shenyang, China.
Department of Oncology, The First Affiliated Hospital of China Medical University, Shenyang, China.
Ann Transl Med. 2021 Aug;9(15):1237. doi: 10.21037/atm-21-3026.
Ovarian cancer is one of the 3 major gynecological malignancies with high mortality, poor prognosis, and lack of specific diagnostic and prognostic markers. Solute-carrier family 27A molecules (SCL27As) play a crucial role in multiple malignant tumors via the regulation of long-chain fatty acid uptake and subsequent regulation of lipid metabolism. To date, the specific mechanisms and roles of SCL27As in epithelial ovarian cancer (EOC) have remained unclear.
The Oncomine and Gene Expression Profiling Interactive Analysis (GEPIA) databases and the Kaplan-Meier plotter were used to explore the differential expression and the prognostic value of SCL27As in EOC. The expression of in 20 normal ovarian tissues and 120 ovarian cancer tissues was detected by immunohistochemistry (IHC). Cell Counting Kit-8 (CCK8) assay and colony-forming experiments were conducted to evaluate the role of in the proliferation of ovarian cancer cells, so as to verify the clinical application value of in the diagnosis and prognosis of ovarian cancer. We extracted the data of for multiple bioinformatics analysis to identify the potential regulatory mechanism of .
The expression levels of and were significantly decreased in ovarian cancer tissues. Prognostic analysis showed that , , , and expression levels were significantly correlated with overall survival (OS) in EOC patients. Moreover, the expression of the SLC27A6 protein was decreased in EOC tissues, which was related to the prognosis. Additionally, knocking down the expression of could significantly enhance the malignant biological behavior of ovarian cancer cells. The gene may be involved in the proteasome, cell cycle, Hippo signaling pathway, and so on.
This study revealed the abnormal expression and prognostic value of in EOC. In addition, it was highlighted that may be a novel biomarker for the diagnosis and prognostication of EOC patients.
卵巢癌是三大妇科恶性肿瘤之一,死亡率高、预后差,且缺乏特异性诊断和预后标志物。溶质载体家族27A分子(SCL27As)通过调节长链脂肪酸摄取及随后的脂质代谢调节,在多种恶性肿瘤中发挥关键作用。迄今为止,SCL27As在上皮性卵巢癌(EOC)中的具体机制和作用仍不清楚。
利用Oncomine和基因表达谱交互式分析(GEPIA)数据库以及Kaplan-Meier绘图仪,探讨SCL27As在EOC中的差异表达及预后价值。采用免疫组织化学(IHC)检测20例正常卵巢组织和120例卵巢癌组织中[具体分子名称未给出]的表达。进行细胞计数试剂盒-8(CCK8)检测和集落形成实验,以评估[具体分子名称未给出]在卵巢癌细胞增殖中的作用,从而验证[具体分子名称未给出]在卵巢癌诊断和预后中的临床应用价值。我们提取[具体分子名称未给出]的数据进行多项生物信息分析以确定其潜在调控机制。
卵巢癌组织中[具体分子名称未给出]和[具体分子名称未给出]的表达水平显著降低。预后分析表明,[具体分子名称未给出]、[具体分子名称未给出]、[具体分子名称未给出]和[具体分子名称未给出]的表达水平与EOC患者的总生存期(OS)显著相关。此外,EOC组织中SLC27A6蛋白表达降低,这与预后相关。另外,敲低[具体分子名称未给出]的表达可显著增强卵巢癌细胞的恶性生物学行为。[具体分子名称未给出]基因可能参与蛋白酶体、细胞周期、Hippo信号通路等。
本研究揭示了[具体分子名称未给出]在EOC中的异常表达及预后价值。此外,强调[具体分子名称未给出]可能是EOC患者诊断和预后的新型生物标志物。