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Expert Opin Drug Discov. 2015 Mar;10(3):269-92. doi: 10.1517/17460441.2015.1009892. Epub 2015 Feb 9.

Drug discovery for alopecia: gone today, hair tomorrow.

Author information

1
Massachusetts General Hospital, Wellman Center for Photomedicine , Boston, MA 02114 , USA +1 617 726 6182 ; +1 617 726 6643 ; hamblin@helix.mgh.harvard.edu.

Abstract

INTRODUCTION:

Hair loss or alopecia affects the majority of the population at some time in their life, and increasingly, sufferers are demanding treatment. Three main types of alopecia (androgenic [AGA], areata [AA] and chemotherapy-induced [CIA]) are very different, and have their own laboratory models and separate drug-discovery efforts.

AREAS COVERED:

In this article, the authors review the biology of hair, hair follicle (HF) cycling, stem cells and signaling pathways. AGA, due to dihydrotesterone, is treated by 5-α reductase inhibitors, androgen receptor blockers and ATP-sensitive potassium channel-openers. AA, which involves attack by CD8(+)NK group 2D-positive (NKG2D(+)) T cells, is treated with immunosuppressives, biologics and JAK inhibitors. Meanwhile, CIA is treated by apoptosis inhibitors, cytokines and topical immunotherapy.

EXPERT OPINION:

The desire to treat alopecia with an easy topical preparation is expected to grow with time, particularly with an increasing aging population. The discovery of epidermal stem cells in the HF has given new life to the search for a cure for baldness. Drug discovery efforts are being increasingly centered on these stem cells, boosting the hair cycle and reversing miniaturization of HF. Better understanding of the molecular mechanisms underlying the immune attack in AA will yield new drugs. New discoveries in HF neogenesis and low-level light therapy will undoubtedly have a role to play.

KEYWORDS:

5-α-reductase inhibitor; alopecia areata; androgenic alopecia; anti-androgen; baldness; chemotherapy-induced alopecia; hair follicle; low-level laser (light) therapy; stem cells; topical immunotherapy

PMID:
25662177
PMCID:
PMC4339524
DOI:
10.1517/17460441.2015.1009892
[Indexed for MEDLINE]
Free PMC Article

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