Evidence map›Paper›PMID 26124566›Full record

ArticleBioinformation2015

An in silico analytical study of lung cancer and smokers datasets from gene expression omnibus (GEO) for prediction of differentially expressed genes.

Atif Noorul Hasan, Mohammad Wakil Ahmad, Inamul Hasan Madar, B Leena Grace, Tarique Noorul Hasan

Open access · hybridAbstract read
In one paragraph

Article in Bioinformation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. A novel role of ADGRF1 (GPR110) in promoting cellular quiescence and chemoresistance in human epidermal growth factor receptor 2-positive breast cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  6. Article
  7. Article
  8. The Emerging Role of Adhesion GPCRs in Cancer.ACS pharmacology & translational science · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Bioinformatic analysis of differential expression and core GENEs in breast cancer.International journal of clinical and experimental pathology · 2018
    Article
  13. Article
  14. Article
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

5 authors at 5 institutions in 3 countries.

Atif Noorul HasanDept. of Bioinformatics, Jamia Millia Islamia, New Delhi, India ; Division of Bioinformatics, Noor-Amna Foundation for Research and Education, Bettiah, Bihar, India.
Mohammad Wakil AhmadDept. of Software Engg, College of Computer Science, King Saud University, Riyadh, Saudi Arabia.
Inamul Hasan MadarDept. of Biotechnology and Bioinformatics, Bishop Heber College, Tiruchirappalli, TN, India.
B Leena GraceDept of Biotechnology, Vinayaka Missions University, Salem, TN, India.
Tarique Noorul HasanDivision of Bioinformatics, Noor-Amna Foundation for Research and Education, Bettiah, Bihar, India ; R & D Center, Bharathiar University, Coimbatore-641046, TN,India.
Bharathiar University · INJamia Millia Islamia · INKing Saud University · SASaint Joseph's College · USVinayaka Missions University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Smoking is the leading cause of lung cancer development and several genes have been identified as potential biomarker for lungs cancer. Contributing to the present scientific knowledge of biomarkers for lung cancer two different data sets, i.e. GDS3257 and GDS3054 were downloaded from NCBI׳s GEO database and normalized by RMA and GRMA packages (Bioconductor). Diffrentially expressed genes were extracted by using and were R (3.1.2); DAVID online tool was used for gene annotation and GENE MANIA tool was used for construction of gene regulatory network. Nine smoking independent gene were found whereas average expressions of those genes were almost similar in both the datasets. Five genes among them were found to be associated with cancer subtypes. Thirty smoking specific genes were identified; among those genes eight were associated with cancer sub types. GPR110, IL1RN and HSP90AA1 were found directly associated with lung cancer. SEMA6A differentially expresses in only non-smoking lung cancer samples. FLG is differentially expressed smoking specific gene and is related to onset of various cancer subtypes. Functional annotation and network analysis revealed that FLG participates in various epidermal tissue developmental processes and is co-expressed with other genes. Lung tissues are epidermal tissues and thus it suggests that alteration in FLG may cause lung cancer. We conclude that smoking alters expression of several genes and associated biological pathways during development of lung cancers.

Identifiers

PMID26124566
PMCPMC4464538
OpenAlexW798726819

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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.