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Article

ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC

  • Authors:
    • Qijian Cheng
    • Ling Zhou
    • Jianping Zhou
    • Huanying Wan
    • Qingyun Li
    • Yun Feng
  • View Affiliations / Copyright

    Affiliations: Department of Respiration, Ruijin Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200025, P.R. China
  • Pages: 1403-1410
    |
    Published online on: July 22, 2016
       https://doi.org/10.3892/or.2016.4967
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Abstract

Angiotensin II (AngII) is a multifunctional bioactive peptide in the renin-angiotensin system (RAS). Angiotensin-converting enzyme 2 (ACE2) is a newly identified component of RAS. We previously reported that ACE2 overexpression may inhibit cell growth and vascular endothelial growth factor (VEGF) production in vitro and in vivo. In the present study, we investigated the effect of ACE2 on tumor-associated angiogen­esis after the development of acquired platinum resistance in non-small cell lung cancer (NSCLC). Four NSCLC cell lines, A549, LLC, A549-DDP and LLC-DDP, were used in vitro, while A549 and A549-DDP cells were used in vivo. A549-DDP and LLC-DDP cells were newly established at our institution as acquired platinum-resistant sublines by culturing the former parent cells in cisplatin (CDDP)-containing conditioned medium for 6 months. These platinum-resistant cells showed significantly higher angiotensin II type 1 receptor (AT1R), ACE and VEGF production and lower ACE2 expression than their corresponding parent cells. We showed that ACE2 overexpression inhibited the production of VEGF in vitro and in vivo compared to their corresponding parent cells. We also found that ACE2 overexpression reduced the expression of AT1R and ACE. Additionally, we confirmed that ACE2 overexpres­sion inhibited cell growth and VEGF production while simultaneously suppressing ACE and AT1R expression in human lung cancer xenografts. Our findings indicate that ACE2 overexpression may potentially suppress angiogenesis in NSCLC after the development of acquired platinum resistance.
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Copy and paste a formatted citation
Spandidos Publications style
Cheng Q, Zhou L, Zhou J, Wan H, Li Q and Feng Y: ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC. Oncol Rep 36: 1403-1410, 2016.
APA
Cheng, Q., Zhou, L., Zhou, J., Wan, H., Li, Q., & Feng, Y. (2016). ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC. Oncology Reports, 36, 1403-1410. https://doi.org/10.3892/or.2016.4967
MLA
Cheng, Q., Zhou, L., Zhou, J., Wan, H., Li, Q., Feng, Y."ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC". Oncology Reports 36.3 (2016): 1403-1410.
Chicago
Cheng, Q., Zhou, L., Zhou, J., Wan, H., Li, Q., Feng, Y."ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC". Oncology Reports 36, no. 3 (2016): 1403-1410. https://doi.org/10.3892/or.2016.4967
Copy and paste a formatted citation
x
Spandidos Publications style
Cheng Q, Zhou L, Zhou J, Wan H, Li Q and Feng Y: ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC. Oncol Rep 36: 1403-1410, 2016.
APA
Cheng, Q., Zhou, L., Zhou, J., Wan, H., Li, Q., & Feng, Y. (2016). ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC. Oncology Reports, 36, 1403-1410. https://doi.org/10.3892/or.2016.4967
MLA
Cheng, Q., Zhou, L., Zhou, J., Wan, H., Li, Q., Feng, Y."ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC". Oncology Reports 36.3 (2016): 1403-1410.
Chicago
Cheng, Q., Zhou, L., Zhou, J., Wan, H., Li, Q., Feng, Y."ACE2 overexpression inhibits acquired platinum resistance-induced tumor angiogenesis in NSCLC". Oncology Reports 36, no. 3 (2016): 1403-1410. https://doi.org/10.3892/or.2016.4967
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