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Co-localization of stanniocalcin-1 ligand and receptor in human breast carcinomas
被引:45
|作者:
McCudden, CR
Majewski, A
Chakrabarti, S
Wagner, GF
[1
]
机构:
[1] Univ Western Ontario, Fac Med & Dent, Dept Physiol & Pharmacol, London, ON N6A 5C1, Canada
[2] Univ Western Ontario, Dept Pathol, London, ON N6A 5C1, Canada
基金:
加拿大自然科学与工程研究理事会;
加拿大健康研究院;
关键词:
breast cancer;
stanniocalcin-1;
ligand;
receptor;
D O I:
10.1016/j.mce.2003.10.042
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Stanniocalcin-1 (STC1) is a new polypeptide hormone that has metabolic effects on target cell mitochondria. Recent studies have shown that the STC1 gene is upregulated in primary breast tumors and co-expressed with the estrogen receptor. In this report we have demonstrated the histological co-localization of STC1 and its receptor in invasive and non-invasive human mammary gland ductal carcinomas. Analysis of 58 malignant breast biopsies revealed that STC1 and its receptor co-localized to cancer cells in 91% of cases. The study therefore reveals that in breast carcinomas STC1 signals in an autocrine feedback loop and opens up the possibility that it may be sequestered by neoplastic cells in much the same manner as it is by non-malignant cells. The data further supports the notion that STC1 plays a role in breast cancer and that it may prove to be a novel diagnostic and prognostic marker, and potential therapeutic target. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
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页码:167 / 172
页数:6
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