Heavy metals interfere with plasma metabolites, including lipids and amino acids, in patients with breast cancer

被引:20
作者
Li, Ling [1 ]
Zhang, Meihua [2 ]
Men, Yuhao [3 ]
Wang, Wei [1 ]
Zhang, Weidong [3 ]
机构
[1] Jining Med Univ, Dept Oncol, Affiliated Tengzhou Cent Peoples Hosp, Tengzhou 277599, Shandong, Peoples R China
[2] Jining Med Univ, Med Image Ctr, Affiliated Tengzhou Cent Peoples Hosp, 181 Xingtan Rd, Tengzhou 277599, Shandong, Peoples R China
[3] Qingdao Agr Univ, Coll Anim Sci & Technol, Qingdao 266109, Shandong, Peoples R China
关键词
breast cancer; heavy metals; metabolome; lipids; TOTAL DIET SAMPLES; CADMIUM EXPOSURE; CELL CHARACTERISTICS; TRACE-ELEMENTS; METABOLOMICS; ZINC; MORTALITY; FEMALE; WATER; ASSOCIATION;
D O I
10.3892/ol.2020.11402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the present study was to examine the association between plasma heavy metals and the metabolome in patients with breast cancer (BC), and the association with cancer development. Nuclear magnetic resonance was used to determine the metabolites involved and an inductively coupled plasma mass spectrometry system was used to quantify the heavy metals in the plasma samples. It was indicated that cadmium was significantly higher in the plasma of patients with BC compared with that in the control population (15-fold increase). Chromium, arsenic and lead were also elevated in the plasma of patients with BC by 3.24, 2.14 and 1.52 fold, respectively. A number of small molecules, including amino acids and salts, were altered in the plasma of patients with BC compared with the control population. Another notable finding in this investigation was that plasma lipid levels were elevated in patients with BC compared with those in the control population. The findings of the present study suggest that exposure to heavy metals, including cadmium, arsenic, chromium and lead, may influence blood lipid levels and other small molecule metabolites, which in turn may be involved in BC development. Further studies surrounding urinary heavy metals and the metabolome are required to further determine the impact of metals on metabolism and on BC development.
引用
收藏
页码:2925 / 2933
页数:9
相关论文
共 65 条
[1]  
Agency for Toxic Substances and Disease Registry (ATSDR), 2007, ATSDR TOX PROF ARS A
[2]  
ALEXOPOULOS CG, 1987, CANCER-AM CANCER SOC, V60, P3065, DOI 10.1002/1097-0142(19871215)60:12<3065::AID-CNCR2820601234>3.0.CO
[3]  
2-Q
[4]  
[Anonymous], 1980, IARC Monogr Eval Carcinog Risk Chem Hum, V23, P1
[5]  
[Anonymous], 2012, IARC MON EV CARC RIS
[6]   Association of cadmium with human breast cancer [J].
Antila, E ;
MussaloRauhamaa, H ;
Kantola, M ;
Atroshi, F ;
Westermarck, T .
SCIENCE OF THE TOTAL ENVIRONMENT, 1996, 186 (03) :251-256
[7]   Magnetic Resonance Metabolomics of Intact Tissue: A Biotechnological Tool in Cancer Diagnostics and Treatment Evaluation [J].
Bathen, Tone F. ;
Sitter, Beathe ;
Sjobakk, Torill E. ;
Tessem, May-Britt ;
Gribbestad, Ingrid S. .
CANCER RESEARCH, 2010, 70 (17) :6692-6696
[8]   Opening up the "Black Box": Metabolic phenotyping and metabolome-wide association studies in epidemiology [J].
Bictash, Magda ;
Ebbels, Timothy M. ;
Chan, Queenie ;
Loo, Ruey Leng ;
Yap, Ivan K. S. ;
Brown, Ian J. ;
de Iorio, Maria ;
Daviglus, Martha L. ;
Holmes, Elaine ;
Stamler, Jeremiah ;
Nicholson, Jeremy K. ;
Elliott, Paul .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 2010, 63 (09) :970-979
[9]   NMR-based metabolomics: From sample preparation to applications in nutrition research [J].
Brennan, Lorraine .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 2014, 83 :42-49
[10]   Metals and Breast Cancer [J].
Byrne, Celia ;
Divekar, Shailaja D. ;
Storchan, Geoffrey B. ;
Parodi, Daniela A. ;
Martin, Mary Beth .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 2013, 18 (01) :63-73