Suppr超能文献

四种肽通过环鸟苷酸降低人结肠腺癌细胞数量并抑制DNA合成。

Four peptides decrease human colon adenocarcinoma cell number and DNA synthesis via cyclic GMP.

作者信息

Gower William R, Vesely Brian A, Alli Abdel A, Vesely David L

机构信息

Department of Internal Medicine, University of South Florida Cardiac Hormone Center and James A. Haley Veterans Medical Center, Tampa, 33612, USA.

出版信息

Int J Gastrointest Cancer. 2005;36(2):77-87. doi: 10.1385/IJGC:36:2:77.

Abstract

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.

摘要

背景

结肠癌导致的死亡率很高,在2005年,采用当前的治疗方法预计有30350人死于结肠癌。长效利钠肽、血管扩张肽、促尿钾排泄肽和心房利钠肽在乳腺癌和胰腺腺癌中具有显著的抗癌作用。

研究目的

这些肽类激素在结肠腺癌细胞中是否具有抗癌作用,以及这些作用是否由环磷酸鸟苷(cGMP)特异性介导,目前尚未确定。

方法

评估这些肽类激素在人结肠腺癌细胞中的抗癌作用,并确定其抗癌作用是否由cGMP特异性介导。

结果

用1 mM的这些肽类激素处理后,24小时内结肠腺癌细胞数量减少了89% - 97%(每种肽激素的p值均<0.001)。这四种肽激素浓度从1 microM增加到1000 microM(即1 mM),每增加10倍,人结肠癌细胞数量就显著减少(p <0.05),且在减少后3天内无任何增殖。同样这些激素使DNA合成减少了65% - 83%(p <0.001)。cGMP抗体抑制了这些肽减少结肠腺癌细胞数量能力的75% - 80%,抑制了其DNA合成作用的92% - 96%以及cGMP作用的97%。蛋白质免疫印迹法首次揭示结肠腺癌细胞中存在利钠肽受体(NPR)A和C。

结论

四种肽类激素在24小时内可消除高达97%的结肠癌细胞,其DNA效应由cGMP特异性介导。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验