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Specific Inhibition of Tumor Cells by Oncogenic EGFR Specific Silencing by RNA interference

Overview of attention for article published in PLOS ONE, August 2013
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About this Attention Score

  • Good Attention Score compared to outputs of the same age (70th percentile)
  • Above-average Attention Score compared to outputs of the same age and source (62nd percentile)

Mentioned by

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2 X users
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1 patent

Citations

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8 Dimensions

Readers on

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13 Mendeley
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Title
Specific Inhibition of Tumor Cells by Oncogenic EGFR Specific Silencing by RNA interference
Published in
PLOS ONE, August 2013
DOI 10.1371/journal.pone.0073214
Pubmed ID
Authors

Masaki Takahashi, Tomoko Chiyo, Takashi Okada, Hirohiko Hohjoh

Abstract

Anticancer agents that have minimal effects on normal cells and tissues are ideal cancer drugs. Here, we show specific inhibition of human cancer cells carrying oncogenic mutations in the epidermal growth factor receptor (EGFR) gene by means of oncogenic allele-specific RNA interference (RNAi), both in vivo and in vitro. The allele-specific RNAi (ASP-RNAi) treatment did not affect normal cells or tissues that had no target oncogenic allele, whereas the suppression of a normal EGFR allele by a conventional in vivo RNAi caused adverse effects, i.e., normal EGFR is vital. Taken together, our current findings suggest that specific inhibition of oncogenic EGFR alleles without affecting the normal EGFR allele may provide a safe treatment approach for cancer patients and that ASP-RNAi treatment may be capable of becoming a safe and effective, anticancer treatment method.

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 3 23%
Student > Bachelor 2 15%
Student > Postgraduate 2 15%
Researcher 2 15%
Student > Ph. D. Student 1 8%
Other 1 8%
Unknown 2 15%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 31%
Pharmacology, Toxicology and Pharmaceutical Science 3 23%
Biochemistry, Genetics and Molecular Biology 3 23%
Medicine and Dentistry 1 8%
Unknown 2 15%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 4. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 02 January 2018.
All research outputs
#6,765,156
of 22,716,996 outputs
Outputs from PLOS ONE
#79,690
of 193,928 outputs
Outputs of similar age
#58,093
of 197,294 outputs
Outputs of similar age from PLOS ONE
#1,749
of 4,810 outputs
Altmetric has tracked 22,716,996 research outputs across all sources so far. This one has received more attention than most of these and is in the 69th percentile.
So far Altmetric has tracked 193,928 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 15.0. This one has gotten more attention than average, scoring higher than 58% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 197,294 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 70% of its contemporaries.
We're also able to compare this research output to 4,810 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 62% of its contemporaries.