TY - GEN
T1 - Correlative imaging techniques reveal organic-inorganic compositions of pathological mineral deposits
AU - Estroff, Lara
AU - Kunitake, Jennie
AU - Vidavsky, Netta
AU - Fischbach, Claudia
AU - Masic, Admir
PY - 2018
Y1 - 2018
N2 - Pathological calcification is a wide-spread phenomenon in the human body, in which calcium minerals form in soft tissues and are found in both normal and damaged tissues. One example are microcalcifications (MCs) found in both benign and malignant breast tissue. Breast cancer is screened using mammography based on MC presence and appearance. Little is known, however, about their materials properties and associated organic matrix, or their correlation to breast cancer prognosis. One of the biggest questions regarding MC formation is whether they form by cell-mediated processes or are the result of cell-independent crystallization that is related to necrosis. We have used a combination of histopathology, Raman microscopy, and electron microscopy to image MCs within snap-frozen human breast tissue and have generated micron-scale resolution correlative maps of crystalline phase, trace metals, particle morphology, and organic matrix chemical signatures within high grade ductal carcinoma in situ (DCIS) and invasive cancer. This multimodal methodology lays the groundwork for establishing MC heterogeneity in the context of breast cancer biology, and has the potential to be applied to other pathological minerals, as well as in vitro models of mineralization. Research reported in this presentation was supported by the National Cancer Institute of the National Institutes of Health under Award Number R01CA173083. This work made use of the Cornell Center for Materials Research Shared Facilities which are supported through the NSF MRSEC program (DMR-1719875). Add.
AB - Pathological calcification is a wide-spread phenomenon in the human body, in which calcium minerals form in soft tissues and are found in both normal and damaged tissues. One example are microcalcifications (MCs) found in both benign and malignant breast tissue. Breast cancer is screened using mammography based on MC presence and appearance. Little is known, however, about their materials properties and associated organic matrix, or their correlation to breast cancer prognosis. One of the biggest questions regarding MC formation is whether they form by cell-mediated processes or are the result of cell-independent crystallization that is related to necrosis. We have used a combination of histopathology, Raman microscopy, and electron microscopy to image MCs within snap-frozen human breast tissue and have generated micron-scale resolution correlative maps of crystalline phase, trace metals, particle morphology, and organic matrix chemical signatures within high grade ductal carcinoma in situ (DCIS) and invasive cancer. This multimodal methodology lays the groundwork for establishing MC heterogeneity in the context of breast cancer biology, and has the potential to be applied to other pathological minerals, as well as in vitro models of mineralization. Research reported in this presentation was supported by the National Cancer Institute of the National Institutes of Health under Award Number R01CA173083. This work made use of the Cornell Center for Materials Research Shared Facilities which are supported through the NSF MRSEC program (DMR-1719875). Add.
M3 - Conference contribution
BT - APS March Meeting 2018
ER -