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两种源自甲胎蛋白的肽的抗前列腺癌和抗乳腺癌活性

Anti-prostate cancer and anti-breast cancer activities of two peptides derived from alpha-fetoprotein.

作者信息

Caceres Gisela, Dauphinee Michael J, Eisele Leslie E, MacColl Robert, Mizejewski Gerald J

机构信息

Rumbaugh-Goodwin Institute for Cancer Research, Inc., 1850 NW 69th Avenue, Suite 5, Plantation, Florida 33313, USA.

出版信息

Anticancer Res. 2002 Sep-Oct;22(5):2817-20.

Abstract

A chemically synthesized 34-amino-acid peptide and a select analog have been studied to determine their activities against the growth of prostate and breast cancer tumors. It was of interest to determine if the peptide has anti-prostate cancer activity. Previously, the peptide was shown to inhibit the growth of breast cancer tumor cells. The peptide inhibited the growth of both breast and prostate tumors. A novel experimental design for the peptide was in a study in which a time-release pellet was used to give daily peptide doses to mice that were subjected to a breast cancer tumor. The peptide was effective in inhibiting the growth of tumors in the mice. The 2 C-->2 A analog peptide, in which the two cysteines were replaced by alanines, was also active in inhibition of the growth of prostate and breast cancer cell lines and in an in vivo assay against breast cancer. A scrambled amino acid sequence of the peptide was used as a control in these tumor studies, and it had virtually no anti-cancer activity.

摘要

一种化学合成的34个氨基酸的肽及其一种特定类似物已被研究,以确定它们对前列腺癌和乳腺癌肿瘤生长的活性。确定该肽是否具有抗前列腺癌活性很有意义。此前,该肽已被证明可抑制乳腺癌肿瘤细胞的生长。该肽抑制了乳腺癌和前列腺癌肿瘤的生长。该肽的一种新颖实验设计是在一项研究中,使用缓释微丸向患有乳腺癌肿瘤的小鼠每日给予肽剂量。该肽在抑制小鼠肿瘤生长方面有效。2 C→2 A类似物肽(其中两个半胱氨酸被丙氨酸取代)在抑制前列腺癌和乳腺癌细胞系生长以及针对乳腺癌的体内试验中也具有活性。该肽的一个氨基酸序列打乱的序列在这些肿瘤研究中用作对照,它几乎没有抗癌活性。

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