Evidence map›Paper›PMID 26721311›Full record

ArticleGenomics2016

Ancestral-derived effects on the mutational landscape of laryngeal cancer.

Meganathan P Ramakodi, Rob J Kulathinal, Yujin Chung, Ilya Serebriiskii, Jeffrey C Liu, Camille C Ragin

Abstract read
In one paragraph

Article in Genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Racial survival disparities in head and neck cancer clinical trials.Journal of the National Cancer Institute · 2023
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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 at 2 institutions in 2 countries.

Meganathan P RamakodiCancer Prevention and Control Program, Fox Chase Cancer Center-Temple Health, Philadelphia, PA 19111, USA; Department of Biology, Temple University, Philadelphia, PA 19122, USA; African-Caribbean Cancer Consortium; Center for Computational Genetics and Genomics, Temple University, Philadelphia, PA 19122, USA.
Rob J KulathinalDepartment of Biology, Temple University, Philadelphia, PA 19122, USA; African-Caribbean Cancer Consortium; Center for Computational Genetics and Genomics, Temple University, Philadelphia, PA 19122, USA.
Yujin ChungDepartment of Biology, Temple University, Philadelphia, PA 19122, USA; Center for Computational Genetics and Genomics, Temple University, Philadelphia, PA 19122, USA.
Ilya SerebriiskiiDevelopmental Therapeutics, Fox Chase Cancer Center- Temple Health, Philadelphia, PA 19111, USA; Kazan Federal University, Kazan, Russia.
Jeffrey C LiuCancer Prevention and Control Program, Fox Chase Cancer Center-Temple Health, Philadelphia, PA 19111, USA; Department of Otolaryngology - Head and Neck Surgery, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Camille C RaginCancer Prevention and Control Program, Fox Chase Cancer Center-Temple Health, Philadelphia, PA 19111, USA; African-Caribbean Cancer Consortium; Department of Otolaryngology - Head and Neck Surgery, Temple University School of Medicine, Philadelphia, PA 19140, USA; College of Public Health, Temple University, Philadelphia, PA 19122, USA. Electronic address: Camille.Ragin@fccc.edu.
Fox Chase Cancer Center · USTemple University · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
NCI NIH HHS CA006927-50NCI NIH HHS P30 CA006927
6 · The paper itself

Abstract

Laryngeal cancer disproportionately affects more African-Americans than European-Americans. Here, we analyze the genome-wide somatic point mutations from the tumors of 13 African-Americans and 57 European-Americans from TCGA to differentiate between environmental and ancestrally-inherited factors. The mean number of mutations was different between African-Americans (151.31) and European-Americans (277.63). Other differences in the overall mutational landscape between African-American and European-American were also found. The frequency of C>A, and C>G were significantly different between the two populations (p-value<0.05). Context nucleotide signatures for some mutation types significantly differ between these two populations. Thus, the context nucleotide signatures along with other factors could be related to the observed mutational landscape differences between two races. Finally, we show that mutated genes associated with these mutational differences differ between the two populations. Thus, at the molecular level, race appears to be a factor in the progression of laryngeal cancer with ancestral genomic signatures best explaining these differences.

Indexed as

Point MutationBlack or African AmericanGene FrequencyGenetic Predisposition to DiseaseGenetics, PopulationHumansLaryngeal NeoplasmsUnited StatesWhite PeopleAfrican-AmericansCancer genomicsContext nucleotidesEuropean-AmericansLaryngeal cancerMutational landscapes

Identifiers

PMID26721311
PMCPMC4761303
OpenAlexW2218992589

What OpenQuestion holds

Textmetadata
LicenceTDM
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.