Literature DB >> 24524765

Angiotensin-(1-7): a peptide hormone with anti-cancer activity.

P E Gallagher, A L Arter, G Deng, E A Tallant1.   

Abstract

The development of peptides as therapeutic agents has progressed such that these small molecules of less than fifty amino acids are currently in use for the treatment of a variety of pathologies. This review focuses on the pre-clinical studies and clinical trials assessing the anti-cancer properties of angiotensin-(1-7) [Ang-(1-7)], an endogenous heptapeptide hormone of the renin-angiotensin system. Ang-(1-7) mediates biological responses by activating mas, a unique G protein- coupled receptor, thereby providing specific targeted actions when used as a therapeutic agent. Studies in in vitro as well as in vivo mouse models demonstrated that the heptapeptide hormone reduced proliferation of human cancer cells and xenograft tumors. This attenuation was concomitant with decreased angiogenesis, cancer associated fibrosis, osteoclastogenesis, tumor-induced inflammation and metastasis as well as altered regulation of growth promoting cellular signaling pathways. In three clinical trials, Ang-(1-7) was well tolerated with limited toxic or quality-of-life side effects and showed clinical benefit in cancer patients with solid tumors. Taken together, these studies suggest that Ang-(1-7) may serve as a first-in-class peptide chemotherapeutic agent, reducing cancer growth and metastases by pleiotrophic mechanisms as well as targeting the tumor microenvironment.

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Year:  2014        PMID: 24524765     DOI: 10.2174/0929867321666140205133357

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  15 in total

Review 1.  Fetal programming and the angiotensin-(1-7) axis: a review of the experimental and clinical data.

Authors:  Andrew M South; Hossam A Shaltout; Lisa K Washburn; Alexa S Hendricks; Debra I Diz; Mark C Chappell
Journal:  Clin Sci (Lond)       Date:  2019-01-08       Impact factor: 6.124

2.  Angiotensin-(1-7): A Novel Peptide to Treat Hypertension and Nephropathy in Diabetes?

Authors:  Ranjit Singh Padda; Yixuan Shi; Chao-Sheng Lo; Shao-Ling Zhang; John S D Chan
Journal:  J Diabetes Metab       Date:  2015-10-14

3.  Identification of dipeptidyl peptidase 3 as the Angiotensin-(1-7) degrading peptidase in human HK-2 renal epithelial cells.

Authors:  Nildris Cruz-Diaz; Bryan A Wilson; Nancy T Pirro; K Bridget Brosnihan; Allyson C Marshall; Mark C Chappell
Journal:  Peptides       Date:  2016-06-15       Impact factor: 3.750

4.  Stabilization of Angiotensin-(1-7) by key substitution with a cyclic non-natural amino acid.

Authors:  Anita Wester; Marc Devocelle; E Ann Tallant; Mark C Chappell; Patricia E Gallagher; Francesca Paradisi
Journal:  Amino Acids       Date:  2017-07-25       Impact factor: 3.789

Review 5.  The ACE2/Angiotensin-(1-7)/Mas Receptor Axis: Pleiotropic Roles in Cancer.

Authors:  Juanjuan Xu; Jinshuo Fan; Feng Wu; Qi Huang; Mengfei Guo; Zhilei Lv; Jieli Han; Limin Duan; Guorong Hu; Lian Chen; Tingting Liao; Wanli Ma; Xiaonan Tao; Yang Jin
Journal:  Front Physiol       Date:  2017-05-08       Impact factor: 4.566

6.  AAV-Mediated angiotensin 1-7 overexpression inhibits tumor growth of lung cancer in vitro and in vivo.

Authors:  Xinglu Chen; Sansan Chen; Nana Pei; Yingying Mao; Shengyao Wang; Renhe Yan; Na Bai; Andrew Li; Yanling Zhang; Hongyan Du; Baihong Chen; Colin Sumners; Jinlong Li; Hongwei Li
Journal:  Oncotarget       Date:  2017-01-03

7.  The pentapeptide Gly-Thr-Gly-Lys-Thr confers sensitivity to anti-cancer drugs by inhibition of CAGE binding to GSK3β and decreasing the expression of cyclinD1.

Authors:  Youngmi Kim; Hyuna Kim; Deokbum Park; Hansoo Lee; Yun Sil Lee; Jongseon Choe; Young Myeong Kim; Doyong Jeon; Dooil Jeoung
Journal:  Oncotarget       Date:  2017-02-21

Review 8.  Involvement of ACE2/Ang-(1-7)/MAS1 Axis in the Regulation of Ovarian Function in Mammals.

Authors:  Kamila Domińska
Journal:  Int J Mol Sci       Date:  2020-06-27       Impact factor: 5.923

9.  Transactivation of ErbB Family of Receptor Tyrosine Kinases Is Inhibited by Angiotensin-(1-7) via Its Mas Receptor.

Authors:  Saghir Akhtar; Bindu Chandrasekhar; Sreeja Attur; Gursev S Dhaunsi; Mariam H M Yousif; Ibrahim F Benter
Journal:  PLoS One       Date:  2015-11-04       Impact factor: 3.240

Review 10.  The Meaning of Mas.

Authors:  Michael Bader; Natalia Alenina; Dallan Young; Robson A S Santos; Rhian M Touyz
Journal:  Hypertension       Date:  2018-11       Impact factor: 10.190

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