Targeting Nitric Oxide: Say NO to Metastasis

Author:

Reddy Tejaswini P.123ORCID,Glynn Sharon A.4ORCID,Billiar Timothy R.5ORCID,Wink David A.6ORCID,Chang Jenny C.23ORCID

Affiliation:

1. 1Texas A&M University Health Science Center, Bryan, Texas.

2. 2Houston Methodist Research Institute, Houston, Texas.

3. 3Houston Methodist Neal Cancer Center, Houston, Texas.

4. 4Prostate Cancer Institute, National University of Ireland Galway, Galway, Ireland.

5. 5Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

6. 6Cancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute, National Institute of Health, Frederick, Maryland.

Abstract

Abstract Utilizing targeted therapies capable of reducing cancer metastasis, targeting chemoresistant and self-renewing cancer stem cells, and augmenting the efficacy of systemic chemo/radiotherapies is vital to minimize cancer-associated mortality. Targeting nitric oxide synthase (NOS), a protein within the tumor microenvironment, has gained interest as a promising therapeutic strategy to reduce metastatic capacity and augment the efficacy of chemo/radiotherapies in various solid malignancies. Our review highlights the influence of nitric oxide (NO) in tumor progression and cancer metastasis, as well as promising preclinical studies that evaluated NOS inhibitors as anticancer therapies. Lastly, we highlight the prospects and outstanding challenges of using NOS inhibitors in the clinical setting.

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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