Xiaomei Zhang

ORCID: 0000-0003-3121-3992
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About
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Research Areas
  • Cytokine Signaling Pathways and Interactions
  • Cancer Mechanisms and Therapy
  • Advanced Breast Cancer Therapies
  • PI3K/AKT/mTOR signaling in cancer
  • Toxin Mechanisms and Immunotoxins
  • Biochemical and Molecular Research
  • Hippo pathway signaling and YAP/TAZ
  • interferon and immune responses
  • Cancer-related Molecular Pathways
  • Cancer, Lipids, and Metabolism
  • Liver Disease Diagnosis and Treatment
  • Cancer-related molecular mechanisms research
  • Cancer, Hypoxia, and Metabolism

The First Affiliated Hospital, Sun Yat-sen University
2023-2024

Sun Yat-sen University
2023-2024

Objective Whether and how the PI3K-AKT pathway, a central node of metabolic homeostasis, is responsible for high-fat-induced non-alcoholic steatohepatitis (NASH) hepatocellular carcinoma (HCC) remain mystery. Characterisation AKT regulation in this setting will provide new strategies to combat HCC. Design Metabolite library screening disclosed that palmitic acid (PA) could activate AKT. In vivo vitro palmitoylation assay were employed detect palmitoylation. Diverse cell mouse models,...

10.1136/gutjnl-2023-330826 article EN Gut 2024-01-08

Abstract The PI3K–AKT signaling pathway is frequently dysregulated in cancer, and it hyperactivated approximately 50% of breast cancers. Although inhibitors directly targeting the axis have been developed, clinical efficacy has limited to only a subset patients. Identification mechanisms underlying AKT-driven tumorigenesis could lead alternative approaches block suppress tumor growth. Mass spectrometry–based analyses demonstrated that salt-inducible kinase 1 (SIK1) binds AKT undergoes...

10.1158/0008-5472.can-22-3407 article EN Cancer Research 2023-02-20

Physiologically, FoxA1 plays a key role in liver differentiation and development, pathologically exhibits an oncogenic prostate breast cancers. However, its upstream regulation tumorigenesis remain unclear. Here, we demonstrate that acts as tumor suppressor cancer. Using CRISPR-based kinome screening approach, noncanonical inflammatory kinase IKBKE has been identified to inhibit transcriptional activity. Notably, directly binds phosphorylates reduce complex formation DNA interaction, leading...

10.1126/sciadv.adk2285 article EN cc-by-nc Science Advances 2024-02-07

<div>Abstract<p>The PI3K-AKT signaling pathway is frequently dysregulated in cancer, and it hyperactivated approximately 50% of breast cancers. While inhibitors directly targeting the axis have been developed, clinical efficacy has limited to only a subset patients. Identification mechanisms underlying AKT-driven tumorigenesis could lead alternative approaches block suppress tumor growth. Mass spectrometry-based analyses demonstrated that salt-inducible kinase 1 (SIK1) binds AKT...

10.1158/0008-5472.c.6599668.v2 preprint EN 2024-09-16

<div>Abstract<p>The PI3K–AKT signaling pathway is frequently dysregulated in cancer, and it hyperactivated approximately 50% of breast cancers. Although inhibitors directly targeting the axis have been developed, clinical efficacy has limited to only a subset patients. Identification mechanisms underlying AKT-driven tumorigenesis could lead alternative approaches block suppress tumor growth. Mass spectrometry–based analyses demonstrated that salt-inducible kinase 1 (SIK1) binds...

10.1158/0008-5472.c.6599668.v1 preprint EN 2023-04-14

<div>Abstract<p>The PI3K-AKT signaling pathway is frequently dysregulated in cancer, and it hyperactivated approximately 50% of breast cancers. While inhibitors directly targeting the axis have been developed, clinical efficacy has limited to only a subset patients. Identification mechanisms underlying AKT-driven tumorigenesis could lead alternative approaches block suppress tumor growth. Mass spectrometry-based analyses demonstrated that salt-inducible kinase 1 (SIK1) binds AKT...

10.1158/0008-5472.c.6599668 preprint EN 2023-04-14
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