Evidence map›Paper›PMID 40741483›Full record

ArticleJournal of solid tumors2024

An investigation for phylogenetic characterization of human pancreatic cancer microbiome by 16S rDNA sequencing and bioinformatics techniques.

Colby Hunter, Khadimou Dia, Julia Boykins, Karrington Perry, Narendra Banerjee, Jazmine Cuffee, Erik Armstrong, Gabrielle Morgan, Hirendra Nath Banerjee, Anasua Banerjee and 1 more

Abstract read
In one paragraph

Article in Journal of solid tumors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Colby HunterDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Khadimou DiaDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Julia BoykinsDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Karrington PerryDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Narendra BanerjeeDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Jazmine CuffeeDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Erik ArmstrongDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Gabrielle MorganDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Hirendra Nath BanerjeeDepartment of Natural Sciences, Elizabeth City State University Campus of The University of North Carolina, Elizabeth City, NC, United States.
Anasua BanerjeeDepartment of Biochemistry, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, United States.
Santanu BhattacharyaDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Jacksonville, FL, United States.

Funding

Elizabeth City State University Minority Access to Research Careers (E-MARC) UndeT34GM100831 · NIGMS · ELIZABETH CITY STATE UNIVERSITY · PI BANERJEE, HIRENDRA N · 2012 to 2022
$1.9M
NIGMS NIH HHS T34 GM100831
6 · The paper itself

Abstract

Pancreatic cancer is a significant public health concern, with increasing incidence rates and limited treatment options. Recent studies have highlighted the role of the human microbiome, particularly the gut microbiota, in the development and progression of this disease. Microbial dysbiosis, characterized by alterations in the composition and function of the gut microbiota, has been implicated in pancreatic carcinogenesis through mechanisms involving chronic inflammation, immune dysregulation, and metabolic disturbances. Researchers have identified specific microbial signatures associated with pancreatic cancer, offering potential biomarkers for early detection and prognostication. By leveraging advanced sequencing and bioinformatics tools, scientists have delineated differences in the gut microbiota between pancreatic cancer patients and healthy individuals, providing insights into disease pathogenesis and potential diagnostic strategies. Moreover, the microbiome holds promise as a therapeutic target in pancreatic cancer treatment. Interventions aimed at modulating the microbiome, such as probiotics, prebiotics, and fecal microbiota transplantation, have demonstrated potential in enhancing the efficacy of existing cancer therapies, including chemotherapy and immunotherapy. These approaches can influence immune responses, alter tumor microenvironments, and sensitize tumors to treatment, offering new avenues for improving patient outcomes and overcoming therapeutic resistance. Overall, understanding the complex interplay between the microbiome and pancreatic cancer is crucial for advancing our knowledge of disease mechanisms and identifying innovative therapeutic strategies. Here we report phylogenetic analysis of the 16S rDNA microbial sequences of the pancreatic cancer mice microbiome and corresponding age matched healthy mice microbiome. We successfully identified differentially abundant microbiota in pancreatic cancer.

Indexed as

16SrRNAMicrobiomePancreatic CancerPhylogeny

Identifiers

PMID40741483
PMCPMC12309466

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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.