Abstract
While sequencing studies have provided an improved understanding of the genetic landscape of head and neck squamous cell carcinomas (HNSCC), there remains a significant lack of genetic data derived from non-Caucasian cohorts. Additionally, there is wide variation in HNSCC incidence and mortality worldwide both between and within various geographic regions. These epidemiologic differences are in part accounted for by varying exposure to environmental risk factors such as tobacco, alcohol, high risk human papilloma viruses and betel quid. However, inherent genetic factors may also play an important role in this variability. As limited sequencing data is available for many populations, the involvement of unique genetic factors in HNSCC pathogenesis from epidemiologically diverse groups is unknown. Here, we review current knowledge about the epidemiologic, environmental, and genetic variation in HNSCC cohorts globally and discuss future studies necessary to further our understanding of these differences. Long-term, a more complete understanding of the genetic drivers found in diverse HNSCC cohorts may help the development of personalized medicine protocols for patients with rare or complex genetic events.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 182-200 |
| Number of pages | 19 |
| Journal | Genes and Cancer |
| Volume | 7 |
| Issue number | 5-6 |
| DOIs | |
| State | Published - May 2016 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2016, Impact Journals LLC. All rights reserved.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Epidemiology
- Head and neck squamous cell carcinoma
- Human papillomavirus
- Personalized medicine
- Sequencing
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