Lauren A. Hapach

ORCID: 0000-0002-9404-8974
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About
Contact & Profiles
Research Areas
  • Cancer Cells and Metastasis
  • Radiopharmaceutical Chemistry and Applications
  • Estrogen and related hormone effects
  • Computational Drug Discovery Methods
  • Cellular Mechanics and Interactions
  • Cancer, Hypoxia, and Metabolism
  • Bone Tissue Engineering Materials
  • Prostate Cancer Treatment and Research
  • Glutathione Transferases and Polymorphisms
  • Extracellular vesicles in disease
  • Metabolism, Diabetes, and Cancer
  • Collagen: Extraction and Characterization
  • Microfluidic and Bio-sensing Technologies
  • Cancer-related molecular mechanisms research
  • Electrospun Nanofibers in Biomedical Applications
  • Gene expression and cancer classification
  • Immune cells in cancer
  • Cancer Genomics and Diagnostics
  • 3D Printing in Biomedical Research
  • Cancer Research and Treatments
  • Microtubule and mitosis dynamics
  • Erythrocyte Function and Pathophysiology
  • Molecular Biology Techniques and Applications
  • Chemical Reactions and Isotopes
  • Immunotherapy and Immune Responses

Saint Meinrad Seminary and School of Theology
2024

Cornell University
2015-2023

Vanderbilt University
2021-2023

Abstract Although intratumoral genomic heterogeneity can impede cancer research and treatment, less is known about the effects of phenotypic heterogeneities. To investigate role cell migration heterogeneities in metastasis, we phenotypically sorted metastatic breast cells into two subpopulations based on ability. typically considered to be associated with when injected orthotopically vivo, weakly migratory subpopulation metastasized significantly more than highly subpopulation. mechanism...

10.1158/0008-5472.can-20-1799 article EN Cancer Research 2021-05-11

Diabetes mellitus is a complex metabolic disorder that associated with an increased risk of breast cancer. Despite this correlation, the interplay between tumor progression and diabetes, particularly regard to stiffening extracellular matrix, still mechanistically unclear. Here, we established murine model where hyperglycemia was induced before development. Using model, in vitro systems, patient samples, show increases growth, matrix stiffness, glycation, epithelial-mesenchymal transition...

10.1126/sciadv.abo1673 article EN cc-by-nc Science Advances 2022-11-16

Intratumor heterogeneity is a well-established hallmark of cancer that impedes research, diagnosis, and treatment. Previously, we phenotypically sorted human breast cells based on migratory potential. When injected into mice, highly were weakly metastatic metastatic. The purpose this study was to determine whether these interact with each other in vitro or vivo.To assess the relationship between cell migration fitness, MDA-MB-231 SUM159PT triple negative subpopulations assayed separately 1:1...

10.1186/s13058-023-01696-3 article EN cc-by Breast Cancer Research 2023-08-30

Intracellular and environmental cues result in heterogeneous cancer cell populations with different metabolic migratory behaviors. Although glucose metabolism epithelial-to-mesenchymal transition have previously been linked, we aim to understand how this relationship fuels migration. We show that while glycolysis drives single-cell migration confining microtracks, fast slow cells display sensitivities oxidative phosphorylation inhibition. Phenotypic sorting of highly weakly subpopulations...

10.1016/j.isci.2022.105190 article EN cc-by-nc-nd iScience 2022-10-01

Cancer cell migration is highly heterogeneous, and the migratory capability of cancer cells thought to be an indicator metastatic potential. It becoming clear that a does not have inherently metastasize, with weakly often found metastatic. However, mechanism through which escape from primary tumor remains unclear. Here, utilizing phenotypically sorted human breast cells, we demonstrate disseminate via communication stromal cells. While are capable single migration, rely on cell-cell...

10.7554/elife.74433 article EN cc-by eLife 2022-12-06

Scaffold mechanical properties are essential in regulating the microenvironment of three-dimensional cell culture. A coupled fiber-matrix numerical model was developed this work for predicting response collagen scaffolds subjected to various levels non-enzymatic glycation and concentrations. The scaffold simulated by a Voronoi network embedded matrix. computational validated using published experimental data. Results indicate that both glycation-induced matrix stiffening fiber density, as...

10.3390/ma8085254 article EN cc-by Materials 2015-08-20

Mounting evidence suggests that the immune landscape within prostate tumors influences progression, metastasis, treatment response, and patient outcomes. In this study, we investigated spatial density of innate cell populations NOD.SCID orthotopic cancer xenografts following microinjection human DU145 cells. Our laboratory has previously developed nanoscale liposomes attach to leukocytes via conjugated E-selectin (ES) kill cells TNF-related apoptosis inducing ligand (TRAIL)....

10.3389/pore.2024.1611586 article EN cc-by Pathology & Oncology Research 2024-04-16

Abstract Cancer cell migration is highly heterogeneous, and the migratory capability of cancer cells thought to be an indicator metastatic potential. It becoming clear that a does not have inherently metastasize, with weakly often found metastatic. However, mechanism through which escape from primary tumor remains unclear. Here, utilizing phenotypically sorted breast cells, we demonstrate disseminate via communication stromal cells. While are capable single migration, rely on cell-cell...

10.1101/2021.10.27.466095 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2021-10-29

<div>Abstract<p>Although intratumoral genomic heterogeneity can impede cancer research and treatment, less is known about the effects of phenotypic heterogeneities. To investigate role cell migration heterogeneities in metastasis, we phenotypically sorted metastatic breast cells into two subpopulations based on ability. Although typically considered to be associated with when injected orthotopically <i>in vivo</i>, weakly migratory subpopulation metastasized...

10.1158/0008-5472.c.6513169.v1 preprint EN 2023-03-31

<div>Abstract<p>Although intratumoral genomic heterogeneity can impede cancer research and treatment, less is known about the effects of phenotypic heterogeneities. To investigate role cell migration heterogeneities in metastasis, we phenotypically sorted metastatic breast cells into two subpopulations based on ability. Although typically considered to be associated with when injected orthotopically <i>in vivo</i>, weakly migratory subpopulation metastasized...

10.1158/0008-5472.c.6513169 preprint EN 2023-03-31
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