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.
引用
收藏
页码:425e1 / 425e13
页数:13
相关论文
共 50 条
  • [21] High-grade urothelial bladder cancer in children: A case report and critical analysis of the literature
    Kral, Milan
    Michalek, Jaroslav
    Skarda, Jozef
    Tichy, Tomas
    Smakal, Oldrich
    Kodet, Roman
    Student, Vladimir
    BIOMEDICAL PAPERS-OLOMOUC, 2016, 160 (04): : 578 - 582
  • [22] Major differences in glycosylation and fucosyltransferase expression in low-grade versus high-grade bladder cancer cell lines
    Ezeabikwa, Bernadette
    Mondal, Nandini
    Antonopoulos, Aristotelis
    Haslam, Stuart M.
    Matsumoto, Yasuyuki
    Martin-Caraballo, Miguel
    Lehoux, Sylvain
    Mandalasi, Msano
    Ishaque, Ali
    Heimburg-Molinaro, Jamie
    Cummings, Richard D.
    Nyame, Anthony K.
    GLYCOBIOLOGY, 2021, 31 (11) : 1444 - 1463
  • [23] Clinical and biological markers for risk-stratification of T1 high-grade non-muscle invasive bladder cancer
    Soria, Francesco
    Dutto, Daniele
    Gontero, Paolo
    CURRENT OPINION IN UROLOGY, 2022, 32 (05) : 517 - 522
  • [24] The impact of positive soft tissue surgical margins following radical cystectomy for high-grade, invasive bladder cancer
    Pantelis Hadjizacharia
    John P. Stein
    Jie Cai
    Gus Miranda
    World Journal of Urology, 2009, 27 : 33 - 38
  • [25] Low- and high-grade bladder cancer appraisal via serum-based proteomics approach
    Bansal, Navneeta
    Gupta, Ashish
    Sankhwar, Satya Narain
    Mandi, Abbas Ali
    CLINICA CHIMICA ACTA, 2014, 436 : 97 - 103
  • [26] Overexpression of long non-coding RNA TUG1 predicts poor prognosis and promotes cancer cell proliferation and migration in high-grade muscle-invasive bladder cancer
    Iliev, Robert
    Kleinova, Renata
    Juracek, Jaroslav
    Dolezel, Jan
    Ozanova, Zuzana
    Fedorko, Michal
    Pacik, Dalibor
    Svoboda, Marek
    Stanik, Michal
    Slaby, Ondrej
    TUMOR BIOLOGY, 2016, 37 (10) : 13385 - 13390
  • [27] Risk-scoring models for individualized prediction of overall survival in low-grade and high-grade endometrial cancer
    AlHilli, Mariam M.
    Mariani, Andrea
    Bakkum-Gamez, Jamie N.
    Dowdy, Sean C.
    Weaver, Amy L.
    Peethambaram, Preema P.
    Keeney, Gary L.
    Cliby, William A.
    Podratz, Karl C.
    GYNECOLOGIC ONCOLOGY, 2014, 133 (03) : 485 - 493
  • [28] Cell-cycle markers do not improve discrimination of EORTC and CUETO risk models in predicting recurrence and progression of non muscle-invasive high-grade bladder cancer
    Passoni, Niccolo
    Gayed, Bishoy
    Kapur, Payal
    Sagalowsky, Arthur I.
    Shariat, Shahrokh F.
    Lotan, Yair
    UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2016, 34 (11) : 485.e7 - 485.e14
  • [29] Histological and immunohistochemical markers for progression prediction in transurethrally resected high-grade non-muscle invasive bladder cancer
    Kim, Kyungeun
    Cho, Yong Mee
    Park, Bong-Hee
    Lee, Jae-Lyun
    Ro, Jae Y.
    Go, Heounjeong
    Shim, Jung Weon
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2015, 8 (01): : 743 - 750
  • [30] Low- and High-Grade Bladder Cancer Determination via Human Serum-Based Metabolomics Approach
    Bansal, Navneeta
    Gupta, Ashish
    Mitash, Nilay
    Shakya, Prashant Singh
    Mandhani, Anil
    Mahdi, Abbas Ali
    Sankhwar, Satya Narain
    Mandal, Sudhir Kumar
    JOURNAL OF PROTEOME RESEARCH, 2013, 12 (12) : 5839 - 5850