Evidence map›Paper›PMID 35834946›Full record

ArticleNeoplasia (New York, N.Y.)2022

Fusobacterium is enriched in oral cancer and promotes induction of programmed death-ligand 1 (PD-L1).

Chieko Michikawa, Vancheswaran Gopalakrishnan, Amani M Harrandah, Tatiana V Karpinets, Rekha Rani Garg, Randy A Chu, Yuk Pheel Park, Sasanka S Chukkapallia, Nikhita Yadlapalli, Kelly C Erikson-Carter and 11 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.1field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
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  6. The role ofFEMS microbes · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 5 institutions in 3 countries.

Chieko MichikawaDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA; Department of Maxillofacial Surgery, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Vancheswaran GopalakrishnanDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Amani M HarrandahDepartment of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, USA; Department of Oral Biology, Umm AlQura University, Makkah, Saudi Arabia.
Tatiana V KarpinetsDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Rekha Rani GargDepartment of Pediatrics, University of Florida, Gainesville, Florida, USA.
Randy A ChuDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA; Institute for Personalized Cancer Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Yuk Pheel ParkDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida, Gainesville, Florida, USA.
Sasanka S ChukkapalliaDepartment of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, USA.
Nikhita YadlapalliDepartment of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, USA.
Kelly C Erikson-CarterDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA; Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA.
Frederico Omar Gleber-NettoDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Elias SayourDepartment of Pediatrics and Neurosurgery, University of Florida, Gainesville, Florida, USA.
Ann Progulske-FoxDepartment of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, USA.
Edward K L ChanDepartment of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, USA.
Xiaogang WuDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Jianhua ZhangDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Christian JobinDepartment of Internal Medicine, University of Florida, Gainesville, FL, USA.
Jennifer A WargoDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Curtis R PickeringDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Jeffrey N MyersDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Natalie SilverCleveland Clinic, Head and Neck Institute/Lerner Research Institute, Cleveland, OH, USA. Electronic address: SILVERN@ccf.org.
The University of Texas MD Anderson Cancer Center · USUniversity of Florida · USCleveland Clinic Lerner College of Medicine · USTokyo Medical and Dental University · JPUmm al-Qura University · SA

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
(PQ10) Enhancing responses to immune checkpoint blockade in melanoma via modulation of the microbiomeR01CA219896 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WARGO, JENNIFER A. · 2018 to 2022
$2.2M
Remodeling host immunity in oral cancer with personalized RNA nanoparticle vaccinesK08DE029503 · NIDCR · UNIVERSITY OF FLORIDA · PI SILVER, NATALIE LEA · 2020 to 2024
$777k
NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA219896NIDCR NIH HHS K08 DE029503
6 · The paper itself

Abstract

Recently, increased number of studies have demonstrated a relationship between the oral microbiome and development of head and neck cancer, however, there are few studies to investigate the role of oral bacteria in the context of the tumor microenvironment in a single head and neck subsite. Here, paired tumor and adjacent normal tissues from thirty-seven oral tongue squamous cell carcinoma (SCC) patients were subjected to 16S rRNA gene sequencing and whole exome sequencing (WES), in addition to RNA sequencing for tumor samples. We observed that Fusobacterium was significantly enriched in oral tongue cancer and that Rothia and Streptococcus were enriched in adjacent normal tissues. A decrease in alpha diversity was found in tumor when compared to adjacent normal tissues. While increased Fusobacterium in tumor samples was not associated with changes in immune cell infiltration, it was associated with increased PD-L1 mRNA expression. Therefore, we examined the effects of Fusobacterium on PD-L1 expression in head and neck SCC cell lines. We demonstrated that infection with Fusobacterium species can increase both PD-L1 mRNA and surface PD-L1 protein expression on head and neck cancer cell lines. The correlation between Fusobacterium and PD-L1 expression in oral tongue SCC, in conjunction with the ability of the bacterium to induce PD-L1 expression in vitro suggests a potential role for Fusobacterium on modulation of the tumor immune microenvironment in head and neck cancer.

Indexed as

Carcinoma, Squamous CellHead and Neck NeoplasmsMouth NeoplasmsTongue NeoplasmsB7-H1 AntigenFusobacteriumHumansRNA, MessengerRNA, Ribosomal, 16SSquamous Cell Carcinoma of Head and NeckTumor MicroenvironmentB7-H1 AntigenCD274 protein, humanRNA, MessengerRNA, Ribosomal, 16SFusobacteriumHead and neck cancerMicrobiomeOral cancerPD-L1Periodontal bacteria

Identifiers

PMID35834946
PMCPMC9287628
OpenAlexW4285040455

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.