scholarly journals Melanogenesis Effect of 7-acetoxy-4-methylcoumarin in B16F10 Melanoma Cells

Cosmetics ◽  
2020 ◽  
Vol 7 (4) ◽  
pp. 94
Author(s):  
Ji-Han Sim ◽  
Sung-Chan Jang ◽  
Tae-Jin Park ◽  
Won-Jae Chi ◽  
Seung-Young Kim
Keyword(s):  
Melanoma Cells ◽  
Hair Follicles ◽  
Dependent Manner ◽  
B16f10 Melanoma ◽  
Melanin Production ◽  
B16f10 Cells ◽  
B16f10 Melanoma Cells ◽  
Diphenyl Tetrazolium Bromide ◽  
Synthetic Derivatives ◽  
Dose Dependent

The increased interest in anti-whitening dyes has enhanced the research interest to identify efficient melanogenic activators. Melanogenesis is the process of melanin production by melanocytes in the hair follicles and skin, which is mediated by several enzymes, such as microphthalmia-associated transcription factor (MITF), tyrosinase (TYR), tyrosinase-related protein (TRP)-1, and TRP-2. This study investigated the melanogenesis-stimulating effect of 4-Methylumbelliferone (4MUMB) and its synthetic derivatives, 7-acetoxy-4-methylcoumarin (7A4MC) and 4-methylheriniarin (4MH) in B16F10 melanoma cells. The cytotoxicity of these compounds was investigated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay, followed by the assessment of the melanin content and the intracellular TYR activity. Finally, the expression levels of the key enzymes involved in melanogenesis were investigated. 7A4MC increased melanin production in B16F10 cells relative to that by 4MUMB and 4MH treated cells in a dose-dependent manner without significant cytotoxicity. Concomitantly, 7A4MC significantly increased TYR activity and enhanced the expression of MITF, which significantly induced the expression of TRP-1, TRP-2, and TYR. Furthermore, 7A4MC stimulated melanogenesis via increased phosphorylation of c-Jun N-terminal kinases (JNK) and reduced phosphorylation of protein kinase B (AKT). These results confirmed the melanogenesis-inducing effects of 7A4MC and indicated its potential use as an anti-hair bleaching agent in cosmetics industries.

scholarly journals Anti-Melanogenic Effects of Hydroxyectoine via MITF Inhibition by JNK, p38, and AKT Pathways in B16F10 Melanoma Cells

2019 ◽  
Vol 14 (6) ◽  
pp. 1934578X1985852 ◽  
Author(s):  
You C. Chung ◽  
Min-Jin Kim ◽  
Eun Y. Kang ◽  
Yun B. Kim ◽  
Bong S. Kim ◽  
...  
Keyword(s):  
Skin Color ◽  
Inhibitory Effect ◽  
Tyrosinase Activity ◽  
Dependent Manner ◽  
Related Protein ◽  
B16f10 Melanoma ◽  
Melanin Production ◽  
B16f10 Cells ◽  
Dose Dependent ◽  
Tyrosinase Related Protein

Melanin plays a role in determining human skin color of a person, and a large amount of melanin makes the skin color look darkened. The proper amount of melanin formation protects our skin from UV radiation, but excessive melanin production causes hyperpigmentation and leads to freckles, melasma, and lentigo. In this study, we investigated the inhibitory effect of hydroxyectoine on melanogenesis and its mechanism in B16F10 cells. Melanin content and cellular tyrosinase activity were determined. The expression of microphthalmia-associated transcription factor (MITF), and the activities of tyrosinase and other melanogenesis-related enzymes, such as tyrosinase-related protein 1 (TRP-1) and tyrosinase-related protein 2, were also examined. Hydroxyectoine treatment significantly inhibited melanin production and intracellular tyrosinase activity in a dose-dependent manner. Western blot analysis showed that hydroxyectoine also reduced the expressions of tyrosinase and TRP-1. In addition, hydroxyectoine significantly reduced the expression of MITF, a major regulator of melanin production, and inhibited the phosphorylation of p38, c-Jun N-terminal kinase, and activated the protein kinase B. The results demonstrated that hydroxyectoine inhibits the expression of MITF through the inhibition or activation of melanin-related signaling pathways and downregulates melanogenesis by inhibiting melanogenic enzyme expression and tyrosinase activity. Hydroxyectoine has potential value in functional cosmetics applications, such as whitening.

scholarly journals Kinetics of Mushroom Tyrosinase and Melanogenesis Inhibition byN-Acetyl-pentapeptides

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Ching-Yi Lien ◽  
Ching-Yu Chen ◽  
Shih-Ting Lai ◽  
Chin-Feng Chan
Keyword(s):  
Kojic Acid ◽  
Lag Time ◽  
Melanoma Cells ◽  
Dependent Manner ◽  
Mushroom Tyrosinase ◽  
Inhibitory Effects ◽  
B16f10 Melanoma ◽  
B16f10 Melanoma Cells ◽  
Kinetics Of ◽  
Dose Dependent

We investigated the kinetics of 4N-acetyl-pentapeptides, Ac-P1, Ac-P2, Ac-P3, and Ac-P4, regarding inhibition of mushroom tyrosinase activity. The peptides sequences of Ac-P1, Ac-P2, Ac-P3, and Ac-P4 were Ac-RSRFK, Ac-KSRFR, Ac-KSSFR, and Ac-RSRFS, respectively. The 4N-acetyl-pentapeptides were able to reduce the oxidation ofL-DOPA by tyrosinase in a dose-dependent manner. Of the 4N-acetyl-pentapeptides, only Ac-P4 exhibited lag time (80 s) at a concentration of 0.5 mg/mL. The tyrosinase inhibitory effects of Ac-P4 (IC500.29 mg/mL) were more effective than those of Ac-P1, Ac-P2, and Ac-P3, in which IC50s were 0.75 mg/mL, 0.78 mg/mL, and 0.81 mg/mL, respectively. Kinetic analysis demonstrated that all 4N-acetyl-pentapeptides were mixed-type tyrosinase inhibitors. Furthermore, 0.1 mg/mL of Ac-P4 exhibited significant melanogenesis inhibition on B16F10 melanoma cells and was more effective than kojic acid. The melanogenesis inhibition of Ac-P4 was dose-dependent and did not induce any cytotoxicity on B16F10 melanoma cells.

scholarly journals Tobramycin Promotes Melanogenesis by Upregulating p38 MAPK Protein Phosphorylation in B16F10 Melanoma Cells

Antibiotics ◽  
2019 ◽  
Vol 8 (3) ◽  
pp. 140 ◽  
Author(s):  
Seung-Hyun Moon ◽  
You Chul Chung ◽  
Chang-Gu Hyun
Keyword(s):  
Protein Phosphorylation ◽  
Melanoma Cells ◽  
Clinical Use ◽  
Melanin Content ◽  
B16f10 Melanoma ◽  
Melanin Production ◽  
B16f10 Cells ◽  
Infection Treatment ◽  
B16f10 Melanoma Cells ◽  
Long Time

Tobramycin is an aminoglycoside-based natural antibiotic derived from Streptomyces tenebrarius, which is primarily used for Gram-negative bacterial infection treatment. Although tobramycin has been utilized in clinical practice for a long time, it has exhibited several side effects, leading to the introduction of more effective antibiotics. Therefore, we conducted our experiments focusing on new possibilities for the clinical use of tobramycin. How tobramycin affects skin melanin formation is unknown. This study used B16F10 melanoma cells to assess the effect of tobramycin on melanin production. After cytotoxicity was assessed by MTT assay, melanin content and tyrosinase activity analyses revealed that tobramycin induces melanin synthesis in B16F10 cells. Next, Western blot analyses were performed to elucidate the mechanism by which tobramycin increases melanin production; phosphorylated p38 protein expression was upregulated. Protein inhibitors have been used to elucidate the mechanism of tobramycin. Kanamycin A and B are structurally similar to tobramycin, and 2-DOS represents the central structure of these antibiotics. The effects of these substances on melanogenesis were evaluated. Kanamycin A reduced melanin production, whereas kanamycin B and 2-DOS had no effect. Overall, our data indicated that tobramycin increases melanin production by promoting p38 protein phosphorylation in B16F10 melanoma cells.

Inhibitory Effects of Dryopteris erythrosora Extract on Tyrosinase Activity and Melanin Production in B16F10 Melanoma Cells

KSBB Journal ◽  
2020 ◽  
Vol 35 (3) ◽  
pp. 228-234
Author(s):  
Yeon-Su Koo ◽  
Taejin Park ◽  
Ji Han Sim ◽  
Min-Seon Kim ◽  
Seung-Young Kim
Keyword(s):  
Melanoma Cells ◽  
Tyrosinase Activity ◽  
Inhibitory Effects ◽  
B16f10 Melanoma ◽  
Melanin Production ◽  
B16f10 Melanoma Cells

scholarly journals Azadirachta indica (Neem) Water Leaf Extract Inhibits Melanin Production and Tyrosinase Activity in B16F10 Melanoma Cells

2021 ◽  
Vol 13 (4) ◽  
pp. 1030-1035
Author(s):  
Thanitsara Songtavisin ◽  
Benjamart Pratoomthai ◽  
Warachin Gangnonngiw ◽  
Jarinyaporn Naowaboot
Keyword(s):  
Azadirachta Indica ◽  
Leaf Extract ◽  
Melanoma Cells ◽  
Tyrosinase Activity ◽  
B16f10 Melanoma ◽  
Melanin Production ◽  
B16f10 Melanoma Cells

scholarly journals SBA-15 mesoporous silica particles loaded with cisplatin induce senescence in B16F10 cells

RSC Advances ◽  
2016 ◽  
Vol 6 (112) ◽  
pp. 111031-111040 ◽  
Author(s):  
David Edeler ◽  
Milena R. Kaluđerović ◽  
Biljana Dojčinović ◽  
Harry Schmidt ◽  
Goran N. Kaluđerović
Keyword(s):  
Mesoporous Silica ◽  
Melanoma Cells ◽  
Silica Particles ◽  
B16f10 Melanoma ◽  
B16f10 Cells ◽  
B16f10 Melanoma Cells

Nanoparticles obtained by loading of cisplatin into mesoporous silica SBA-15 (SBA-15|CP) change the phenotype of surviving B16F10 melanoma cells from malignant to senescent.

scholarly journals Antimelanogenic activities of piperlongumine derived from Piper longum on murine B16F10 melanoma cells in vitro and zebrafish embryos in vivo: its molecular mode of depigmenting action

2019 ◽  
Vol 62 (1) ◽  
Author(s):  
Hwang-Ju Jeon ◽  
Kyeongnam Kim ◽  
Yong-Deuk Kim ◽  
Sung-Eun Lee
Keyword(s):  
Melanoma Cells ◽  
Positive Control ◽  
Zebrafish Embryos ◽  
B16f10 Melanoma ◽  
Melanin Production ◽  
Melanocyte Stimulating Hormone ◽  
B16f10 Melanoma Cells ◽  
Pharmaceutical Industries

Abstract In this study, the antimelanogenic activity of piperlongumine in murine B16F10 melanoma cells and zebrafish was investigated, and its mode of antimelanogenic action was elucidated using quantitative reverse transcription-polymerase chain reaction. A melanocyte-stimulating hormone (α-MSH, 200 nM) was used to induce melanin production in B16F10 melanoma cells, and kojic acid (200 μM) was used as a positive control. Piperlongumine had no inhibitory effects on cell growth at the treated concentrations (3 and 6 μM), and it significantly reduced total melanin production. Piperlongumine decreased the expression of Mitf, Tyr, Trp-1, and Trp-2 and tyrosinase activity was also dramatically reduced by the piper amide addition under α-MSH treatment. With these findings, zebrafish embryos were used to confirm antimelanogenic activity of piperlongumine, and it showed the potent antimelanogenic activity at the concentration of 1 μM. Altogether, piperlongumine has potent antimelanogenic activity, and these results support it as a candidate for natural depigmentation agent in a cosmetic and pharmaceutical industries.

scholarly journals L-765,314 Suppresses Melanin Synthesis by Regulating Tyrosinase Activity

Molecules ◽  
2019 ◽  
Vol 24 (4) ◽  
pp. 773 ◽  
Author(s):  
Jinhwan Kim ◽  
Yo-Han Kim ◽  
Seunghyun Bang ◽  
Hanju Yoo ◽  
InKi Kim ◽  
...  
Keyword(s):  
Defense Mechanism ◽  
Tyrosinase Activity ◽  
Dependent Manner ◽  
Skin Damage ◽  
B16f10 Melanoma ◽  
Melanin Production ◽  
Self Defense ◽  
Kinase C ◽  
Promising Strategy ◽  
Dose Dependent

Although melanin production is a key self-defense mechanism against ultraviolet radiation (UVR)-induced skin damage, uneven or excessive deposition of melanin causes hyperpigmentary disorders. Currently available whitening agents are unsatisfactory because of issues with efficacy and safety. To develop more effective depigmenting agents, we performed high-throughput melanin content assay screening using the B16F10 melanoma cell line and identified L-765,314 as a drug that suppressed melanin production in cultured melanocytes in a dose-dependent manner as well as cAMP- or 12-O-tetradecanoylphorbol 13-acetate (TPA)-stimulated melanin production without cytotoxicity. Interestingly, melanogenic gene expression was not altered by L-765,314. Rather, diminished melanin production by L-765,314 appeared to be caused by downregulation of tyrosinase activity via inhibition of protein kinase C (PKC). Because L-765,314 did not show any adverse effect in melanocytes, altogether our data suggest that L-765,314 could be a potential therapeutic candidate for skin hyperpigmentary disorders and further discovery of selective inhibitors targeting PKC might be a promising strategy for the development of depigmenting agents to treat hyperpigmentary disorders.

scholarly journals Pleurochrysis carterae Hot-Water Extract Inhibits Melanogenesis in Murine Melanoma Cells

Cosmetics ◽  
2019 ◽  
Vol 6 (4) ◽  
pp. 60
Author(s):  
Kazuomi Sato ◽  
Yuji Yamaguchi ◽  
Setsuko Sakaki ◽  
Hiroyuki Takenaka
Keyword(s):  
Water Extract ◽  
Melanoma Cells ◽  
Hot Water ◽  
Mrna Levels ◽  
Dependent Manner ◽  
Melanin Synthesis ◽  
B16f10 Melanoma ◽  
Hot Water Extract ◽  
B16f10 Melanoma Cells ◽  
Pleurochrysis Carterae

In this study, we examined the effect of a hot-water extract of coccolithophore Pleurochrysis carterae on melanogenesis in B16F1 and B16F10 melanoma cells. P. carterae extract inhibited the α-melanocyte-stimulating hormone (α-MSH)-enhanced melanin synthesis in B16F1 melanoma cells. P. carterae also inhibited unstimulated melanin synthesis in B16F10 melanoma cells. Western blotting showed that the P. carterae extract inhibited tyrosinase and microphthalmia-associated transcription factor (MITF) in a dose-dependent manner. The reporter assay also revealed a decline in the tyrosinase promoter activity in the presence of P. carterae extract. Furthermore, quantitative real-time RT-PCR analysis showed that P. carterae extract downregulated the mRNA levels of tyrosinase and MITF. Finally, our study demonstrated that the hot-water extract of P. carterae inhibits melanin synthesis via the down-regulation of MITF mRNA level. Our findings indicate that P. carterae extract could be a possible cosmetic ingredient.

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