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Related Experiment Video

Updated: Aug 26, 2025

Assessment of the Metabolic Profile of Primary Leukemia Cells
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Src: coordinating metabolism in cancer.

Sara G Pelaz1, Arantxa Tabernero2

  • 1Instituto de Neurociencias de Castilla y León (INCYL), Departamento de Bioquímica y Biología Molecular, Universidad de Salamanca, Instituto de Investigación Biomédica de Salamanca (IBSAL), Calle Pintor Fernando Gallego 1, Salamanca, 37007, Spain.

Oncogene
|October 10, 2022
PubMed
Summary
This summary is machine-generated.

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Cx43 levels guide apicobasal polarity in regenerating airway epithelial cells.

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The Src inhibitor peptide TAT-Cx43<sub>266-283</sub> improves survival in an intracranial murine model of lung cancer brain metastasis.

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Single-nucleus RNA sequencing reveals a preclinical model for the most common subtype of glioblastoma.

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EGFR amplification and EGFRvIII predict and participate in TAT-Cx43266-283 antitumor response in preclinical glioblastoma models.

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Impairment of Autophagic Flux Participates in the Antitumor Effects of TAT-Cx43<sub>266-283</sub> in Glioblastoma Stem Cells.

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The Src oncoprotein regulates cancer cell metabolism, including glucose uptake and glycolysis, to support tumor progression and plasticity. Understanding this link is crucial for developing new cancer therapies.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Metabolism

Background:

  • Cellular metabolism is critical for cancer cell functions like proliferation and migration.
  • Src is a key signaling node regulating numerous biological processes, including metabolism.
  • Dysregulated metabolism is a hallmark of cancer, contributing to tumor growth and progression.

Purpose of the Study:

  • To summarize recent advancements in understanding Src's role in cancer glucose metabolism.
  • To elucidate the connection between Src, cancer cell metabolic plasticity, and tumor progression.
  • To discuss current challenges and future opportunities in this research area.

Main Methods:

  • Literature review of recent studies on Src and cancer metabolism.
  • Analysis of signaling pathways regulated by Src impacting metabolic processes.

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  • Integration of data on metabolic plasticity and tumor progression linked to Src activity.
  • Main Results:

    • Src influences key metabolic pathways, including glucose uptake, glycolysis, the pentose-phosphate pathway, and oxidative phosphorylation.
    • Src acts as a central coordinator of metabolic reprogramming in cancer cells.
    • Src-mediated metabolic regulation is linked to enhanced cancer cell proliferation, migration, and stemness.

    Conclusions:

    • Src plays a pivotal role in fine-tuning cancer cell metabolism to support various oncogenic activities.
    • Targeting Src offers a potential strategy for modulating cancer cell metabolism and inhibiting tumor progression.
    • Further research is needed to fully exploit the therapeutic potential of targeting the Src-metabolism axis in cancer.