

Author: Rotenberg Susan Mirkin Michael
Publisher: Springer Publishing Company
ISSN: 1083-3021
Source: Journal of Mammary Gland Biology and Neoplasia, Vol.9, Iss.4, 2004-10, pp. : 375-382
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Scanning electrochemical microscopy (SECM) can be used to measure the redox activity of individual human breast cells. A chemical mediator (e.g. quinone) that rapidly crosses the membrane participates in intracellular redox reactions that are recorded on a microsecond timescale by an ultramicroelectrode positioned close to the membrane. Measurements of redox reactivity yield rate constants that are different for cancerous and non-transformed human breast cells. With non-transformed or metastatic cells, rate constants are modulated by altered expression or activity of protein kinase Cα, an enzyme involved in the mechanism of cell metastasis. When used in two-dimensional scanning, SECM produces a spatially resolved redox map of an individual cell or field of cells and can detect individual breast cancer cells in a field of non-transformed cells. These studies identify a new technology for cancer detection and establish a framework for future analysis of malignant cells in human breast tissues and biopsies.
Related content




Detection of Epithelial Cells in Hematopoietic Organs of Patients with Breast Cancer
Acta Haematologica, Vol. 105, Iss. 3, 2001-07 ,pp. :



