Enzymatic activity of HIV-1 protease defines migration of tumor cells in vitro and enhances their metastatic activity in vivo

被引:1
作者
Isaguliants, M. [1 ]
Zhitkevich, A. [2 ]
Petkov, S. [1 ]
Gorodnicheva, T. [3 ]
Mezale, D. [1 ]
Fridrihsone, I. [1 ]
Kuzmenko, Y. [4 ]
Kostyushev, D. [5 ]
Kostyusheva, A. [5 ]
Gordeychuk, I. [1 ,2 ]
Bayurova, E. [1 ,2 ]
机构
[1] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, S-77777 Stockholm, Sweden
[2] Russian Acad Sci, Chumakov Fed Sci Ctr Res & Dev Immune and Biol Pro, Moscow 708879, Russia
[3] Pirogov Russian Natl Res Med Univ, Inst Translat Med, Moscow 777997, Russia
[4] Acad Sci Russian Federat, Engelhardt Inst Mol Biol, Moscow 779997, Russia
[5] Sechenov Univ, Martsinovsky Inst Med Parasitol Trop & Vector Born, Moscow 779997, Russia
关键词
HIV-1; protease; Enzymatic activity; Cell migration; Tumorigenicity; Metastatic activity; HUMAN-IMMUNODEFICIENCY-VIRUS; EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-CANCER; MICROENVIRONMENTAL REGULATION; DIMERIZATION INHIBITION; TYPE-1; PROTEASE; REACTIVE OXYGEN; DARUNAVIR; FLUORESCENT; PROGRESSION;
D O I
10.1016/j.biochi.2024.08.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Overexpression of aspartic proteases, as cathepsin D, is an independent marker of poor prognosis in breast cancer, correlated with the incidence of clinical metastasis. We aimed to find if HIV-1 aspartic protease (PR) can play a similar role. Murine adenocarcinoma 4T1luc2 cells were transduced with lentivirus encoding inactivated drug-resistant PR, generating subclones PR20.1 and PR20.2. Subclones were assessed for production of reactive oxygen species (ROS), expression of epithelial-mesenchymal transition (EMT) factors, and in vitro migratory activity in the presence or absence of antioxidant Nacetyl cysteine and protease inhibitors. Tumorigenic activity was evaluated by implanting cells into BALB/c mice and following tumor growth by calipering and bioluminescence imaging in vivo, and metastases, by organ imaging ex vivo. Both subclones expressed PR mRNA, and PR20.2, also the protein detected by Western blotting. PR did not induce production of ROS, and had no direct effect on cell migration rate, however, treatment with inhibitors of drug-resistant PR suppressed the migratory activity of both subclones. Furthermore, expression of N-cadherin and Vimentin in PR20.2 cells and their migration were enhanced by antioxidant treatment. Sensitivity of in vitro migration to protease inhibitors and to antioxidant, known to restore PR activity, related the effects to the enzymatic activity of PR. In vivo, PR20.2 cells demonstrated higher tumorigenic and metastatic activity than PR20.1 or parental cells. Thus, HIV-1 protease expressed in breast cancer cells determines their migration in vitro and metastatic activity in vivo. This effect may aggravate clinical course of cancers in people living with HIV-1. (c) 2024 Elsevier B.V. and Soci & eacute;t & eacute; Fran & ccedil;aise de Biochimie et Biologie Mol & eacute;culaire (SFBBM). All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页码:32 / 43
页数:12
相关论文
共 84 条
[1]  
Abolins A, 2011, POL J PATHOL, V62, P65
[2]   Multiscale profiling of protease activity in cancer [J].
Amini, Ava P. ;
Kirkpatrick, Jesse D. ;
Wang, Cathy S. ;
Jaeger, Alex M. ;
Su, Susan ;
Naranjo, Santiago ;
Zhong, Qian ;
Cabana, Christina M. ;
Jacks, Tyler ;
Bhatia, Sangeeta N. .
NATURE COMMUNICATIONS, 2022, 13 (01)
[3]   Detection of HIV-1 and Human Proteins in Urinary Extracellular Vesicles from HIV+ Patients [J].
Anyanwu, Samuel I. ;
Doherty, Akins ;
Powell, Michael D. ;
Obialo, Chamberlain ;
Huang, Ming B. ;
Quarshie, Alexander ;
Mitchell, Claudette ;
Bashir, Khalid ;
Newman, Gale W. .
ADVANCES IN VIROLOGY, 2018, 2018
[4]   Luciferase Expression Allows Bioluminescence Imaging But Imposes Limitations on the Orthotopic Mouse (4T1) Model of Breast Cancer [J].
Baklaushev, V. P. ;
Kilpelainen, A. ;
Petkov, S. ;
Abakumov, M. A. ;
Grinenko, N. F. ;
Yusubalieva, G. M. ;
Latanova, A. A. ;
Gubskiy, I. L. ;
Zabozlaev, F. G. ;
Starodubova, E. S. ;
Abakumova, T. O. ;
Isaguliants, M. G. ;
Chekhonin, V. P. .
SCIENTIFIC REPORTS, 2017, 7
[5]   HIV-1 Reverse Transcriptase Promotes Tumor Growth and Metastasis Formation via ROS-Dependent Upregulation of Twist [J].
Bayurova, Ekaterina ;
Jansons, Juris ;
Skrastina, Dace ;
Smirnova, Olga ;
Mezale, Dzeina ;
Kostyusheva, Anastasiya ;
Kostyushev, Dmitry ;
Petkov, Stefan ;
Podschwadt, Philip ;
Valuev-Elliston, Vladimir ;
Sasinovich, Sviataslau ;
Korolev, Sergey ;
Warholm, Per ;
Latanova, Anastasia ;
Starodubova, Elizaveta ;
Tukhvatulin, Amir ;
Latyshev, Oleg ;
Selimov, Renat ;
Metalnikov, Pavel ;
Komarov, Alexander ;
Ivanova, Olga ;
Gorodnicheva, Tatiana ;
Kochetkov, Sergey ;
Gottikh, Marina ;
Strumfa, Ilze ;
Ivanov, Alexander ;
Gordeychuk, Ilya ;
Isaguliants, Maria G. .
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2019, 2019
[6]   Cell killing by HIV-1 protease [J].
Blanco, R ;
Carrasco, L ;
Ventoso, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (02) :1086-1093
[7]   HIV-1 protease: mechanism and drug discovery [J].
Brik, A ;
Wong, CH .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2003, 1 (01) :5-14
[8]   Cellular Targets of HIV-1 Protease: Just the Tip of the Iceberg? [J].
Centazzo, Matteo ;
Manganaro, Lara ;
Alvisi, Gualtiero .
VIRUSES-BASEL, 2023, 15 (03)
[9]   Role of Matrix Metalloproteinases in Epithelial Migration [J].
Chen, Peter ;
Parks, William C. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2009, 108 (06) :1233-1243
[10]   A SHORT-TERM STUDY OF THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF RITONAVIR, AN INHIBITOR OF HIV-1 PROTEASE [J].
DANNER, SA ;
CARR, A ;
LEONARD, JM ;
LEHMAN, LM ;
GUDIOL, F ;
GONZALES, J ;
RAVENTOS, A ;
RUBIO, R ;
BOUZA, E ;
PINTADO, V ;
AGUADO, AG ;
DELOMAS, JG ;
DELGADO, R ;
BORLEFFS, JCC ;
HSU, A ;
VALDES, JM ;
BOUCHER, CAB ;
COOPER, DA ;
GIMENO, C ;
CLOTET, B ;
TOR, J ;
FERRER, E ;
MARTINEZ, PL ;
MORENO, S ;
ZANCADA, G ;
ALCAMI, J ;
NORIEGA, AR ;
PULIDO, F ;
GLASSMAN, HN .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (23) :1528-1533