Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai
Reexamination Certificate
1999-03-09
2004-01-27
Low, Christopher S. F. (Department: 1644)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Peptide containing doai
C514S009100, C514S011400, C514S012200, C514S013800, C514S014800, C514S015800, C514S016700, C514S017400, C530S300000, C530S326000, C530S328000, C530S329000, C530S330000
Reexamination Certificate
active
06683048
ABSTRACT:
TECHNICAL FIELD
The present invention relates generally to compounds and methods for use in stimulating &bgr;-catenin mediated gene expression and cellular differentiation. The invention is more specifically related to modulating agents capable of increasing the level of free &bgr;-catenin in a cell cytoplasm, and to therapeutic methods employing such agents.
BACKGROUND OF THE INVENTION
&bgr;-catenin is a cytoplasmic protein that is critical for classical cadherin-mediated intercellular adhesion. Inside the cell, a &bgr;-catenin/&agr;-catenin complex interacts with the second cytoplasmic domain (CP2) of the classical cadherins. In the absence of this &bgr;-catenin/&agr;-catenin complex, the classical cadherins cannot promote cell adhesion (see Wheelock et al.,
Current Topics in Membranes
43:169-185, 1996).
&bgr;-Catenin is composed of 13 domains, referred to as arm repeats (FIG.
3
). The arm repeat closest to the amino terminus of &bgr;-catenin (designated as the first arm repeat) is known to contain the &agr;-catenin binding site. The specific amino acids that are directly involved in mediating the interaction between &bgr;-catenin and &agr;-catenin have not previously been identified.
In addition to its role in cell adhesion, &bgr;-catenin also appears to be a key component of certain cellular signaling pathways, leading to activation of gene expression and a variety of developmental processes, such as differentiation. In particular, &bgr;-catenin functions in Wnt-mediated signaling, associating with LEF-1/TCF DNA binding proteins to form a transcription factor. The level of signal transduction appears to correlate with the level of free &bgr;-catenin in the cytoplasm of the cell (see Willert and Nusse,
Genetics and Development
8:95-102, 1998).
Wnt-mediated signaling is involved in a variety of developmental processes, including cellular differentiation. For example, skin cells expressing a stabilized form of &bgr;-catenin display increased hair growth (Gat et al.,
Cell
95:605-614, 1998; Ono et al.,
Cell
95:575-578, 1998). Thus, therapies based on increasing the level of free &bgr;-catenin in the cytoplasm have potential for stimulating Wnt-mediated signal transduction, resulting in differentiation and, in certain instances, enhanced hair growth. However, there are presently no available therapies for modulating Wnt-mediated signaling.
Accordingly, there is a need in the art for improved methods for inducing Wnt-mediated signal transduction and cellular differentiation. The present invention fulfills this need and further provides other related advantages.
SUMMARY OF THE INVENTION
The present invention provides methods for stimulating &bgr;-catenin mediated gene transcription and cellular differentiation. Within certain aspects, the present invention provides modulating agents capable of increasing the level of free &bgr;-catenin in a cell. In one such aspect, the modulating agent comprises an internalization moiety and one or more of: (a) the amino acid sequence KHAVV (SEQ ID NO: 1); (b) a peptide analogue or peptidomimetic of the amino acid sequence KHAVV (SEQ ID NO: 1); or (c) an antibody or antigen-binding fragment thereof that specifically binds to a peptide comprising the amino acid sequence KHAVV (SEQ ID NO: 1). Within certain embodiments, the modulating agent comprises the sequence KHAVV (SEQ ID NO:1) within a linear peptide or a cyclic peptide ring. Such modulating agents may, within certain embodiments, comprise a linear or cyclic peptide ranging from 3 to 16 amino acid residues in length. The internalization moiety may comprise, within certain embodiments, an internalization sequence covalently linked to the modulating agent, a liposome that encapsulates the modulating agent or an antibody or ligand that binds to a cell surface receptor.
Within further embodiments, any of the above modulating agents may be linked to a targeting agent and/or a drug.
Within other aspects, the present invention provides pharmaceutical compositions comprising a modulating agent as described above, in combination with a pharmaceutically acceptable carrier.
The present invention further provides, within other aspects, methods for increasing the level of &bgr;-catenin in a cell, comprising contacting a cell with a modulating agent as described above.
Within further related aspects, the present invention provides methods for stimulating the activation of &bgr;-catenin mediated gene transcription in a cell, comprising contacting a cell with a modulating agent as described above.
Within further related aspects, the present invention provides methods for stimulating differentiation of a cell, comprising contacting a cell with a modulating agent as described above. In certain embodiments, the cell is a skin cell, such as a keratinocyte.
In other aspects, methods are provided for stimulating hair growth or reducing hair loss on a mammal, comprising administering to a mammal a modulating agent as described above. Such administration may be topical, and the skin cells may be present on the scalp of the mammal.
The present invention further provides, within other aspects, methods for stimulating exfoliation of skin on a mammal, comprising administering to a mammal a modulating agent as described above.
REFERENCES:
patent: 5972884 (1999-10-01), Cohen et al.
patent: WO 98/42296 (1998-10-01), None
patent: WO 98/45319 (1998-10-01), None
Bullions et al., “The role of beta-catenin in cell adhesion, signal transduction, and cancer,”Current Opinion in Oncology 10(1): 81-87, 1998.
Gat et al., “De Novo Hair Follicle Morphogenesis and Hair Tumors in Mice Expressing a Truncated &bgr;-Catenin in Skin,”Cell 95: 605-614, 1998.
Nagahara et al., “Transduction of full-length TAT fusion proteins into mammalian cells: TAT-p27Kip1induces cell migration,”Nature Medicine 4(12): 1449-1452, 1998.
Oro and Scott, “Splitting Hairs: Dissecting Roles of Signaling Systems in Epidermal Development,”Cell 95: 575-578, 1998.
Willert and Roel Nusse, “&bgr;-catenin: a key mediator of Wnt signaling,”Current Opinions in Genetics&Development 8: 95-102, 1998.
Blaschuk Orest W.
Gour Barbara J.
Kam Chih-Min
Low Christopher S. F.
McGill University
Seed IP Law Group PLLC
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