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[[Information on nutritional supplements people with ALS have been taking]]
 
[[Information on nutritional supplements people with ALS have been taking]]
  
* [https://en.wikipedia.org/wiki/Pu-erh_tea Wikipedia page]
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[https://en.wikipedia.org/wiki/Pu-erh_tea Wikipedia page]
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== Effects on ALS ==
 
== Effects on ALS ==
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Pu-erh tea may have beneficial health effects, including preventing the onset of FET family protein-associated neurodegenerative diseases and delaying the progression of ALS by inhibiting the cytoplasmic aggregation of FET family proteins.
 
Pu-erh tea may have beneficial health effects, including preventing the onset of FET family protein-associated neurodegenerative diseases and delaying the progression of ALS by inhibiting the cytoplasmic aggregation of FET family proteins.
  
FET family proteins consist of fused in sarcoma/translocated in liposarcoma (FUS/TLS), Ewing's sarcoma (EWS), and TATA-binding protein-associated factor 15 (TAF15). Mutations in the copper/zinc superoxide dismutase (SOD1), TAR DNA-binding protein 43 (TDP-43), and FET family proteins are associated with the development of ALS.{{#pmid: 24804206|Yu2014}}
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FET family proteins consist of fused in sarcoma/translocated in liposarcoma (FUS/TLS), Ewing's sarcoma (EWS), and TATA-binding protein-associated factor 15 (TAF15). Mutations in the copper/zinc superoxide dismutase (SOD1), TAR DNA-binding protein 43 (TDP-43), and FET family proteins are associated with the development of ALS. [1]
  
 
== Discussion threads on the ALSTDI forum ==
 
== Discussion threads on the ALSTDI forum ==
  
 
== Regulated pathways ==
 
== Regulated pathways ==
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== References ==
 
== References ==
  
[[Category:Supplement data pages]]
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[1]
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<bibtex>
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@article{Yu2014,
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abstract = {FET family proteins consist of fused in sarcoma/translocated in liposarcoma (FUS/TLS), Ewing's sarcoma (EWS), and TATA-binding protein-associated factor 15 (TAF15). Mutations in the copper/zinc superoxide dismutase (SOD1), TAR DNA-binding protein 43 (TDP-43), and FET family proteins are associated with the development of amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease. There is currently no cure for this disease and few effective treatments are available. Epidemiological studies indicate that the consumption of tea is associated with a reduced risk of developing neurodegenerative diseases. The results of this study revealed that components of a pu-erh tea extract (PTE) interacted with FET family proteins but not with TDP-43 or SOD1. PTE induced the degradation of FET family proteins but had no effects on TDP-43 or SOD1. The most frequently occurring ALS-linked FUS/TLS mutant protein, R521C FUS/TLS, was also degraded in the presence of PTE. Furthermore, ammonium chloride, a lysosome inhibitor, but not lactacystin, a proteasome inhibitor, reduced the degradation of FUS/TLS protein by PTE. PTE significantly reduced the incorporation of R521C FUS/TLS into stress granules under stress conditions. These findings suggest that PTE may have beneficial health effects, including preventing the onset of FET family protein-associated neurodegenerative diseases and delaying the progression of ALS by inhibiting the cytoplasmic aggregation of FET family proteins.},
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author = {Yang Yu, huhei Hayashi, Xianbin Cai, Chongye Fang, Wei Shi, Hiroko Tsutsui and Jun Sheng},
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doi = {10.1155/2014/254680},
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issn = {},
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journal = {Biomed Res Int.},
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keywords = {},
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mendeley-groups = {},
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month = apr,
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number = {},
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pages = {},
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pmid = {3997874},
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title = {{Pu-Erh Tea Extract Induces the Degradation of FET Family Proteins Involved in the Pathogenesis of Amyotrophic Lateral Sclerosis.}},
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url = {http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997874/},
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volume = {},
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year = {2014}
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}
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</bibtex>

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