Evidence map›Paper›PMID 30747051›Full record

ArticleThyroid : official journal of the American Thyroid Association2019

Microsatellite Instability Occurs in a Subset of Follicular Thyroid Cancers.

Luke K Genutis, Jerneja Tomsic, Ralf A Bundschuh, Pamela L Brock, Michelle D Williams, Sameek Roychowdhury, Julie W Reeser, Wendy L Frankel, Mohammed Alsomali, Mark J Routbort and 5 more

Abstract read
In one paragraph

Article in Thyroid : official journal of the American Thyroid Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
4.2field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 40 citations in OpenAlex.

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  14. Thyroid cancer harboringFrontiers in oncology · 2022
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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

15 authors at 4 institutions in 1 country.

Luke K Genutis1 Department of Cancer Biology and Genetics, The Ohio State University Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Jerneja Tomsic2 Division of Biomarkers Early Detection Prevention, City of Hope Comprehensive Cancer Center, Duarte, California.
Ralf A Bundschuh3 Department of Physics and Department of Chemistry and Biochemistry, Division of Hematology, Department of Internal Medicine, Center for RNA Biology, The Ohio State University, Columbus, Ohio.
Pamela L Brock4 Department of Internal Medicine, The Ohio State University, Columbus, Ohio.
Michelle D Williams5 Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Sameek Roychowdhury4 Department of Internal Medicine, The Ohio State University, Columbus, Ohio.
Julie W Reeser4 Department of Internal Medicine, The Ohio State University, Columbus, Ohio.
Wendy L Frankel6 Department of Pathology, The Ohio State University, Columbus, Ohio.
Mohammed Alsomali6 Department of Pathology, The Ohio State University, Columbus, Ohio.
Mark J Routbort7 Department of Hematopathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Russell R Broaddus5 Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Paul E Wakely6 Department of Pathology, The Ohio State University, Columbus, Ohio.
John E Phay8 Department of Surgery, The Ohio State University Wexner Medical Center, The Ohio State University, Columbus, Ohio.
Christopher J Walker1 Department of Cancer Biology and Genetics, The Ohio State University Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Albert de la Chapelle1 Department of Cancer Biology and Genetics, The Ohio State University Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
The Ohio State University · USThe University of Texas MD Anderson Cancer Center · USCity of Hope · USThe Ohio State University Wexner Medical Center · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Selective Modulation of Thyroidal RadioiodineP01CA124570 · NCI · OHIO STATE UNIVERSITY · PI RINGEL, MATTHEW D · 2008 to 2017
$23.4M
The Ohio State University and MD Anderson Cancer Center Thyroid Cancer SPOREP50CA168505 · NCI · OHIO STATE UNIVERSITY · PI DE LA CHAPELLE, ALBERT · 2013 to 2017
$10.9M
Detection of microsatellite instability biomarkers for therapeutic clinical trial eligibilityUH3CA216432 · NCI · OHIO STATE UNIVERSITY · PI ROYCHOWDHURY, SAMEEK · 2019 to 2021
$942k
NCI NIH HHS P01 CA124570NCI NIH HHS P30 CA016058NCI NIH HHS P50 CA168505NCI NIH HHS UH3 CA216432
6 · The paper itself

Abstract

backgroundInactivation of DNA mismatch repair (MMR) and the resulting microsatellite instability (MSI) are frequently observed in endometrial, stomach, and colorectal cancers, as well as more rarely in other solid tumor types. The prevalence of MSI in thyroid cancer has not been explored in depth, although recent studies utilizing data from large cancer sequencing efforts such as The Cancer Genome Atlas indicate that MSI is absent or at least very rare in the most common and most well studied histologic subtype, papillary thyroid carcinoma. This study aimed to determine the prevalence of MSI in thyroid cancer by using a large series comprising all major histological subtypes.

methodsA total of 485 thyroid cancer patients were screened for MSI/MMR deficiency, including all major histologic subtypes (195 papillary thyroid carcinoma, 156 follicular thyroid carcinoma [FTC], 50 anaplastic thyroid carcinoma, 65 medullary thyroid carcinoma, and 17 poorly differentiated thyroid carcinomas) by using a combination of polymerase chain reaction-based detection, immunohistochemistry, and next-generation sequencing.

resultsA total of four tumors were MSI-high and had loss of MMR protein expression, all of which were from FTC patients. Whole-exome sequencing was performed on two MSI-high FTCs and revealed a hemizygous loss of function mutation in MSH2 in one tumor.

conclusionsBased on these data, it is estimated that the overall prevalence of MSI in FTC is 2.5%, and MSI is either entirely absent or rare in other histology subtypes of thyroid carcinoma. These findings highlight the importance of testing for MSI in FTC.

Indexed as

DNA Mismatch RepairMicrosatellite InstabilityAdenocarcinoma, FollicularBiomarkers, TumorGenetic Predisposition to DiseaseHemizygoteHumansLoss of HeterozygosityMutationMutS Homolog 2 ProteinPhenotypeRisk FactorsThyroid NeoplasmsBiomarkers, TumorMSH2 protein, humanMutS Homolog 2 ProteinDNA mismatch repairfollicular thyroid cancerLynch syndromemicrosatellite instabilitypapillary thyroid carcinoma

Identifiers

PMID30747051
PMCPMC6457885
OpenAlexW2912355711

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.