| Literature DB >> 29331419 |
Hamed Mirzaei1, Hossein Salehi2, Reza Kazemi Oskuee1, Ali Mohammadpour3, Hamid Reza Mirzaei4, Mohammad Reza Sharifi5, Reza Salarinia6, Hossein Yousofi Darani7, Mojgan Mokhtari8, Aria Masoudifar9, Amirhossein Sahebkar10, Rasoul Salehi11, Mahmoud Reza Jaafari12.
Abstract
Interferon γ-induced protein 10 kDa (IP-10) is a potent chemoattractant and has been suggested to enhance antitumor activity and mediate tumor regression through multiple mechanisms of action. Multiple lines of evidence have indicated that genetically-modified adult stem cells represent a potential source for cell-based cancer therapy. In the current study, we assessed therapeutic potential of human adipose derived mesenchymal stem cells (hADSC) genetically-modified to express IP-10 for the treatment of lung metastasis in an immunocompetent mouse model of metastatic melanoma. A Piggybac vector encoding IP-10 was employed to transfect hADSC ex vivo. Expression and bioactivity of the transgenic protein from hADSCs expressing IP-10 were confirmed prior to in vivo studies. Our results indicated that hADSCs expressing IP-10 could inhibit the growth of B16F10 melanoma cells and significantly prolonged survival. Immunohistochemistry analysis, TUNEL assay and western blot analysis indicated that hADSCs expressing IP-10 inhibited tumor cell growth, hindered tumor infiltration of Tregs, restricted angiogenesis and significantly prolonged survival. In conclusion, our results demonstrated that targeting metastatic tumor sites by hADSC expressing IP-10 could reduce melanoma tumor growth and lung metastasis.Entities:
Keywords: CXCL10; Human adipose derived mesenchymal stem cells; Melanoma; Metastasis
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Year: 2018 PMID: 29331419 DOI: 10.1016/j.canlet.2018.01.029
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679