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Related Concept Videos

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...

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Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
11:42

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells

Published on: April 7, 2017

S-MED: sarcoma microRNA expression database.

Aaron L Sarver1, Rasik Phalak, Venugopal Thayanithy

  • 1Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.

Laboratory Investigation; a Journal of Technical Methods and Pathology
|March 10, 2010
PubMed
Summary
This summary is machine-generated.

Researchers created a new database, the Sarcoma microRNA Expression Database (S-MED), to catalog microRNA (miRNA) expression patterns in human sarcomas. This resource aids in understanding sarcoma biomarkers and improving diagnosis.

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Area of Science:

  • Oncology
  • Genomics
  • Bioinformatics

Background:

  • Human sarcomas are diverse cancers lacking specific diagnostic markers.
  • MicroRNAs (miRNAs) show potential as biomarkers for cancer diagnosis, classification, and prognosis.
  • Current understanding of miRNA expression in sarcomas is limited, with no centralized data repository.

Purpose of the Study:

  • To systematically profile miRNA expression across various human sarcoma types.
  • To develop a publicly accessible bioinformatics resource for sarcoma miRNA data.
  • To facilitate research into novel miRNA biomarkers for sarcoma diagnosis and classification.

Main Methods:

  • Generated miRNA expression profiles from over 300 tumor tissue samples across 22 sarcoma types.
  • Developed the Sarcoma microRNA Expression Database (S-MED), a web-accessible repository.
  • Included data search functionalities (heat map, text/numerical) and statistical analysis (fold changes, P-values) for differential miRNA expression.

Main Results:

  • Comprehensive miRNA expression profiles for 22 human sarcoma types are now available.
  • S-MED provides detailed statistical data on differentially expressed miRNAs compared to normal tissues.
  • Experimental validation of differentially expressed miRNAs was performed for angiosarcoma and other sarcoma types.

Conclusions:

  • S-MED is the first dedicated database for miRNA expression patterns in human sarcomas.
  • The database serves as a valuable resource for advancing biological knowledge and bioinformatics infrastructure in sarcoma research.
  • This resource is expected to accelerate the discovery and development of novel miRNA-based biomarkers for sarcomas.