Paper Details 
Original Abstract of the Article :
As many societies age, primary osteoporosis (PO) is increasingly a major health problem. Current drug treatments such as alendronate and risedronate have known side effects. We took an agnostic empirical approach to find PO therapeutic compounds. We examined 13,548,960 probe data-points from mesench...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299905/

データ提供:米国国立医学図書館(NLM)

Finding New Therapies for Osteoporosis: A Desert Oasis of Bone Health

Osteoporosis, a condition that weakens bones and increases fracture risk, is a major health concern, particularly as populations age. Current treatments for osteoporosis have known side effects, making the search for new therapies a priority. This study, like a quest for a hidden oasis in the desert, explores a novel approach to identifying potential therapeutic compounds for primary osteoporosis.

Mining the Desert of Gene Expression: A Search for Therapeutic Targets

The researchers, like intrepid desert explorers, analyzed gene expression data from mesenchymal stromal cell (hMSC) lines, searching for genes that are differentially regulated in osteoporosis. They identified a set of genes that were either up-regulated or down-regulated in osteoporosis, offering potential targets for therapeutic intervention.

Identifying New Compounds: A Promise of Bone Health

Using pharmacophore models, the researchers screened a vast library of chemical compounds, searching for those that could bind to the identified targets. This approach, like a meticulous sifting of desert sands, led to the identification of five novel therapeutic compounds that could potentially treat osteoporosis.

Dr. Camel's Conclusion

This study offers a promising new approach to identifying therapeutic compounds for osteoporosis. By exploring the landscape of gene expression and employing sophisticated screening techniques, the researchers have uncovered potential new avenues for treating this debilitating condition.

Date :
  1. Date Completed n.d.
  2. Date Revised 2020-09-30
Further Info :

Pubmed ID

30647616

DOI: Digital Object Identifier

PMC6299905

Related Literature

SNS
PICO Info
in preparation
Languages

English

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