Expression of Attractin and Its Differential Enzyme Activity in Glioma Cells
Biochemical and Biophysical Research Communications, ISSN: 0006-291X, Vol: 284, Issue: 2, Page: 289-294
2001
- 16Citations
- 11Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations16
- Citation Indexes16
- 16
- CrossRef14
- Captures11
- Readers11
- 11
Article Description
Attractin/ mahogany protein was previously shown to be involved in a number of physiological and pathological events, including immune system regulation, body weight control, pigmentation, myelinization, and tumor susceptibility. Human attractin has an enzymatic activity resembling dipeptidyl peptidase IV (DPP-IV). In the central nervous system, attractin has been detected in neurons but not in glial cells up to now. We show the expression of attractin mRNA and protein in glioma cell lines at different degree of transformation. In human U373 and U87 glioma cells (Grades III and IV), membrane-bound attractin displays hydrolytic activity amounting to 5 and 25% of total cellular DPP-IV-like enzyme activity, respectively. Such activity has not been observed in the rat C6 glioma cells (Grade I). Attractin presence in glioma, but not in normal glial cells, together with its differential enzymatic activity, suggests its role in growth properties of tumors of glial cell origin.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0006291X01949563; http://dx.doi.org/10.1006/bbrc.2001.4956; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0034811757&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/11394875; https://linkinghub.elsevier.com/retrieve/pii/S0006291X01949563; https://dx.doi.org/10.1006/bbrc.2001.4956
Elsevier BV
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