Liang‐I Kang

ORCID: 0000-0001-7025-3095
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About
Contact & Profiles
Research Areas
  • Cancer Immunotherapy and Biomarkers
  • Immunotherapy and Immune Responses
  • Phagocytosis and Immune Regulation
  • Epigenetics and DNA Methylation
  • Pancreatic and Hepatic Oncology Research
  • Retinopathy of Prematurity Studies
  • Protein Degradation and Inhibitors
  • Tissue Engineering and Regenerative Medicine
  • Ferroptosis and cancer prognosis
  • Cancer Genomics and Diagnostics
  • Liver physiology and pathology
  • Immune cells in cancer
  • CAR-T cell therapy research
  • Meningioma and schwannoma management
  • Liver Disease Diagnosis and Treatment
  • MicroRNA in disease regulation
  • RNA modifications and cancer
  • Pancreatic function and diabetes
  • Histone Deacetylase Inhibitors Research
  • Neuroendocrine Tumor Research Advances
  • Liver Disease and Transplantation
  • Pancreatitis Pathology and Treatment
  • Organ Transplantation Techniques and Outcomes
  • Viral gastroenteritis research and epidemiology
  • Gastrointestinal Tumor Research and Treatment

Ministry of Agriculture and Rural Affairs
2025

Anhui Agricultural University
2025

Washington University in St. Louis
2018-2024

Hebei University
2024

Hunter New England Local Health District
2023

University of Newcastle Australia
2023

Hunter Medical Research Institute
2023

Jewish Hospital
2022

Barnes-Jewish Hospital
2019-2022

Fiona Stanley Hospital
2020

Pancreatic ductal adenocarcinoma (PDAC) therapeutic resistance is largely attributed to a unique tumor microenvironment embedded with an abundance of cancer-associated fibroblasts (CAF). Distinct CAF populations were recently identified, but the phenotypic drivers and specific impact heterogeneity remain unclear. In this study, we identify subpopulation senescent myofibroblastic CAFs (SenCAF) in mouse human PDAC. These SenCAFs are phenotypically distinct subset that localize near ducts...

10.1158/2159-8290.cd-23-0428 article EN Cancer Discovery 2024-04-26

Antimicrobial peptides (AMPs) are small that play an important role in disease defense. As the problem of pathogen resistance caused by misuse antibiotics intensifies, identification AMPs as alternatives to has become a hot topic. Accurately identifying using computational methods been key issue field bioinformatics recent years. Although there many machine learning-based AMP tools, most them do not focus on or only few functional activities. Predicting multiple activities antimicrobial can...

10.1021/acs.jcim.4c01913 article EN Journal of Chemical Information and Modeling 2025-01-10

Liver regeneration is a complex phenomenon aimed at maintaining constant liver mass in the event of injury resulting loss hepatic parenchyma. Partial hepatectomy followed by series events involving multiple signaling pathways controlled mitogenic growth factors (HGF, EGF) and their receptors (MET EGFR). In addition cytokines other molecules contribute to orchestration signal which drives hepatocytes into DNA synthesis. The cell types receive transmit signals so that, end regenerative...

10.3390/cells1041261 article EN cc-by Cells 2012-12-13

Exogenous interleukin 6 (IL-6), synthesized at the initiation of acute phase response, is considered responsible for signaling hepatocytes to produce proteins. It widely posited that IL-6 either delivered liver in an endocrine fashion from immune cells site injury, or alternatively, a paracrine manner by hepatic within liver. A recent publication showed there was muted response lipopolysaccharide (LPS)-injured mice when nuclear NFκB specifically inactivated hepatocytes. This indicates...

10.1371/journal.pone.0096053 article EN cc-by PLoS ONE 2014-04-24

Abstract The effects of radiotherapy (RT) on tumor immunity in pancreatic ductal adenocarcinoma (PDAC) are not well understood. To better understand if RT can prime antigen-specific T-cell responses, we analyzed human PDAC tissues and mouse models. In both settings, there was little evidence RT-induced priming. Using vitro systems, found that tumor–stromal components, including fibroblasts collagen, cooperate to blunt efficacy impair interferon signaling. Focal adhesion kinase (FAK)...

10.1158/2159-8290.cd-22-0192 article EN Cancer Discovery 2022-09-27

Recent investigations of the meninges have highlighted importance dura layer in central nervous system immune surveillance beyond a purely structural role. However, our understanding largely stems from use pre-clinical models rather than human samples.

10.1186/s13073-022-01051-9 article EN cc-by Genome Medicine 2022-05-09

Non–small cell lung cancer (NSCLC) is a leading cause of cancer-related deaths. Immune checkpoint blockade has improved survival for many patients with NSCLC, but most fail to obtain long-term benefit. Understanding the factors reduced immune surveillance in NSCLC critical improving patient outcomes. Here, we show that human harbors large amounts fibrosis correlates T infiltration. In murine models, induction led increased progression, impaired surveillance, and failure efficacy. Associated...

10.1126/scitranslmed.adh8005 article EN Science Translational Medicine 2023-06-07

<p>Supplementary Figure S4. CK5 and CK17 do not predict treatment response or time to recurrence. A) Combining GATA6 IHC does overall survival. B) high, low tumors display improved survival compared low, high tumors. C) Kaplan-Meier curves for positive negative treated with first-line gemcitabine chemotherapy. D) E) status F) show longer recurrence than tumors, the opposite phenotype expected from basal subtype.</p>

10.1158/1078-0432.28431507 preprint EN cc-by 2025-02-17

<p>Supplementary Figure S3. Consort Diagram and Mixed Populations. A) diagram of analyzed samples. For survival analyses, all patients with intact cores (n = 491) were assessed. treatment response further subdivided by type chemotherapy received, neoadjuvant-treated samples considered separately 51). B) (HMGA2+ GATA6+) double negative (HMGA2- GATA6-) populations show intermediate between basal classical tumors.</p>

10.1158/1078-0432.28431510 preprint EN cc-by 2025-02-17

<p>Supplementary Figure S6. GATA6 expression predicts chemotherapy response to GnP but not mFFX. A) GATA6low metastatic tumors have significantly worse overall survival when treated with combination first-line chemotherapy. B) status does predict patients receive first line mFFX chemotherapy.</p>

10.1158/1078-0432.28431501 preprint EN cc-by 2025-02-17

<div>AbstractPurpose:<p>The purpose of this study was to establish HMGA2 as a marker basal-like disease in pancreatic ductal adenocarcinoma (PDAC) and explore its use biomarker for prognosis treatment resistance.</p>Experimental Design:<p>We identified high-mobility group A2 (HMGA2) protein expression basal PDAC cells single-cell RNA sequencing (RNA-seq) atlas 172 patient samples. We then analyzed expression, along with the classic GATA-binding factor 6 (GATA6),...

10.1158/1078-0432.c.7676155 preprint EN 2025-02-17

<p>Supplementary Figure S6. GATA6 expression predicts chemotherapy response to GnP but not mFFX. A) GATA6low metastatic tumors have significantly worse overall survival when treated with combination first-line chemotherapy. B) status does predict patients receive first line mFFX chemotherapy.</p>

10.1158/1078-0432.28428097 preprint EN cc-by 2025-02-17
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