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NHERF (Na+/H+ exchanger regulatory factor) gene mutations in human breast cancer
Jia Le Dai1, Lei Wang, Aysegul A Sahin
1Department of Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. jldai@mdanderson.org
Abstract:
Yeast two-hybrid screening was used to explore novel proteins that interact with a breast tumor or metastasis suppressor, SYK (spleen tyrosine kinase). The screening yielded NHERF (Na+/H+ exchanger regulatory factor, also known as NHERF1 or EBP-50) that binds to the interdomain B of SYK. NHERF is an estrogen-responsive gene that encodes an inhibitory factor for epithelial Na+/H+ exchanger isoform 3 (NHE3). We found intragenic mutation of the NHERF gene accompanied by loss of heterzygosity (LOH) in approximately 3% (3/85) of breast cancer cell lines and primary breast tumors. Mutations occurred at the conserved PDZ domains at NHERF NH2-terminus that bound to SYK, or at its COOH-terminus motif that binds to MERLIN, the product of Neurofibromatosis 2 (NF2) tumor suppressor gene. NHERF tumorigenic mutations decreased or abolished its interaction with SYK or MERLIN, suggesting a pathway link among these three molecules that may play a critical role in mammary neoplastic progression. Primary breast tumors with LOH at the NHERF locus had clinical presentations of higher aggressiveness, indicating that deregulated NHERF signaling may be associated with disease progression. Moreover, the LOH was inversely correlated with SYK promoter methylation, suggesting that NHERF and SYK may transduce a common suppressive signal. Taken together, the results indicated NHERF to be a candidate tumor suppressor gene in human breast carcinoma that may be interconnected to the SYK and MERLIN suppressors.
Insights
Na+/H+ exchanger regulatory factor (NHERF) interacts with spleen tyrosine kinase (SYK), a breast cancer suppressor. Mutations in NHERF are linked to aggressive breast cancer, suggesting NHERF acts as a tumor suppressor gene.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Spleen tyrosine kinase (SYK) is a known breast tumor suppressor.
- Na+/H+ exchanger regulatory factor (NHERF) is an estrogen-responsive gene involved in regulating ion transport.
Purpose of the Study:
- To identify novel proteins interacting with SYK.
- To investigate the role of NHERF in breast cancer development and progression.
Main Methods:
- Yeast two-hybrid screening to identify SYK-interacting proteins.
- Mutation analysis and loss of heterozygosity (LOH) studies on the NHERF gene in breast cancer samples.
- Correlation analysis between NHERF LOH, SYK promoter methylation, and clinical presentation.
Main Results:
- NHERF was identified as a SYK-binding protein.
- Intragenic mutations and LOH in NHERF were found in 3% of breast cancer cell lines and tumors.
- These mutations disrupted NHERF interactions with SYK and MERLIN, a NF2 tumor suppressor.
- NHERF LOH correlated with increased tumor aggressiveness and was inversely associated with SYK promoter methylation.
Conclusions:
- NHERF functions as a candidate tumor suppressor gene in human breast carcinoma.
- NHERF, SYK, and MERLIN may form a critical pathway in mammary neoplastic progression.
- Deregulated NHERF signaling is associated with breast cancer progression and aggressiveness.
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