Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Jan 29;20(3):2392.
doi: 10.3390/ijerph20032392.

Tumour Genetic Heterogeneity in Relation to Oral Squamous Cell Carcinoma and Anti-Cancer Treatment

Affiliations
Review

Tumour Genetic Heterogeneity in Relation to Oral Squamous Cell Carcinoma and Anti-Cancer Treatment

Gal Feller et al. Int J Environ Res Public Health. .

Abstract

Oral squamous cell carcinoma (SCC) represents more than 90% of all oral cancers and is the most frequent SCC of the head and neck region. It may affect any oral mucosal subsite but most frequently the tongue, followed by the floor of the mouth. The use of tobacco and betel nut, either smoked or chewed, and abuse of alcohol are the main risk factors for oral SCC. Oral SCC is characterized by considerable genetic heterogeneity and diversity, which together have a significant impact on the biological behaviour, clinical course, and response to treatment and on the generally poor prognosis of this carcinoma. Characterization of spatial and temporal tumour-specific molecular profiles and of person-specific resource availability and environmental and biological selective pressures could assist in personalizing anti-cancer treatment for individual patients, with the aim of improving treatment outcomes. In this narrative review, we discuss some of the events in cancer evolution and the functional significance of driver-mutations in carcinoma-related genes in general and elaborate on mechanisms mediating resistance to anti-cancer treatment.

Keywords: cancer-evolution; driver mutation; genetic diversity; genetic heterogeneity; natural selection; oral squamous cell carcinoma; passenger mutation; resistance to anti-cancer treatment.

PubMed Disclaimer

Conflict of interest statement

All authors declare no competing interest to the authorship and/or publication of this article.

Figures

Figure 1
Figure 1
Schematic presentation of the cancerization process adapted from Feller et al., 2013 (12).

References

    1. Turajlic S., Sottoriva A., Graham T., Swanton C. Resolving genetic heterogeneity in cancer. Nat. Rev. Genet. 2019;20:404–416. doi: 10.1038/s41576-019-0114-6. - DOI - PubMed
    1. Andor N., Graham T.A., Jansen M., Xia L.C., Aktipis C.A., Petritsch C., Ji H.P., Maley C.C. Pan-cancer analysis of the extent and consequences of intratumor heterogeneity. Nat. Med. 2016;22:105–113. doi: 10.1038/nm.3984. - DOI - PMC - PubMed
    1. Gerlinger M., Rowan A.J., Horswell S., Larkin J., Endesfelder D., Gronroos E., Martinez P., Matthews N., Stewart A., Tarpey P. Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N. Engl. J. Med. 2012;366:883–892. doi: 10.1056/NEJMoa1113205. - DOI - PMC - PubMed
    1. Welch D.R. Tumor heterogeneity—A ‘contemporary concept’founded on historical insights and predictions. Cancer Res. 2016;76:4–6. doi: 10.1158/0008-5472.CAN-15-3024. - DOI - PMC - PubMed
    1. Sottoriva A., Barnes C.P., Graham T.A. Catch my drift? Making sense of genomic intra-tumour heterogeneity. Biochim. Biophys. Acta Rev. Cancer. 2017;1867:95–100. doi: 10.1016/j.bbcan.2016.12.003. - DOI - PMC - PubMed

MeSH terms