Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Aug 6;19(8):11679-721.
doi: 10.3390/molecules190811679.

Review of natural compounds for potential skin cancer treatment

Affiliations
Review

Review of natural compounds for potential skin cancer treatment

Tawona N Chinembiri et al. Molecules. .

Abstract

Most anti-cancer drugs are derived from natural resources such as marine, microbial and botanical sources. Cutaneous malignant melanoma is the most aggressive form of skin cancer, with a high mortality rate. Various treatments for malignant melanoma are available, but due to the development of multi-drug resistance, current or emerging chemotherapies have a relatively low success rates. This emphasizes the importance of discovering new compounds that are both safe and effective against melanoma. In vitro testing of melanoma cell lines and murine melanoma models offers the opportunity for identifying mechanisms of action of plant derived compounds and extracts. Common anti-melanoma effects of natural compounds include potentiating apoptosis, inhibiting cell proliferation and inhibiting metastasis. There are different mechanisms and pathways responsible for anti-melanoma actions of medicinal compounds such as promotion of caspase activity, inhibition of angiogenesis and inhibition of the effects of tumor promoting proteins such as PI3-K, Bcl-2, STAT3 and MMPs. This review thus aims at providing an overview of anti-cancer compounds, derived from natural sources, that are currently used in cancer chemotherapies, or that have been reported to show anti-melanoma, or anti-skin cancer activities. Phytochemicals that are discussed in this review include flavonoids, carotenoids, terpenoids, vitamins, sulforaphane, some polyphenols and crude plant extracts.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
A scheme showing the anti-melanoma actions of the compounds and extracts discussed in this review.
Figure 2
Figure 2
Chemical structures of selected flavonoids possessing anti-cancer potential: (a) quercetin, (b) kaempferol, (c) EGCG, (d) apigenin and (e) daidzein.
Figure 3
Figure 3
Chemical structures of selected carotenoids: (a) β-carotene, (b) retinol, (c) lycopene and (d) fucoxanthin.
Figure 4
Figure 4
Chemical structures of (a) vitamin A, (b) vitamin C, (c) vitamin D3 and (d) vitamin E (α-tocopherol).
Figure 5
Figure 5
Chemical structure of resveratrol.
Figure 6
Figure 6
Chemical structure of curcumin.
Figure 7
Figure 7
Chemical structure of sulforaphane.

References

    1. Kachuri L., De P., Ellison L.F., Semenciw R., Advisory Committee on Canadian Cancer Statistics Cancer incidence, mortality and survival trends in Canada, 1970–2007. Chronic Dis. Inj. Can. 2013;33:69–80. - PubMed
    1. Erb P., Ji J., Wernli M., Kump E., Glaser A., Büchner S.A. Role of apoptosis in basal cell and squamous cell carcinoma formation. Immunol. Lett. 2005;100:68–72. doi: 10.1016/j.imlet.2005.06.008. - DOI - PubMed
    1. Lippens S., Hoste E., Vandenabeele P., Declercq W. Cell death in skin. In: Reed J.C., Green D.R., editors. Apoptosis: Physiology and Pathology. Cambridge University Press; Cambridge, UK: 2011. pp. 323–332.
    1. Marks V.J., Hanson N.W. Non-melanoma skin cancer. In: Hall B.J., Hall J.C., editors. Sauer’s Manual of Skin Diseases. Volume 10. Wolters Kluwer Health; Philadelphia, PA, USA: 2010. pp. 305–312.
    1. Freedman M.L., Nierodzik M.L.R. Cancer and age. In: Birren J.E., editor. Encyclopedia of Gerontology. 2nd ed. Volume 1. Elsevier; New York, NY, USA: 2007. pp. 191–212.

Publication types

MeSH terms