Targeting cellular metabolism in head and neck cancer precision medicine era: A promising strategy to overcome therapy resistance

Oral Dis. 2023 Nov;29(8):3101-3120. doi: 10.1111/odi.14411. Epub 2022 Nov 6.

Abstract

Head and neck squamous cell carcinoma (HNSCC) is among the most prevalent cancer worldwide, with the most severe impact on quality of life of patients. Despite the development of multimodal therapeutic approaches, the clinical outcomes of HNSCC are still unsatisfactory, mainly caused by relatively low responsiveness to treatment and severe drug resistance. Metabolic reprogramming is currently considered to play a pivotal role in anticancer therapeutic resistance. This review aimed to define the specific metabolic programs and adaptations in HNSCC therapy resistance. An extensive literature review of HNSCC was conducted via the PubMed including metabolic reprogramming, chemo- or immune-therapy resistance. Glucose metabolism, fatty acid metabolism, and amino acid metabolism are closely related to the malignant biological characteristics of cancer, anti-tumor drug resistance, and adverse clinical results. For HNSCC, pyruvate, lactate and almost all lipid categories are related to the occurrence and maintenance of drug resistance, and targeting amino acid metabolism can prevent tumor development and enhance the response of drug-resistant tumors to anticancer therapy. This review will provide a better understanding of the altered metabolism in therapy resistance of HNSCC and promote the development of new therapeutic strategies against HNSCC, thereby contribute to a more efficacious precision medicine.

Keywords: cancer drug resistance; combination therapy; head and neck cancer; metabolic regulations; tumor metabolism.

Publication types

  • Review

MeSH terms

  • Amino Acids / therapeutic use
  • Carcinoma, Squamous Cell* / pathology
  • Head and Neck Neoplasms* / drug therapy
  • Humans
  • Precision Medicine
  • Quality of Life
  • Squamous Cell Carcinoma of Head and Neck

Substances

  • Amino Acids