Evidence map›Paper›PMID 29672635›Full record

ArticlePloS one2018

Differential transmission of the molecular signature of RBSP3, LIMD1 and CDC25A in basal/ parabasal versus spinous of normal epithelium during head and neck tumorigenesis: A mechanistic study.

Shreya Sarkar, Neyaz Alam, Syam Sundar Mandal, Kabita Chatterjee, Supratim Ghosh, Susanta Roychoudhury, Chinmay Kumar Panda

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Shreya SarkarDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, India.
Neyaz AlamDepartment of Surgical Oncology, Chittaranjan National Cancer Institute, Kolkata, India.
Syam Sundar MandalDepartment of Epidemiology and Biostatistics, Chittaranjan National Cancer Institute, Kolkata, India.
Kabita ChatterjeeDepartment of Oral and Maxillofacial Pathology, Buddha Institute of Dental Sciences and Hospital, Patna, India.
Supratim GhoshDepartment of Oral and Maxillofacial Pathology, Burdwan Dental College and Hospital, Burdwan, India.
Susanta RoychoudhuryBasic Research, Saroj Gupta Cancer Centre and Research Institute, Kolkata, India.
Chinmay Kumar PandaDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, India.ORCID 0000-0002-0854-6978
Chittaranjan National Cancer Institute · INBurdwan Medical College & Hospital · INGautam Buddha University · INSaroj Gupta Cancer Centre & Research Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a global disease and mortality burden, necessitating the elucidation of its molecular progression for effective disease management. The study aims to understand the molecular profile of three candidate cell cycle regulatory genes, RBSP3, LIMD1 and CDC25A in the basal/ parabasal versus spinous layer of normal oral epithelium and during head and neck tumorigenesis. Immunohistochemical expression and promoter methylation was used to determine the molecular signature in normal oral epithelium. The mechanism of alteration transmission of this profile during tumorigenesis was then explored through additional deletion and mutation in HPV/ tobacco etiological groups, followed byclinico-pathological correlation. In basal/parabasal layer, the molecular signature of the genes was low protein expression/ high promoter methylation of RBSP3, high expression/ low methylation of LIMD1 and high expression of CDC25A. Dysplastic epithelium maintained the signature of RBSP3 through high methylation/ additional deletion with loss of the signatures of LIMD1 and CDC25A via deletion/ additional methylation. Similarly, maintenance and / or loss of signature in invasive tumors was by recurrent deletion/ methylation. Thus, differential patterns of alteration of the genes might be pre-requisite for the development of dysplastic and invasive lesions. Etiological factors played a key role in promoting genetic alterations and determining prognosis. Tobacco negative HNSCC patients had significantly lower alterations of LIMD1 and CDC25A, along with better survival among tobacco negative/ HPV positive patients. Our data suggests the necessity for perturbation of normal molecular profile of RBSP3, LIMD1 and CDC25A in conjunction with etiological factors for head and neck tumorigenesis, implying their diagnostic and prognostic significance.

Indexed as

AdultAgedCarcinoma, Squamous Cellcdc25 PhosphatasesCell Transformation, NeoplasticDNA MethylationEpitheliumFemaleHead and Neck NeoplasmsHumansImmunohistochemistryIntracellular Signaling Peptides and ProteinsLIM Domain ProteinsMaleMiddle AgedMutationCDC25A protein, humancdc25 PhosphatasesCTDSPL protein, humanIntracellular Signaling Peptides and ProteinsLIMD1 protein, humanLIM Domain ProteinsTumor Suppressor Proteins

Identifiers

PMID29672635
PMCPMC5909606
OpenAlexW2801869517

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.