Discriminant analysis of trace elements in normal, benign and malignant breast tissues measured by total reflection X-ray fluorescence
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2009
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Resumo |
In this work total reflection X-ray fluorescence spectrometry has been employed to determine trace element concentrations in different human breast tissues (normal, normal adjacent, benign and malignant). A multivariate discriminant analysis of observed levels was performed in order to build a predictive model and perform tissue-type classifications. A total of 83 breast tissue samples were studied. Results showed the presence of Ca, Ti, Fe, Cu and Zn in all analyzed samples. All trace elements, except Ti, were found in higher concentrations in both malignant and benign tissues, when compared to normal tissues and normal adjacent tissues. In addition, the concentration of Fe was higher in malignant tissues than in benign neoplastic tissues. An opposite behavior was observed for Ca, Cu and Zn. Results have shown that discriminant analysis was able to successfully identify differences between trace element distributions from normal and malignant tissues with an overall accuracy of 80% and 65% for independent and paired breast samples respectively, and of 87% for benign and malignant tissues. (C) 2009 Elsevier B.V. All rights reserved. |
Identificador |
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, v.64, n.6, p.587-592, 2009 0584-8547 http://producao.usp.br/handle/BDPI/20034 10.1016/j.sab.2009.05.026 |
Idioma(s) |
eng |
Publicador |
PERGAMON-ELSEVIER SCIENCE LTD |
Relação |
Spectrochimica Acta Part B-atomic Spectroscopy |
Direitos |
restrictedAccess Copyright PERGAMON-ELSEVIER SCIENCE LTD |
Palavras-Chave | #Total reflection X-ray fluorescence #Breast cancer #Trace elements #Discriminant analysis #NEUTRON-ACTIVATION ANALYSIS #SYNCHROTRON-RADIATION #HEALTHY TISSUES #SAMPLES #CANCER #XRF #DISTRIBUTIONS #SPECTROMETRY #CARCINOMA #DIAGNOSIS #Spectroscopy |
Tipo |
article proceedings paper publishedVersion |