Publications by authors named "Keyong Sun"

Article Synopsis
  • Researchers are exploring targeted therapies for cancer by focusing on neoantigens, but these are difficult to detect on tumor cells due to their low expression.
  • Chimeric antigen receptors (CARs) are significantly less sensitive (10-100 times) than T cell receptors (TCRs) when it comes to targeting specific neoantigens like p53 presented by HLA class I.
  • Introducing synthetic receptors like STARs shows promise as they mimic TCR sensitivity better, proving more effective in redirecting T cells to attack tumors with low neoantigen density, leading to improved cancer cell killing in lab studies and better tumor control in animal models.
View Article and Find Full Text PDF
Article Synopsis
  • Identifying T-cell receptors (TCRs) and virus epitopes is vital due to the rapid mutations of viruses like SARS-CoV-2, necessitating the development of a cost-effective and scalable workflow for this task.
  • The study employs a tandem minigene (TMG) system and peptide-major histocompatibility complex-displaying yeasts to streamline epitope identification, avoiding the need for time-consuming peptide synthesis.
  • Results show that 75% of individuals recovered from COVID-19 have T cells targeting a specific shared epitope from the virus, suggesting that some TCRs can cross-react with mutant strains, which may help in providing lasting immune responses.
View Article and Find Full Text PDF

Bone metastasis is a lethal consequence of breast cancer. Here we used single-cell transcriptomics to investigate the molecular mechanisms underlying bone metastasis colonization-the rate-limiting step in the metastatic cascade. We identified that lymphotoxin-β (LTβ) is highly expressed in tumour cells within the bone microenvironment and this expression is associated with poor bone metastasis-free survival.

View Article and Find Full Text PDF

Currently, the dynamic accessible elements that determine regulatory programs responsible for the unique identity and function of each cell type during zebrafish embryogenesis lack detailed study. Here we present SPATAC-seq: a split-pool ligation-based assay for transposase-accessible chromatin using sequencing. Using SPATAC-seq, we profiled chromatin accessibility in more than 800,000 individual nuclei across 20 developmental stages spanning the sphere stage to the early larval protruding mouth stage.

View Article and Find Full Text PDF

Organogenesis is a highly complex and precisely regulated process. Here we profiled the chromatin accessibility in >350,000 cells derived from 13 mouse embryos at four developmental stages from embryonic day (E) 10.5 to E13.

View Article and Find Full Text PDF

Janus hydrogels with different properties on the two surfaces have considerable potential in the field of material engineering applications. Various Janus hydrogels have been developed, but there are still some problems, such as stress mismatch caused by the double-layer structure and Janus failure caused by material diffusion in the gradient structure. Here, we report a Janus adhesive-tough hydrogel with polydopamine-decorated FeO nanoparticles (FeO@PDA) at one side induced by magnetic field to avoid uncontrollable material diffusion in the cross-linking polymerization of acrylamide with alginate-calcium.

View Article and Find Full Text PDF

The tumor microenvironment (TME) in gastric cancer (GC) has been shown to be important for tumor control but the specific characteristics for GC are not fully appreciated. We generated an atlas of 166,533 cells from 10 GC patients with matched paratumor tissues and blood. Our results show tumor-associated stromal cells (TASCs) have upregulated activity of Wnt signaling and angiogenesis, and are negatively correlated with survival.

View Article and Find Full Text PDF

Immune checkpoint inhibitor (ICI) therapy is generating remarkable responses in individuals with cancer, but only a small portion of individuals with breast cancer respond well. Here we report that tumor-derived Jagged1 is a key regulator of the tumor immune microenvironment. Jagged1 promotes tumorigenesis in multiple spontaneous mammary tumor models.

View Article and Find Full Text PDF

Hi-C is a genome-wide assay based on Chromosome Conformation Capture and high-throughput sequencing to decipher 3D chromatin organization in the nucleus. However, computational methods to detect functional interactions utilizing Hi-C data face challenges including the correction for various sources of biases and the identification of functional interactions with low counts of interacting fragments. We present Chrom-Lasso, a lasso linear regression model that removes complex biases assumption-free and identifies functional interacting loci with increased power by combining information of local reads distribution surrounding the area of interest.

View Article and Find Full Text PDF

Increasing evidence has supported the crucial role of CARD14 in the pathogenesis of psoriasis, whereas the precise cellular signaling involved in skin physiopathology remains poorly understood. In this article, we show that neither genetic ablation of nor elimination of T cells was sufficient to restrain the skin inflammation in a CARD14-E138A-mutation-induced psoriasis-like mouse model, whereas depletion of , which extremely blocked the IL-23/T17 axis, was more effective. Targeting CBM complex by conditional deletion of MALT1 or BCL10 in keratinocytes abrogated both the cutaneous and systemic inflammation of heterozygous mice.

View Article and Find Full Text PDF

The expression level of folate receptor alpha (FRα) is located highly rate in ovarian cancer though it is remained absent in normal tissues. This highly tumor restricted expression profile makes FRα a promising target for tumor therapy and diagnosis. In this research we report a FRα binding peptide C7(Met-His-Thr-Ala-Pro-Gly-Trp-Gly-Tyr-Arg-Leu-Ser) discovered by phage display and this peptide showed specific binding to FRα expressing cells by cell ELISA and flow cytometry.

View Article and Find Full Text PDF

Phage peptide display is a powerful technique for discovery of various target-specific ligands. However, target-unrelated peptides can often be obtained and cause ambiguous results. Peptide PB-TUP has been isolated repeatedly in our laboratory on different targets and we conducted a research on PB-TUP phage to investigate their binding properties and rate of propagation.

View Article and Find Full Text PDF