@article{132366, keywords = {Animals, Humans, Membrane Proteins, Cell Line, Female, Nuclear Proteins, Neoplasm Proteins, Breast Neoplasms, Lung Neoplasms, Survival Rate, Cell Adhesion Molecules, Dogs, RNA-Binding Proteins, Neoplasm Metastasis, Endonucleases, Disease-Free Survival}, author = {Mario Andres Blanco and Masa Ale{\v c}kovi{\'c} and Yuling Hua and Tuo Li and Yong Wei and Zhen Xu and Ileana Cristea and Yibin Kang}, title = {Identification of staphylococcal nuclease domain-containing 1 (SND1) as a Metadherin-interacting protein with metastasis-promoting functions}, abstract = {
Metastasis is the deadliest and most poorly understood feature of malignant diseases. Recent work has shown that Metadherin (MTDH) is overexpressed in over 40\% of breast cancer patients and promotes metastasis and chemoresistance in experimental models of breast cancer progression. Here we applied mass spectrometry-based screen to identify staphylococcal nuclease domain-containing 1 (SND1) as a candidate MTDH-interacting protein. After confirming the interaction between SND1 and MTDH, we tested the role of SND1 in breast cancer and found that it strongly promotes lung metastasis. SND1 was further shown to promote resistance to apoptosis and to regulate the expression of genes associated with metastasis and chemoresistance. Analyses of breast cancer clinical microarray data indicated that high expression of SND1 in primary tumors is strongly associated with reduced metastasis-free survival in multiple large scale data sets. Thus, we have uncovered SND1 as a novel MTDH-interacting protein and shown that it is a functionally and clinically significant mediator of metastasis.
}, year = {2011}, journal = {J Biol Chem}, volume = {286}, pages = {19982-92}, month = {06/2011}, issn = {1083-351X}, doi = {10.1074/jbc.M111.240077}, language = {eng}, }