Department of Clinical Laboratory, Yunnan Molecular Diagnostic Center, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.
Chinese Academy of Medical Sciences and Institute of Medical Biology, Peking Union Medical College, Kunming, China.
Med Oncol. 2023 Aug 22;40(9):274. doi: 10.1007/s12032-023-02143-1.
TROAP, interacts with trophinin and bystin, polys a key role in embryo implantation. TROAP is required for spindle assembly and centrosome integrity during the mitosis. TROAP has been described to promote tumorigenesis in a diverse range of cancer. We performed this study to assess the biological and clinical significance of TROAP in Non-small cell lung cancer. Forty-eight pairs of lung adenocarcinoma (LUAD) tissues and paraneoplastic tissues were collected. RT-qPCR, western bolt and immunohistochemistry assay was used to test TROAP RNA and protein expression not in LUAD tissues and paraneoplastic tissues but in LUAD cell lines and control cell lines. TROAP knockdown and overexpression vector were constructed and transfected into lung cancer cells. CCK-8, transwell, and wound healing assays were used to assess cell viability, migration, and invasion. The expression of PI3K/AKT and EMT signaling proteins and METTL3 were determined by western blot. We found the TROAP was enriched in NSCLC tissues and cell lines. TROAP knockdown inhibited cell proliferation, migration, invasion compared with control group in NSCLC. Mechanism analysis revealed that TROAP activated PI3K/AKT and EMT signaling pathway. To a certain extent, TROAP was regulated by METTL3. In a word, TROAP accelerated the progression of NSCLC through PI3K/AKT and EMT pathway, and TROAP might be considered as a novel target for NSCLC therapy.
TROAP 与 trophinin 和 bystin 相互作用,在胚胎植入中发挥关键作用。TROAP 在有丝分裂过程中对纺锤体组装和中心体完整性至关重要。TROAP 已被描述为在多种癌症中促进肿瘤发生。我们进行这项研究是为了评估 TROAP 在非小细胞肺癌中的生物学和临床意义。收集了 48 对肺腺癌(LUAD)组织和癌旁组织。使用 RT-qPCR、western bolt 和免疫组织化学检测 LUAD 组织和癌旁组织中 TROAP RNA 和蛋白表达,同时也在 LUAD 细胞系和对照细胞系中进行检测。构建了 TROAP 敲低和过表达载体,并转染到肺癌细胞中。使用 CCK-8、transwell 和划痕愈合实验评估细胞活力、迁移和侵袭。通过 western blot 测定 PI3K/AKT 和 EMT 信号通路蛋白和 METTL3 的表达。我们发现 TROAP 在 NSCLC 组织和细胞系中富集。与对照组相比,TROAP 敲低组 NSCLC 细胞增殖、迁移和侵袭能力受到抑制。机制分析表明,TROAP 激活了 PI3K/AKT 和 EMT 信号通路。在一定程度上,TROAP 受 METTL3 调控。总之,TROAP 通过 PI3K/AKT 和 EMT 通路加速了 NSCLC 的进展,TROAP 可能被认为是 NSCLC 治疗的一个新靶点。