Evidence map›Paper›PMID 27757712›Full record

ArticleCytotechnology2016

RNA interference mediated downregulation of human telomerase reverse transcriptase (hTERT) in LN18 cells.

Ch Lavanya, M K Sibin, M M Srinivas Bharath, M Jeru Manoj, Manjunatha M Venkataswamy, Dhananjaya I Bhat, K V L Narasinga Rao, G K Chetan

Open access · bronzeAbstract read
In one paragraph

Article in Cytotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 25% 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

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

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Cellular senescence in glioma.Journal of neuro-oncology · 2023
    Review
  6. Review
  7. 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

8 authors at 1 institution in 1 country.

Ch LavanyaDepartment of Human Genetics, National Institute of Mental Health and Neuro Sciences, Bangalore, 560029, India.
M K SibinDepartment of Human Genetics, National Institute of Mental Health and Neuro Sciences, Bangalore, 560029, India.
M M Srinivas BharathDepartment of Neuro-chemistry, National Institute of Mental Health and Neuro Sciences, Bangalore, 560029, India.
M Jeru ManojDepartment of Human Genetics, National Institute of Mental Health and Neuro Sciences, Bangalore, 560029, India.
Manjunatha M VenkataswamyDepartment of Neurovirology, National Institute of Mental Health and Neuro Sciences, Bangalore, 560029, India.
Dhananjaya I BhatDepartment of Neurosurgery, National Institute of Mental Health and Neuro Sciences, Bangalore, India.
K V L Narasinga RaoDepartment of Neurovirology, National Institute of Mental Health and Neuro Sciences, Bangalore, 560029, India.
G K ChetanDepartment of Human Genetics, National Institute of Mental Health and Neuro Sciences, Bangalore, 560029, India. drchetangk@gmail.com.
National Institute of Mental Health and Neurosciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human telomerase reverse transcriptase (hTERT) gene is a biomarker for the targeted therapy in various cancers. Presence of increased telomerase activity is a common feature of all cancers including glioblastoma. Both RNA and catalytic subunits of hTERT are the target sites for blocking its activity. The current study focuses on the expression of hTERT in glioblastoma and its regulation using two different novel siRNAs (small interfering RNA). Our patient data demonstrated increased expression of hTERT, which could be correlated with carcinogenesis in glioma. In vitro studies in siRNA transfected LN18 cells confirmed significant cell death (p < 0.05) as evidenced by MTT and trypan blue exclusion assay. These results were further supported by flow cytometry data, which showed significant increase in early and late apoptosis. The hTERT mRNA expression was effectively downregulated by 45 and 39 % with siRNA1 and siRNA2, respectively. These results were further confirmed by immunoblotting analysis (p < 0.05). Our results suggest that both the siRNAs effectively down regulated the expression of hTERT at mRNA and protein levels, thereby decreasing cell viability and proliferation rate. Hence siRNA mediated downregulation of hTERT could be a potential therapeutic avenue in glioblastoma.

Indexed as

ApoptosisGlioblastomahTERTLN18 cell lineSmall interfering RNA

Identifiers

PMID27757712
PMCPMC5101301
OpenAlexW2532783625

What OpenQuestion holds

Textmetadata
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.