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Biology subjects

Thakar, D.

Publications and source records attributed to Thakar, D..

2 recordsLinked to original sources

Magnitude and Kinetics of a set of Neuroanatomic Volume and Thickness together with White Matter Hyperintensity is definitive of Cognitive Status and Brain Age

In an aging population, a subset of individuals at a given age group have low white matter hyperintensity (WMH) while another subset has intermediate to high WMH load. WMH load quantification together with comprehensive neuroanatomic volumetry needs to be examined together for establishing a unique precise and optimal number of brain features as a noninvasive indicator of Brain Age and cognitive status. Here, a comprehensive neuroanatomic volumetry together with WMH quantification using longitudinal MRI and cognitive measurements from two aging cohorts have been performed together with machine learning modeling of the quantitative changes with aging to establish Optimal unique brain events discriminative of cognitive status and estimative of Brain Age. A set of Three optimal brain-associated quantities; wherein two are neuroanatomic features Total brain volume; CSF volume, and the third is the extent of microvascular pathology WMH load, provide highly precise discrimination of cognitive status as cognitively normal (CN), impaired (CI) and AD (CI-AD). While medial cortical thinning of Parahippocampal gyrus is an early age event discriminative between CI and CI-AD but loss of hippocampus, gray matter and white matter volume lacks sensitivity to discriminate between CI and CI-AD. The Brain Age estimation using the neuroanatomic volumetry and periventricular and deep WMH load indicates that elevated WMH load in the brain led to an increased Brain Age gap than the brain with low WMH at a given chronological age. Increased Brain Age gap with elevated WMH load at the early age groups is suggestive of profound vascular insult arising from WMH to the brain structure and function.

neuroscience↗

Mechanosensitive hormone signaling promotes mammary progenitor expansion and breast cancer progression

Tissue stem-progenitor cell frequency has been implicated in tumor risk and progression. Tissue-specific factors linking stem-progenitor cell frequency to cancer risk and progression remain ill defined. Using a genetically engineered mouse model that promotes integrin mechanosignaling with syngeneic manipulations, spheroid models, and patient-derived xenografts we determined that a stiff extracellular matrix and high integrin mechanosignaling increase stem-progenitor cell frequency to enhance breast tumor risk and progression. Studies revealed that high integrin-mechanosignaling expands breast epithelial stem-progenitor cell number by potentiating progesterone receptor-dependent RANK signaling. Consistently, we observed that the stiff breast tissue from women with high mammographic density, who exhibit an increased lifetime risk for breast cancer, also have elevated RANK signaling and a high frequency of stem-progenitor epithelial cells. The findings link tissue fibrosis and integrin mechanosignaling to stem-progenitor cell frequency and causally implicate hormone signaling in this phenotype. Accordingly, inhibiting RANK signaling could temper the tumor promoting impact of fibrosis on breast cancer and reduce the elevated breast cancer risk exhibited by women with high mammographic density. SummaryElevated mechano-signaling and matrix stiffness promote progesterone and RANK mediated expansion of mammary progenitors and breast cancer risk and progression.

cancer biology↗