Breast Cancer and Arsenic Anticancer Effects: Systematic Review of the Experimental Data from In Vitro Studies

被引:5
作者
Skoczynska, Anna [1 ]
Skoczynska, Marta [2 ]
机构
[1] Wroclaw Med Univ, Dept Internal & Occupat Dis Hypertens & Clin Oncol, Pasteura 1, PL-50556 Wroclaw, Poland
[2] Lower Siles Specialist Hosp, Dept Rheumatol & Internal Dis, Fieldorfa 2, PL-54049 Wroclaw, Poland
关键词
ACUTE PROMYELOCYTIC LEUKEMIA; INHIBITS CELL-GROWTH; METHYLATION CAPACITY; OXIDATIVE STRESS; DRINKING-WATER; RETINOIC ACID; UP-REGULATION; MCF-7; CELLS; TRIOXIDE; APOPTOSIS;
D O I
10.1155/2022/8030931
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Arsenic is a known environmental carcinogenic agent. However, under certain circumstances, it may exert anticancer effects. In this systematic review, we aim to provide information on recent developments in studies on arsenic antitumor effects in breast cancer. Research included in the review refers to experimental data from in vitro studies. The data was collected using search terms "breast cancer," "arsenic," and "anticancer" (25.05.2021). Only studies in English and published in the last 10 years were included. The search identified 123 studies from the EBSCOhost, PubMed, and Scopus databases. In the selection process, thirty full-texts were evaluated as eligible for the review. The literature of the last decade provides a lot of information on mechanisms behind anticancer effects of arsenic on breast cancer. Similar to arsenic-induced carcinogenesis, these mechanisms include the activation of the redox system and the increased production of free radicals. Targets of arsenic action are systems of cell membranes, mitochondria, pathways of intracellular transmission, and the genetic apparatus of the cell. Beneficial effects of arsenic use are possible due to significant metabolic differences between cancer and healthy cells. Further efforts are needed in order to establish modes and doses of treatment with arsenic that would provide anticancer activity with minimal toxicity.
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页数:16
相关论文
共 71 条
[1]   A Novel Nanoparticulate Formulation of Arsenic Trioxide with Enhanced Therapeutic Efficacy in a Murine Model of Breast Cancer [J].
Ahn, Richard W. ;
Chen, Feng ;
Chen, Haimei ;
Stern, Stephan T. ;
Clogston, Jeffrey D. ;
Patri, Anil K. ;
Raja, Meera R. ;
Swindell, Elden P. ;
Parimi, Vamsi ;
Cryns, Vincent L. ;
O'Halloran, Thomas V. .
CLINICAL CANCER RESEARCH, 2010, 16 (14) :3607-3617
[2]   Inhibition of PI3K pathway using BKM120 intensified the chemo-sensitivity of breast cancer cells to arsenic trioxide (ATO) [J].
Alipour, Faranak ;
Riyahi, Niknam ;
Safaroghli-Azar, Ava ;
Sari, Soyar ;
Zandi, Zahra ;
Bashash, Davood .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2019, 116
[3]  
[Anonymous], 2007, Human papillomaviruses, V90, P1, DOI DOI 10.1097/MEG.0B013E32835A870B
[4]   Arsenic trioxide in the treatment of a patient with multiply recurrent, ATRA-resistant promyelocytic leukemia: A case report [J].
Bergstrom, SK ;
Gillan, E ;
Quinn, JJ ;
Altman, AJ .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1998, 20 (06) :545-547
[5]   Nutritional Influences on One-Carbon Metabolism: Effects on Arsenic Methylation and Toxicity [J].
Bozack, Anne K. ;
Saxena, Roheeni ;
Gamble, Mary V. .
ANNUAL REVIEW OF NUTRITION, VOL 38, 2018, 38 :401-429
[6]  
Changizi V, 2020, IRAN J PUBLIC HEALTH, V49, P1555, DOI 10.18502/ijph.v49i8.3901
[7]  
Chung Jin-Yong, 2014, J Prev Med Public Health, V47, P253, DOI 10.3961/jpmph.14.036
[8]   Acute Promyelocytic Leukemia: A Paradigm for Oncoprotein-Targeted Cure [J].
de The, Hugues ;
Pandolfi, Pier Paolo ;
Chen, Zhu .
CANCER CELL, 2017, 32 (05) :552-560
[9]  
Dharani Sundarmurthy Dharani Sundarmurthy, 2017, National Journal of Physiology, Pharmacy and Pharmacology, V7, P685, DOI [10.5455/njppp.2017.7.0202628022017, 10.5455/njppp.2017.7.0202628022017]
[10]   Arsenic Induces Functional Re-Expression of Estrogen Receptor α by Demethylation of DNA in Estrogen Receptor-Negative Human Breast Cancer [J].
Du, Juan ;
Zhou, Nannan ;
Liu, Hongxia ;
Jiang, Fei ;
Wang, Yubang ;
Hu, Chunyan ;
Qi, Hong ;
Zhong, Caiyun ;
Wang, Xinru ;
Li, Zhong .
PLOS ONE, 2012, 7 (04)