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Dove Medical Press

Roles of dopamine receptors and their antagonist thioridazine in hepatoma metastasis

Overview of attention for article published in OncoTargets and therapy, June 2015
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • Good Attention Score compared to outputs of the same age (77th percentile)
  • High Attention Score compared to outputs of the same age and source (95th percentile)

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1 X user
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2 patents

Citations

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41 Mendeley
Title
Roles of dopamine receptors and their antagonist thioridazine in hepatoma metastasis
Published in
OncoTargets and therapy, June 2015
DOI 10.2147/ott.s77373
Pubmed ID
Authors

Meiling Lu, Jinghua Li, Zaili Luo, Shuai Zhang, Shaobo Xue, Kesheng Wang, Yan Shi, Cunzhen Zhang, Haiyang Chen, Zhong Li

Abstract

Tumor metastasis is the most common cause of death and poor prognosis for cancer patients. Therapeutics that prevent tumor metastasis are the key to prolonging the lifespan of cancer patients. Cancer stem cells are believed to be critical in the metastatic process. Recently, drug screening for cancer stem cells reports that antipsychotic drugs displayed potential anticancer activity. Thioridazine, one of the antipsychotic drugs for dopamine receptors (DRs), is shown to induce the differentiation of cancer stem cells in leukemic disease and breast cancer, but it is not known if this drug would affect liver cancer. In this study, expression of DR5 was higher in tumors than in nontumor adjacent tissues, while DR1 was lower in human hepatocellular carcinoma (HCC) than those in the adjacent tissues. Other DRs were very low or undetectable. Treatment of HCC cells with thioridazine displays a dose-dependent response in HCC cell lines SNU449, LM3, and Huh7. Thioridazine treatment reduced cell viability and sphere formation of HCC cell lines through induction of G0/G1 cell cycle arrest and suppression of stemness genes CD133, OCT4, and EpCam. It also inhibited cell migration via suppression of epithelial-mesenchymal transition (EMT)-related genes such as twist2 and E-cadherin. Thioridazine-pretreated LM3 cells decreased the capacity of tumorigenesis in nude mice. Taken together, our data suggest that thioridazine may have the potential role in treatment of HCC.

X Demographics

X Demographics

The data shown below were collected from the profile of 1 X user 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 41 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Ghana 1 2%
Unknown 40 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 27%
Student > Ph. D. Student 7 17%
Student > Master 5 12%
Student > Bachelor 3 7%
Professor 2 5%
Other 6 15%
Unknown 7 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 14 34%
Pharmacology, Toxicology and Pharmaceutical Science 6 15%
Psychology 4 10%
Medicine and Dentistry 3 7%
Agricultural and Biological Sciences 2 5%
Other 5 12%
Unknown 7 17%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 7. 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 12 January 2021.
All research outputs
#5,340,716
of 25,584,565 outputs
Outputs from OncoTargets and therapy
#261
of 2,967 outputs
Outputs of similar age
#61,787
of 281,752 outputs
Outputs of similar age from OncoTargets and therapy
#4
of 64 outputs
Altmetric has tracked 25,584,565 research outputs across all sources so far. Compared to these this one has done well and is in the 79th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 2,967 research outputs from this source. They receive a mean Attention Score of 3.0. This one has done particularly well, scoring higher than 90% 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 281,752 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 77% of its contemporaries.
We're also able to compare this research output to 64 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 95% of its contemporaries.