含主要促进因子超家族结构域 12 在肺癌中过度表达,并在肺腺癌细胞中发挥致癌作用。

DNA and cell biology Pub Date : 2024-07-01 Epub Date: 2024-04-30 DOI:10.1089/dna.2023.0378
Weijun Zhao, Xilin Hu, Zixuan Chen, Xinjian Li
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引用次数: 0

摘要

含主要促进剂超家族结构域12(MFSD12)调节溶酶体半胱氨酸的输入,并促进黑色素瘤细胞的增殖和存活。然而,MFSD12在其他癌症,尤其是肺癌中的表达和功能仍不清楚。研究人员使用 TIMER 检测了 MFSD12 在各类癌症和相应对照组织中的表达情况。利用 UALCAN 分析了肺腺癌(LUAD)中 MFSD12 的表达及其与 LUAD 患者不同临床病理特征的相关性。使用 R 软件包 survival 评估了 MFSD12 表达与 LUAD 患者生存期之间的相关性,并使用 CIBERSORT 研究了 MFSD12 表达与 LUAD 免疫浸润状态之间的关系。此外,还敲除了 PC9 LUAD 细胞中 MFSD12 的表达,并通过 CCK-8 试验、集落形成试验、7-AAD 染色、Annexin V/PI 染色和 Transwell 试验分别评估了它们的增殖、扩增能力、细胞周期、细胞凋亡和迁移/侵袭。这些PC9细胞的干性是通过Western印迹、流式细胞术和肿瘤球形成试验确定的。在包括LUAD在内的多种癌症中,MFSD12 mRNA水平明显升高。MFSD12的表达还与LUAD的癌症分期、结节转移和各种免疫细胞的浸润呈正相关,MFSD12的高水平预示着LUAD患者的生存率较低。在 PC9 细胞中敲除 MFSD12 会导致 PC9 细胞增殖减少、集落形成能力减弱、细胞周期停滞、凋亡增加、迁移/侵袭受损和干性降低。MFSD12是LUAD的致癌基因。
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Major Facilitator Superfamily Domain Containing 12 Is Overexpressed in Lung Cancer and Exhibits an Oncogenic Role in Lung Adenocarcinoma Cells.

Major facilitator superfamily domain containing 12 (MFSD12) regulates lysosomal cysteine import and promotes the proliferation and survival of melanoma cells. However, the expression and function of MFSD12 in other cancers, particularly in lung cancer, remain unclear. The expression of MFSD12 across various types of cancers and corresponding control tissues was examined using TIMER. MFSD12 expression in lung adenocarcinoma (LUAD) and its correlation with distinct clinicopathological features of LUAD patients were analyzed with UALCAN. The correlation between MFSD12 expression and survival of LUAD patients was assessed using the R package, survival, and the relationship between MFSD12 expression and immune infiltration status in LUAD was investigated using CIBERSORT. In addition, MFSD12 expression was knocked down in PC9 LUAD cells and their proliferation, capacity for expansion, cell cycle, apoptosis, and migration/invasion were evaluated through CCK-8 assays, colony formation assays, 7-AAD staining, Annexin V/PI staining, and Transwell assays, respectively. The stemness of these PC9 cells was determined through Western blotting, flow cytometry, and tumor sphere formation assays. MFSD12 mRNA levels were significantly elevated in multiple types of cancers, including LUAD. MFSD12 expression was also positively correlated with cancer stage, nodal metastasis, and infiltration of various immune cells in LUAD, and high MFSD12 levels predicted poor survival among LUAD patients. Knockdown of MFSD12 in PC9 cells resulted in decreased proliferation, attenuated colony formation capacity, cell cycle arrest, elevated apoptosis, impaired migration/invasion, and reduced stemness in PC9 cells. MFSD12 is an oncogene in LUAD.

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