Wan Jun Lim

ORCID: 0000-0003-2252-879X
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About
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Research Areas
  • Cancer Immunotherapy and Biomarkers
  • Immunotherapy and Immune Responses
  • Cancer Genomics and Diagnostics
  • Cancer, Hypoxia, and Metabolism
  • Autophagy in Disease and Therapy
  • Angiogenesis and VEGF in Cancer
  • RNA modifications and cancer
  • Hepatitis B Virus Studies
  • Adipose Tissue and Metabolism
  • Genetic factors in colorectal cancer
  • Cancer Cells and Metastasis
  • Muscle Physiology and Disorders
  • Ferroptosis and cancer prognosis
  • Single-cell and spatial transcriptomics
  • Immune Cell Function and Interaction
  • CAR-T cell therapy research
  • Colorectal Cancer Treatments and Studies

St. Jude Children's Research Hospital
2021

National Cancer Centre Singapore
2016-2021

Abstract Profiling of circulating tumor DNA (ctDNA) may offer a non-invasive approach to monitor disease progression. Here, we develop quantitative method, exploiting local tissue-specific cell-free (cfDNA) degradation patterns, that accurately estimates ctDNA burden independent genomic aberrations. Nucleosome-dependent cfDNA at promoters and first exon-intron junctions is strongly associated with differential transcriptional activity in tumors blood. A model, based on just 6 regulatory...

10.1038/s41467-021-22463-y article EN cc-by Nature Communications 2021-04-13

e15531 Background: Response to immune checkpoint inhibition is dismal in colorectal cancer (CRC). There are limited experimental models evaluate immunotherapy human CRC. We developed an ex vivo co-culture system interrogate pharmacologic or genetic perturbations that modulate anti-cancer immunotoxicity Methods: Our uses expanded CD8+ TILs & peripheral blood mononuclear cells (PBMC), cultured up 6 weeks with engineered auxotrophic K562 aPCs, as effector cells. For target cells, we use both...

10.1200/jco.2018.36.15_suppl.e15531 article EN Journal of Clinical Oncology 2018-05-20

Abstract Background: Immunotherapy has so far had limited success in colorectal cancer (CRC), with its efficacy restricted to a subset of microsatellite instability high (MSI-H) tumors. A comprehensive interrogation the CRC tumor immune microenvironment (TME) is urgently needed. We present here an ongoing multi-platform study on early stage colon and rectal cancers, where immuno-genomic profiling tumors patient-derived cell models epithelia, cancer-associated fibroblasts tumor-infiltrating...

10.1158/1538-7445.am2020-3990 article EN cc-by-nc Cancer Research 2020-08-15

In the context of hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC), despite a range possibilities, antigen specificities tumor-infiltrating T cells and their relevance to control is largely unknown. Using highly multiplexed peptide-MHC tetramer staining unexpanded from blood, liver tumor tissues 46 HCC patients, we detected 91 different CD8 cell populations specific for epitopes derived HBV, tumor-associated neoantigens (NeoAg), as well disease-unrelated antigens. Parallel...

10.2139/ssrn.3760654 article EN SSRN Electronic Journal 2021-01-01
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