The role of autophagy dysregulation in low and high-grade nonmuscle invasive bladder cancer: A survival analysis and clinicopathological association

被引:0
作者
Kumar, Anil [1 ]
Singh, Mukul Kumar [1 ]
Singh, Vishwajeet [1 ]
Shrivastava, Ashutosh [2 ]
Sahu, Dinesh Kumar [3 ]
Bisht, Dakshina [4 ]
Singh, Shubhendu [4 ]
机构
[1] King Georges Med Univ, Dept Urol, Lucknow, Uttar Pradesh, India
[2] King Georges Med Univ, Fac Med, Ctr Adv Res, Lucknow, Uttar Pradesh, India
[3] Post Grad Inst Child Hlth, Cent Res Facil, Noida, Uttar Pradesh, India
[4] Santosh Deemed Be Univ, Dept Microbiol, Ghaziabad, Uttar Pradesh, India
关键词
Autophagy; NMIBC; low and high grade; Survival outcome; Prognostic; BECLIN; 1; CELL-DEATH; EXPRESSION; ULK1; PROTEIN; LC3; INHIBITION; PROGNOSIS; CARCINOMA; OUTCOMES;
D O I
10.1016/j.urolonc.2024.07.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Bladder cancer disproportionately affects men and often presents as nonmuscle-invasive bladder cancer (NMIBC). Despite initial treatments, the recurrence and progression of NMIBC are linked to autophagy. This study investigates the expression of autophagy genes (mTOR, ULK1, Beclin1, and LC3) in low and high-grade NMIBC, providing insights into potential prognostic markers and therapeutic targets. Material and methods: A total of 115 tissue samples (n = 85 NMIBC (pTa, pT1, and CIS) and n = 30 control from BPH patients) were collected. The expression level of autophagy genes (mTOR, ULK1, Beclin1, and LC3) and their proteins were assessed in low and highgrade NMIBC, along with control tissue samples using quantitative real-time polymerase chain reaction and western blotting. Association with clinicopathological characteristics and autophagy gene expression was analyzed by multivariate and univariate survival analysis using SPSS. Result: In high-grade NMIBC, ULK1, P = 0.0150, Beclin1, P = 0.0041, and LC3, P = 0.0014, were substantially downregulated, whereas mTOR, P = 0.0006, was significantly upregulated. The KM plots show significant survival outcomes with autophagy genes. The clinicopathological characters, high grade (P = 0.019), tumor stage (CIS P = 0.039, pT1 P = 0.018, P = 0.045), male (P = 0.010), lymphovascular invasion (P = 0.028) and autophagy genes (ULK1 P = 0.002, beclin1 (P = 0.010, P = 0.022) were associated as risk factors for survival outcome in NMIBC patients. Conclusion: The upregulated mTOR, downregulated ULK1, and beclin1 expression is linked to a high-grade, CIS and pT1 stage, resulting in poor recurrence-free survival and progression-free survival and highlights the prognostic significance of autophagy gene in non- muscle-invasive bladder cancer. (c) 2024 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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收藏
页码:425e1 / 425e13
页数:13
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