Evidence map›Paper›PMID 27285764›Full record

ArticleOncotarget2016

WHSC1L1 drives cell cycle progression through transcriptional regulation of CDC6 and CDK2 in squamous cell carcinoma of the head and neck.

Vassiliki Saloura, Theodore Vougiouklakis, Makda Zewde, Kazuma Kiyotani, Jae-Hyun Park, Guimin Gao, Theodore Karrison, Mark Lingen, Yusuke Nakamura, Ryuji Hamamoto

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. 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
2.4field-weighted citation impact, top 11% 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, 43 citations in OpenAlex.

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  12. The role of NSD1, NSD2, and NSD3 histone methyltransferases in solid tumors.Cellular and molecular life sciences : CMLS · 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

10 authors at 2 institutions in 1 country.

Vassiliki SalouraDepartment of Medicine, University of Chicago, Chicago, IL, USA.
Theodore VougiouklakisDepartment of Medicine, University of Chicago, Chicago, IL, USA.
Makda ZewdeDepartment of Medicine, University of Chicago, Chicago, IL, USA.
Kazuma KiyotaniDepartment of Medicine, University of Chicago, Chicago, IL, USA.
Jae-Hyun ParkDepartment of Medicine, University of Chicago, Chicago, IL, USA.
Guimin GaoDepartment of Public Health Sciences, University of Chicago, Chicago, IL, USA.
Theodore KarrisonDepartment of Public Health Sciences, University of Chicago, Chicago, IL, USA.
Mark LingenDepartment of Pathology, University of Chicago, Chicago, IL, USA.
Yusuke NakamuraDepartment of Medicine, University of Chicago, Chicago, IL, USA.
Ryuji HamamotoDepartment of Medicine, University of Chicago, Chicago, IL, USA.
University of Chicago · USChicago Department of Public Health · US

Funding

Developing an Oncology Workforce for the 21st Century - Renewal 01K12CA139160 · NCI · UNIVERSITY OF CHICAGO · PI OLOPADE, OLUFUNMILAYO F., SMITH, SONALI · 2010 to 2024
$10.6M
NCI NIH HHS K12 CA139160
6 · The paper itself

Abstract

Wolf-Hisrchhorn Syndrome Candidate 1-Like 1 (WHSC1L1) is a protein lysine methyltransferase that is recurrently amplified (8p11.23) in patients with squamous cell carcinoma of the head and neck (SCCHN). In this study, we investigated the oncogenic role of WHSC1L1 in SCCHN. Using immunohistochemistry on tissue microarrays of patients with locoregionally advanced SCCHN, we found that WHSC1L1 is significantly overexpressed in patients with SCCHN, and is associated with poor grade and heavy smoking history. Knockdown of WHSC1L1 expression resulted in significant growth suppression and reduction of H3K36 dimethylation (H3K36me2) in SCCHN cells. Chromatin immunoprecipitation analysis showed that WHSC1L1 and H3K36me2 are enriched in the gene bodies of the cell cycle-related genes CDC6 and CDK2, implying that WHSC1L1 directly regulates the transcription of these genes. According to the importance of CDC6 and CDK2 for G1 to S transition, WHSC1L1 knockdown induced strong G0/G1 arrest which was rescued by introduction of wild-type WHSC1L1 but not by that of enzyme-inactive WHSC1L1. Our results imply that WHSC1L1 and its product H3K36me2 are essential for the transition from G1 to S phase in SCCHN cells and that WHSC1L1 could serve as a rational target for anticancer drug development for patients with head and neck cancer.

Indexed as

Gene Expression Regulation, NeoplasticCarcinoma, Squamous CellCell CycleCell Cycle ProteinsCell SurvivalChromatin ImmunoprecipitationCyclin-Dependent Kinase 2DNA MethylationGenetic VectorsHead and Neck NeoplasmsHistone-Lysine N-MethyltransferaseHistonesHumansNuclear ProteinsSmokingSquamous Cell Carcinoma of Head and NeckCDC6 protein, humanCDK2 protein, humanCell Cycle ProteinsCyclin-Dependent Kinase 2Histone-Lysine N-MethyltransferaseHistonesNSD3 protein, humanNuclear ProteinsCDC6CDK2H3K36me2squamous cell carcinoma of the head and neckWHSC1L1

Identifiers

PMID27285764
PMCPMC5173153
OpenAlexW2409525301

What OpenQuestion holds

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LicenceCC BY
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.