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 -