Dissecting the Impact of Chemotherapy on the Human Hair Follicle
Keratinocytes
0301 basic medicine
Fibroblast Growth Factor 7
Gene Expression
Alopecia
Antineoplastic Agents
Apoptosis
DNA, Mitochondrial
Models, Biological
Culture Media, Serum-Free
3. Good health
Mice
03 medical and health sciences
Organ Culture Techniques
Animals
Humans
Biological Assay
Hair Diseases
Cyclophosphamide
Hair Follicle
Oxidation-Reduction
Cell Proliferation
Sequence Deletion
DOI:
10.2353/ajpath.2007.061164
Publication Date:
2007-09-07T00:48:14Z
AUTHORS (7)
ABSTRACT
Chemotherapy-induced alopecia represents one of the major unresolved problems of clinical oncology. The underlying molecular pathogenesis in humans is virtually unknown because of the lack of adequate research models. Therefore, we have explored whether microdissected, organ-cultured, human scalp hair follicles (HFs) in anagen VI can be exploited for dissecting and manipulating the impact of chemotherapy on human HFs. Here, we show that these organ-cultured HFs respond to a key cyclophosphamide metabolite, 4-hydroperoxycyclophosphamide (4-HC), in a manner that resembles chemotherapy-induced HF dystrophy as it occurs in vivo: namely, 4-HC induced melanin clumping and melanin incontinence, down-regulated keratinocyte proliferation, massively up-regulated apoptosis of hair matrix keratinocytes, prematurely induced catagen, and up-regulated p53. In addition, 4-HC induced DNA oxidation and the mitochondrial DNA common deletion. The organ culture system facilitated the identification of new molecular targets for chemotherapy-induced HF damage by microarray technology (eg, interleukin-8, fibroblast growth factor-18, and glypican 6). It was also used to explore candidate chemotherapy protectants, for which we used the cytoprotective cytokine keratinocyte growth factor as exemplary pilot agent. Thus, this novel system serves as a powerful yet pragmatic tool for dissecting and manipulating the impact of chemotherapy on the human HF.
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