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磷脂酰肌醇3激酶/蛋白激酶B/雷帕霉素哺乳动物靶标通路相关蛋白在肺鳞状细胞癌中的表达及其与淋巴结转移的相关性

Phosphatidylinositol 3-Kinase/Protein Kinase B/Mammalian Target of the Rapamycin Pathway-Related Protein Expression in Lung Squamous Cell Carcinoma and Its Correlation with Lymph Node Metastasis.

作者信息

Shi Fang, Li Ling

机构信息

Department of Oncology, Jiangxi Chest Hospital, Nanchang 330006, Jiangxi, China.

Department of Oncology, Second Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.

出版信息

J Oncol. 2022 Aug 23;2022:4537256. doi: 10.1155/2022/4537256. eCollection 2022.

Abstract

The targeted therapy of lung squamous cell carcinoma (LSCC), a pathological type of non-small-cell lung cancer, is relatively lacking by contrast with lung adenocarcinoma. The overexpression or inhibition of intracellular signaling pathways leads to disease. To evaluate genes for a targeted therapy in LSCC, we analyzed PI3K pathway components in LSCC tissues and found elevated PI3K levels in LSCC tissues compared with adjacent counterparts. A comparison of PI3K levels in tissues with and without metastasis revealed that the PI3K pathway activity was greatly increased in metastatic tissues. Our findings suggest that the metastasis of cancer cells in patients with LSCC is closely related to the overexpression of PI3K pathway components in cancer tissues. We performed cell culture experiments and found that inhibition of PI3K activity decreased proliferation and increased apoptosis in H520 cells, suggesting that PI3K pathway inhibition limits LSCC cell proliferation. We hypothesize that LSCC metastasis is related to the overexpression of PI3K pathway components and inhibiting this pathway may help reduce the risk of lymph node metastasis in LSCC patients.

摘要

肺鳞状细胞癌(LSCC)是一种非小细胞肺癌的病理类型,与肺腺癌相比,其靶向治疗相对较少。细胞内信号通路的过度表达或抑制会导致疾病。为了评估用于LSCC靶向治疗的基因,我们分析了LSCC组织中的PI3K通路成分,发现与相邻组织相比,LSCC组织中PI3K水平升高。对有转移和无转移组织中PI3K水平的比较显示,转移组织中PI3K通路活性大大增加。我们的研究结果表明,LSCC患者癌细胞的转移与癌组织中PI3K通路成分的过度表达密切相关。我们进行了细胞培养实验,发现抑制PI3K活性可降低H520细胞的增殖并增加其凋亡,这表明抑制PI3K通路可限制LSCC细胞增殖。我们推测,LSCC转移与PI3K通路成分的过度表达有关,抑制该通路可能有助于降低LSCC患者发生淋巴结转移的风险。

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