Intratumoral Microbiome of Adenoid Cystic Carcinomas and Comparison with Other Head and Neck Cancers

Author:

Karpinets Tatiana V.1,Mitani Yoshitsugu1,Chang Chia-Chi1,Wu Xiaogang1,Song Xingzhi1,Flores Ivonne I1,McDaniel Lauren K1,Hoballah Yasmine M1,Veguilla Fabiana J1,Ferrarotto Renata1,Colbert Lauren E1,Ajami Nadim J1,Jenq Robert R1,Zhang Jianhua1,Futreal Andrew P1,El-Naggar Adel K.1

Affiliation:

1. The University of Texas MD Anderson Cancer Center

Abstract

Abstract Background: Adenoid cystic carcinoma (ACC) is a rare, usually slow-growing yet aggressive head and neck malignancy. Despite its clinical significance, our understanding of the cellular evolution and microenvironment in ACC remains limited. Methods: We investigated the intratumoral microbiomes of 50 ACC tumor tissues and 33 adjacent normal tissues using 16S rRNA gene sequencing. This allowed us to characterize the bacterial communities within the ACC and explore potential associations between the bacterial community structure, patient clinical characteristics, and tumor molecular features obtained through RNA sequencing. Results: The bacterial composition in the ACC was significantly different from that in adjacent normal salivary tissue, and the ACC exhibited diverse levels of species richness. We identified two main microbial subtypes within the ACC: oral-like and gut-like. Oral-like microbiomes, characterized by increased diversity and abundance of Neisseria, Leptotrichia, Actinomyces, Streptococcus, Rothia, and Veillonella(commonly found in healthy oral cavities), were associated with a less aggressive ACC-II molecular subtype and improved patient outcomes. Notably, we identified the same oral genera in oral cancer and head and neck squamous cell carcinomas. In both cancers, they were part of shared oral communities associated with a more diverse microbiome, less aggressive tumor phenotype, and better survival. Conversely, gut-like intratumoral microbiomes, which feature low diversity and colonization by gut mucus layer-degrading species, such as Bacteroides, Akkermansia, Blautia, Bifidobacterium, and Enterococcus, were associated with poorer outcomes. Elevated levels of Bacteroides thetaiotaomicron were independently associated with significantly worse survival, regardless of other clinical and molecular factors. Furthermore, these associations were positively correlated with tumor cell biosynthesis of glycan-based cell membrane components. Conclusions: Our study identified specific intratumoral oral genera as potential pancancer biomarkers for favorable microbiomes in ACC and other head and neck cancers. These findings highlight the pivotal role of the intratumoral microbiome in influencing ACC prognosis and disease biology.

Publisher

Research Square Platform LLC

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