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Old 03-09-2007, 04:00 AM   #1
RhondaH
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Exclamation Upregulation of CXCR4 is essential for HER2-mediated tumor metastasis.

Ok, now we know what CAUSES the metastatis, now what to prevent it.


http://www.ncbi.nlm.nih.gov/entrez/q...&dopt=Abstract

More info on CXCR4
http://en.wikipedia.org/wiki/CXCR4

Rhonda
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Dx 2/1/05, Stage 1, 0 nodes, Grade 3, ER/PR-, HER2+ (3.16 Fish)
2/7/05, Partial Mastectomy
5/18/05 Finished 6 rounds of dose dense TEC (Taxotere, Epirubicin and Cytoxan)
8/1/05 Finished 33 rads
8/18/05 Started Herceptin, every 3 weeks for a year (last one 8/10/06)

2/1/13...8 year Cancerversary and I am "perfect" (at least where cancer is concerned;)


" And in the end, it's not the years in your life that count. It's the life in your years."- Abraham Lincoln
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Old 03-09-2007, 05:31 AM   #2
jhandley
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also interesting....

Hi rhonda

I found this reference on CXCR4. I was particularly interested in the sentences I have highlighted. If this MAb turns off CXCR4 then it might stop her 2 mets as well as HIV.



Food for thought.

Jackie

FUSIN ANTISERA

Background:Fusin (CXCR4) (subject to patent by University of Pa) is a seven-transmembrane domain G-protein linked chemokine receptor. It has the highest degree of sequence homology with IL-8 receptors. Fusin is expressed on a wide variety of CD4+ and CD4- cells including those from spleen, brain and lung. The gene is located on chromosome 2 close to other chemokine receptor genes. The CXC chemokine, stromal cell-derived factor-1 (SDF-1), was recently identified as the ligand for Fusin . This molecule is strongly chemotactic for monocytes and lymphocytes. Messenger RNA for SDF-1 has been detected in a wide range of tissues and it has been suggested that it may have a role in immune surveillance or lymphocyte recirculation, rather than in inflammation. SDF-1 is highly conserved in human and mouse and studies on SDF-1 knockout mice reveal an essential function in development, as the mice show defects in B cell lymphopoiesis, bone marrow myelopoiesis and in the structure of the heart.
Fusin functions as a cofactor for infection with T-cell tropic strains of HIV-1. Immunoprecipitation of Fusin with the HIVgp120-CD4 complex suggests a direct mode of action for Fusin as a co-receptor. The monoclonal antibody (mAb), 12G5, is specific for Fusin. Some HIV-2 isolates can utilize Fusin as a receptor for CD4-independent infection. 12G5 blocks both CD4-independent infection by HIV-2, and CD4-dependent infection by certain T-cell tropic isolates of HIV-11-5 and does not cross-react with IL8RA (CXCR1), IL8RB (CXCR2), CCR1, CCR2, CCR3, CCR4 or CCR5 or the murine SDF-1 receptor.

REFERENCES

1. Loetscher, M., T. Geiser, T. O'Reilly, et al. 1994. Cloning of a human seven-transmembrane domain receptor, LESTR, that is highly expressed in leukocytes. J. Biol. Chem. 269: 232.


2. Simmons, G., D. Wilkinson, J.D. Reeves, et al. 1996. Primary, syncytium-inducing human immunodeficiency virus type 1 isolates are dual-tropic and most can use either Lestr or CCR5 as coreceptors for virus entry. J. Virol. 70: 8355.


3. Nagasawa, T., T. Nakajima, K. Tachibana, et al. 1996. Molecular cloning and characterization of a murine pre-B-cell growth-stimulating factor/stromal cell-derived factor 1 receptor, a murine homolog of the human immunodeficiency virus 1 entry coreceptor fusin. Proc. Natl. Acad. Sci. USA 93: 14726.


4. Endres, M.J., P.R. Clapham, M. Marsh, et al. 1996. CD4-independent infection by HIV-2 is mediated by fusin/CXCR4. Cell 87: 745.
5. Feng, Y., C.C. Broder, P.E. Kennedy, et al. 1996. HIV-1 entry cofactor: functional cDNA cloning of a seven-transmembrane, G-protein-coupled receptor. Science 272:809.
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