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Literature DB >> 16613575

Towards the targeted therapy of melanoma.

Abstract

Novel anti-cancer treatments use knowledge about the underlying biology of the tumor to find suitable molecular targets. The recent years have seen great advances in understanding the biology of melanoma. In the current review we discuss the most promising molecular targets for melanoma and suggest possible strategies for overcoming resistance.

Entities: Disease

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Year: 2006 PMID： 16613575 DOI： 10.2174/138955706776361402

Source DB: PubMed Journal: Mini Rev Med Chem ISSN： 1389-5575 Impact factor: 3.862

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Cited

11 in total

1. Targeting sphingosine kinase-1 to inhibit melanoma.

Authors: SubbaRao V Madhunapantula; Jeremy Hengst; Raghavendra Gowda; Todd E Fox; Jong K Yun; Gavin P Robertson
Journal: Pigment Cell Melanoma Res Date: 2012-03 Impact factor: 4.693

2. Glutathione and Bcl-2 targeting facilitates elimination by chemoradiotherapy of human A375 melanoma xenografts overexpressing bcl-xl, bcl-2, and mcl-1.

Authors: Salvador Mena; María L Rodriguez; Angel Ortega; Sonia Priego; Elena Obrador; Miguel Asensi; Ignacio Petschen; Miguel Cerdá; Bob D Brown; José M Estrela
Journal: J Transl Med Date: 2012-01-10 Impact factor: 5.531

Towards the targeted therapy of melanoma.

1. Targeting sphingosine kinase-1 to inhibit melanoma.

2. Glutathione and Bcl-2 targeting facilitates elimination by chemoradiotherapy of human A375 melanoma xenografts overexpressing bcl-xl, bcl-2, and mcl-1.

3. Zinc oxide nanoparticles induce apoptosis and autophagy in human ovarian cancer cells.

4. Liposome encapsulation of doxorubicin and celecoxib in combination inhibits progression of human skin cancer cells.

Review 5. Impact of nanoparticles on neuron biology: current research trends.

Review 6. ZnO Nanoparticles: A Promising Anticancer Agent.

7. Extracts of Clove (Syzygium aromaticum) Potentiate FMSP-Nanoparticles Induced Cell Death in MCF-7 Cells.

8. Use of Nanotechnology to Develop Multi-Drug Inhibitors For Cancer Therapy.

9. Chitosan-based thermoreversible hydrogel as an in vitro tumor microenvironment for testing breast cancer therapies.

10. Registered Report: COT drives resistance to RAF inhibition through MAP kinase pathway reactivation.