Shuguang Clinical Medical College of Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Department of Cardiovascular Medicine, Shuguang Hospital Affiliated to Shanghai University of Chinese Medicine, Shanghai, China.
J Healthc Eng. 2022 Mar 25;2022:2209979. doi: 10.1155/2022/2209979. eCollection 2022.
This study aimed to elucidate how SPINK5 affects the malignant phenotypes of NSCLC and the molecular mechanism. NSCLC and adjacent normal tissues were collected to detect the differential level of SPINK5. The influence of SPINK5 on pathological indicators of NSCLC was analyzed. Cellular functions of NSCLC cells overexpressing SPINK5 were assessed by CCK-8, EdU, and transwell assay. By confirming the downstream target of SPINK5, its molecular mechanism on regulating NSCLC was finally explored through rescue experiments. SPINK5 was lowly expressed in NSCLC tissues, and it predicted tumor staging and lymphatic metastasis. In vitro overexpression of SPINK5 declined proliferative and migratory rates in NSCLC cells. PSIP1 was verified as the target gene binding SPINK5, and they displayed a negative correlation in NSCLC tissues. Overexpression of PSIP1 was able to reverse the inhibited proliferative and migratory potentials in NSCLC cells overexpressing SPINK5. SPINK5 level has a close relation to tumor staging and lymphatic metastasis in NSCLC. It serves as a tumor-suppressor gene that inhibits proliferation and migration of NSCLC through negatively regulating PSIP1.
本研究旨在阐明 SPINK5 如何影响 NSCLC 的恶性表型及其分子机制。收集 NSCLC 及相邻正常组织,检测 SPINK5 的差异水平。分析 SPINK5 对 NSCLC 病理指标的影响。通过 CCK-8、EdU 和 Transwell 实验评估过表达 SPINK5 的 NSCLC 细胞的细胞功能。通过确认 SPINK5 的下游靶标,最终通过挽救实验探索其调节 NSCLC 的分子机制。SPINK5 在 NSCLC 组织中低表达,且其预测肿瘤分期和淋巴转移。体外过表达 SPINK5 可降低 NSCLC 细胞的增殖和迁移率。PSIP1 被验证为与 SPINK5 结合的靶基因,它们在 NSCLC 组织中呈负相关。过表达 PSIP1 能够逆转过表达 SPINK5 的 NSCLC 细胞中被抑制的增殖和迁移潜能。SPINK5 在 NSCLC 中的水平与肿瘤分期和淋巴转移密切相关。它作为一种肿瘤抑制基因,通过负调控 PSIP1 抑制 NSCLC 的增殖和迁移。