Please use this identifier to cite or link to this item: https://doi.org/10.1023/A:1010658907462
Title: Metallothionein 1F mRNA expression correlates with histological grade in breast carcinoma
Authors: Jin, R.
Bay, B.-H. 
Chow, V.T.-K. 
Tan, P.-H.
Keywords: Breast cancer
Histological grade
Immunohistochemistry
Metallothionein
Reverse transcription polymerase chain reaction (RT-PCR)
Issue Date: 2001
Citation: Jin, R., Bay, B.-H., Chow, V.T.-K., Tan, P.-H. (2001). Metallothionein 1F mRNA expression correlates with histological grade in breast carcinoma. Breast Cancer Research and Treatment 66 (3) : 265-272. ScholarBank@NUS Repository. https://doi.org/10.1023/A:1010658907462
Abstract: Immunohistochemical expression of metallothioneins (MTs), a group of intracellular metal-binding proteins, is well documented in breast cancer. However, there is a paucity of information on the expression of the different MT isoforms in breast cancer tissues. The dichotomous association of MT overexpression with turnout types and progression led us to examine the role of the MT-1F mRNA isoform in breast cancer. We evaluated MT expression in 48 primary invasive ductal breast cancer tissues by immunohistochemistry, and the corresponding MT-1F mRNA expression via a semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) assay. The specificity of the RT-PCR products was confirmed by direct cycle sequencing and restriction enzyme digestion. Immunohistochemical analysis of MT revealed a significantly higher MT expression in histological grade 3 tumours as compared to grade 1 and 2 tumours (p = 0.021). Similarly, MT-1F mRNA expression was found to be significantly higher in grade 3 tumours (p < 0.001). The results suggest that the MT-1F isoform influences histological differentiation in invasive ductal breast cancer. The converse is also true in that the histological grade may determine the level of MT-1F expression in breast cancer.
Source Title: Breast Cancer Research and Treatment
URI: http://scholarbank.nus.edu.sg/handle/10635/120845
ISSN: 01676806
DOI: 10.1023/A:1010658907462
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