• 제목/요약/키워드: melan-A

검색결과 65건 처리시간 0.029초

개에서 발생한 구강 멜라닌결핍 악성흑색종 예 : Melan A 면역화학조직 염색 고찰 (Oral Amelanotic Malignant Melanoma in a Dog: Melan A Immunohistochemical Findings)

  • 강민희;박철;박희명
    • 한국임상수의학회지
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    • 제26권6호
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    • pp.612-615
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    • 2009
  • 10년령의 수컷 잡종견이 3개월 간의 구강내 궤양성 종양을 주증으로 내원하였다. 신체검사상 오른쪽 상악 잇몸에서 돌출된 구강내 종양이 관찰되었다. 내원당시 전이소견은 관찰되지 않았으며 구강 종양의 절제생검을 통한 조직검사결과 전반적인 상피양 세포와 일부 방추세포를 가진 전형적인 신경내분비종으로 의심되는 소견이 관찰되었다. 멜라닌 과립으로 추정되는 소견은 관찰되지 않았지만 악성종양에서 관찰되는 세포의 유사분열은 다수 관찰되었다. 확진을 위해 조직 절제 단면에 Melan A를 이용한 면역화학조직 염색을 실시하였으며, 그 결과는 강한 양성반응을 나타내었다. 조직검사와 조직면역염색을 통하여 종양은 멜라닌 결핍 악성흑색종으로 진단되었다. 결론적으로 본 증례의 경우 개에서 멜라닌결핍 악성흑색종의 진단에 Melan A를 이용한 면역화학조직염색이 유용함을 보여준다고 생각된다.

Sarsasapogenin Increases Melanin Synthesis via Induction of Tyrosinase and Microphthalmia-Associated Transcription Factor Expression in Melan-a Cells

  • Moon, Eun-Jung;Kim, Ae-Jung;Kim, Sun-Yeou
    • Biomolecules & Therapeutics
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    • 제20권3호
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    • pp.340-345
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    • 2012
  • Sarsasapogenin (SAR) is a steroidal sapogenin that is used as starting material for the industrial synthesis of steroids. It has various pharmacological benefits, such as antitumor and antidepressant activities. Since its effect on melanin biosynthesis has not been reported, we used murine melanocyte melan-a cells to investigate whether SAR influences melanogenesis. In this study, SAR significantly increased the melanin content of the melan-a cells from 1 to 10 ${\mu}M$. Based on an enzymatic activity assay using melan-a cell lysate, SAR had no effect on tyrosinase and DOPAchrome tautomerase activities. It also did not affect the protein expression of tyrosinase-related protein 1 and DOPAchrome tautomerase. However, protein levels of tyrosinase and microphthalmia-associated transcription factor were strongly stimulated by treatment with SAR. Therefore, our reports suggest that SAR treatment may induce melanogenesis through the stimulation of tyrosinase and microphthalmia-associated transcription factor expression in melan-a cells.

삼릉 에탄올추출물의 in vitro 피부 미백 유효성 (Effectiveness of Scirpi rhizoma Ethanol Extract on Skin Whitening Using in vitro Test)

  • 고주영;김영철
    • Environmental Analysis Health and Toxicology
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    • 제25권1호
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    • pp.69-77
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    • 2010
  • The purpose of this study is to evaluate the effectiveness of Scirpi rhizoma ethanol extract (SREE) on skin whitening using in vitro test. In the antioxidative activities, it was found that SREE contains 38.9 mg/g of polyphenol and 74.5 mg/g of flavonoid in total. In the electron donating ability, SREE showed a dose-dependent response, showing a high antioxidative capacity of 86.1% at 1000 ppm. It was found that the maximum permissible level of SREE to Melan-a cells was over 200 ppm, showing a quite low toxicity of SREE against Melan-a cells. Both in the inhibitory measurement for tyrosinase activity and melanogenesis using Melan-a cells, SREE presented a dose-dependent response with excellent efficacy.

두경부에서 발생한 점막피부 혈관근육지방종 3예 : HMB-45와 Melan-A에 대한 면역화학검사 특징 (Three Cases of Mucocutaneous Angiomyolipoma in the Head and Neck Region with Reference to the HMB-45 and Melan-A Immunohistochemistry)

  • 김나래;김동영;차흥억;하승연
    • 대한두경부종양학회지
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    • 제25권2호
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    • pp.150-152
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    • 2009
  • 혈관근육지방종은 지방, 평활근, 두꺼운 벽의 혈관이 다양한 비율로 구성된 흔하지 않은 과오종이며, 이는 결정 경화증을 동반하거나 산발적으로 발생한다. 저자들은 혈관근육지방종이 드물게 발생하는 두경부에서 발생한 귓바퀴 1예, 구개점막 2예의 혈관근육지방종을 보고하고자 한다. 병리소견상, 3예 모두에서 성숙지방조직, 불규칙한 혈관, 그리고 HMB-45와 Melan-A에 음성을 보이는 평활근육세포로 이루어진 조직소견을 보였으며, 여러군데에서 림프구 침윤이 3예 모두에서 관찰되었다. 점막피부 혈관근육지방종으로 진단하였다. 세증례 모두 결절경화증은 동반되지 않았다. 점막피부 혈관근육지방종에서는 혈관주변세포가 HMB-45와 Melan-A에서 음성을 보였으며, 이는 간이나 신장의 혈관근육지방종에서의 특징적인 양성반응과는 다른 점이었다. 간이나 신장에서 생긴 혈관근육지방종과 다른 임상병리적 특징을 비교 기술하고자 두경부에서 발생한 점막피부 혈관근육지방종 3예를 보고한다.

Quercetin이 Melan-a 멜라닌세포의 멜라닌합성에 미치는 영향 (Effect of Quercetin on Melanogenesis in Melan-a Melanocyte Cells)

  • 최원형;백승화;우원홍;천현자
    • 생약학회지
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    • 제33권3호통권130호
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    • pp.245-251
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    • 2002
  • Flavonoid seems to have various biological effects. Quercetin is a kind of natural plant flavonoids and has multiple biological effects such as antioxidant, antimutagenic and anticarcinogenec agent. Melanogenesis is a physiological process resulting in the synthesis of melanin pigments, which play a crucial protective role against skin photocarcinogenesis. This present study was designed to investigate effect of quercetin on proliferation and melanogenesis in Melan-a melanocyte cells. After 48h treatment of cells with quercetin, the cells exhibited a dose-dependent inhibition in their proliferation without apoptosis. Therefore, thε growth retardation by the extract may be due to the cell arrest or cell differentiation. We also investigated the effect of quercetin on melanogenesis of this cells. Melan-a melanocyte cells were grown for 48h in the presence of $0.01-60\;{\mu}g/ml$ quercetin and the total melanin content and activity of tyrosinase were measured. Quercetin stimulated melanization of the cells in low concentrations $(0.01-1.0\;{\mu}g/ml)$, whereas it inhibited melanization in high concentrations $(5.0-30\;{\mu}g/ml)$. It was observed that quercetin differently regulates melanogenesis of Melan-a melanocyte cells dependent on Its concentrations.

Detection of Circulating Melanoma Cells by a Two-marker Polymerase Chain Reaction Assay in Relation to Therapy

  • Bitisik, Ozlem;Camlica, Hakan;Duranyildiz, Derya;Tas, Faruk;Kurul, Sidika;Dalay, Nejat
    • BMB Reports
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    • 제36권2호
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    • pp.173-178
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    • 2003
  • Malignant melanoma is one of the most rapidly increasing cancer types, and patients with metastatic disease have a very poor prognosis. Detection of metastatic melanoma cells in circulation may aid the clinician in assessing tumor progression, metastatic potential, and response to therapy. Tyrosinase is a key enzyme in melanine biosynthesis. The gene is actively expressed in melanocytes and melanoma cells. Melan A is a differentiation antigen that is expressed in melanocytes. The presence of these molecules in blood is considered a marker for circulating melanoma cells. In this study, we analyzed the usefulness of this marker combination I evaluating the response to therapy in the blood of 30 patients with malignant melanoma. Circulating cells were detected by a reverse-transcriptase-polymerase-chain reaction. The tyrosinase expression was observed in 9 (30%) patients and Melan A in 19 (63.3%) patients before therapy. Following treatment, the tyrosinase mRNA was detected in only one patient, while Melan A transcripts were still present in 14 patients. We suggest that this molecular assay can identify circulating melanoma cells that express melanoma-associated antigens and may provide an early indication of therapy effectiveness.

도깨비부채 뿌리 추출물의 멜라닌 생성억제효과 (Inhibitory Effects of Root Extracts on Melanin Biosynthesis in Rodgersia podophylla A. Gray)

  • 최상윤;강난주;김호철
    • 한국약용작물학회지
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    • 제14권1호
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    • pp.27-30
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    • 2006
  • 도깨비 뿌리 추출물의 멜라닌 생성 억제효과를 검증하기 위하여 melan-a 세포주에서의 세포독성 및 멜라닌 생성량을 측정하고 멜라닌 생합성에 관여하는 주된 효소인 tyrosinase의 활성에 미치는 영향과 자외선에 대한 흡수도를 검색하여 다음과 같은 결과를 얻었다. 도깨비 뿌리 추출물을 $100\;{\mu}g/ml$ 농도로 melan-a 세포에 처리시 뚜렷한 독성 없이 멜라닌 생성을 24.6% 감소시켰으며 melan-a 세포로부터 추출된 tyrosinase 활성억제 효과실험에서 농도 의존적인 활성억제 효과를 보였다. 또한 도깨비 뿌리추출물은 일광화상의 원인인 UV-B 영역의 자외선을 흡수하였다. 이상의 결과를 바탕으로 볼 때 도깨비 부채 뿌리 추출물은 피부 미백 및 자외선 차단을 목적으로 하는 기능성 원료로써의 높은 활용 가능성을 가지는 것으로 판단된다.

소목의 부탄올 추출물에 의한 Melan-a 세포의 멜라닌생성 억제효과 (Inhibitory Effects of Butyl Alcohol Extract from Caesalpinia sappan L. on Melanogenesis in Melan-a Cells)

  • 황상구;이진선;백승화;전병훈;우원홍;천현자
    • 생약학회지
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    • 제33권2호통권129호
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    • pp.130-136
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    • 2002
  • Melanogenesis is a physiological process resulting in the synthesis of melanin pigments, which play a crucial protective role against skin photocarcinogenesis. The heart wood of Caesalpinia sappan L.(C. sappan) has long been commonly used in Oriental folk medicines to promote blood circulation, and as an emmenagogue, analgesic or anti-inflammatory agent as well as a remedy for thrombosis. From the heartwood, many constituents have been purified and among them, brazilin and hematoxylin are two of the most abundant. This present study was designed to investigate the inhibitory effect of butanol extract from C. sappan on proliferation and melanogenesis in Melan-a cells. After 48 h treatment of these cells with various concentrations of butanol extract, the cells showed a dose-dependent inhibition in their proliferation without apoptotic cell death. Therefore, the growth retardation by the extract may be due to the cell arrest or cell differentiation. We also estimated total melanin content as a final product and activity of tyrosinase, a key enzyme, of melanogenesis in Melan-a cells. The melanin content and tyrosinase activity were deσeased in extract-treated cells in a dose dependent manner compared to control group. The butanol extract also resulted in a decrease of melanin content in ${\alpha}-melanocyte-stimulating$ hormone (MSH)-induced melanogenesis, indicating that butanol extract of C. sappan could be developed as skin whitening components of cosmetics.

Modulation of Melanin Synthesis by Amaranthus spp. L Seed Extract in Melan-a Cells

  • Seo, Jae Ok;Do, Moon Ho;Lee, Jae Hak;Lee, Taek Hwan;Wahedi, Hussain Mustatab;Park, Yong Un;Kim, Sun Yeou
    • Natural Product Sciences
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    • 제22권3호
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    • pp.168-174
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    • 2016
  • Anti-melanogenic effects of amaranth (AT), one of the key source of squalene, were investigated in melanocytes. Amaranth seed powder was extracted with water and melan-a cells were treated with various concentrations of AT. By using HPLC, content of myo-inositol, one of potential active components, was measured in the crude extract of AT.AT reduced the melanin content in melan-a melanocytes and down-regulated melanogenic enzyme activity such as tyrosinase, TRP-1 and TRP-2. By regulating melanogenic enzyme activity, AT may be a potential natural source for whitening agent. Myo-inositol was detected in AT by HPLC and may be one of the active compounds from AT involved in the regulation of anti-melanogenesis. In this study, we demonstrated that AT has anti-melanogenesis properties. This new function of amaranth may be useful in the development of new skin-whitening products and its value as food.

오디씨 에탄올 추출물의 멜라닌 합성 억제효과 (Melanogenesis Inhibitory Activities of Mulberry Seed Ethanol Extracts)

  • 정용태;강민주;김진희
    • 대한화장품학회지
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    • 제41권3호
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    • pp.263-268
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    • 2015
  • 본 연구는 오디씨 에탄올 추출물(MSE)의 멜라닌 합성 저해 효과를 밝히는 것이다. 먼저 MSE의 melan-a 세포를 이용한 멜라닌 합성 저해 실험결과, 독성을 보이지 않는 $10{\mu}g/mL$의 농도까지 멜라닌 합성 저해 효과를 나타내었다. 또한 tyrosinase, tyrosinase-related protein-1 (TRP-1) 단백질의 발현이 저해되었으며, extracelluar signal-regulated protein kinase (ERK)의 발현을 농도 의존적으로 증가시키는 MSE의 기전을 확인하였다. 뿐만 아니라, 제브라피쉬를 이용한 in vivo 모델의 실험에서도 색소 발생이 저해됨을 관찰하였다. 따라서 오디씨로 부터 획득한 에탄올 추출물이 ERK 단백질의 발현으로 인해 멜라닌 생합성을 억제할 수 있음을 밝혔다.