Evidence map›Paper›PMID 24403859›Full record

ArticleNeoplasia (New York, N.Y.)2013

Tumor evolution and intratumor heterogeneity of an oropharyngeal squamous cell carcinoma revealed by whole-genome sequencing.

Xinyi Cindy Zhang, Chang Xu, Ryan M Mitchell, Bo Zhang, Derek Zhao, Yao Li, Xin Huang, Wenhong Fan, Hongwei Wang, Luisa Angelica Lerma and 4 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 89 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. FMISO-Based Adaptive Radiotherapy in Head and Neck Cancer.Journal of personalized medicine · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. PET/MRI and genetic intrapatient heterogeneity in head and neck cancers.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2020
    Article
  12. Article
  13. Prognostic impact of intra-field heterogeneity in oral squamous cell carcinoma.Virchows Archiv : an international journal of pathology · 2020
    Article
  14. Article
  15. Review
  16. Review
  17. Cancer evolution and heterogeneity.Annals of gastroenterological surgery · 2018
    Review
  18. Review
  19. Review
  20. Article
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

14 authors at 2 institutions in 1 country.

Xinyi Cindy ZhangDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
Chang XuDepartment of Otolaryngology-Head and Neck Surgery, University of Washington School of Medicine, Seattle, WA ; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Ryan M MitchellDepartment of Otolaryngology-Head and Neck Surgery, University of Washington School of Medicine, Seattle, WA.
Bo ZhangDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
Derek ZhaoDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
Yao LiDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
Xin HuangDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
Wenhong FanDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
Hongwei WangDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
Luisa Angelica LermaDepartment of Otolaryngology-Head and Neck Surgery, University of Washington School of Medicine, Seattle, WA.
Melissa P UptonDepartment of Pathology, University of Washington School of Medicine, Seattle, WA.
Ashley HayDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
Eduardo MéndezDepartment of Otolaryngology-Head and Neck Surgery, University of Washington School of Medicine, Seattle, WA ; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA ; Surgery and Perioperative Care Service, VA Puget Sound Health Care System, Seattle, WA.
Lue Ping ZhaoDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA ; Department of Biostatistics, University of Washington School of Public Health, Seattle, WA.
Fred Hutch Cancer Center · USUniversity of Washington · US

Funding

Research Training in OtolaryngologyT32DC000018 · NIDCD · UNIVERSITY OF WASHINGTON · PI STONE, JENNIFER S. · 1989 to 2023
$7.8M
An integrated computational and functional genomics discovery engine for precliniU01CA176303 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KEMP, CHRISTOPHER J · 2013 to 2016
$4.1M
Designs and Methods for Sequence-Based Validation AnalysisR01MH084621 · NIMH · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ZHAO, LUE PING · 2008 to 2012
$1.8M
Methods for Assessing Genetic Association with Time-Varying PhenotypeR01CA119225 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ZHAO, LUE PING · 2007 to 2010
$1.3M
NCI NIH HHS CA119225NCI NIH HHS R01 CA119225NCI NIH HHS R01CA124574-01NCI NIH HHS U01 CA176303NIDCD NIH HHS 5T32DC000018-29NIDCD NIH HHS T32 DC000018NIMH NIH HHS MH084621NIMH NIH HHS R01 MH084621NIMH NIH HHS R01MH084621-03S2
6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is characterized by significant genomic instability that could lead to clonal diversity. Intratumor clonal heterogeneity has been proposed as a major attribute underlying tumor evolution, progression, and resistance to chemotherapy and radiation. Understanding genetic heterogeneity could lead to treatments specific to resistant and metastatic tumor cells. To characterize the degree of intratumor genetic heterogeneity within a single tumor, we performed whole-genome sequencing on three separate regions of an human papillomavirus (HPV)-positive oropharyngeal squamous cell carcinoma and two separate regions from one corresponding cervical lymph node metastasis. This approach achieved coverage of approximately 97.9% of the genome across all samples. In total, 5701 somatic point mutations (SPMs) and 4347 small somatic insertions and deletions (indels)were detected in at least one sample. Ninety-two percent of SPMs and 77% of indels were validated in a second set of samples adjacent to the discovery set. All five tumor samples shared 41% of SPMs, 57% of the 1805 genes with SPMs, and 34 of 55 cancer genes. The distribution of SPMs allowed phylogenetic reconstruction of this tumor's evolutionary pathway and showed that the metastatic samples arose as a late event. The degree of intratumor heterogeneity showed that a single biopsy may not represent the entire mutational landscape of HNSCC tumors. This approach may be used to further characterize intratumor heterogeneity in more patients, and their sample-to-sample variations could reveal the evolutionary process of cancer cells, facilitate our understanding of tumorigenesis, and enable the development of novel targeted therapies.

Indexed as

AgedCarcinoma, Squamous CellDNA Mutational AnalysisGenes, NeoplasmGenome, HumanHigh-Throughput Nucleotide SequencingHumansINDEL MutationLymphatic MetastasisMaleMolecular Sequence AnnotationOpen Reading FramesOropharyngeal Neoplasms

Identifiers

PMID24403859
PMCPMC3884528
OpenAlexW1907421893

What OpenQuestion holds

Textmetadata
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.