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Method for enhancing epithelial cell proliferation and uses thereof

a technology of epithelial cells and epithelial cells, which is applied in the field can solve the problems of keratinocyte proliferation, keratinocyte proliferation, and keratinocyte proliferation, and achieve the effects of enhancing epithelial cell proliferation

Inactive Publication Date: 2007-01-11
GLIAMED
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0015] The present invention is further directed to a method for enhancing epithelial cell proliferation, by contacting epithelial tissue with an amount of an immunophilin ligand effective to enhance epithelial cell proliferation.
[0016] The present invention also provides a use of an immunophilin ligand to enhance epithelial cell proliferation, wherein epithelial tissue is contacted with an amount of the immunophilin ligand effective to enhance epithelial cell proliferation.

Problems solved by technology

Dysfunctions associated with one or more of these components can lead to anatomical changes of intact skin and / or alterations in the ability of wounded epithelium to regain its normal histology and function.
Such an alteration may result in either the accumulation of inhibitory molecules—which would then negatively affect keratinocyte growth—or a reduction in the delivery of one or more growth factors to the dermal / epidermal boundaries—which might also reduce keratinocyte proliferation.
However, while it is an attractive hypothesis, it lacks support in the literature.
While the dogma holds that decubital ulcers are the result of poor blood flow and blood pooling in the skin, this has never been demonstrated or tested rigorously.
Refractory skin lesions present a huge therapeutic challenge in patients with a range of underlying pathologies, including diabetic ulcers, venous stasis ulcers, pressure ulcers, burns, and trauma.
This approach, while offering some benefit, is limited, as epidermis will break down in the absence of repair of the underlying tissue.

Method used

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  • Method for enhancing epithelial cell proliferation and uses thereof
  • Method for enhancing epithelial cell proliferation and uses thereof
  • Method for enhancing epithelial cell proliferation and uses thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

GM-284 Promotes Wound Healing

[0078] In recent studies, the inventor demonstrated myelin and axonal hypertrophy following mechanical transection of the sciatic nerve. These studies required surgical exposure of the right lower quadrant of all study animals. Following exposure of the sciatic nerve from the sciatic notch to the knee, and manipulation of the nerve, the muscle and overlaying skin were closed with suture material. Each animal was subsequently treated with a daily gavage of either GM-284 (5 mg / kg), FK506 (5 mg / kg), or methylcellulose vehicle alone. During the post-operative course, it was noted by an investigator who was blinded to the treatment groups that the surgical wounds of one group of animals appeared to be qualitatively improved over those of the other two groups, with less erythemia and more rapid closure. Following unblinding of the investigator, it was learned that the group demonstrating improved healing had received treatment with GM-284.

[0079] To determine...

example 2

GM-284 Doubles the Keratinocyte Proliferative Index

[0082] As detailed above, keratinocyte proliferation is influenced by a number of factors, including innervation (Hsieh and Lin, Modulation of keratinocyte proliferation by skin innervation. J. Invest. Dermatol., 113:579-86, 1999) and growth-factor treatment (Castagnino et al., Neu differentiation factor / heregulin induction by hepatocyte and keratinocyte growth factors. Oncogene, 19:640-48, 2000; and reviewed by Werner and Smola, Paracrine regulation of keratinocyte proliferation and differentiation. Trends Cell Biol., 11:143-46, 2001). Thus, by culturing human-foreskin keratinocytes with increasing concentrations of GM-284, the inventor investigated the possibility that GM-284 was able to influence keratinocyte growth. As shown in FIG. 3, treatment with 1 gM of GM-284 increased the rate of keratinocyte proliferation by more than 150% after 14 days of treatment. Not surprisingly, a comparison of the growth rates of keratinocytes gr...

example 3

Topical Treatment with GM-284 Increases Epidermal Thickness In Vivo

[0083] The increased rate of wound closure in the presence of GM-284, taken with the accelerated keratinocyte proliferation, suggested to the inventor the possibility that GM-284 treatment might alter epidermal thickness in vivo. To examine this possibility, 5-mm, full-skin thickness biopsies were taken from the hindquarters of both male and female ICR retired breeders. The wounds were treated daily, for 8 days, with topical administration of either the DMSO-based vehicle, or FK506 or GM-284 in the vehicle. Thereafter, the original biopsy site was rebiopsied. Comparison of epidermal thickness of the FK506- and vehicle-treated animals showed no observable differences (cf. FIG. 4, panels a and b). In contrast, the epidermis of the GM-284-treated animals was much thicker, and appeared to be much more cellular, than the epidermis of animals under the other two conditions (FIG. 4, panel c). Without being bound by theory,...

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Abstract

The present invention is directed to uses of GM-284 for enhancing epithelial cell proliferation. The present invention is also provides methods for treating a keratinocyte-associated disorder in a subject in need of treatment.

Description

[0001] This application is a divisional of U.S. Ser. No. 10 / 290,657 which was filed on Nov. 8, 2002.BACKGROUND OF THE INVENTION [0002] Healing of wounds in skin and other epithelia involves a complex set of interactions between numerous components, including epithelial cells, peripheral nerves, and immune cells, as well as soluble and matrix molecules contributed by the various cell types (reviewed in Hom et al., Growth factor therapy to improve soft tissue healing. Facial Plast. Surg., 18:41-52, 2002). Dysfunctions associated with one or more of these components can lead to anatomical changes of intact skin and / or alterations in the ability of wounded epithelium to regain its normal histology and function. For example, sensory denervation of skin results in alterations in skin anatomy, including thinning of the epidermis, decreases in epidermal proliferation, and changes in the gene expression of Langerhans cells (Huang et al., Influence of cutaneous nerves on keratinocyte prolifer...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/4745A61K38/13
CPCA61K38/13
Inventor WEINSTEIN, DAVID
Owner GLIAMED
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