Mutation signature analysis identifies increased mutation caused by tobacco smoke associated DNA adducts in larynx squamous cell carcinoma compared with oral cavity and oropharynx

被引:15
|
作者
South, Andrew P. [1 ,2 ,3 ]
den Breems, Nicoline Y. [4 ]
Riche, Tony [5 ]
Nwagu, Uche [5 ]
Zhan, Tingting [3 ,6 ]
Poojan, Shiv [1 ]
Martinez-Outschoorn, Ubaldo [3 ,7 ]
Johnson, Jennifer M. [3 ,7 ]
Luginbuhl, Adam J. [3 ,5 ]
Curry, Joseph M. [3 ,5 ]
机构
[1] Thomas Jefferson Univ, Dept Dermatol & Cutaneous Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Joan & Joel Rosenbloom Res Ctr Fibrot Dis, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[4] Lincoln Univ, Ctr Adv Comp C fACS, Lincoln 7647, New Zealand
[5] Thomas Jefferson Univ, Dept Otolaryngol Head & Neck Surg, Philadelphia, PA 19107 USA
[6] Thomas Jefferson Univ, Dept Pharmacol & Expt Therapeut, Philadelphia, PA 19107 USA
[7] Thomas Jefferson Univ, Dept Oncol, Philadelphia, PA 19107 USA
关键词
HUMAN-PAPILLOMAVIRUS; NECK-CANCER; PREDICT SURVIVAL; HEAD; RISK; FEATURES; APOBEC; TUMORS;
D O I
10.1038/s41598-019-55352-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Squamous cell carcinomas of the head and neck (HNSCC) arise from mucosal keratinocytes of the upper aero-digestive tract. Despite a common cell of origin and similar driver-gene mutations which divert cell fate from differentiation to proliferation, HNSCC are considered a heterogeneous group of tumors categorized by site of origin within the aero-digestive mucosa, and the presence or absence of HPV infection. Tobacco use is a major driver of carcinogenesis in HNSCC and is a poor prognosticator that has previously been associated with poor immune cell infiltration and higher mutation numbers. Here, we study patterns of mutations in HNSCC that are derived from the specific nucleotide changes and their surrounding nucleotide context (also known as mutation signatures). We identify that mutations linked to DNA adducts associated with tobacco smoke exposure are predominantly found in the larynx. Presence of this class of mutation, termed COSMIC signature 4, is responsible for the increased burden of mutation in this anatomical sub-site. In addition, we show that another mutation pattern, COSMIC signature 5, is positively associated with age in HNSCC from non-smokers and that larynx SCC from non-smokers have a greater number of signature 5 mutations compared with other HNSCC sub-sites. Immunohistochemistry demonstrates a significantly lower Ki-67 proliferation index in size matched larynx SCC compared with oral cavity SCC and oropharynx SCC. Collectively, these observations support a model where larynx SCC are characterized by slower growth and increased susceptibility to mutations from tobacco carcinogen DNA adducts.
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页数:9
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