Highly metastatic cancer cells are more likely to escape and form metastases, and only minimal improvements in treatment can be achieved. Despite metas- tases being the primary cause of cancer-related mortality, they often proceed unnoticed. Current imaging modalities rely solely on the morphological fea- tures of the tumor for characterization, rather than cellular differences. Our goal is to develop an MR cellular imaging capability for characterizing the po- tential of breast cancer cells to metastasize and enable early cancer detection using manganese. Experiments on breast cell lines demonstrated that aggres- sive cancer cells significantly enhanced on T1 -weighted MR images as a result of a higher uptake and retention of manganese. These results suggest that dif- ferences in uptake of manganese can help the detection and characterization of breast cancers. The proposed technique can also be useful for other cancers, and could bring a critically needed dimension to cancer imaging.

Highly metastatic cancer cells are more likely to escape and form metastases, and only minimal improvements in treatment can be achieved. Despite metas- tases being the primary cause of cancer-related mortality, they often proceed unnoticed. Current imaging modalities rely solely on the morphological fea- tures of the tumor for characterization, rather than cellular differences. Our goal is to develop an MR cellular imaging capability for characterizing the po- tential of breast cancer cells to metastasize and enable early cancer detection using manganese. Experiments on breast cell lines demonstrated that aggres- sive cancer cells significantly enhanced on T1 -weighted MR images as a result of a higher uptake and retention of manganese. These results suggest that dif- ferences in uptake of manganese can help the detection and characterization of breast cancers. The proposed technique can also be useful for other cancers, and could bring a critically needed dimension to cancer imaging.