Background: To analyze the prognostic factors of combined small cell lung cancer (CSCLC) and construct a nomogram model for CSCLC. Methods: A total of 978 patients diagnosed with CSCLC from 2010 to 2015 were collected based on the SEER database. According to the ratio of 7:3, the patients were divided into the modeling group and the testing group. Univariate and multivariate Cox regression analyses were performed on the patients in the modeling group to analyze the independent factors affecting the prognosis of CSCLC patients and construct a nomogram prediction model, which was verified by the C-index and calibration curve in the training cohort and the validation cohort, respectively. Results: Univariate and multivariate Cox regression analysis showed that N stage, M stage, surgery, chemotherapy, radiotherapy, age, brain metastases, lung metastases, liver metastases, bone metastases, and tumor size were independent risk factors affecting the prognosis of CSCLC patients (P<0.05). A nomogram prediction model was constructed based on the above 10 risk factors through visual analysis, and the C-index was 0.753 (95%CI: 0.727~0.750). The calibration curves showed good agreement between the 1 -, 2 -, and 3-year predicted and actual survival rates of the prediction model constructed in this study. The AUC of the 1-, 2-, and 3-year prediction models was 0.813, 0.814, and 0.802, respectively. DCA showed that the nomogram model had more clinical application value in predicting survival prognosis than TNM staging. Finally, according to the total score of the nomogram survival prediction model, all the included cases were divided into low-risk, intermediate-risk, and high-risk strata and these three survival curves of each risk stratification showed significant survival differences (p< 0.05). Conclusions: The nomogram prediction model constructed in this study has higher accuracy and clinical application value than the traditional TNM staging. It can predict the 1 -, 2 - and 3-year OS of patients individually and provide a new tool for clinicians to evaluate the survival prognosis of CSCLC. The risk stratification system established by this model can identify high-risk patients more quickly, and make follow-up plans and subsequent treatment plans more targeted.
Objective: To study the mechanism of lncRNA p21 inhibiting the growth and metastasis of human gastric cancer SGC7901/GES-1 cells by mediating the Wnt/β-catenin signaling pathway. Methods: Lentiviral overexpression of lncRNA-p21 in human gastric cancer SGC7901/GES-1 cell transfections was observed and analyzed for in vitro migration, invasion, cell morphology and proliferation. Besides. Wnt/β-catenin signaling pathway was tested for direct involvement in lncRNA-p21-mediated inhibition of gastric cancer cell growth and proliferation. Wnt/β-catenin signaling pathway was validated using Li-C1. Results: Gastric cancer SGC7901/GES-1 cells in the overexpression of lncRNA-p21 showed changes in stellate morphology, low invasion, or spindle-shaped morphology. LncRNA-p21 inhibited the growth and proliferation of gastric cancer SGC7901/GES-1 cells both in vivo and in vitro, and Wnt/β-catenin signaling pathway mediated the proliferation, invasion, and migration of lncRNA-p21 on gastric cancer SGC7901/GES-1 cells. Conclusion: LncRNA-p21 can inhibit the growth and metastasis of gastric cancer SGC7901/GES-1 cells in vitro and in vivo, and the inhibition of lncRNA p21 is mainly mediated by inhibiting the Wnt/β-catenin signaling pathway.
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