Amy Zhang

ORCID: 0000-0002-6536-3609
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About
Contact & Profiles
Research Areas
  • Pancreatic and Hepatic Oncology Research
  • Cancer Genomics and Diagnostics
  • Epigenetics and DNA Methylation
  • Cancer Research and Treatments
  • PARP inhibition in cancer therapy
  • Cancer Immunotherapy and Biomarkers
  • Bone health and treatments
  • Renal cell carcinoma treatment
  • CAR-T cell therapy research
  • Ferroptosis and cancer prognosis
  • Genetic factors in colorectal cancer
  • Single-cell and spatial transcriptomics
  • Phagocytosis and Immune Regulation
  • Neuroendocrine Tumor Research Advances
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Mitochondrial Function and Pathology
  • Gut microbiota and health
  • Cancer Cells and Metastasis
  • Advanced biosensing and bioanalysis techniques
  • Glaucoma and retinal disorders
  • Effects of Radiation Exposure
  • Colorectal Cancer Treatments and Studies
  • Cancer, Lipids, and Metabolism
  • Immunotherapy and Immune Responses
  • Spectroscopy Techniques in Biomedical and Chemical Research

Stanford University
2024-2025

University of Michigan–Ann Arbor
2024-2025

Ontario Institute for Cancer Research
2017-2024

Yale University
2020-2024

Center for Neurosciences
2024

Indiana University – Purdue University Indianapolis
2014-2024

National Institutes of Health
2019-2024

Indiana University Indianapolis
2024

Institute of Cancer Research
2017-2024

Princess Margaret Cancer Centre
2023

Purpose: To perform real-time whole genome sequencing (WGS) and RNA (RNASeq) of advanced pancreatic ductal adenocarcinoma (PDAC) to identify predictive mutational transcriptional features for better treatment selection.Experimental Design: Patients with PDAC were prospectively recruited prior first-line combination chemotherapy. Fresh tumor tissue was acquired by image-guided percutaneous core biopsy WGS RNASeq. Laser capture microdissection performed all cases. Primary endpoint feasibility...

10.1158/1078-0432.ccr-17-2994 article EN Clinical Cancer Research 2017-12-29

Abstract Purpose: To determine the impact of basal-like and classical subtypes in advanced pancreatic ductal adenocarcinoma (PDAC) to explore GATA6 expression as a surrogate biomarker. Experimental Design: Within COMPASS trial, patients proceeding chemotherapy for PDAC undergo tumor biopsy RNA-sequencing (RNA-seq). Overall response rate (ORR) overall survival (OS) were stratified by according received. Correlation with using gene profiling, situ hybridization (ISH) was explored. Results:...

10.1158/1078-0432.ccr-19-3724 article EN Clinical Cancer Research 2020-03-10

Abstract The most prominent homozygous deletions in cancer affect chromosome 9p21.3 and eliminate CDKN2A/B tumor suppressors, disabling a cell-intrinsic barrier to tumorigenesis. Half of deletions, however, also encompass type I interferon (IFN) gene cluster; the consequences this co-deletion remain unexplored. To functionally dissect other large genomic we developed flexible deletion engineering strategy, MACHETE (molecular alteration chromosomes with engineered tandem elements). Applying...

10.1038/s43018-022-00443-5 article EN cc-by Nature Cancer 2022-11-07

The molecular drivers of antitumor immunity in pancreatic ductal adenocarcinoma (PDAC) are poorly understood, posing a major obstacle for the identification patients potentially amenable immune-checkpoint blockade or other novel strategies. Here, we explore association chemokine expression with effector T-cell infiltration PDAC.Discovery cohorts comprised 113 primary resected PDAC and 107 liver metastases. Validation 182 from Cancer Genome Atlas 92 PDACs Australian International Consortium....

10.1158/1078-0432.ccr-19-2803 article EN Clinical Cancer Research 2020-01-21

Abstract The degree of metastatic disease varies widely among patients with cancer and affects clinical outcomes. However, the biological functional differences that drive extent metastasis are poorly understood. We analyzed primary tumors paired metastases using a multifluorescent lineage-labeled mouse model pancreatic ductal adenocarcinoma (PDAC)—a tumor type in which most present metastases. Genomic transcriptomic analysis revealed an association between burden gene amplification or...

10.1158/2159-8290.cd-20-1826 article EN cc-by-nc-nd Cancer Discovery 2021-09-22

Germline BRCA-associated pancreatic ductal adenocarcinoma (glBRCA PDAC) tumors are susceptible to platinum and PARP inhibition. The clinical outcomes of 125 patients with glBRCA PDAC were stratified based on the spectrum response platinum/PARP inhibition: (i) refractory [overall survival (OS) <6 months], (ii) durable followed by acquired resistance (OS <36 months), (iii) long-term responders >36 months). Patient-derived xenografts (PDX) generated from 25 at different time points. Response...

10.1158/2159-8290.cd-22-0412 article EN cc-by-nc-nd Cancer Discovery 2023-07-14

Abstract Reported is a new shell‐based spectroscopic platform, named mechanical trap surface‐enhanced Raman spectroscopy (MTSERS), for simultaneous capture, profiling, and 3D microscopic mapping of the intrinsic molecular signatures on membrane single live cells. By leveraging functionalization inner surfaces MTs with plasmonic gold nanostars, conformal contact cell membrane, MTSERS permits excellent signal enhancement, reliably detects signatures, allows non‐perturbative, multiplex surface...

10.1002/anie.201700695 article EN Angewandte Chemie International Edition 2017-02-15

While localized prostate cancer (PCa) can be effectively cured, metastatic disease inevitably progresses to a lethal state called castration-resistant (CRPC). Emerging evidence suggests that aberrant epigenetic repression by the polycomb group (PcG) complexes fuels PCa progression, providing novel therapeutic opportunities.In search for potential drivers of CRPC, we analyzed molecular profile PcG members in patient-derived xenografts and clinical samples. Overall, our results identify...

10.1186/s13148-016-0182-9 article EN cc-by Clinical Epigenetics 2016-02-12

Thyroid disorders have emerged as one of the most common immune-related adverse events (irAE), yet optimum management and biomarkers to predict vulnerable individuals remain be explored. High-dose glucocorticoid (HDG) therapy is routinely recommended for irAEs. However, systematic analysis impact on outcome immune-checkpoint inhibitor (ICI)-induced thyroid lacking. We analyzed 151 patients with or without ICI-related disorders. divided into two subgroups: those HDG treatment. Our results...

10.1158/2326-6066.cir-18-0613 article EN Cancer Immunology Research 2019-05-14

To describe the clinical, pathological and genomic characteristics of pancreatic cancer with DNA mismatch repair deficiency (MMRD) proficiency (MMRP).We identified patients MMRD MMRP in a clinical cohort (N=1213, 519 genetic testing, 53 immunohistochemistry (IHC)) (N=288 whole-genome sequencing (WGS)).12 out 1213 (1.0%) were by IHC or WGS. Of 14 Lynch syndrome, 3 (21.4%) had an IHC, 4 (28.6%) excluded because tissue was unavailable for testing. cancers longer overall survival after surgery...

10.1136/gutjnl-2020-320730 article EN Gut 2020-09-15

Pancreatic ductal adenocarcinoma (PDAC) has the worst prognosis among solid malignancies and improved therapeutic strategies are needed to improve outcomes. Patient-derived xenografts (PDX) patient-derived organoids (PDO) serve as promising tools identify new drugs with potential in PDAC. For these preclinical disease models be effective, they should both recapitulate molecular heterogeneity of PDAC validate patient-specific sensitivities. To date however, deep characterization PDX PDO...

10.1371/journal.pcbi.1006596 article EN cc-by PLoS Computational Biology 2019-01-10

Abstract Pancreatic cancer metastasis is a leading cause of cancer-related deaths, yet very little understood regarding the underlying biology. As result, targeted therapies to inhibit are lacking. Here, we report that parathyroid hormone–related protein (PTHrP encoded by PTHLH) frequently amplified as part KRAS amplicon in patients with pancreatic cancer. PTHrP upregulation drives growth both primary and metastatic tumors mice highly enriched ductal adenocarcinoma metastases. Loss...

10.1158/2159-8290.cd-20-1098 article EN Cancer Discovery 2021-02-15

Reward and representation learning are two long-standing challenges for an expanding set of robot manipulation skills from sensory observations. Given the inherent cost scarcity in-domain, task-specific data, large, diverse, offline human videos has emerged as a promising path towards acquiring generally useful visual control; however, how these can be used general-purpose reward remains open question. We introduce $\textbf{V}$alue-$\textbf{I}$mplicit $\textbf{P}$re-training (VIP),...

10.48550/arxiv.2210.00030 preprint EN other-oa arXiv (Cornell University) 2022-01-01

Nucleoporins (nups) in the nuclear pore complex (NPC) form a selective barrier that suppresses diffusion of most macromolecules while enabling rapid transport receptor (NTR)–bound cargos. Recent studies have shown NPC may dilate and constrict, but how altering diameter affects its properties remains unclear. Here, we build DNA nanopores with programmable diameters nup arrangements to model constricted dilated NPCs. We find Nup62 proteins dynamic cross-channel impermeable hepatitis B virus...

10.1126/sciadv.adq8773 article EN cc-by-nc Science Advances 2024-11-13

Precis: Current optical coherence tomography normative sample data may not represent diverse human optic nerve anatomy to accurately classify all individuals with true glaucomatous neuropathy. Purpose: To compare head (ONH) measurements between published values from an (OCT) database and a more cohort of healthy individuals. Patients Methods: ONH parameters participants the Michigan Screening Intervention for Glaucoma Eye Health through Telemedicine (MI-SIGHT) program Topcon Maestro-1 were...

10.1097/ijg.0000000000002545 article EN Journal of Glaucoma 2025-01-29

Commensals shape host physiology through molecular crosstalk with receptors. Identifying specific microbial factors that causally influence immunity is key to understanding homeostasis at the host-microbe interface and advancing microbial-based therapeutics. Here, we identify trehalose monocorynomycolate (TMCM) from Corynebacterium mastitidis ( C. mast ) as a potent stimulator of IL-17 production by γδ T cells ocular surface. Mechanistically, TMCM-driven responses require both IL-1 signals...

10.1101/2025.03.17.643820 preprint EN public-domain bioRxiv (Cold Spring Harbor Laboratory) 2025-03-18
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