Evidence map›Paper›PMID 30527230›Full record

ArticleOral oncology2018

The genomic landscape of UM-SCC oral cavity squamous cell carcinoma cell lines.

Megan L Ludwig, Aditi Kulkarni, Andrew C Birkeland, Nicole L Michmerhuizen, Susan K Foltin, Jacqueline E Mann, Rebecca C Hoesli, Samantha N Devenport, Brittany M Jewell, Andrew G Shuman and 4 more

Abstract read
In one paragraph

Article in Oral oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

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  2. E7Science advances · 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

14 authors at 4 institutions in 2 countries.

Megan L LudwigDepartment of Otolaryngology - Head and Neck Surgery, United States; Program in Cellular and Molecular Biology, United States.
Aditi KulkarniDepartment of Otolaryngology - Head and Neck Surgery, United States.
Andrew C BirkelandDepartment of Otolaryngology - Head and Neck Surgery, United States.
Nicole L MichmerhuizenDepartment of Otolaryngology - Head and Neck Surgery, United States; Department of Pharmacology, United States.
Susan K FoltinDepartment of Otolaryngology - Head and Neck Surgery, United States.
Jacqueline E MannDepartment of Otolaryngology - Head and Neck Surgery, United States; Department of Pathology, United States.
Rebecca C HoesliDepartment of Otolaryngology - Head and Neck Surgery, United States.
Samantha N DevenportDepartment of Otolaryngology - Head and Neck Surgery, United States; Program in Cellular and Molecular Biology, United States.
Brittany M JewellDepartment of Otolaryngology - Head and Neck Surgery, United States.
Andrew G ShumanDepartment of Otolaryngology - Head and Neck Surgery, United States; Center for Bioethics and Social Sciences in Medicine, United States; Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI. University of Michigan Medical School, Ann Arbor, MI, United States.
Matthew E SpectorDepartment of Otolaryngology - Head and Neck Surgery, United States; Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI. University of Michigan Medical School, Ann Arbor, MI, United States.
Thomas E CareyDepartment of Otolaryngology - Head and Neck Surgery, United States; Department of Pharmacology, United States; Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI. University of Michigan Medical School, Ann Arbor, MI, United States.
Hui JiangDepartment of Biostatistics, United States; Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI. University of Michigan Medical School, Ann Arbor, MI, United States.
J Chad BrennerDepartment of Otolaryngology - Head and Neck Surgery, United States; Department of Pharmacology, United States; Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI. University of Michigan Medical School, Ann Arbor, MI, United States. Electronic address: chadbren@umich.edu.
Pediatrics and Genetics · USUniversity of Michigan · USCellular Research (United States) · USInstitute of Pharmacology · CZ

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
Proteogenomics of Cancer Training ProgramT32CA140044 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAO, ARVIND, SARTOR, MAUREEN AGNES · 2010 to 2024
$3.9M
Dissecting Co-Dependent Pathways in Oral CancersU01DE025184 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BRENNER, JOHN CHADWICK, CAREY, THOMAS E. · 2015 to 2018
$3.7M
Molecular Mechanisms of Tumor Behavior and Response to Therapy in HPV-positive Oropharyngeal CancerR01CA194536 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CAREY, THOMAS E. · 2016 to 2021
$2.8M
Not so sweet: Investigating the role of c-Kit in sweet cell homeostasisF31DC020634 · NIDCD · UNIVERSITY OF COLORADO DENVER · PI PIAROWSKI, CHRISTINA M · 2022 to 2024
$108k
Advancing Mechanistic Concepts of FGFR1-Regulated Adaptive PDL1 Expression in HNSCCF31DE027600 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MANN, JACQUELINE · 2017 to 2019
$99k
Investigating the Mechanisms of Resistance to EGFR-Targeted Therapy in Head and Neck Squamous Cell CarcinomaF31CA206341 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUDWIG, MEGAN LOREE · 2017 to 2019
$93k
NCI NIH HHS F31 CA206341NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA194536NCI NIH HHS T32 CA140044NIDCD NIH HHS F31 DC020634NIDCR NIH HHS F31 DE027600NIDCR NIH HHS U01 DE025184
6 · The paper itself

Abstract

objectivesWe sought to describe the genetic complexity of 14 UM-SCC oral cavity cancer cell lines that have remained uncharacterized despite being used as model systems for decades. MATERIALS AND

methodsWe performed exome sequencing on 14 oral cavity UM-SCC cell lines and denote the mutational profile of each line. We used a SNP array to profile the multiple copy number variations of each cell line and use immunoblotting to compare alterations to protein expression of commonly amplified genes (EGFR, PIK3CA, etc.). RNA sequencing was performed to characterize the expression of genes with copy number alterations.

resultsThe cell lines displayed a highly complex network of genetic aberrations that was consistent with alterations identified in the HNSCC TCGA project including PIK3CA amplification, CDKN2A deletion, as well as TP53 and CASP8 mutations, enabling genetic stratification of each cell line in the panel. Copy number FISH and spectral karyotyping analysis demonstrate that cell lines retain chromosomal heterogeneity.

conclusionsCollectively, we developed an important resource for future oral cavity HNSCC cell line studies and highlight the complexity of genomic aberrations in cell lines.

Indexed as

Caspase 8Cell Line, TumorClass I Phosphatidylinositol 3-KinasesCyclin-Dependent Kinase Inhibitor p16DNA Copy Number VariationsExome SequencingHumansKaryotypingMouth NeoplasmsMutationSquamous Cell Carcinoma of Head and NeckTumor Suppressor Protein p53CASP8 protein, humanCaspase 8CDKN2A protein, humanClass I Phosphatidylinositol 3-KinasesCyclin-Dependent Kinase Inhibitor p16PIK3CA protein, humanTP53 protein, humanTumor Suppressor Protein p53Cell LinesExomeHNSCCOral cancerUM-SCC

Identifiers

PMID30527230
PMCPMC6349383
OpenAlexW2899763802

What OpenQuestion holds

Textmetadata
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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.