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4-S-半胱氨酰苯酚对黑鼠毛囊黑素细胞的选择性细胞毒性:其应用于黑色素瘤化疗的合理依据。

Selective cytotoxicity of 4-S-cysteaminylphenol on follicular melanocytes of the black mouse: rational basis for its application to melanoma chemotherapy.

作者信息

Ito Y, Jimbow K

出版信息

Cancer Res. 1987 Jun 15;47(12):3278-84.

PMID:3107807
Abstract

We have previously shown that 4-S-cysteaminylphenol (4-S-CAP) causes a significant inhibition of in vivo melanoma growth. To clarify the mechanism of the in vivo antimelanoma effect, this study evaluated the cellular and subcellular changes of follicular melanocytes after s.c. administration of 4-S-CAP on the lumbar areas of black and albino mice. 4-S-CAP produced a prompt, selective swelling and lysis of melanocytes, resulting eventually in the necrosis of melanocytes and the depigmentation of black hair follicles. None of the degenerative changes were seen in melanocytes and keratinocytes of control albino follicles. Comparison of melanocytes in black and albino follicles revealed that melanin synthesis is highly active in the melanocytes of black follicles while melanin and tyrosinase synthesis is not seen in the melanocytes of albino follicles. The findings indicate that the selective melanocytotoxicity of 4-S-CAP is manifested by lysis and necrosis of cells which are actively engaged in melanin synthesis. 4-S-CAP appears to provide a new modality for rational chemotherapy of malignant melanoma.

摘要

我们之前已经表明,4-S-半胱氨酰苯酚(4-S-CAP)能显著抑制体内黑色素瘤的生长。为了阐明其体内抗黑色素瘤作用的机制,本研究评估了在黑色和白化小鼠的腰部皮下注射4-S-CAP后,毛囊黑素细胞的细胞和亚细胞变化。4-S-CAP可使黑素细胞迅速、选择性地肿胀并溶解,最终导致黑素细胞坏死和黑色毛囊色素脱失。对照白化毛囊的黑素细胞和角质形成细胞未见任何退行性变化。对黑色和白化毛囊中的黑素细胞进行比较发现,黑色毛囊中的黑素细胞黑色素合成高度活跃,而白化毛囊中的黑素细胞未见黑色素和酪氨酸酶合成。这些发现表明,4-S-CAP的选择性黑素细胞毒性表现为活跃参与黑色素合成的细胞的溶解和坏死。4-S-CAP似乎为恶性黑色素瘤的合理化疗提供了一种新的方法。

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Selective cytotoxicity of 4-S-cysteaminylphenol on follicular melanocytes of the black mouse: rational basis for its application to melanoma chemotherapy.4-S-半胱氨酰苯酚对黑鼠毛囊黑素细胞的选择性细胞毒性:其应用于黑色素瘤化疗的合理依据。
Cancer Res. 1987 Jun 15;47(12):3278-84.
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引用本文的文献

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A Sulfur Containing Melanogenesis Substrate, -Pr-4--CAP as a Potential Source for Selective Chemoimmunotherapy of Malignant Melanoma.一种含硫黑色素生成底物,-Pr-4--CAP,有望成为恶性黑素瘤选择性化学免疫治疗的潜在来源。
Int J Mol Sci. 2023 Mar 9;24(6):5235. doi: 10.3390/ijms24065235.
2
Molecular Events in the Melanogenesis Cascade as Novel Melanoma-Targeted Small Molecules: Principle and Development.黑色素生成级联反应中的分子事件作为新型黑色素瘤靶向小分子:原理与开发
Cancers (Basel). 2022 Nov 14;14(22):5588. doi: 10.3390/cancers14225588.
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Immunomodulation of Melanoma by Chemo-Thermo-Immunotherapy Using Conjugates of Melanogenesis Substrate NPrCAP and Magnetite Nanoparticles: A Review.
用黑色素生成底物 NPrCAP 和磁铁纳米粒子的化学-热-免疫疗法对黑色素瘤的免疫调节:综述。
Int J Mol Sci. 2022 Jun 9;23(12):6457. doi: 10.3390/ijms23126457.
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Melanoma-targeted chemo-thermo-immuno (CTI)-therapy using N-propionyl-4-S-cysteaminylphenol-magnetite nanoparticles elicits CTL response via heat shock protein-peptide complex release.使用 N-丙酰基-4-S-半胱氨酸基苯酚-磁铁矿纳米粒子进行黑素瘤靶向化疗-热疗-免疫(CTI)治疗,通过热休克蛋白-肽复合物的释放引发 CTL 反应。
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