Biomolecules & Therapeutics 2021; 29(5): 545-550
ER71/ETV2 Promotes Hair Regeneration from Chemotherapeutic Drug-Induced Hair Loss by Enhancing Angiogenesis
Tae-Jin Lee1,2,†, Hee-Kyoung Kang3,4,†,*, Jeffrey C. Berry5, Hong-Gu Joo6, Changwon Park7, Mark J. Miller5 and Kyunghee Choi1,*
1Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA
2Department of Bio-Health Convergence, Kangwon National University, Chuncheon 24341, Republic of Korea
3Department of Pharmacology, School of Medicine, Jeju National University, Jeju 63243, Republic of Korea
4Jeju Research Center for Natural Medicine, Jeju National University, Jeju 63243, Republic of Korea
5Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA
6College of Veterinary Medicine, Jeju National University, Jeju 63243, Republic of Korea
7Department of Molecular and Cellular Physiology, Louisiana State University Health Science Center, Shreveport, LA 71103, USA
*E-mail: (Kang HK), (Choi K)
Tel: +82-64-754-3846 (Kang HK), +1-314-362-8716 (Choi K)
Fax: +82-64-702-2687 (Kang HK), +1-314-362-8888 (Choi K)
The first two authors contributed equally to this work.
Received: January 27, 2021; Revised: February 19, 2021; Accepted: March 15, 2021; Published online: April 5, 2021.
© The Korean Society of Applied Pharmacology. All rights reserved.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Chemotherapy-induced alopecia and hair loss can be stressful in patients with cancer. The hair grows back, but sometimes the hair tends to stay thin. Therefore, understanding mechanisms regulating hair regeneration may improve the management of chemotherapy-induced alopecia. Previous studies have revealed that chemotherapeutic agents induce a hair follicle vascular injury. As hair growth is associated with micro-vessel regeneration, we postulated that the stimulation of angiogenesis might enhance hair regeneration. In particular, mice treated with 5-fluorouracil (5-FU) showed delayed anagen initiation and reduced capillary density when compared with untreated controls, suggesting that the retardation of anagen initiation by 5-FU treatment may be attributed to the loss of perifollicular micro-vessels. We investigated whether the ETS transcription factor ETV2 (aka ER71), critical for vascular development and regeneration, can promote angiogenesis and hair regrowth in a 5-FU-induced alopecia mouse model. Tie2-Cre; Etv2 conditional knockout (CKO) mice, which lack Etv2 in endothelial cells, presented similar hair regrowth rates as the control mice after depilation. Following 5-FU treatment, Tie2-Cre; Etv2 CKO mice revealed a significant reduction in capillary density, anagen induction, and hair restoration when compared with controls. Mice receiving lentiviral Etv2 injection after 5-FU treatment showed significantly improved anagen induction and hair regrowth. Two-photon laser scanning microscopy revealed that enforced Etv2 expression restored normal vessel morphology after 5-FU mediated vessel injury. Our data suggest that vessel regeneration strategies may improve hair regrowth after chemotherapeutic treatment.
Keywords: Angiogenesis, Chemotherapy-induced alopecia, ETS transcription factor, ETV2/ER71, Hair regeneration, 5-FU

Hair follicles continuously cycle through anagen (growth), catagen (regression), and telogen (resting) stages (Schneider et al., 2009). These cyclic changes involve rapid remodeling of both epithelial and dermal components (Paus and Cotsarelis, 1999). Hair growth is associated with perifollicular angiogenesis, which is highly active during the anagen phase (Mecklenburg et al., 2000; Yano et al., 2001). The interaction of vascular endothelial growth factor (VEGF) with its receptors plays a critical role in angiogenesis. VEGF receptor 2 (VEGFR2; FLK1), the primary receptor for VEGF, mediates most of the mitogenic, survival, and vascular permeability effects of VEGF. Consistently, VEGF delivery into the dorsal subcutaneous tissue of mice significantly promotes angiogenesis and hair follicle growth (Ozeki and Tabata, 2002). Notably, the perivascular niche in the upper bulge maintains the hair follicle stem cells (Xiao et al., 2013).

Chemotherapy or radiation therapy, which targets rapidly dividing cancer cells, frequently leads to visibly distressing side effects such as hair loss. Chemotherapy-induced alopecia, ranging from mild to severe, often causes patients to refuse chemotherapy (Yeager and Olsen, 2011; Dunnill et al., 2018). Hair loss can occur from a few days to weeks after chemotherapy, and distinct hair loss patterns can be observed based on severity (Rossi et al., 2020). Chemotherapy-induced alopecia most prominently disturbs the highly proliferative activity of matrix keratinocytes in anagen hair follicles (Trüeb, 2010; Paus et al., 2013). Telogen hair follicles are less sensitive to chemotherapy than anagen hair follicles, presumably because of their low proliferative activity. In certain instances, hair-follicle stem cells are also injured, leading to permanent hair loss (Trüeb, 2010; Paus et al., 2013). Several drugs or devices have been used to prevent or treat chemotherapy-induced alopecia; however, the results have been unsatisfactory in several cases (Rubio-Gonzalez et al., 2018).

5-Fluorouracil (5-FU) is an antimetabolite anticancer drug widely used to treat gastrointestinal, breast, gynecological, and head and neck cancers (Grem, 1997). However, patients receiving 5-FU treatment commonly display endovascular injury in various organs (Jensen and Sørensen, 2012; Focaccetti et al., 2015). As chemotherapeutic agents induce vascular damage to the hair follicle (Amoh et al., 2007), we hypothesized that the stimulation of vascular regeneration might enhance hair regrowth. The ETS transcription factor ETV2 (ER71) is essential for hematopoietic and vessel development (Lee et al., 2008). Etv2 is reactivated in endothelial cells and upregulates Flk1 expression in an ischemic hindlimb vascular regeneration model (Park et al., 2016). In the present study, we investigated whether Etv2/Er71 can promote perifollicular angiogenesis and hair regrowth in a mouse model of 5-FU induced alopecia. We revealed that endothelial Etv2 enhanced hair regeneration by promoting vessel regeneration after 5-FU mediated vascular injury and hair loss.


Generation of CKO mice

Tie2-Cre; Etv2 CKO (Tie2-Cre; Etv2flox/flox) mice were generated from Tie2-Cre; Etv2flox/+×Etv2flox/flox mating, as previously reported (Park et al., 2016). Tie2-Cre mice were purchased from the Jackson Laboratory (Bar Harbor, ME, USA); the generation of Etv2flox/flox mice has been previously described (Lee et al., 2011). Animal husbandry, generation, handling, and experimentation were performed in accordance with protocols (20170245) approved by the Institutional Animal Care and Use Committee of Washington University School of Medicine in St. Louis (MO, USA).

Depilation induced hair growth measurement

Synchronized anagen was induced in the dorsal skin of approximately 7-week-old (P50-53) C57BL/6 mice by depilation, as previously described (Paus et al., 1990; Yano et al., 2001). The dorsal skin surface was photographed at days 12 and 18 after depilation, followed by quantitative assessment of anagen induction by dotmatrix planimetry. Areas that were in different stages (pink, telogen; anagen, black) were marked on a mouse photo, and the percentage of anagen induction was calculated using the equation [(black skin/total skin)×100]. Data are presented as mean ± standard deviation (SD) (n=4-8).

5-FU treatment

P50-53 wild-type C57BL/6 mice and Tie2cre; Etv2 CKO mice were intraperitoneally injected with 200 mg/kg or 250 mg/kg of 5-FU or phosphate-buffered saline (PBS) at day 0 after depilation.

Lentiviral particle production

Lentivirus was produced as previously reported (Park et al., 2016). Briefly, 293T cells were transfected with pCSII-EF1α-ETV2-IRES-VENUS (pCSII-EF1α-IRES-VENUS or pCSII-EF1α-FLK1), pCAG-HIVgp, and pCMV-VSV-G-RSV-Rev (4:3:1) using the calcium phosphate method. Sixteen hours after transfection, the medium was changed, and cells were grown for an additional 48 h. Subsequently, the supernatant was harvested and concentrated using a Lenti-X-Concentrator (Clontech, Mountain View, CA, USA). The virus titer was determined using a Lenti-X™ p24 Rapid Titer Kit (Clontech). For the injection study, the IFU was approximately 3×107/mL.

Lentiviral Etv2 injection

P50-53 C57BL/6 mice were depilated and intraperitoneally injected with 250 mg/kg 5-FU or PBS. Lentiviral Etv2 (or control) (100 μL) was intradermally injected the following day.


In brief, the dorsal skin was excised at day 13 (late anagen) after depilation and fixed using 4% paraformaldehyde in PBS. The skins were then frozen in optimal cutting temperature compound (Tissue-Tek, Sakura Finetk, Torrance, CA, USA) at −20°C, and cut into 10-µm thick sections using a Cryostat Cryocut Microtome (CM1850, Leica, Nussloch, Germany). For CD31 staining, tissue sections were incubated overnight at 4°C with rat anti-platelet endothelial cell adhesion molecule (CD31, PECAM-1) (1:25) antibody (BD Bioscience, San Jose, CA, USA), followed by staining with Alexa Fluor 594-labeled goat anti-rat (1:200) for 1 h at room temperature (Molecular Probes, Grand Island, NY, USA). Nuclei were counterstained with 4,6 diamidino-2-phenylindole (DAPI, Vector Laboratories, Burlingame, CA, USA) and examined using a fluorescence microscope (Axiovert 200M, ZEISS, Göttingen, Germany). At least eight images were randomly selected from each slide, and fluorescent vessels were counted to quantify CD31 positive vessels in the skin.


The dorsal skins were excised on day 13 after depilation, fixed in 4% paraformaldehyde in PBS, dehydrated in a graded ethanol series, and embedded in paraffin. Tissue sections (4-μm thick) were stained with hematoxylin and eosin. Five images were randomly selected from each slide (n=1). The skin thickness was measured in at least five different regions and averaged per image using ImageJ (National Institutes of Health, Bethesda, MD, USA).

Two-photon imaging analysis

Mice were injected intravenously with 70 kDa rhodamine-dextran (50 μL) on day 13 after depilation. A two-photon laser tuned to 890 nm was used to excite dextran. In each experiment, a total of 50 two-dimensional (2D) slices were obtained at 2.5 μm steps and extrapolated into a three-dimensional (3D) volume using the Imaris software. Blood vessel diameters and volumes were measured from 3D rendering using Imaris’s FilamentTracer module (OXFORD Instruments, Zurich, Switzerland). The fractal dimension of the vasculature was calculated in MATLAB using an iterative box-counting algorithm on the maximum intensity projection of the 3D volume. Data are presented as the mean ± standard error (SE) (n=7-8, z-stack images).

Statistical analysis

Statistical analysis of blood vessel density measurements and quantification of anagen induction was performed using analysis of variance (ANOVA). For 2P image quantification, repeated measures analysis of covariance (ANCOVA) was performed using SAS statistical software (Campus Drive, Cary, NC, USA) with proc mixed. Multiple images per mouse were obtained, and model-fitting statistics, such as AIC and log-likelihood, suggested that a diagonal variance component matrix best fits the repeated measures effect. Outcome variables were adjusted for covariance from naturally occurring predictor variables (e.g., longer vessels have higher curvature regardless of treatment). Statistical contrasts were performed to assess within-group differences, and a p-value of <0.05 was considered significant.


5-FU treatment delays anagen induction

Previous studies have revealed that depilation (shaving) induces anagen in telogenic mice (Yano et al., 2001). Consistently, on inducing the hair cycle by depilation in 7-week-old C57BL/6 mice, which were almost exclusively in the telogenic hair follicle phase, anagen was initiated in 77.3 ± 15.4% of the depilated dorsal skin on day 12. The coat was almost fully restored by the end of anagen (day 18, 98.1 ± 2.2%, Fig. 1). In contrast, mice treated with 5-FU (200 mg/kg) after depilation showed delayed anagen initiation when compared with untreated controls, as indicated by the decreased percentage of black skin observed at day 12 (42.9 ± 10.3%) and day 18 (77.5 ± 26.1%). In a cohort of mice administered a higher dose of 5-FU dosage (250 mg/kg), anagen induction and hair regeneration were decreased further to 31.4 ± 12.5% on day 12 and 52.1 ± 27.8% on day 18, indicating that 5-FU treatment resulted in retarded anagen induction (Fig. 2A, 2B). Importantly, 5-FU treatment resulted in reduced capillary density (Fig. 2C, 2D, Supplementary Fig. 1).

Figure 1. Etv2 is required for hair follicle anagen induction after 5-FU injury. (A) Representative images of the depilated dorsal skin of wild-type and Tie2-Cre; Etv2 CKO mice, with or without 5-FU treatment, at days 12 and 18. (B) Quantification of anagen induction in (A). *p<0.05; ***p<0.001. 5-FU, 5-fluorouracil.
Figure 2. Etv2 enhances hair follicle anagen induction by angiogenesis. (A) Representative images of the depilated dorsal skin surface in 5-FU treated mice ± Etv2 at days 12 and 18. (B) Quantification of anagen induction in (A). Mean values ± standard error (SE) (n≥4); *p<0.05; **p<0.01; ***p<0.001. (C) Representative images of the CD31 immunohistochemistry in the 5-FU-treated perifollicular region after lentiviral Etv2 Injection. The nuclei were stained with DAPI (blue). Scale bars: 100 µm. (D) Quantitative analysis of CD31-positive vessels in (C). Mean values ± standard deviation (SD); ***p<0.001. At least 8 fields generated from n≥2 mice were examined. 5-FU, 5-fluorouracil.

Endothelial Etv2 deletion leads to delayed hair regeneration after 5-FU treatment

As Etv2 is required for vascular regeneration after ischemic injuries (Park et al., 2016), we determined whether Etv2 is also necessary for hair regeneration. First, we assessed hair regrowth after depilation in Tie2-Cre; Etv2 conditional knockout (CKO) mice, which lack Etv2 in endothelial cells. Tie2-Cre; Etv2 CKO mice displayed similar hair regrowth rates as compared with control mice after depilation, as shown by the similar anagen initiation (day 12, C57BL/6, 77.3 ± 15.4%; Tie2-Cre; Etv2 CKO, 65.8 ± 10.1%) and the fully restored hair by the end of anagen (day 18, C57BL/6, 98.1 ± 2.2%; Tie2-Cre; Etv2 CKO, 98.6 ± 0.6%) (Fig. 1). These results indicate that in addition to being dispensable for maintaining steady-state blood vessels (Park et al., 2016), Etv2 is dispensable for normal hair regrowth by steady-state blood vessels. However, when wild-type and Tie2-Cre; Etv2 CKO mice underwent depilation and treatment with 5-FU at 200 mg/kg, a dosage that allows substantial hair regrowth in wild-type mice by day 18 (Fig. 1), Tie2-Cre; Etv2 CKO mice showed diminished anagen (day 12, 26.6 ± 11.1% vs. 42.9 ± 10.3%, respectively), as well as reduced capillary density (Supplementary Fig. 1). Although hair regrowth in control mice reached 77.5 ± 26.1% by day 18, 5-FU-treated Tie2-Cre; Etv2 CKO mice showed significantly delayed hair regrowth (63.5 ± 27.0%).

Lentiviral Etv2 gene delivery enhances vessel regeneration and hair regrowth

In a mouse hindlimb ischemic injury model, lentiviral Etv2 gene delivery robustly enhances vessel angiogenesis and tissue repair (Park et al., 2016). Thus, we determined whether Etv2 gene delivery could augment vessel regeneration and enhance hair regrowth. Telogen C57BL/6 mice were depilated and administered 5-FU at 250 mg/kg, a dosage that severely impairs hair regrowth in wild-type mice; this was followed by intradermal lentiviral Etv2 injection. We confirmed the lentiviral infection of endothelial cells by assessing the co-expression of CD31 and lentiviral-encoded GFP (Supplementary Fig. 2). Mice receiving lentiviral Etv2 injection revealed significantly improved anagen induction and hair regrowth (62.6 ± 23.2% at day 12 and 86.6 ± 14.2% at day 18) (Fig. 2A, 2B), while the lentiviral vector control group showed no improvement when compared with controls (not shown). Notably, hair-follicle-associated micro-vessel density, decreased in the 5-FU treatment group, was increased to control levels following the Etv2 injection (control, 40.0 ± 10.7; 5-FU, 18.9 ± 6.2; 5-FU and Etv2, 41.2 ± 9.1; Fig. 2C, 2D).

Moreover, the 5-FU treatment decreased the thickness of the dermis and subcutaneous tissue of the dorsal skin, and Etv2 injected mice showed a similar thickness of the whole dermis and subcutaneous tissue to that of normal dorsal skin (Fig. 3). We employed in vivo two-photon laser scanning microscopy to assess the impact of Etv2 on the morphology and density of vessels in depilated dorsal skin (Fig. 4). Vessels in 5-FU treated mice appeared discontinuous and fragmented (Fig. 4A). Additionally, vessels in 5-FU-treated mouse skin revealed decreased vascular volume when compared with those in the control mouse skin. However, lentiviral expression of Etv2 rescued 5-FU mediated vessel defects and restored normal vessel morphology in terms of tortuosity and branching, as measured by the fractal dimension (Fig. 4B-4D).

Figure 3. Etv2 increases dorsal skin thickness after 5-FU injury. (A) Hematoxylin and eosin staining of histological dorsal skin samples at day 13 after depilation. Scale bars: 500 µm. (B) Quantification of skin thickness in (A) (n=1). 5-FU, 5-fluorouracil.
Figure 4. Etv2 enhances perifollicular angiogenesis after 5-FU injury. (A) Two-photon microscopy images of dorsal skin at day 13 after depilation. Red colors indicate vascular signal. Hair shafts display auto-fluorescence. Scale bars: 50 µm. (B) Vessel diameter from Z-stacks of two-photon images of dorsal skin at day 13 after depilation. Data are presented as the mean ± standard error (SE) (n=7-8 z-stack images). ***p<0.001. (C) Vessel volume from Z-stacks of two-photon images of dorsal skin at day 13 after depilation. Data are presented as the mean ± SE (n=7-8 Z-stack images). **p<0.01; ***p<0.001. (D) Fractal dimension of vessels from the Z-stacks of two-photon images at day 13 after depilation. ***p<0.001. 5-FU, 5-fluorouracil.

Approximately 80% of patients with cancer have reported that chemotherapy-induced alopecia is a severe problem associated with cancer treatment after nausea and vomiting (Yeager and Olsen, 2011). Accordingly, several patients refuse to undergo cancer chemotherapy (Yeager and Olsen, 2011). Understanding hair loss mechanisms and hair regeneration after chemotherapy can improve the quality of life in patients undergoing cancer treatment.

Chemotherapeutic agents reportedly cause vascular damage to hair follicles (Amoh et al., 2007). Angiogenesis is essential for regulating the hair follicle cycle and hair regrowth (Yano et al., 2001). During the anagen phase, the vascular network is highly developed (Mecklenburg et al., 2000). Hair follicle dermal papilla and outer root sheath keratinocytes are known to secrete VEGF at higher levels, thereby controlling hair growth (Man et al., 2009). Moreover, VEGF can induce hair follicle growth by promoting angiogenesis (Ozeki and Tabata, 2002). These studies support the notion that angiogenic stimulation may promote hair regeneration. In the present study, we examined whether hair regeneration could be promoted by enhancing angiogenesis. We specifically tested whether Etv2 deficiency affected chemotherapy-induced alopecia. Our data indicate that 5-FU treated Tie2-Cre; Etv2 CKO mice showed delayed anagen initiation when compared with control mice after 5-FU treatment (Fig. 1). Additionally, lentiviral Etv2 injected mice demonstrated significantly improved anagen induction and hair regrowth (Fig. 2, 4). We confirmed lentiviral Etv2 gene delivery to endothelial cells (Supplementary Fig. 2). These results indicate that hair regeneration after 5-FU treatment can be facilitated by enhancing perifollicular capillary angiogenesis and anagen initiation.

Etv2 is critical for vascular development and regeneration (Lee et al., 2008; Park et al., 2016). Previously, we showed that endothelial Etv2/Er71 reactivation was essential for angiogenesis in hindlimb ischemia and a tumor model (Park et al., 2016; Kabir et al., 2018). Etv2 was reactivated in endothelial cells at the site of hindlimb ischemic injury in wild-type mice, while Etv2 expression and angiogenesis decreased in Etv2 CKO mice, such as Tie2-Cre; Etv2 CKO mice (Park et al., 2016). Additionally, Etv2 gene delivery to endothelial cells by lentiviral Etv2 injection enhanced angiogenesis and reduced the fibrosis area in a mouse hindlimb ischemic injury model (Park et al., 2016). In contrast, Etv2 shRNA inhibited angiogenesis and tumor growth when Etv2 shRNA was delivered to the tumor (Kabir et al., 2018). In the present study, 5-FU treatment in Tie2-Cre; Etv2 CKO mice delayed anagen induction and reduced capillary density. Lentiviral Etv2 gene delivery rescued impaired angiogenesis at the anagen stage, as well as hair regeneration in 5-FU treated wild-type mice. Therefore, Etv2 reactivation in endothelial cells induced angiogenesis, which was followed by hair regrowth. Hair growth is associated with perifollicular angiogenesis (Mecklenburg et al., 2000; Yano et al., 2001). Several studies have shown that angiogenesis promotes hair growth. VEGF delivery and platelet-rich plasma (Ozeki and Tabata, 2002; Cheng et al., 2017) successfully enhanced angiogenesis and hair growth. Based on previous reports, the difference in anagen induction in 5-FU treated Tie2-Cre; Etv2 CKO mice and 5-FU treated, lentiviral Etv2 gene-delivered mice is dependent on angiogenesis. Therefore, Etv2 can regulate hair regeneration via angiogenesis in hair loss induced by vascular injury.

In the present study, we were unable to confirm the effect of Etv2 on the regulation of the normal hair cycle; however, Etv2 activation might also enhance hair regeneration under normal conditions. ER71 promotes FLK1+ mesoderm formation by directly activating Flk1 gene expression (Lee et al., 2008). Furthermore, Er71 deficient mice demonstrated considerably reduced FLK1 expression, died early during gestation, and displayed severe blood and vessel defects (Lee et al., 2008). Reportedly, Etv2 regulates FLK1 expression in endothelial cells (Park et al., 2016; Kabir et al., 2018). Endothelial cells derived from Etv2 deletion mice revealed reduced FLK1 expression when compared with endothelial cells derived from normal mice (Park et al., 2016; Kabir et al., 2018). Endothelial cells derived from Etv2 deficient mice showed reduced VEGF response, while an increase in Etv2 expression enhanced FLK1 expression (Kabir et al., 2018). It has been reported that VEGF is produced at higher levels during the anagen phase by dermal papilla and outer root sheath keratinocytes, which control hair growth (Kozlowska et al., 1998; Man et al., 2009). Therefore, the reactivation of Etv2 in endothelial cells increased the VEGF response secreted from dermal papilla and outer root sheath keratinocytes and could enhance angiogenesis, which can accelerate anagen induction and improve hair growth.

In conclusion, our data demonstrated that Etv2 deficiency in endothelial cells reduces hair regeneration. Conversely, enforced Etv2 expression led to improved angiogenesis and hair regeneration after 5-FU treatment. Our data support the notion that Etv2-mediated enhanced vascularization may offer a novel approach for hair regeneration after chemotherapy. Our studies further support the idea that vessel regeneration strategies may be integrated into future tissue regeneration therapies.


We thank the lab members for constructive criticism and discussions of this work. This work was supported by the NIH grants HL119291 (C.P), HL149954 and HL55337 (K.C), and the 2020 Research Grant from Kangwon National University (520200067) (T. L.).


The authors have declared that no competing interest exists.

  1. Amoh, Y., Li, L., Katsuoka, K. and Hoffman, R. M. (2007) Chemotherapy targets the hair-follicle vascular network but not the stem cells. J. Invest. Dermatol. 127, 11-15.
    Pubmed CrossRef
  2. Cheng, H., Zhang, J., Li, J., Jia, M., Wang, Y. and Shen, H. (2017) Platelet-rich plasma stimulates angiogenesis in mice which may promote hair growth. Eur. J. Med. Res. 22, 39.
    Pubmed KoreaMed CrossRef
  3. Dunnill, C. J., Al-Tameemi, W., Collett, A., Haslam, I. S. and Georgopoulos, N. T. (2018) A clinical and biological guide for understanding chemotherapy-induced alopecia and its prevention. Oncologist 23, 84-96.
    Pubmed KoreaMed CrossRef
  4. Focaccetti, C., Bruno, A., Magnani, E., Bartolini, D., Principi, E., Dallaglio, K., Bucci, E. O., Finzi, G., Sessa, F., Noonan, D. M. and Albini, A. (2015) Effects of 5-fluorouracil on morphology, cell cycle, proliferation, apoptosis, autophagy and ROS production in endothelial cells and cardiomyocytes. PLoS ONE 10, e0115686.
    Pubmed KoreaMed CrossRef
  5. Grem, J. L. (1997) Mechanisms of action and modulation of fluorouracil. Semin. Radiat. Oncol. 7, 249-259.
    Pubmed CrossRef
  6. Jensen, S. A. and Sørensen, J. B. (2012) 5-fluorouracil-based therapy induces endovascular injury having potential significance to development of clinically overt cardiotoxicity. Cancer Chemother. Pharmacol. 69, 57-64.
    Pubmed CrossRef
  7. Kabir, A. U., Lee, T. J., Pan, H., Berry, J. C., Krchma, K., Wu, J., Liu, F., Kang, H. K., Hinman, K., Yang, L., Hamilton, S., Zhou, Q., Veis, D. J., Mecham, R. P., Wickline, S. A., Miller, M. J. and Choi, K. (2018) Requisite endothelial reactivation and effective siRNA nanoparticle targeting of Etv2/Er71 in tumor angiogenesis. JCI Insight 3, e97349.
    Pubmed KoreaMed CrossRef
  8. Kozlowska, U., Blume-Peytavi, U., Kodelja, V., Sommer, C., Goerdt, S., Majewski, S., Jablonska, S. and Orfanos, C. E. (1998) Expression of vascular endothelial growth factor (VEGF) in various compartments of the human hair follicle. Arch. Dermatol. Res. 290, 661-668.
    Pubmed CrossRef
  9. Lee, D., Kim, T. and Lim, D. S. (2011) The Er71 is an important regulator of hematopoietic stem cells in adult mice. Stem Cells 29, 539-548.
    Pubmed CrossRef
  10. Lee, D., Park, C., Lee, H., Lugus, J. J., Kim, S. H., Arentson, E., Chung, Y. S., Gomez, G., Kyba, M., Lin, S., Janknecht, R., Lim, D. S. and Choi, K. (2008) ER71 acts downstream of BMP, Notch, and Wnt signaling in blood and vessel progenitor specification. Cell Stem Cell 2, 497-507.
    Pubmed KoreaMed CrossRef
  11. Man, X. Y., Yang, X. H., Cai, S. Q., Bu, Z. Y., Wu, X. J., Lu, Z. F. and Zheng, M. (2009) Expression and localization of vascular endothelial growth factor and vascular endothelial growth factor receptor-2 in human epidermal appendages: a comparison study by immunofluorescence. Clin. Exp. Dermatol. 34, 396-401.
    Pubmed CrossRef
  12. Mecklenburg, L., Tobin, D. J., Müller-Röver, S., Handjiski, B., Wendt, G., Peters, E. M., Pohl, S., Moll, I. and Paus, R. (2000) Active hair growth (anagen) is associated with angiogenesis. J. Invest. Dermatol. 114, 909-916.
    Pubmed CrossRef
  13. Ozeki, M. and Tabata, Y. (2002) Promoted growth of murine hair follicles through controlled release of vascular endothelial growth factor. Biomaterials 23, 2367-2373.
    Pubmed CrossRef
  14. Park, C., Lee, T. J., Bhang, S. H., Liu, F., Nakamura, R., Oladipupo, S. S., Pitha-Rowe, I., Capoccia, B., Choi, H. S., Kim, T. M., Urao, N., Ushio-Fukai, M., Lee, D. J., Miyoshi, H., Kim, B. S., Lim, D. S., Apte, R. S., Ornitz, D. M. and Choi, K. (2016) Injury-mediated vascular regeneration requires endothelial ER71/ETV2. Arterioscler. Thromb. Vasc. Biol. 36, 86-96.
    Pubmed KoreaMed CrossRef
  15. Paus, R. and Cotsarelis, G. (1999) The biology of hair follicles. N. Engl. J. Med. 341, 491-497.
    Pubmed CrossRef
  16. Paus, R., Haslam, I. S., Sharov, A. A. and Botchkarev, V. A. (2013) Pathobiology of chemotherapy-induced hair loss. Lancet Oncol. 14, e50-e59.
    Pubmed CrossRef
  17. Paus, R., Stenn, K. S. and Link, R. E. (1990) Telogen skin contains an inhibitor of hair growth. Br. J. Dermatol. 122, 777-784.
    Pubmed CrossRef
  18. Rossi, A., Caro, G., Fortuna, M. C., Pigliacelli, F., D'Arino, A. and Carlesimo, M. (2020) Prevention and treatment of chemotherapy-induced alopecia. Dermatol. Pract. Concept. 10, e2020074.
    Pubmed KoreaMed CrossRef
  19. Rubio-Gonzalez, B., Juhász, M., Fortman, J. and Mesinkovska, N. A. (2018) Pathogenesis and treatment options for chemotherapy-induced alopecia: a systematic review. Int. J. Dermatol. 57, 1417-1424.
    Pubmed CrossRef
  20. Schneider, M. R., Schmidt-Ullrich, R. and Paus, R. (2009) The hair follicle as a dynamic miniorgan. Curr. Biol. 19, R132-R142.
    Pubmed CrossRef
  21. Trüeb, R. M. (2010) Chemotherapy-induced hair loss. Skin Therapy Lett. 15, 5-7.
  22. Xiao, Y., Woo, W. M., Nagao, K., Li, W., Terunuma, A., Mukouyama, Y. S., Oro, A. E., Vogel, J. C. and Brownell, I. (2013) Perivascular hair follicle stem cells associate with a venule annulus. J. Invest. Dermatol. 133, 2324-2331.
    Pubmed KoreaMed CrossRef
  23. Yano, K., Brown, L. F. and Detmar, M. (2001) Control of hair growth and follicle size by VEGF-mediated angiogenesis. J. Clin. Invest. 107, 409-417.
    Pubmed KoreaMed CrossRef
  24. Yeager, C. E. and Olsen, E. A. (2011) Treatment of chemotherapy-induced alopecia. Dermatol. Ther. 24, 432-442.
    Pubmed CrossRef

This Article

Cited By Articles
  • CrossRef (0)

Funding Information
  • National Institutes of Health
      HL119291, HL149954, HL55337
  • Kangwon National University

Social Network Service