Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives
Reexamination Certificate
2009-04-01
2011-10-25
Vivlemore, Tracy (Department: 1635)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carbohydrates or derivatives
C514S04400A
Reexamination Certificate
active
08044193
ABSTRACT:
Objective methods for detecting and diagnosing breast cancer (BRC) are described herein. In one embodiment, the diagnostic method involves determining the expression level of a BRC-associated gene that discriminates between BRC cells and normal cells. In another embodiment, the diagnostic method involves determining the expression level of a BRC-associated gene that discriminates among BRC cells, between DCIS and IDC cells. The present invention further provides means for predicting and preventing breast cancer metastasis using BRC-associated genes having unique altered expression patterns in breast cancer cells with lymph-node metastasis. Finally, the present invention provides methods of screening for therapeutic agents useful in the treatment of breast cancer, methods of treating breast cancer and method for vaccinating a subject against breast cancer.
REFERENCES:
patent: 6365358 (2002-04-01), Hillman et al.
patent: 2003/0104418 (2003-06-01), Zhang et al.
patent: 2003/0157544 (2003-08-01), Gish et al.
patent: 2004/0005563 (2004-01-01), Mack et al.
patent: 2005/0064402 (2005-03-01), Goldsworthy et al.
patent: WO 02/04514 (2002-01-01), None
patent: WO 02/29104 (2002-04-01), None
patent: WO 2004/031410 (2004-04-01), None
patent: WO 2006/085684 (2006-08-01), None
patent: WO 2008/018642 (2008-02-01), None
Pages 1-35 and 182 of WO 2004094636 A1 (38 pages total).
U.S. Appl. No. 12/377,024, which is a U.S. Nat'l Phase of PCT/JP2007/065992, filed Aug. 10, 2007, 221 pgs.
U.S. Appl. No. 12/673,432, which is a U.S. Nat'l Phase of PCT/JP2008/064437, filed Aug. 12, 2008, 83 pgs.
U.S. Appl. No. 12/673,434, which is a US National Stage (371) of PCT/JP2008/060837, 102 pgs.
Abe, Y., et al., “Cloning and expression of a novel MAPKK-like protein kinase, lymphokine-activated killer T-cell originated protein kinase, specifically expressed in the testis and activated lymphoid cells,”The Journal of Biological Chemistry, 275(28):21525-21531 (Jul. 14, 2000).
Adam, Paul J. et al.; “ArylamineN-acetyltransferase-1 is highly expressed in breast cancers and conveys enhanced growth and resistance to etoposide in vitro”;Molecular Cancer Research1:826-835 (Sep. 2003).
Database EBI Accession No. AAM56211; “Sequence 1 from patent US 6365358” Jun. 20, 2002.
Database; EBI Accession No. AX369194; “Sequence from patent WO0204514”; Feb. 15, 2002.
Dermer, 1994, Bio/technology, 12: 320.
Dressman, Marlene A. et al.; “Gene expression in profiling detects gene amplification and differentiates tumor types in breast cancer”;Cancer Research63:2194-2199 (May 1, 2003).
Freshney (Culture of Animal Cells, A Manual of Basic Technique, Alan R. Liss, Inc. 1983, New York, p. 4).
Gaudet, S., et al., “Characterization of PDZ-binding kinase, a mitotic kinase,”Proc. Natl. Acad. Sci. USA, 97(10): 5167-5172 (May 9, 2000).
Geylan, Y.S. et al.; “Arylamine N-acetyltransferase activities in human breast cancer tissues”;Neoplasma48(2):108-111 (2001).
Gura, “Cancer Models: Systems for Identifying New Drugs Are Often Faulty,” 1997, Science, 278: pp. 1041-1042.
Lipkowitz, Stan; “The role of ubiquitination-proteasome pathway in breast cancer: Ubiquitin mediated degradation of growth factor receptors in the pathogenesis and treatment of cancer”;Breast Cancer Research5(1):8-15 (2003).
Matsumoto et al., Biochemical and Biophysical Research Communications, Dec. 2004, 32:997-1004.
Orlowski, Robert Z. and E. Claire Dees; “The role of ubiquitination-proteasome pathway in breast cancer: Applying drugs that affect the ubiquitin-proteasome pathway to the therapy of breast cancer”;Breast Cancer Research5(1):1-7 (2003).
Perou, Charles M. et al.; “Molecular portraits of human breast tumors”;Nature406:747-752 (Aug. 17, 2000).
Sgroi, Dennis C. et al.; “In vivo gene expression profile analysis of human breast cancer progression”;Cancer Research59:5656-5661 (Nov. 15, 1999).
Zhao, S., et al., “PDZ-binding kinase participates in spermatogenesis,”Int. J. of Biochem.&Cell Biol., 33(6): 631-636 (Jun. 2001).
Keydar, I., et al., “Establishment of Characterization of a Cell Line of Human Breast Carcinoma Origin,”Eur. J. Cancer, vol. 15(5), pp. 659-670 (May 1979).
Park, J-H., et al., “PDZ-Binding Kinase/T-LAK Cell-Originated Protein Kinase, a Putative Cancer/Testis Antigen with an Oncogenic Activity in Breast Cancer,”Cancer Res., vol. 66(18), pp. 9186-8195 (Sep. 15, 2006).
Park, J-H., et al., “PBK/TOPK (PDZ-binding kinase/T-LAK cell-originated protein kinase) as a novel molecular target for breast cancer therapy,”Proceedings of the 66thAnnual Meeting of the Japanese Cancer Association, p. 78, Abstract No. EW17-4 (Aug, 25, 2007).
Watanabe, T., et al., “Identification and characterization of a novel geneCXADRL1whose expression is frequently up-regulated in differentiated-type of gastric cancer,”Proceedings of the 61stAnnual Meeting of the Japanese Cancer Association, p. 77, Abstract No. 2027 (Aug. 25, 2002).
Katagiri Toyomasa
Nakamura Yusuke
Nakatsuru Shuichi
Kilpatrick Townsend & Stockton LLP
Oncotherapy Science, Inc.
Vivlemore Tracy
LandOfFree
Short interfering RNAs targeted to T-LAK cell-originated... does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Short interfering RNAs targeted to T-LAK cell-originated..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Short interfering RNAs targeted to T-LAK cell-originated... will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-4276119