Evidence map›Paper›PMID 29224811›Full record

ArticleOral oncology2017

Cancer stem cell and its niche in malignant progression of oral potentially malignant disorders.

Subin Surendran, Gangotri Siddappa, Amrutha Mohan, Wesley Hicks, Vijayvel Jayaprakash, Christina Mimikos, Mohammed Mahri, Fatima Almarzouki, Kayla Morrell, Ravindra Ravi and 9 more

Open access · greenAbstract read
In one paragraph

Article in Oral oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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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

19 authors at 3 institutions in 2 countries.

Subin SurendranHead and Neck Surgery, Roswell Park Cancer Institute, Buffalo, USA.
Gangotri SiddappaIntegrated Head and Neck Oncology Research Program, Mazumdar Shaw Centre for Translational Research, Mazumdar Shaw Medical Foundation, Bangalore, India.
Amrutha MohanHead and Neck Surgery, Roswell Park Cancer Institute, Buffalo, USA; Department of Medicine, Roswell Park Cancer Institute, Buffalo, USA.
Wesley HicksHead and Neck Surgery, Roswell Park Cancer Institute, Buffalo, USA.
Vijayvel JayaprakashHead and Neck Surgery, Roswell Park Cancer Institute, Buffalo, USA.
Christina MimikosHead and Neck Surgery, Roswell Park Cancer Institute, Buffalo, USA.
Mohammed MahriHead and Neck Surgery, Roswell Park Cancer Institute, Buffalo, USA.
Fatima AlmarzoukiHead and Neck Surgery, Roswell Park Cancer Institute, Buffalo, USA.
Kayla MorrellDepartment of Biostatistics, Roswell Park Cancer Institute, Buffalo, USA.
Ravindra RaviIntegrated Head and Neck Oncology Research Program, Mazumdar Shaw Centre for Translational Research, Mazumdar Shaw Medical Foundation, Bangalore, India; Head and Neck Oncology, Mazumdar Shaw Medical Centre, Bangalore, India.
Sindhu GovindanIntegrated Head and Neck Oncology Research Program, Mazumdar Shaw Centre for Translational Research, Mazumdar Shaw Medical Foundation, Bangalore, India.
C N SushmaDepartment of Oral Medicine and Radiology, KLE Institute of Dental Sciences, Dental Hospital and Research Centre, Bangalore, India.
Nisheena RaghavanDepartment of Pathology, Mazumdar Shaw Medical Center, Bangalore, India.
Praveen BirurDepartment of Oral Medicine and Radiology, KLE Institute of Dental Sciences, Dental Hospital and Research Centre, Bangalore, India.
Jeyaram IlayarajaDepartment of Clinical Research, Mazumdar Shaw Medical Center, Bangalore, India.
Mihai MerzianuPathology, Roswell Park Cancer Institute, Buffalo, USA.
Mary ReidDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, USA.
Amritha SureshIntegrated Head and Neck Oncology Research Program, Mazumdar Shaw Centre for Translational Research, Mazumdar Shaw Medical Foundation, Bangalore, India; Head and Neck Oncology, Mazumdar Shaw Medical Centre, Bangalore, India; Mazumdar Shaw Medical Centre-Roswell Park Collaboration Program, Roswell Park Cancer Institute, Buffalo, USA.
Moni Abraham KuriakoseHead and Neck Surgery, Roswell Park Cancer Institute, Buffalo, USA; Integrated Head and Neck Oncology Research Program, Mazumdar Shaw Centre for Translational Research, Mazumdar Shaw Medical Foundation, Bangalore, India; Head and Neck Oncology, Mazumdar Shaw Medical Centre, Bangalore, India; Mazumdar Shaw Medical Centre-Roswell Park Collaboration Program, Roswell Park Cancer Institute, Buffalo, USA. Electronic address: moni.kuriakose@roswellpark.org.
Roswell Park Comprehensive Cancer Center · USMazumdar Shaw Medical Foundation · INMazumdar Shaw Medical Centre · IN

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
Informatic Methods for Differential Signaling and Immune Co-Regulatory ExpressionK01LM012100 · NLM · ROSWELL PARK CANCER INSTITUTE CORP · PI ENG, KEVIN HASEGAWA · 2015 to 2017
$502k
NCI NIH HHS P30 CA016056NLM NIH HHS K01 LM012100
6 · The paper itself

Abstract

objectiveThe purpose of this study was to determine association between cancer stem cells (CSCs) and their niche with progression of oral potentially malignant disorders. MATERIALS AND

methodsPatients with histologically confirmed oral potentially malignant disorders, stratified into high/low risk lesions based on the degree of dysplasia and oral cancer were included in this study. Immunohistochemical profiling of markers of CSCs (CD44), endothelial cells (CD31) and CSC-vascular niche cross-talk (CXCR4 and SDF1) were carried out. Statistical analysis was performed to correlate the relationship of markers with histopathology grade (ANOVA, and χ

resultsThe study included 550 samples (349 patients) and analysis showed progressive increase in expression levels of CSC and its niche markers with increase in grade of dysplasia as compared to the normal cohort (p < 0.05). Co-expression analysis revealed that, in comparison to the normal cohort, a larger percentage of patients showed increased expression of CD31 and CD44 (CD31

conclusionThe increased expression of CSCs, the vascular niche and their cross talk markers are associated with increase in severity of dysplasia suggesting their role in the progression of oral potentially malignant disorders and may hence be used in identifying high-risk OPMD.

Indexed as

Disease ProgressionAdultAgedAged, 80 and overBiomarkers, TumorChemokine CXCL12Cohort StudiesFemaleHumansHyaluronan ReceptorsImmunohistochemistryMaleMiddle AgedMouth NeoplasmsNeoplastic Stem CellsPlatelet Endothelial Cell Adhesion Molecule-1Biomarkers, TumorCD44 protein, humanChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanHyaluronan ReceptorsPlatelet Endothelial Cell Adhesion Molecule-1Receptors, CXCR4Cancer stem cellsCD31CD44CSC-niche interactionCXCR4Oral cancerOral potentially malignant disordersSDF1Vascular niche

Identifiers

PMID29224811
PMCPMC5880641
OpenAlexW2767440441

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.