Evidence map›Paper›PMID 39502024›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2025

Black Raspberry Modulates Cecal and Oral Microbiomes at the Early Stage of a Dibenzo[def,p]chrysene-Induced Murine Oral Cancer Model.

Jingcheng Zhao, Yuan-Wan Sun, Kun-Ming Chen, Cesar Aliaga, Jordan E Bisanz, Karam El-Bayoumy

Abstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

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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

3 citing papers in PubMed.

  1. Article
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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

6 authors.

Jingcheng ZhaoDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, Pennsylvania.ORCID 0009-0004-0447-6652
Yuan-Wan SunDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, College of Medicine, Hershey, Pennsylvania.ORCID 0000-0002-2028-3533
Kun-Ming ChenDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, College of Medicine, Hershey, Pennsylvania.ORCID 0000-0002-3820-6149
Cesar AliagaDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, College of Medicine, Hershey, Pennsylvania.ORCID 0009-0003-0370-9875
Jordan E BisanzDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, Pennsylvania.ORCID 0000-0002-8649-1706
Karam El-BayoumyDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, College of Medicine, Hershey, Pennsylvania.ORCID 0000-0002-4198-0696

Funding

Chemoprevention by Black Raspberry of Oral Cancer Induced by Tobacco Carcinogens: Translational StudiesR01CA173465 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI EL-BAYOUMY, KARAM E · 2013 to 2024
$3.1M
Decoding Microbial Diversity in the Human Gut MicrobiomeR35GM151045 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Jordan Adam Bisanz · 2023 to 2026
$1.5M
Huck Institutes of the Life Sciences (Huck Institutes)NCI NIH HHS R01 CA173465NIGMS NIH HHS R35 GM151045
6 · The paper itself

Abstract

While tobacco smoking is a risk factor in the development of oral squamous cell carcinoma (OSCC), only a fraction of smokers develop the disease. Compelling evidence shows that microbial community composition is associated with carcinogenesis, suggesting that the microbiome may play a role in cancer development of smokers. We previously showed that black raspberry (BRB) protects against OSCC induced by the tobacco constituent dibenzo[def,p]chrysene (DBP) via alteration of genetic and epigenetic markers in a manner consistent with its cancer preventive activity. In the present study, we conducted a mouse experiment to investigate the effects of BRB and DBP individually and in combination on the oral and gut microbiota. DBP-induced DNA damage in the mouse oral cavity is an essential step for the development of OSCC in mice. 16S rRNA gene sequencing revealed that BRB significantly increased microbial diversity and shifted microbiome composition in the gut and oral cavity, whereas DBP had no significant effect. In both gut and oral microbiota, Akkermansia muciniphila was significantly reduced after BRB treatment; however, this was not consistent with pure culture in vitro assays suggesting that the impact of BRB on A. muciniphila may be mediated through indirect mechanisms including the host or other microbes. Indeed BRB, but not DBP, was found to modulate the growth kinetics of human gut microbes in vitro including lactic acid bacteria and Bacteroides spp. The results of the current study further emphasize the interplay of microbiome and environmental factors in the development and prevention of OSCC. Prevention Relevance: Our work clearly demonstrates the modulatory impact of BRB on both gut and oral microbiomes within a DBP-induced OSCC mouse model and paves the way for future research examining a causal role of BRB-microbiota interactions at different stages of disease progression.

Indexed as

BenzopyrenesCecumDisease Models, AnimalMouth NeoplasmsRubusAnimalsCarcinoma, Squamous CellFemaleGastrointestinal MicrobiomeHumansMaleMiceMice, Inbred C57BLMicrobiotaMouthPlant ExtractsBenzopyrenesdibenzo(a,l)pyrenePlant ExtractsRNA, Ribosomal, 16S

Identifiers

PMID39502024
PMCPMC11703685

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Registered trials

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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.