US2018100157A1PendingUtilityA1

Reduction of tgf beta signaling in myeloid cells in the treatment of cancer

Assignee: US HEALTHPriority: Aug 18, 2011Filed: Dec 11, 2017Published: Apr 12, 2018
Est. expiryAug 18, 2031(~5 yrs left)· nominal 20-yr term from priority
Inventors:Li Yang
C12N 15/1138G01N 33/5091A01K 67/0276A01K 2227/105A61K 31/4025A61K 31/5377A61K 35/28A61K 31/7088A01K 2217/075C12Q 1/6886A01K 2267/0331C07K 14/71G01N 2333/71C12N 15/85C12N 2320/30A61P 35/04C12Q 2600/158C12N 2310/14C12N 15/86A01K 2217/206G01N 33/5759G01N 33/57492A61K 40/42A61K 40/10A61K 2239/49
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Claims

Abstract

Methods of inhibiting metastasis in cancer patients are provided, wherein the methods comprise reducing TGFβ signaling, for example, by reducing TGFβ receptor II expression in myeloid cells. Vectors comprising a TGFβ receptor II RNAi nucleic acid sequence operably linked to a myeloid specific promoter also are provided. A method of diagnosing cancer in an individual by determining TGFβ receptor II expression in myeloid cells in the individual is provided. Additionally, a method of modulating TGFβ activity in myeloid cells in a cancer patient comprising administering a regulator of at least one of the GSK3 and PI3K pathways to the patient is provided.

Claims

exact text as granted — not AI-modified
1 .- 14 . (canceled) 
     
     
         15 . A vector comprising a TGFβ receptor II RNAi nucleic acid sequence operably linked to a myeloid-specific promoter. 
     
     
         16 . The vector of  claim 15 , wherein the vector is a viral vector, a plasmid, a yeast, or a nanoparticle. 
     
     
         17 . (canceled) 
     
     
         18 . A method of modulating TGFβ activity in myeloid cells in a cancer patient comprising administering a regulator of at least one of the GSK3 and PI3K pathways to the patient. 
     
     
         19 . The method of  claim 18 , wherein TGFβ activity in myeloid cells is reduced by administering an inhibitor of PI3K or an enhancer of GSK3. 
     
     
         20 . The method of  claim 18 , wherein the PI3K inhibitor is LY294002.

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