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通过抑制多巴脱羧酶增强左旋多巴掺入黑色素瘤的能力。

Enhancement of L-dopa incorporation into melanoma by dopa decarboxylase inhibition.

作者信息

Wick M M, Kramer R A, Gorman M

出版信息

J Invest Dermatol. 1978 Jun;70(6):358-60. doi: 10.1111/1523-1747.ep12543559.

Abstract

Melanoma cells possess a special biochemical pathway for the conversion of L-dopa to melanin. Selective incorparation of exogenous L-dopa into melanoma cells in vivo has been limited by extensive decarboxylation to dopamine. Pretreatment of animals bearing the S-91 Cloudman or ACI melanomas with Ro4-4602, a potent dopa decarboxylase inhibitor limited incorporation of label into adrenal tissue and enhanced entry of label into tumor. Six hours following pretreatment, the ratio of tumor to adrenal specific activities was altered from 0.25 to 1.5 for the S-91 melanoma and 0.68 to 1.99 for the ACI melanoma indicating diversion of metabolism away from catecholamine formation. The possibility of a selective diagnostic and/or therapeutic approach is proposed.

摘要

黑色素瘤细胞拥有一条将左旋多巴转化为黑色素的特殊生化途径。外源性左旋多巴在体内选择性掺入黑色素瘤细胞的过程一直受到广泛脱羧转化为多巴胺的限制。用强效多巴脱羧酶抑制剂Ro4 - 4602对携带S - 91克劳德曼或ACI黑色素瘤的动物进行预处理,可限制标记物掺入肾上腺组织,并增强标记物进入肿瘤的能力。预处理6小时后,S - 91黑色素瘤的肿瘤与肾上腺比活性从0.25变为1.5,ACI黑色素瘤从0.68变为1.99,这表明代谢从儿茶酚胺形成方向发生了转移。文中提出了一种选择性诊断和/或治疗方法的可能性。

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