Evidence map›Paper›PMID 27034264›Full record

ArticleMedical oncology (Northwood, London, England)2016

Cyclin D1 and cyclin E2 are differentially expressed in gastric cancer.

Soni Kumari, Puneet, Shyam Babu Prasad, Suresh Singh Yadav, Mohan Kumar, A Khanna, V K Dixit, Gopal Nath, Sunita Singh, Gopeshwar Narayan

Abstract read
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In one paragraph

Article in Medical oncology (Northwood, London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

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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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  7. Expression of p27 and p16 and their clinical significance in gastric cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Article
  8. Article
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  14. Molecular biology and immunology of gastric cancer peritoneal metastasis.Translational gastroenterology and hepatology · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Network Pharmacology-Based Approach to Investigate the Mechanisms ofEvidence-based complementary and alternative medicine : eCAM · 2018
    Article
  20. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Soni KumariCancer Genetics Laboratory, Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi, 221 005, India.
PuneetDepartment of General Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221 005, India.
Shyam Babu PrasadCancer Genetics Laboratory, Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi, 221 005, India.
Suresh Singh YadavCancer Genetics Laboratory, Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi, 221 005, India.
Mohan KumarDepartment of Pathology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221 005, India.
A KhannaDepartment of General Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221 005, India.
V K DixitDepartment of Gastroenterology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221 005, India.
Gopal NathDepartment of Microbiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221 005, India.
Sunita SinghDepartment of Zoology, Mahila Mahavidyalaya, Banaras Hindu University, Varanasi, 221 005, India.
Gopeshwar NarayanCancer Genetics Laboratory, Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi, 221 005, India. gnarayan@bhu.ac.in.
Banaras Hindu University · INInstitute of Medical Sciences · INJawaharlal Nehru University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell cycle regulators cyclin D1 and cyclin E2 function in G1/S transition by activating downstream cyclin-dependent kinases. Deregulated expression of these cyclins has been reported in various cancers. However, little is known about their clinical significance in gastric carcinoma. We aimed to explore that whether there is differential expression of these cyclins in clinically distinct gastric cancer patients. In this study we recruited a total of 92 subjects including 20 controls and 72 cases of histopathologically proven gastric carcinoma. Expression profiling at transcript level was done by semiquantitative RT-PCR and of protein by immunohistochemistry. Receiver operator characteristics analysis was done for determining diagnostic utility of cyclin D1 and cyclin E2. We demonstrate that cyclins D1 and E2 are frequently overexpressed in early stages of gastric carcinoma. Interestingly, expression of cyclins D1 and E2 significantly correlates with different clinical parameters such as gender, histological type (intestinal and diffuse), tumor location (proximal, middle, and distal), tumor differentiation (differentiated and undifferentiated), tumor invasion (serosal, lymphatic, and venous) and tumor metastasis (lymph node, peritoneal, ascites, and liver). Cyclin D1 has significantly higher sensitivity and specificity as diagnostic biomarker than cyclin E2. Our results suggest that overexpression of cyclin D1 and cyclin E2 is an early event in gastric carcinogenesis. The differential expression of these cyclins may be useful as diagnostic biomarkers for early detection of gastric carcinoma.

Indexed as

Biomarkers, TumorCase-Control StudiesCyclin D1CyclinsFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryMaleReverse Transcriptase Polymerase Chain ReactionROC CurveSensitivity and SpecificityStomach NeoplasmsBiomarkers, TumorCCND1 protein, humanCCNE2 protein, humanCyclin D1CyclinsClinical correlationCyclin D1Cyclin E2Gastric cancer

Identifiers

PMID27034264
OpenAlexW2322598197

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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.