Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/51332
Title: A comparative study of Ki-67 antigen expression between luminal A and triple-negative subtypes of breast cancer
Authors: Borges, Umbelina Soares
Costa-Silva, Danylo Rafhael
da Silva-Sampaio, Joao Paulo
Escorcio-Dourado, Carla Solange
Conde, Airton Mendes, Jr.
Campelo, Viriato
Gebrim, Luiz Henrique [UNIFESP]
da Silva, Benedito Borges
Lopes-Costa, Pedro Vitor
Keywords: Breast cancer
Molecular subtypes
Luminal A
Triple-negative
Ki-67
Issue Date: 2017
Publisher: Humana Press Inc
Citation: Medical Oncology. Totowa, v. 34, n. 9, p. -, 2017.
Abstract: Tumor biomarkers such as hormone receptors, HER-2 and Ki-67 are used routinely in clinical practice for classification of molecular subtypes of breast cancer. Cell proliferation evaluated by Ki-67 antigen expression is important to determine tumor aggressiveness. However, there is a paucity of studies comparing Ki-67 expression in an expressive number of cells among molecular subtypes of breast cancer, particularly among less and more aggressive tumors, such as luminal A and triple-negative, which have led us to the present study. The current study included invasive ductal carcinoma samples of 59 patients, which were divided into two groups: luminal A (n = 29) and triple-negative (n = 30). For immunohistochemical reaction, the samples were incubated with monoclonal anti-Ki-67 antibody (clone MIB1) and cells expressing Ki-67 protein were identified by dark brown staining of the nuclei, counting at least 600 cells per slide. The mean percentages of stained nuclei were analyzed by Student's t test (p < 0.05). The mean percentage of nuclei stained with anti-ki-67 was 10.14 and 77.22 in luminal A and triple-negative breast cancers, respectively (p < 0.0001). Our study showed a high cell proliferation of triple-negative breast cancer in comparison with luminal A, justifying its aggressiveness and poor clinical outcome.
URI: http://repositorio.unifesp.br/handle/11600/51332
ISSN: 1357-0560
Other Identifiers: http://dx.doi.org/10.1007/s12032-017-1019-x
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