Evidence map›Paper›PMID 31516387›Full record

ArticleCancer cell international2019

miR-145 supports cancer cell survival and shows association with DDR genes, methylation pattern, and epithelial to mesenchymal transition.

Siddharth Manvati, Kailash Chandra Mangalhara, Ponnuswamy Kalaiarasan, Rupali Chopra, Gaurav Agarwal, Rakesh Kumar, Sunil Kumar Saini, Monika Kaushik, Ankita Arora, Usha Kumari and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Article
  5. miRNAs in Signal Transduction of SMAD Proteins in Breast Cancer.International journal of molecular sciences · 2024
    Article
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  7. Article
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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

12 authors at 4 institutions in 2 countries.

Siddharth Manvati1School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.
Kailash Chandra Mangalhara2National Centre of Applied Human Genetics, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Ponnuswamy Kalaiarasan1School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.
Rupali Chopra2National Centre of Applied Human Genetics, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Gaurav Agarwal3Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Rakesh Kumar4School of Biotechnology, Shri Mata Vaishno Devi University, Kakryal, Katra, Jammu and Kashmir India.
Sunil Kumar Saini1School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.
Monika Kaushik1School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.
Ankita Arora1School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.
Usha Kumari5Faculty of Medicine, AIMST University, Bedong, Malaysia.
Rameshwar Nath Koul Bamezai2National Centre of Applied Human Genetics, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Pawan Kumar Dhar1School of Biotechnology, Jawaharlal Nehru University, New Delhi, India.
Jawaharlal Nehru University · INAIMST University · MYSanjay Gandhi Post Graduate Institute of Medical Sciences · INShri Mata Vaishno Devi University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite several reports describing the dual role of miR-145 as an oncogene and a tumor suppressor in cancer, not much has been resolved and understood.

methodIn this study, the potential targets of miR-145 were identified bio-informatically using different target prediction tools. The identified target genes were validated in vitro by dual luciferase assay. Wound healing and soft agar colony assay assessed cell proliferation and migration. miR-145 expression level was measured quantitatively by RT-PCR at different stages of breast tumor. Western blot was used to verify the role of miR-145 in EMT transition using key marker proteins.

resultWound healing and soft agar colony assays, using miR-145 over-expressing stably transfected MCF7 cells, unraveled its role as a pro-proliferation candidate in cancerous cells. The association between miR-145 over-expression and differential methylation patterns in representative target genes (

conclusionOur results demonstrate miR-145 as a pro-cancerous candidate, evident from the phenotypes of aggressive cellular proliferation, epithelial to mesenchymal transition, hypermethylation of CpG sites in DDR and apoptotic genes and upregulation of miR-145 in later stages of tumor tissues.

Indexed as

BRCA2DR5Epithelial–mesenchymal transitionMethylationmiR-145SMAD3Vimentin

Identifiers

PMID31516387
PMCPMC6731614
OpenAlexW2971858615

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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.