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Molecular Pathways: Inhibiting Steroid Biosynthesis in Prostate Cancer

Overview of attention for article published in Clinical Cancer Research, June 2013
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (80th percentile)
  • Above-average Attention Score compared to outputs of the same age and source (62nd percentile)

Mentioned by

twitter
3 X users
patent
5 patents

Readers on

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122 Mendeley
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1 CiteULike
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Article details
Title
Molecular Pathways: Inhibiting Steroid Biosynthesis in Prostate Cancer
Published in
Clinical Cancer Research, June 2013
DOI 10.1158/1078-0432.ccr-12-0931
Pubmed ID
Authors
Abstract

A significant proportion of castration-resistant prostate cancers (CRPC) remains driven by ligand activation of the androgen receptor. Although the testes are the primary source of testosterone, testosterone can also be produced from peripheral conversion of adrenal sex hormone precursors DHEA and androstenedione in the prostate and other tissues. CYP17A1 catalyzes two essential reactions in the production of DHEA and androstenedione: the hydroxylation (hydroxylase activity) and the subsequent cleavage of the C17-20 side chain (lyase activity). Potent and selective inhibition of CYP17A1 by abiraterone depletes residual nongonadal androgens and is an effective treatment for CRPC. Elucidation of the mechanisms that underlie resistance to abiraterone will inform the development of novel therapeutic strategies post-abiraterone. Preclinical evidence that androgen biosynthesis in prostate cancer cells does not necessarily follow a single dominant pathway, and residual androgens or alternative ligands (including administered glucocorticoids) can reactivate androgen receptor signaling, supports cotargeting of more than one enzyme involved in steroidogenesis and combining a CYP17A1 inhibitor with an antiandrogen. Furthermore, given the drawbacks of 17α-hydroxylase inhibition, there is considerable interest in developing new CYP17A1 inhibitors that more specifically inhibit lyase activity and are therefore less likely to require glucocorticoid coadministration.

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X Demographics

X Demographics

The data shown below were collected from the profiles of 3 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 122 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
Japan 1 <1%
Germany 1 <1%
Canada 1 <1%
Unknown 119 98%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Student > Master 19 16%
Researcher 19 16%
Student > Bachelor 17 14%
Student > Ph. D. Student 14 11%
Other 11 9%
Other 16 13%
Unknown 26 21%
Readers by discipline
Readers by discipline Count As %
Medicine and Dentistry 26 21%
Biochemistry, Genetics and Molecular Biology 18 15%
Agricultural and Biological Sciences 13 11%
Pharmacology, Toxicology and Pharmaceutical Science 11 9%
Chemistry 9 7%
Other 12 10%
Unknown 33 27%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 8. 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 31 August 2021.
All research outputs
#6,505,287
of 34,054,827 outputs
Outputs from Clinical Cancer Research
#6,959
of 17,666 outputs
Outputs of similar age
#47,113
of 239,635 outputs
Outputs of similar age from Clinical Cancer Research
#67
of 187 outputs
Altmetric has tracked 34,054,827 research outputs across all sources so far. Compared to these this one has done well and is in the 80th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 17,666 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 12.0. This one has gotten more attention than average, scoring higher than 60% 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 239,635 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 80% of its contemporaries.
We're also able to compare this research output to 187 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.