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细胞程序性死亡蛋白5与宫颈癌患者病理特征的关系 及对淋巴结转移发生风险的评估价值.

Authors :
杨光
张丹凤
冯晓娜
张燕
Source :
Journal of Practical Medicine / Shiyong Yixue Zazhi. 12/25/2023, Vol. 39 Issue 24, p3210-3213. 4p.
Publication Year :
2023

Abstract

Objective To explore the expression of programmed cell death protein 5 in cervical cancer and its relationship with lymph node metastasis. Methods 98 cases of cervical cancer patients admitted to our hospital were selected as the observation group, and 98 cases of cervical benign lesions were selected as the control group. The expression levels of PDCD5 in serum and lesion tissues of the two groups were compared to analyze the relationship between PDCD5 and pathological features of cervical cancer, and the diagnostic value of PDCD5 in lymph node metastasis of patients with cervical cancer was analyzed by ROC curve. Results The expression levels of PDCD5 in serum and lesion tissue of observation group were lower than those of control group (P < 0.05) . With the increase of clinical stage and pathological grade of cervical cancer, the expression of PDCD5 in serum and lesion tissue was significantly decreased (P < 0.05) . Among the 98 patients with cervical cancer, 32 had lymph node metastasis. The expression levels of PDCD5 in serum and lesion tissue of lymph node metastasis group were lower than those of non-lymph node metastasis group (P < 0.05) . ROC curve results showed that the AUCs of PDCD5 in serum and lesion tissue to predict lymph node metastasis of cervical cancer patients were 0.810 and 0.850, respectively, with no statistical significance (P > 0.05) . Conclusion The Programmed cell death protein 5 is closely related to the pathological features of patients with cervical cancer, and it has a good predictive effect on lymph node metastasis, which is worthy of further study and application. [ABSTRACT FROM AUTHOR]

Details

Language :
Chinese
ISSN :
10065725
Volume :
39
Issue :
24
Database :
Academic Search Index
Journal :
Journal of Practical Medicine / Shiyong Yixue Zazhi
Publication Type :
Academic Journal
Accession number :
174722576
Full Text :
https://doi.org/10.3969/j.issn.1006-5725.2023.24.011