Reactive Oxygen Species as Mediators of Disease Progression and Therapeutic Response in Colorectal Cancer

被引:11
作者
Lyons, Nicholas J. [1 ]
Giri, Rabina [1 ]
Begun, Jakob [1 ,2 ]
Clark, David [3 ]
Proud, David [4 ]
He, Yaowu [1 ]
Hooper, John D. [1 ]
Kryza, Thomas [1 ]
机构
[1] Univ Queensland, Mater Res Inst, Translat Res Inst, Woolloongabba, Australia
[2] Mater Hosp Brisbane, South Brisbane, Brisbane, Australia
[3] Royal Brisbane & Womens Hosp, Brisbane, Australia
[4] Austin Hosp, Melbourne, Australia
关键词
colorectal cancer; reactive oxygen species; photodynamic therapy; sonodynamic therapy; radiodynamic therapy; NF-KAPPA-B; GLUTATHIONE S-TRANSFERASES; STEM-LIKE CELLS; PHOTODYNAMIC THERAPY; COLON-CANCER; OXIDATIVE STRESS; NITRIC-OXIDE; SONODYNAMIC THERAPY; PROTOPORPHYRIN IX; IN-VITRO;
D O I
10.1089/ars.2022.0127
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
Significance: Reactive oxygen species (ROS) are critical to normal cellular function with redox homeostasis achieved by balancing ROS production with removal through detoxification mechanisms. Many of the conventional chemotherapies used to treat colorectal cancer (CRC) derive a proportion of their cytotoxicity from ROS generation, and resistance to chemotherapy is associated with elevated detoxification mechanisms. Furthermore, cancer stem cells demonstrate elevated detoxification mechanisms making definitive treatment with existing chemotherapy challenging. In this article, we review the roles of ROS in normal and malignant colonic cell biology and how existing and emerging therapies might harness ROS for therapeutic benefit.Recent Advances: Recent publications have elucidated the contribution of ROS to the cytotoxicity of conventional chemotherapy alongside the emerging approaches of photodynamic therapy (PDT), sonodynamic therapy (SDT), and radiodynamic therapy (RDT), in which ROS are generated in response to excitatory light, sound, or X-ray stimuli to promote cancer cell apoptosis.Critical Issues: The majority of patients with metastatic CRC have a very poor prognosis with a 5-year survival of similar to 13% making the need for new or more effective treatments an imperative.Future Directions: Modulation of ROS through a combination of new and emerging therapies may improve the efficacy of current chemotherapy providing novel approaches to treat the otherwise resistant disease.
引用
收藏
页码:186 / 205
页数:20
相关论文
共 198 条
[1]   Sono-photodynamic modality for cancer treatment using biodegradable bio-conjugated sonnelux nanocomposite in tumor-bearing mice: Activated cancer therapy using light and ultrasound [J].
Abd El-Kaream, Samir Ali ;
Abd Elsamie, Gihan Hosny ;
Abd-Alkareem, Azhar Salim .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 503 (02) :1075-1086
[2]  
Abulafi AM, 1997, BRIT J SURG, V84, P368, DOI 10.1002/bjs.1800840329
[3]  
AIHW, 2021, CANC AUSTR 2021 SUMM, P1
[4]   Redox signaling regulates commensal-mediated mucosal homeostasis and restitution and requires formyl peptide receptor 1 [J].
Alam, A. ;
Leoni, G. ;
Wentworth, C. C. ;
Kwal, J. M. ;
Wu, H. ;
Ardita, C. S. ;
Swanson, P. A. ;
Lambeth, J. D. ;
Jones, R. M. ;
Nusrat, A. ;
Neish, A. S. .
MUCOSAL IMMUNOLOGY, 2014, 7 (03) :645-655
[5]   Glucocorticoid receptor signaling represses the antioxidant response by inhibiting histone acetylation mediated by the transcriptional activator NRF2 [J].
Alam, Md. Morshedul ;
Okazaki, Keito ;
Nguyen, Linh Thi Thao ;
Ota, Nao ;
Kitamura, Hiroshi ;
Murakami, Shohei ;
Shima, Hiroki ;
Igarashi, Kazuhiko ;
Sekine, Hiroki ;
Motohashi, Hozumi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2017, 292 (18) :7519-7530
[6]   Molecular mechanisms of action and prediction of response to oxaliplatin in colorectal cancer cells [J].
Arango, D ;
Wilson, AJ ;
Shi, Q ;
Corner, GA ;
Arañes, MJ ;
Nicholas, C ;
Lesser, M ;
Mariadason, JM ;
Augenlicht, LH .
BRITISH JOURNAL OF CANCER, 2004, 91 (11) :1931-1946
[7]   Short-course radiotherapy followed by chemotherapy before total mesorectal excision (TME) versus preoperative chemoradiotherapy, TME, and optional adjuvant chemotherapy in locally advanced rectal cancer (RAPIDO): a randomised, open-label, phase 3 trial [J].
Bahadoer, Renu R. ;
Dijkstra, Esmee A. ;
van Etten, Boudewijn ;
Marijnen, Corrie A. M. ;
Putter, Hein ;
Kranenbarg, Elma Meershoek-Klein ;
Roodvoets, Annet G. H. ;
Nagtegaal, Iris D. ;
Beets-Tan, Regina G. H. ;
Blomqvist, Lennart K. ;
Fokstuen, Tone ;
ten Tije, Albert J. ;
Capdevila, Jaume ;
Hendriks, Mathijs P. ;
Edhemovic, Ibrahim ;
Cervantes, Andres ;
Nilsson, Per J. ;
Glimelius, Bengt ;
van de Velde, Cornelis J. H. ;
Hospers, Geke A. P. .
LANCET ONCOLOGY, 2021, 22 (01) :29-42
[8]   Nitric oxide (NO) induces nitration of protein kinase Cε (PKCε), facilitating PKCε translocation via enhanced PKCε-RACK2 interactions -: A novel mechanism of NO-triggered activation of PKCε [J].
Balafanova, Z ;
Bolli, R ;
Zhang, J ;
Zheng, YT ;
Pass, JM ;
Bhatnagar, A ;
Tang, XL ;
Wang, OL ;
Cardwell, E ;
Ping, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (17) :15021-15027
[9]   Gene Expression: Protein Interaction Systems Network Modeling Identifies Transformation-Associated Molecules and Pathways in Ovarian Cancer [J].
Bapat, Sharmila A. ;
Krishnan, Anagha ;
Ghanate, Avinash D. ;
Kusumbe, Anjali P. ;
Kalra, Rajkumar S. .
CANCER RESEARCH, 2010, 70 (12) :4809-4819
[10]   The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology [J].
Bedard, Karen ;
Krause, Karl-Heinz .
PHYSIOLOGICAL REVIEWS, 2007, 87 (01) :245-313