Hui Zhao

ORCID: 0009-0009-2818-2911
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About
Contact & Profiles
Research Areas
  • Cancer Genomics and Diagnostics
  • RNA modifications and cancer
  • Bacterial biofilms and quorum sensing
  • Genetic Associations and Epidemiology
  • Cancer, Hypoxia, and Metabolism
  • Antimicrobial Peptides and Activities
  • Genetic factors in colorectal cancer
  • Epigenetics and DNA Methylation
  • BRCA gene mutations in cancer
  • RNA and protein synthesis mechanisms
  • Cell Adhesion Molecules Research
  • Biochemical and Structural Characterization
  • Reproductive System and Pregnancy
  • RNA Research and Splicing
  • Blood disorders and treatments
  • Mitochondrial Function and Pathology
  • Gene expression and cancer classification
  • Lymphoma Diagnosis and Treatment
  • Angiogenesis and VEGF in Cancer
  • DNA Repair Mechanisms
  • Protein Hydrolysis and Bioactive Peptides
  • Bacteriophages and microbial interactions
  • ATP Synthase and ATPases Research
  • Platelet Disorders and Treatments
  • Genetic Mapping and Diversity in Plants and Animals

Cancer Research UK
2021-2025

Cancer Research UK Cambridge Center
2021-2025

Guizhou Normal University
2025

Shanxi Medical University
2025

Taian City Central Hospital
2025

Second Hospital of Shanxi Medical University
2025

University of Cambridge
2021-2025

First Affiliated Hospital of Kunming Medical University
2008-2024

Kunming Medical University
2008-2024

Osaka University
2024

10.1038/nature06258 article EN Nature 2007-10-01

Salmonella enterica serovar Typhimurium is a main cause of bacterial food-borne diseases. As can form biofilms in which it better protected against antimicrobial agents on wide diversity surfaces, interest to explore ways inhibit biofilm formation. Brominated furanones, originally extracted from the marine alga Delisea pulchra, are known interfere with formation several pathogens. In this study, we have synthesized small focused library brominated furanones and tested their activity S. We...

10.1128/aem.01262-08 article EN Applied and Environmental Microbiology 2008-09-13

For a comprehensive understanding of cells or tissues, it is important to enable multiple studies under the controllable microenvironment chip. In this report, we present an integrated microfluidic cell culture platform in which endothelial (ECs) are static conditions exposed pulsatile and oscillatory shear stress. Through integration microgap, self-contained flow loop, pneumatic pumps, valves, novel chip achieved functions: fluid circulation, trapping, culture, formation ECs barrier, adding...

10.1039/b909312e article EN Lab on a Chip 2009-01-01

Long non-coding RNAs (lncRNAs), representing a large proportion of transcripts across the human genome, are evolutionally conserved and biologically functional. At least one-third phenotype-related loci identified by genome-wide association studies (GWAS) mapped to intervals. However, relationships between lncRNAs largely unknown. Utilizing 1000 Genomes data, we compared single-nucleotide polymorphisms (SNPs) within sequences lncRNA protein-coding genes as defined in Ensembl database. We...

10.1093/carcin/bgr187 article EN Carcinogenesis 2011-08-19

AGS-16C3F is an antibody-drug conjugate (ADC) against ectonucleotide pyrophosphatase/phosphodiesterase 3 (ENPP3) containing the mcMMAF linker-payload currently in development for treatment of metastatic renal cell carcinoma. and other ADCs have been reported to cause ocular toxicity patients by unknown mechanisms. To investigate this toxicity, we developed vitro assay using human corneal epithelial cells (HCEC) show that HCECs internalized macropinocytosis, causing inhibition proliferation....

10.1158/0008-5472.can-17-3202 article EN Cancer Research 2018-01-30

DNA replication errors that persist as mismatch mutations make up the molecular fingerprint of repair (MMR)-deficient tumors and convey them with resistance to standard therapy. Using whole-genome whole-exome sequencing, we here confirm an MMR-deficient mutation signature is distinct from other tumor genomes, but surprisingly similar germ-line DNA, indicating a substantial fraction human genetic variation arises through escaping MMR. Moreover, identify large set recurrent indels may serve...

10.7554/elife.02725 article EN cc-by eLife 2014-08-01
Dylan M. Glubb Mel Maranian Kyriaki Michailidou Karen A. Pooley Kerstin B. Meyer and 95 more Siddhartha Kar Saskia Carlebur Martin O’Reilly Joshua A. Betts Kristine M. Hillman Susanne Kaufmann Jonathan Beesley Sander Canisius John L. Hopper Melissa C. Southey Helen Tsimiklis Carmel Apicella Marjanka K. Schmidt Annegien Broeks Frans B.L. Hogervorst C. Ellen van der Schoot Kenneth Muir Artitaya Lophatananon Sarah Stewart‐Brown Pornthep Siriwanarangsan Peter A. Fasching Matthias Ruebner Arif B. Ekici Matthias W. Beckmann Julian Peto Isabel dos‐Santos‐Silva Olivia Fletcher Nichola Johnson Paul D.P. Pharoah Manjeet K. Bolla Sophia Wang Joe Dennis Elinor J. Sawyer Ian Tomlinson Michael J. Kerin Nicola Miller Barbara Burwinkel Frederik Marmé Rongxi Yang Harald Surowy Pascal Guénel Thérèse Truong F. Ménégaux Marie-Pierre Sanchez Stig E. Bojesen Børge G. Nordestgaard Sune F. Nielsen Henrik Flyger Anna González‐Neira Javier Benı́tez M. Pilar Zamora José Ignacio Arias Pérez Hoda Anton‐Culver Susan L. Neuhausen Hermann Brenner Aida Karina Dieffenbach Volker Arndt Christa Stegmaier Alfons Meindl Rita K. Schmutzler Hiltrud Brauch Yon‐Dschun Ko Thomas Brüning Heli Nevanlinna Taru Muranen Kristiina Aittomäki Carl Blomqvist Keitaro Matsuo Hidemi Ito Hiroji Iwata Hideo Tanaka Thilo Dörk Natalia Bogdanova Sonja Helbig Annika Lindblom Sara Margolin Graham J. Mann Vesa Kataja Veli-Matti Kosma Jaana M. Hartikainen Anna H. Wu Chiu-Chen Tseng David Van Den Berg Daniel O. Stram Diether Lambrechts Hui Zhao Caroline Weltens Erik Van Limbergen Jenny Chang‐Claude Dieter Flesch‐Janys Anja Rudolph Petra Seibold Paolo Radice Paolo Peterlongo Monica Barile

Genome-wide association studies (GWASs) have revealed SNP rs889312 on 5q11.2 to be associated with breast cancer risk in women of European ancestry. In an attempt identify the biologically relevant variants, we analyzed 909 genetic variants across 103,991 individuals and control from 52 Breast Cancer Association Consortium. Multiple logistic regression analyses identified three independent signals: strongest associations were 15 correlated (iCHAV1), where minor allele best candidate,...

10.1016/j.ajhg.2014.11.009 article EN cc-by-nc-nd The American Journal of Human Genetics 2014-12-19

Candidate gene studies have reported CYP19A1 variants to be associated with endometrial cancer and estradiol (E 2 ) concentrations. We analyzed 2937 single nucleotide polymorphisms (SNPs) in 6608 cases 37 925 controls report the first genome wide-significant association between a SNP (rs727479 intron 2, P =4.8×10 −11 ). rs727479 was also among those most strongly circulating E concentrations 2767 post-menopausal ( =7.4×10 −8 The observed odds ratio per A-allele (1.15, CI=1.11–1.21) is...

10.1530/erc-15-0386 article EN cc-by Endocrine Related Cancer 2015-11-16

Neutropenia is a common adverse event in cancer patients treated with antibody-drug conjugates (ADC) and we aimed to elucidate the potential mechanism of this toxicity. To investigate whether ADCs affect neutrophil production from bone marrow, an vitro assay was developed which hematopoietic stem cells (HSC) were differentiated neutrophils. Several antibodies against targets absent HSCs neutrophils conjugated MMAE via cleavable valine-citrulline linker (vcMMAE-ADC) or MMAF noncleavable...

10.1158/1535-7163.mct-17-0133 article EN Molecular Cancer Therapeutics 2017-05-19

Abstract Analysis of circulating tumor DNA (ctDNA) to monitor cancer dynamics and detect minimal residual disease has been an area increasing interest. Multiple methods have proposed but few studies compared the performance different approaches. Here, we compare detection ctDNA in serial plasma samples from patients with breast using tumor‐informed tumor‐naïve assays designed structural variants (SVs), single nucleotide (SNVs), and/or somatic copy‐number aberrations, by multiplex PCR, hybrid...

10.15252/emmm.202216505 article EN cc-by EMBO Molecular Medicine 2023-05-10

Effectiveness of marker-assisted selection (MAS) and quantitative trait locus (QTL) mapping using population-wide linkage disequilibrium (LD) between markers QTLs depends on the extent LD how it declines with distance in a population. Marker–QTL can be predicted from markers. Our previous work evaluated measures multi-allelic as predictors usable QTLs. Since single nucleotide polymorphisms (SNPs) are current marker choice for high-density genotyping LD-mapping QTLs, objective this study was...

10.1017/s0016672307008634 article EN Genetics Research 2007-02-01

Abstract Thrombocytopenia is a common adverse event in cancer patients treated with antibody–drug conjugates (ADC), including AGS-16C3F, an ADC targeting ENPP3 (ectonucleotide pyrophosphatase/phosphodiesterase-3) and trastuzumab emtansine (T-DM1). This study aims to elucidate the mechanism of action ADC-induced thrombocytopenia. expression platelets megakaryocytes (MK) was investigated shown be negative. The direct effect AGS-16C3F on evaluated using platelet rich plasma following activation...

10.1158/1535-7163.mct-16-0710 article EN Molecular Cancer Therapeutics 2017-06-28

Protection against endothelial damage is recognized as a frontline approach to preventing the progression of cytokine release syndrome (CRS). Accumulating evidence has demonstrated that interleukin-6 (IL-6) promotes vascular during CRS, although molecular mechanisms remain be fully elucidated. Targeting IL-6 receptor signaling delays CRS progression; however, current options are limited by persistent inhibition immune system. Here, we show trans-signaling promoted and inflammatory responses...

10.1073/pnas.2315898120 article EN Proceedings of the National Academy of Sciences 2024-01-02
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