AU2003257264B2 - Repair of DNA mutagenic damage - Google Patents

Description

WO 2004/022023 PCT/AU2003/001152 -1- REPAIR OF DNA MUTAGENIC DAMAGE The present invention relates to the use of equol, dehydroequol and isoflav-3-ene and isoflavan compounds in promoting repair ofDNA mutagenic damage.

Metallothioneins (MT) are proteins synthesised or over expressed in response to DNA damaging agents e.g. UVR (Hansen et al 1997). In most of the studies in animals and tissue cultures, high does of radiation were used to induce MT, and therefore, it is difficult to extrapolate these results to low level or repeated exposures to UVR in humans (Cai et al 1999). Induced synthesis of MT is considered as one of the mechanisms involved in the adaptive response to low dose UVR exposure, and increased levels of MT appear to be associated with protection from UVR, possibly mediated through scavenging of ROS in the skin (Hanada, et al 1992). As well, MT is implicated in protecting against the immunosuppressive effects of UVR on cell-mediated responses as demonstrated in MT=I and II knockout mice (Reeve, et al 2000). UVR induces immunohistochemically detectable MT in keratinocytes and dermal fibroblasts concurrently with the photoconduction of p53, which suggests the these protein systems are protective and complimentary in function. MT is detectable in dermal fibroblasts from 2 hours post-UV (Anstey, et al 1996).

Equol, dehydroequol, isofla-3-ene and isoflavan compounds and methods for producing the same are described in copending International Patent Application PCT/AU03/00427 and WO 98/08503 which are incorporated herein by reference.

UV exposed skin causes damage in DNA which may give rise to carcinogenesis. The most common tumour in humans is the basal cell carcinoma (BCC) followed by squamous cell carcinoma (SCC), and more rarely malignant melanoma.

It has now been found by the applicant that compounds of the present invention, when applied to the skin, result in elevation of metallothioneins production in the skin, particularly the basal layer of irradiated skin.

P\WPI)OCS'CRNNXlSp ll252300 I spa doc-20,08/207 -2- SAs mentioned above, metallothioneins affect and promote repair of DNA mutagenic damage of skin subject to UV exposure, and/or enhancing defence against UV-induced DNA mutagenic damage in skin.

Disclosed herein is the use of equol, dehydroequol, isoflav-3-ene or isoflavan structures for protecting skin from DNA mutagenic damage associated with UV exposure.

(N

SAlso disclosed herein is the use of equol, dehydroequol, isoflav-3-ene or isoflavan structures for the over expression of metallothioneins in the skin, particularly the basal layer of skin.

Further disclosed herein is a method for protecting skin from UV induced DNA mutagenic damage which comprises applying to skin a composition containing one or more of equol, dehydroequol, isoflav-3-ene, or isoflavan compounds in admixture with a dermally acceptable carrier.

Isoflav-3-ene and isoflavan compounds may be represented by the general formula (II)

R,

R2 X r R8 R (II) 4R R7 in which RI, R 2

R

3 and R 4 are independently hydrogen, hydroxy, OR), OC(O)Rlo, OS(O)Rio, CHO, C(O)Rio, COOH, C0 2 Rio, CONRIIRi 2 alkyl, haloalkyl, arylalkyl, alkenyl, alkynyl, aryl, heteroaryl, alkylaryl, alkoxyaryl, thio, alkylthio, amino, alkylamino, dialkylamino, nitro or halo, or WO 2004/022023 PCT/AU2003/001152 -3-

R

3 and R 4 are as previously defined, and RI and R 2 taken together with the carbon atoms to which they are attached form a five-membered ring selected from T 0 o 0 V-

R

1 and R 4 are as previously defined, and R 2 and R3 taken together with the carbon atoms to which they are attached form a five-membered ring selected from 0 0 TO>< or RI and R 2 are as previously defined, and R 3 and R 4 taken together with the carbon atoms to which they are attached form a five-membered ring selected from T 0 and wherein

R

6 and R7 are independently hydrogen, hydroxy, OR 9 OC(O)Rio, OS(O)Rio, CHO, C(O)Rio, COOH, C0 2 Rio, CONRIjR 12 alkyl, haloalkyl, arylalkyl, alkenyl, alkynyl, aryl, heteroaryl, thio, alkylthio, amino, alkylamino, dialkylanmino, nitro or halo, Rg is hydrogen, hydroxy, alkyl, aryl, amino, thio, NR 1

IR

1 2

CONRIIR

1 2, C(O)R 1 3 where R13 is hydrogen, alkyl, aryl, arylalkyl or an amino acid, or C0 2

R

1 4 where R14 is hydrogen, alkyl, haloalkyl, aryl or arylalkyl, P \WPI)OCS'CRNlNX-\Spec125230l sp~I dxo-2208/2007 0-4- R is alkyl, haloalkyl, aryl, arylalkyl, C(O)Ri3 where Ri 3 is as previously defined, or Si(Ris)3 where each R 1 5 is independently hydrogen, alkyl or aryl, Rl) is hydrogen, alkyl, haloalkyl, amino, aryl, arylalkyl, an amino acid, alkylamino or dialkylamino,

\O

C 5 Ril is hydrogen, alkyl, arylalkyl, alkenyl, aryl, an amino acid, C(O)RI 3 where Ri3 is as n) previously defined, or CO 2

R

1 4 where Ri 4 is as previously defined, c R 1 2 is hydrogen, alkyl or aryl, or SR1I and Ri2 taken together with the nitrogen to which they are attached comprise pyrrolidinyl or piperidinyl, the drawing represents either a single bond or a double bond, preferably a double bond, T is independently hydrogen, alkyl or aryl, and X is O, NR 1 2 or S, preferably O, including pharmaceutically acceptable salts and derivatives thereof.

Equol corresponds to the formula (II) wherein Ri, R 3

R

4

R

7 and Rs are hydrogen, R 2 and R 5 are hydroxy, X is 0, and is a single bond. Dehydroequol corresponds to formula (II) when R 1

R

3

R

4 R7 and R 8 are hydrogen, R2 and Rs are hydroxy, X is O and is a double bond.

In a first aspect, the present invention provides a method for promoting repair of UVinduced DNA mutagenic damage in skin and/or enhancing defence against UV-induced DNA mutagenic damage in skin which comprises administering topically to the skin a composition comprising one or more compounds of the formula (II) as defined above.

In a second aspect, the present invention provides use of one or more compounds of the formula (II) as defined above, including pharmaceutically acceptable salts and derivatives thereof in admixture with a dermatologically acceptable carrier for the manufacture of a topical composition for promoting repair of UV-induced DNA mutagenic damage in skin, and/or enhancing defence against UV-induced DNA mutagenic damage in skin.

P \WPX)C S'(R S M, 1I2 S2I p dm 2 0:082(X)7 -4a- In a third aspect, the present invention provides use of compounds of the formula (11) as defined above, for promoting repair of UV-induced DNA mutagenic damage in skin and/or enhancing defence against UV-induced DNA mutagenic damage in skin.

Dermally acceptable carriers and lotions are well known in the art, and are described for example in Remington's Pharmaceutical Sciences, Gennaro A. 18th Ed., Mack Publishing Co., Easton, PA, 1990, pp. 1492-1517. Any dermatologically acceptable carrier can be used in the compositions of the invention. As used herein, "dermatologically acceptable carrier" refers to vehicles, diluents, carriers, which can include adjuvants, additives, or excipients, known for use in dermatological compositions. The compositions of the invention include, but are not limited to, creams, ointments, solutions, sticks, wipes, cleansers and/or gels. The compounds of the present invention may be simply mixed, admixed or blended with suitable carriers to give compositions suitable for application to the skin. Dermally acceptable carriers may include one or more sunscreen agents.

Sunscreens include those materials commonly used to block ultraviolet light. Illustrative WO 2004/022023 PCT/AU2003/001152 compounds include the derivatives of cinnamate, PABA, and salicylate. For example, octyl methoxycinnamate and 2-hydroxy-4-methoxy benzophenone (also known as oxybenzone) can be used. Octyl methoxycinnamate and 2-hydroxy-4-methoxy benzophenone are commercially available under the trademarks, Parsol MCX and Benzophenone-3, respectively. The exact amount of sunscreen employed can vary depending upon the degree of protection desired from the sun's UV irradiation.

In a preferred embodiment one or more compounds of the formula (II) are formulated into cosmetic preparations. Examples of cosmetic formulations include creams, gels, powders, pastes, cakes and the like. Typically such cosmetics may be referred to as "make-up", and/or foundation (typically used to provide a smooth, even appearance to skin and as a base for coloured cosmetics).

Compounds of the formula (II) may be used in the compositions in an amount from 0.001% to 100%, preferably from 0.1% to 20%, most preferably from 0.1% to 10% w/w.

For example, compositions may comprise 1 pm to 500 mmol equol or other compounds of the formula such as 20 gm to 400 tm. The remainder of the composition will comprise one or more dermatologically acceptable carriers and excipients as are well known in the art. One or more compounds may be utilised in the compositions, with equol and dehydroequol being particularly preferred. Compositions may be administered topically to the skin before, during and/or after sun exposure. Typically, doses of between about 1 to 500 mg per day, with doses between 2 to 100 mg per day being preferred.

In accordance with another aspects of this invention there is provided a method for the treatment, or amelioration or preventing the formation of skin cancer, such as basal cell carcinoma (BCC), squamous cell carcinoma (SCC) and malignant melanoma, which comprises applying to the skin of a subject a composition containing one or more of equol, dehydroequol, or an isoflav-3-ene or isoflavan compounds of the general formula (II).

In another aspect of this invention there is provided a method for increasing metallothionein production in the skin, such as the basal layer of skin, which comprises WO 2004/022023 PCT/AU2003/001152 -6applying to skin one or more of equol, dehydroequol, isoflav-3-ene or isoflavan compound in association with a dermally acceptable carrier.

The applicant has further found that the compounds according to this invention promote DNA repair. The promotion of DNA repair may be by one or more of increasing the rate of repair of cyclobutane pyrimidine dimers (CPDs), promoting DNA repair by decreasing P53 expression, and/or by promoting the formation ofmetallothionein (MT).

The formation of CPD is considered to be an important lethal and mutagenic consequence of UVR exposure (Mitchell et al, 1989; Liardet et al, 2000). Animal models have demonstrated an inverse relationship between epidermal CPD repair and skin carcinogenesis (Young et al, 1996). The P53 protein (TP53) is expressed after DNA damage by UV irradiation. P53 is a transcription factor which blocks cellular progression from G1 to S phase, thus preventing replication of damaged DNA (Campbell et al, 1993).

The P53 protein may act as a tumour promoting agent (Murphey et al, 2001).

This invention will be described with reference to the following, non-limiting examples.

Example 1 The effect of equol on the induction of CPD was examined in the skin of hairless mice (a standard model for human dermatological investigations) exposed to solar simulated ultraviolet radiation (SSUV). At various time points after SSUV, dorsal skin was excised, fixed for 6hr in a standard fixing medium (HistoChoice

M

Amersco Inc, Solon, Ohio, USA), processed and paraffin-embedded. Pyrimidine dimers were detected immunohistochemically using citric acid antigen retrieval and the H3 anti-pyrimidine dimer antibody. The number ofdimer-positive cells was counted manually in 30 fields per mouse, at 40x magnification.

When equol lotion (containing 20 pM equol) was applied daily for 7 days prior to and following irradiation with 1 x 3MED of SSUV, the effect of equol was to reduce the initial WO 2004/022023 PCT/AU2003/001152 -7induction of dimers, and to enhance the rate of their repair, as evidenced by a reduced number of dimers at 24 hr (Table 1).

Table 1: Induction of epidermal CPD-positive cells following UV irradiation Time of collection Treatment CPD +ve cells/linear cm Normal skin 0 lhr post-SSUV Vehicle SSUV 300 18 equol SSUV 238 22 24r post-SSU Vehicle SSUV 340 equol24hr post-SSUV167 equol SSUV 167 17 Application of equol immediately after SSUV exposure (and continuing for 5d) resulted in significantly reduced dimers at 1 day post-irradiation (a significant reduction of and at 2d (a significant reduction of 42% -data not shown).

When equol lotion (20gM) was applied for both 7 days prior and 5 days after SSUV exposure, the reduction in CPD numbers was evident immediately and at 1, 24 and 48 hours after (p 0.05; 54%, 50% and 26% reduction in the number of CPD respectively) compared with the control group (vehicle alone).

Example 2 Equol was applied to the skin of five human volunteers immediately after, and at 4 hours and 6 hours post-UV irradiation. A control lotion was also used containing no equol.

Twenty-four hours after UV irradiation, skin biopsies were taken and MT production was measured using immunohistochemistry.

Table 2 shows the counts of cells in the basal epidermis and superficial dermis that demonstrated positive staining for MT. Approximately half of the cells in the basal epidermis constitutively expressed MT at baseline, whereas almost none of the cells in the WO 2004/022023 PCT/AU2003/001152 -8more superficial layers of the epidermis expressed MT. At 24 hrs after exposure to MED SSUV, there were apparent differences in the expression of MT in the basal layers of the epidermis between sections treated with equol and those treated with DMSO in base lotion (vehicle). In all 5 participants, the expression of MT was higher in the skin treated with equol, with the magnitude of the difference ranging from to +21%.

Table 2: Proportion of cells staining positively for MT in the epidermis of five human volunteers, by treatment group Total epidermis Upper epidermis Basal epidermis Subject treatment neg pos neg pos neg pos NOIDWH Baseline 303 201 40 99 0 0 204 201 mins 255 179 41 72 0 0 183 179 49 DMSO 282 185 40 70 0 0 212 185 47 equol 303 382 56 185 2 1 118 380 76 NO3PPA Baseline 227 109 32 97 0 0 130 109 46 mins 231 237 51 77 4 5 154 233 DMSO 317 236 43 96 4 4 221 232 51 equol 270 271 50 82 0 0 188 271 59 NO6MED Baseline 420 413 50 169 0 0 251 413 62 mins 437 565 56 168 1 1 269 564 68 DMSO 440 442 50 130 6 4 310 436 58 equol 315 539 63 76 8 10 239 531 69 N13PDO Baseline 267 217 45 112 0 0 155 217 58 mins 468 703 60 270 10 4 198 693 78 DMSO 465 405 47 144 0 0 321 405 56 equol 323 527 62 169 5 3 154 522 77 N14GBO Baseline 270 127 32 113 0 0 157 127 mins 381 242 39 247 0 0 134 242 64 DMSO 276 217 44 111 4 3 165 213 56 equol 225 234 '51 68 1 1 157 233 Note: "Baseline" refers to the skin sections from the punch biopsy taken prior to exposure to 2.5 MED SSUV.

mins" refers to the skin sections from the punch biopsy taken 10 mins after exposure to MED SSUV. The skin was not treated with either DMSO in base lotion (vehicle) or equol at 200 jtM.

"DMSO" refers to the skin sections from the punch biopsy taken 24 hrs after exposure to MED SSUV. The skin was from the grid treated with DMSO in base lotion (vehicle).

WO 2004/022023 PCT/AU2003/001152 -9- "Equol" refers to the skin sections from the punch biopsy taken 24 hrs after exposure to MED SSUV. The skin was from the grid treated with equol at 200 pM.

The increase of MT immunoreactivity in basal and suprabasal keratinocytes of recently UV-exposed individuals was highest in skin that had been treated with equol.

Example 3 The skin biopsies from the five human volunteers from Example 2 were tested for cyclobutane pyrimidine dimer formation using immunohistochemistry.

Table 3 presents the counts and percentages of cells staining positively with an antibody directed against CPD. These data demonstrate that, as expected, there were essentially no CPD-positive cells in the epidermis prior to irradiation with 2.5 MED. However, skin sections taken from all of the participants 10 mins after UV exposure showed high levels of DNA damage, with the proportion of positively-staining cells ranging from 36% (participants N01DWH and N03PPA) to 87% (participant N14GBO).

Skin sections taken 24 hrs after UV exposure showed substantially lower levels of CPD damage in all subjects. For 4 out of 5 participants, the skin sections treated with equol lotion had proportionally less CPD-positive cells than the skin sections treated with DMSO in base lotion (vehicle).

WO 2004/022023 PCT/AU2003/001152 Table 3: Proportion of cells staining positively for CPDs in the epidermis of five human volunteers, by treatment group Total epidermis Upper epidermis Basal epidermis Subject treatment neg pos neg pos neg pos NO1DWH Baseline 345 0 0 134 0 0 211 0 0 mins 162 107 40 64 51 44 98 56 36 DMSO 231 105 31 81 47 37 150 58 28 equol 164 39 19 70 23 25 94 16 NO3PPA Baseline 309 0 0 104 0 0 205 0 0 mins 204 191 48 56 106 65 148 85 36 DMSO 179 25 12 55 20 27 124 5 4 equol 349 18 5 70 17 20 279 1 0 NO6MED Baseline 309 0 0 90 0 0 219 0 0 mins 136 364 73 19 198 91 117 166 59 DMSO 339 65 16 112 59 35 227 6 3 equol 279 92 25 98 71 42 181 21 N13PDO Baseline 205 0 0 60 0 0 145 0 0 mins 69 195 74 20 94 82 49 101 67 DMSO 105 68 39 78 51 40 27 17 39 equol 213 94 31 79 50 39 134 44 N14GBO Baseline 255 0 0 98 0 0 157 0 0 mins 34 389 92 0 157 100 34 232 87 DMSO 240 131 35 93 69 43 147 62 equol 188 85 31 63 44 41 125 41 Note: "Baseline" refers to the skin sections from the punch biopsy taken prior to exposure to 2.5 MED SSUV. "10 mins" refers to the skin sections from the punch biopsy taken mins after exposure to 2.5 MED SSUV. The skin was not treated with either DMSO in base lotion (vehicle) or equol at 200 pM.

"DMSO" refers to the skin sections from the punch biopsy taken 24 hrs after exposure to MED SSUV. The skin was from the grid treated with DMSO in base lotion (vehicle).

"Equol" refers to the skin sections from the punch biopsy taken 24 hrs after exposure to MED SSUV. The skin was from the grid treated with lotion containing equol at 200 gM.

When data from all participants were pooled, it can be seen that skin sections treated with equol had moderately lower levels of CPD damage at 24 hours.

WO 2004/022023 PCT/AU2003/001152 -11 Example 4 The skin biopsies from the five human volunteers from Example 2 were tested for P53 staining following UV irradiation. Results are shown in Table 4.

Table 4: Proportion of cells staining positively for p53 in the epidermis of five human volunteers, by treatment group Total epidermis Upper epidermis Basal epidermis Subject treatment neg pos neg pos neg pos NO1DWH Baseline 261 0 0 115 0 0 146 0 0 lOmins 343 1 0 154 1 1 189 0 0 DMSO 187 12 6 79 4 5 108 8 7 equol 270 94 26 109 48 31 161 46 22 NO3PPA Baseline 274 2 1 112 1 1 162 1 1 minls 316 2 1 114 2 2 202 0 0 DMSO 223 55 20 81 31 28 142 24 14 equol 337 87 21 165 72 30 172 15 8 N06MED Baseline 412 1 0 134 0 0 278 1 0 mills 402 3 1 153 1 1 249 2 1 DMSO 462 133 22 165 77 32 297 56 16 equol 500 50 9 250 19 7 250 31 11 N13PDO Baseline 325 0 0 141 0 0 184 0 0 lOmins 304 0 0 140 0 0 164 0 0 DMSO 222 45 17 109 8 7 113 37 equol 287 13 4 147 4 3 140 9 6 N14GBO Baseline 321 0 0 149 0 0 172 0 0 lOmins 292 4 1 185 2 1 107 2 2 DMSO 217 190 47 106 106 50 111 84 43 equol 227 76 25 109 35 24 118 41 26 Note: "Baseline" refers to the skin sections from the punch biopsy taken prior to exposure to 2.5 MED SSUV.

"10 mins" refers to the skin sections fromn the punch biopsy taken 10 mins after exposure to MED SSUV. The skin was not treated with either DMSO in base lotion (vehicle) or equol at 200 ,IM.

"DMSO" refers to the skin sections from the punch biopsy taken 24 hrs after exposure to MED SSUV. The skin was from the grid treated with DMSO in base lotion (vehicle).

WO 2004/022023 PCT/AU2003/001152 -12- "Equol" refers to the skin sections from the punch biopsy taken 24 hrs after exposure to MED SSUV. The skin was from the grid treated with equol at 200 M.

As expected, there were essentially no cells in the epidermis expressing p53 prior to irradiation with 2.5 MED for any of the participants. Similarly, skin sections taken from participants 10 mins after UV exposure showed negligible levels of p53 expression, in accordance with the literature.

Skin sections taken 24 hrs after UV exposure showed substantially higher levels of p53 expression in all subjects. The percentage of p53 expression in upper and/or basal epidermis was reduced in four out of five equol treated subjects. For example, in subjects N13PDO and N14GBO the percentage of p53 staining was reduced significantly (generally more than 50%) compared with vehicle controls.

Conclusions The biomarkers assessed in these experiments were selected based on their biological associations with skin cancer (which is directly associated with UV-induced DNA mutagenic damage).

UV-induced oxidative damage is now recognised as a potentially important causal factor in skin cancer. MTs are molecules with anti-oxidant properties that are specifically induced in response to UV exposure. This study found consistent evidence that human skin treated with equol, and it is believed other compounds of the formula induce more MT than skin treated with base lotion.

CPDs are the earliest indicator of molecular damage following exposure to UV radiation, and if not repaired, lead to fixed mutations in the DNA of skin cells. Thus one mechanism of action of a post-exposure treatment would be to increase the rate of repair of these lesions. The experiments conducted here suggest that CPD repair may be enhanced by topical equol compositions, and other compositions containing one or more compounds of the formula (II).

WO 2004/022023 PCT/AU2003/001152 -13- P53 is clearly an important regulatory gene that is commonly mutated in epidermal skin cancers. Moreover, in normal skin cells, p53 is up-regulated following UV exposure to prevent mitosis until DNA damage is repaired. Equol modulated the expression of p53 in this study causing a reduction in the number of cells in the upper or basal epidermis expressing p53 for four of five subjects.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The reference to any prior art in this specification is not, and should not be taken as an acknowledgment or any form of suggestion that that prior art forms part of the common general knowledge in Australia.

WO 2004/022023 PCT/AU2003/001152 -14-

REFERENCES

Anstey, R. Marks, C. Long, H. Navabi. A. Pearse, D. Wynford-Thomas and B. e.

Jasani (1996). "In vivo photoinduction of metallothionein in human skin by ultraviolet irradiation." Journal ofPathology 178(1): 84-8.

Berne, J. Ponten and F. Ponten (1998). "Decreased p53 expression in chronically sunexposed human skin after topical photoprotection." Photodermatology, Photoimmnunology Photomedicine 14(5-6): 148-53.

Cai, Satoh, C. Tohyama and M. G. Cherian (1999). "Metallothionein in radiation exposure: its induction and protective role." Toxicology 132(2-3): 85-98.

Campbell, A. G. Quinn, B. Angus, P. M. Farr and J. L. Rees (1993). "Wavelength specific patterns of p53 induction in human skin following exposure to UV radiation." Cancer Research 53(12): 2697-9.

Hanada, T. Baba, I. Hashimoto, R. Fukui and S. Watanabe (1992). "Possible role of cutaneous metallothioncin in protection against photo-oxidative stress--epidermal localization and scavenging activity for superoxide and hydroxyl radicals." Photodermatology, Photoimmunology Photomedicine 209-13.

Hansen, E. Ablett, A. Green, R. A. Stunn, I. S. Dunn, D. P. Fairlie, M. L. West and P.

G. Parsons (1997). "Biphasic response of the metallothionein promoter to ultraviolet radiation in human melanoma cells." Photochemistry Photobiology 65(3): 550-5.

Liardet, C. Scaletta, R. Panizzon. P. Hohlfeld and L. Laurent-Applegate (2001).

"Protection against pyrimidine dimers, p53, and 8-hydroxy-2'-deoxyguaosine expression in ultraviolet-irradiated human skin by sunscreens: Difference between UVB UVA and UVA alone sunscreens." Journal of Investigative Dermatology 117:1437-1441.

WO 2004/022023 PCT/AU2003/001152 Mitchell, D. L. and R. S. Nair (1989). "The biology of the photoproduct." Photochemistry Photobiology 49(6): 805-19.

Murphy, A. R. Young, H. C. Wulf, D. Kulms and T. Schwarz (2001). "The molecular determinants of sunburn cell formation." ExperimentalDermatology 10(3): 155-60.

Ponten, B. Berne, Z. P. Ren, M. Nister and J. Ponten (1995). "Ultraviolet light induces expression of p53 and p21 in human skin: effect of sunscreen and constitutive p21 expression in skin appendages." Journal ofInvestigative Dermatology 105(3): 402- 6.

Reeve, V. N. Nishimura, M. Bosnic. A. E. Michalska and K. H. Choo (2000). "Lack of metallothionein-I and -II exacerbates the immunosuppressive effect of ultraviolet B radiation and cis-urocanic acid in mice." Immunology 100(3): 399-404.

Rich, R. L. Allen and A. H. Wyllie (2000). "Defying death after DNA damage." Nature 407(6805): 777-83.

Seite, D. Moyal, M. P. Verdier, C. Hourseau and A. Fourtanier (2000). "Accumulated p53 protein and UVA protection level of sunscreens." Photodermatology, Photoimmunology Photomedicine 16(1): 3-9.

Vainio, H. and F. Bianchini, Eds. (2001). Sunscreens. IARC Handbooks of Cancer Prevention. Lyon, International Agency for Research on Cancer.

Young, A. C. A. Chadwick, G. I. Harrison, J. L. Hawk, O. Nikaido and C. S. Potten (1996). "The in situ repair kinetics of epidermal thymine dimers and 6-4 photoproducts in human skin types land II." Journal of Investigative Dermatology 106(6): 1307-13.

Claims (21)

1. A method for promoting repair of UV-induced DNA mutagenic damage in skin and/or enhancing defence against UV-induced DNA mutagenic damage in skin which comprises administering topically to the skin a composition comprising one or more compounds of the general formula (II): RR R2\ Xf\ x R Rg (II) R4 R4 R R7 in which RI,R 2 R 3 and R 4 are independently hydrogen, hydroxy, OR 9 OC(O)Rlo, OS(O)R 1 o, CHO, C(O)Rio, COOH, C0 2 Rio, CONRIIRi 2 alkyl, haloalkyl, arylalkyl, alkenyl, alkynyl, aryl, heteroaryl, alkylaryl, alkoxyaryl, thio, alkylthio, amino, alkylamino, dialkylamino, nitro or halo, or R 3 and R 4 are as previously defined, and R, and R 2 taken together with the carbon atoms to which they are attached form a five-membered ring selected from T 0 0 0 v WO 2004/022023 PCT/AU2003/001152 -17- RI and R 2 are as previously defined, and R 3 and R4 taken together with the carbon atoms to which they are attached form a five-membered ring selected from T O O T 0 and wherein Rs, Re and R7 are independently hydrogen, hydroxy, OR9, OC(O)Rio, OS(O)Rio, CHO, C(O)Rio, COOH, CO 2 Rio, CONRIIR 1 2 alkyl, haloalkyl, arylalkyl, alkenyl, alkynyl, aryl, heteroaryl, thio, alkylthio, amino, alkylamino, dialkylamino, nitro or halo, Rs is hydrogen, hydroxy, alkyl, aryl, amino, thio, NRIR12, CONRIR12, C(O)Ri3 where R13 is hydrogen, alkyl, aryl, arylalkyl or an amino acid, or C0 2 R 14 where R14 is hydrogen, alkyl, haloalkyl, aryl or arylalkyl, R 9 is alkyl, haloalkyl, aryl, arylalkyl, C(O)Ri 3 where R13 is as previously defined, or Si(R 1 5 3 where each Ris is independently hydrogen, alkyl or aryl, RIO is hydrogen, alkyl, haloalkyl, amino, aryl, arylalkyl, an amino acid, alkylamino or dialkylamino, Rn is hydrogen, alkyl, arylalkyl, alkenyl, aryl, an amino acid, C(O)R 13 where R13 is as previously defined, or CO 2 R 4 where R14 is as previously defined, R12 is hydrogen, alkyl or aryl, or R11 and R12 taken together with the nitrogen to which they are attached comprise pyrrolidinyl or piperidinyl, the drawing represents either a single bond or a double bond, preferably a double bond, T is independently hydrogen, alkyl or aryl, and X is O, NR 12 or S, preferably O, P \WP\l)OC\K RN'NXISpc\I523lI sp.ec dX:22/S20821)7 -18- including pharmaceutically acceptable salts and derivatives thereof in admixture with a dermatologically acceptable carrier.

2. A method according to claim 1 wherein said one or more compounds of the fonnula (II) comprise equol and dehydroequol.

3. A method according to claim 1 which is a method for preventing the formation of skin cancer.

4. A method according to claim 3 wherein skin cancer is selected from basal cell carcinoma, squamous cell carcinoma and malignant melanoma.

A method according to claim 1 wherein skin is protected from UV-induced mutagenic damage by one or more of increasing the rate of repair of cyclobutane pyrimidine dimers, promoting the formation of metallothionein, and decreasing p53 expression.

6. A method according to any one of. claims 1 to 5 wherein the composition is administered before, during and/or after UV exposure.

7. A method according to claim 6 wherein the composition is administered before UV exposure.

8. A method according to claim 6 wherein the composition is administered before and after UV exposure.

9. A method according to any one of claims 1 to 8 wherein the composition comprises m to 500 mmol of compounds of the formula (11).

10. Use of one or more compounds of the formula (II) WO 2004/022023 PCT/AU2003/001152 -19- R2\ X R 8 R (II) R3 R4 R R7 in which RI,R 2 R 3 and R 4 are independently hydrogen, hydroxy, OR 9 OC(O)Rlo, OS(O)Rio, CHO, C(O)Rio, COOH, C0 2 R 10 CONRn 1 R12, alkyl, haloalkyl, arylalkyl, alkenyl, alkynyl, aryl, heteroaryl, alkylaryl, alkoxyaryl, thio, alkylthio, amino, alkylamino, dialkylamino, nitro or halo, or R 3 and R 4 are as previously defined, and R 1 and R 2 taken together with the carbon atoms to which they are attached form a five-membered ring selected from T 0 O o RI and R 4 are as previously defined, and R 2 and R 3 taken together with the carbon atoms to which they are attached form a five-membered ring selected from TO 0 RI and R 2 are as previously defined, and R 3 and R 4 taken together with the carbon atoms to which they are attached form a five-membered ring selected from PCT/AU03/01152 Received 16 July 2004 P:\WPDOCS\CRN\SET\Spec\78268493.nw pages.doc-15/07/04 0 o T O and wherein R 5 R 6 and R 7 are independently hydrogen, hydroxy, OR 9 OC(O)Ro, OS(O)Rio, CHO, C(O)Rio, COOH, CO 2 Ro 1 CONRi1R 1 2 alkyl, haloalkyl, arylalkyl, alkenyl, alkynyl, aryl, heteroaryl, thio, alkylthio, amino, alkylamino, dialkylamino, nitro or halo, Rs is hydrogen, hydroxy, alkyl, aryl, amino, thio, NR 11 R 12 CONRIR 1 2 C(O)R 1 3 where R 13 is hydrogen, alkyl, aryl, arylalkyl or an amino acid, or C0 2 R 14 where R 14 is hydrogen, alkyl, haloalkyl, aryl or arylalkyl, R 9 is alkyl, haloalkyl, aryl, arylalkyl, C(O)R 1 3 where R 13 is as previously defined, or Si(R 15 3 where each R 1 5 is independently hydrogen, alkyl or aryl, R 10 is hydrogen, alkyl, haloalkyl, amino, aryl, arylalkyl, an amino acid, alkylamino or dialkylamino, R 11 is hydrogen, alkyl, arylalkyl, alkenyl, aryl, an amino acid, C(O)R 13 where R 1 3 is as previously defined, or C0 2 R 14 where R 14 is as previously defined, R 12 is hydrogen, alkyl or aryl, or R 11 and R 1 2 taken together with the nitrogen to which they are attached comprise pyrrolidinyl or piperidinyl, the drawing represents either a single bond or a double bond, preferably a double bond, T is independently hydrogen, alkyl or aryl, and X is O, NR 12 or S, preferably O, including pharmaceutically acceptable salts and derivatives thereof in admixture with a dermatologically acceptable carrier for the manufacture of a topical composition for promoting repair of UV-induced DNA mutagenic damage in skin, and/or enhancing defence against UV induced DNA mutagenic damage in skin. Ai"-I7DSDB ez P IWPl)OCS'CRN'NXL'Spc\I2523l I spc doc-22,Ogi'20)7 -21-

11. Use according to claim 10 wherein said one or more compounds of the formula (II) comprise equol and dehydroequol.

12. Use according to claim 10 which is a method for preventing the fonnation of skin cancer.

13. Use according to claim 12 wherein skin cancer is selected from basal cell carcinoma, squamous cell carcinoma and malignant melanoma.

14. Use according to claim 10 wherein skin is protected from DNA mutagenic damage by one or more of increasing the rate of repair of cyclobutane pyrimidine dimers, promoting the formation of metallothionein, and decreasing p53 expression.

Use according to any one of claims 10 to 14 wherein the composition is administered before, during and/or after UV exposure.

16. Use according to claim 15 wherein the composition is administered before UV exposure.

17. Use according to claim 15 wherein the composition is administered before and after UV exposure.

18. Use according to any one of claims 10 to 17 wherein the composition comprises upm to 500 mmol of compounds of the formula (II).

19. Use of compounds of the formula (II) for promoting repair of UV-induced DNA mutagenic damage in skin and/or enhancing defence against UV induced DNA mutagenic damage in skin.

20. A method according to any one of claims 1 to 9 where the composition comprises a cosmetic or sunscreen composition. 11 A% PWCSICRN\NXLSp\223I W g- d. 22,082007 -22-

21. A use according to any one of claims 10 to 19 wherein the composition comprises a cosmetic or sunscreen comnposition.