四种肽通过环GMP减少人大肠癌细胞数量和DNA合成。

William R Gower, Brian A Vesely, Abdel A Alli, David L Vesely
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引用次数: 41

摘要

背景:结肠癌的死亡率很高,在目前的治疗下,2005年预计有30,350例结肠癌死亡。长效利钠肽、血管扩张剂、钾利尿肽和心房利钠肽对乳腺癌和胰腺腺癌有显著的抗癌作用。研究目的:目前尚不清楚这些肽激素对结肠癌细胞是否具有抗癌作用,以及这种作用是否由环GMP特异性介导。方法:评价这些肽激素对人结肠腺癌细胞的抗癌作用,并确定其抗癌作用是否由环GMP特异性介导。结论:4种肽激素可在24 h内清除高达97%的结肠癌细胞,其DNA作用是由环GMP特异性介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Four peptides decrease human colon adenocarcinoma cell number and DNA synthesis via cyclic GMP.

Background: Mortality from colon cancer is significant with an expected 30,350 colon cancer deaths in 2005 with current treatment(s). Long-acting natriuretic peptide, vessel dilator, kaliuretic peptide, and atrial natriuretic peptide have significant anticancer effects in breast and pancreatic adenocarcinomas.

Aim of study: Whether these peptide hormones have anticancer effects in colon adenocarcinoma cells and whether these effects are specifically mediated by cyclic GMP has not been determined.

Methods: These peptide hormones were evaluated for anticancer effects in human colon adenocarcinoma cells and to determine whether their anticancer effects are specifically mediated by cyclic GMP.

Results: There was a 89-97% decrease (p <0.001 for each) in colon adenocarcinoma cells within 24 h with 1 mM of these peptide hormones. There was a significant (p <0.05) decrease in human colon cancer cell number with each 10-fold increase in concentration from 1 to 1,000 microM (i.e., 1 mM) of these four peptide hormones without any proliferation in the 3 d following this decrease. These same hormones decreased DNA synthesis 65-83% (p <0.001). Cyclic GMP antibody inhibited 75- 80% of these peptides' ability to decrease colon adenocarcinoma cell number and inhibited 92-96% of their DNA synthesis effects and 97% of cyclic GMP's effects. Western blots revealed that for the first time natriuretic peptide receptors (NPR) A and C were present in colon adenocarcinoma cells.

Conclusions: Four peptide hormones eliminate up to 97% of colon cancer cells within 24 h with their DNA effects specifically mediated by cyclic GMP.

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