US2011086800A1PendingUtilityA1

Screening method for predicting susceptibility to breast cancer

Individually held — no corporate assignee on recordPriority: May 10, 2000Filed: Nov 30, 2010Published: Apr 14, 2011
Est. expiryMay 10, 2020(expired)· nominal 20-yr term from priority
G01N 33/6854C12Q 2600/106C12N 2501/395G01N 33/5011C12N 2500/14C12N 5/0693C12N 2500/25A61K 2039/545G01N 2333/71A61K 31/566C07K 16/12C07K 14/70567C12N 2501/392C12N 2500/99A61K 39/0008A61K 2039/505A61P 35/00Y10T436/25A61K 31/453C07K 2317/73C07K 16/26A61K 31/568C12N 2510/04C12N 5/0629A61K 31/138C12N 5/0631G01N 33/96A61K 2039/542C07K 16/00A61K 31/437C07K 16/065A61K 35/16C12N 2500/24C12N 2501/39A61K 31/4188C12Q 1/6886G01N 33/743C07K 2317/52C12N 2503/02G01N 33/575
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Claims

Abstract

A method to aid in identifying a familial or sporadic pattern of risk in at least one individual for developing cancer of a mucosal epithelial tissue, the method comprising screening said at least one individual for heterozygosity or homozygosity for a mutation in a gene coding for a Poly-Ig (Fc) receptor or a Poly-Ig-like (Fc) receptor capable of mediating inhibition of cancer cell growth by an immunoglobulin inhibitor. A method of treating an individual so identified includes enhancing the amount of immunoglobulin inhibitor contacting a mucosal epithelial tissue of said individual, and, especially in individuals homozygous for the defective receptor, may also include prophylactic surgery. Other methods include implementation of a risk reduction or prevention program in individuals identified as being at risk.

Claims

exact text as granted — not AI-modified
1 - 27 . (canceled) 
     
     
         28 . A method of treating an individual identified as heterozygous or homozygous for a mutation in a gene coding for a Poly-Ig (Fc) receptor or a Poly-Ig-like (Fc) receptor capable of mediating estrogen reversible inhibition of breast cancer cell growth by an immunoglobulin inhibitor, comprising enhancing the amount of immunoglobulin inhibitor contacting a mucosal epithelial tissue of said individual. 
     
     
         29 . The method of  claim 28 , wherein said individual is identified as homozygous for said mutation, the method comprising prophylactic administration to said individual of an anti-estrogen compound. 
     
     
         30 . The method of  claim 29 , wherein said anti-estrogen compound is chosen from the group consisting of Tamoxifen, Toremifene, ICI 16384, ICI 182780, EM-800, RU 58688 and EM-139. 
     
     
         31 . The method of  claim 28 , wherein said individual is identified as homozygous for said mutation, the method comprising prophylactic surgical removal of non-cancerous breast tissue. 
     
     
         32 . The method of  claim 28 , comprising employing a breast cancer risk reduction or prevention program comprising enhancing the amount of immunoglobulin inhibitor of cancer cell growth that contacts the breast ductal tissue of said individuals, and/or administering an immunoglobulin inhibitor mimicking compound; and at least one of the following treatments:
 (a) administering an anti-estrogenic compound;   (b) administering an aromatase inhibitor;   (c) enhancing the number of B immunocytes producing IgA or IgM in breast tissue;   (d) immunizing individuals at risk of developing breast cancer against microorganisms known to or suspected of causing breast cancer.   
     
     
         33 . The method of  claim 32 , wherein said immunoglobulin inhibitor mimicking compound is chosen from the group consisting of Tamoxifen, MER-25 and chemically substituted or modified derivatives thereof. 
     
     
         34 . The method of  claim 33 , comprising co-administering a hormone capable of reducing side effects of said MER-25 or derivative thereof 
     
     
         35 . The method of  claim 32 , wherein enhancing the number of B immunocytes producing IgA or IgM in breast tissue comprises administering an immune enhancing agent. 
     
     
         36 . The method of  claim 35 , wherein said immune enhancing agent is chosen from the group consisting of Levimisole, Imiquimod, Picibanil and DHEA.

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