<abstract xmlns="http://www.w3.org/1999/xhtml"> Background: Epithelial to mesenchymal transition (EMT) not only confers tumor cells with a distinct advantage for metastatic dissemination, but also it provides tumor cells for proliferation and chemotherapy resistance. Thus, inhibiting this process using single or multiple agents, remains a field of intensive research. The development of EMT has been implicated in not only conferring cancer cells distant metastasis, but also providing tumor cells advantages for proliferation and chemotherapy resistance.Objective: We investigated whether axitinib synergistic interaction with AG490 could effectively block the growth and EMT-mediated tumor metastasis in cervical cancer in vitro.Methods: We addressed synergism effects on tumor growth, axitinib, AG490 alone and in any possible combinations on cell viability, apoptosis and cell cycle distribution were evaluated by XTT assay, Annexin V/propidium iodide staining and flow cytometric analysis. To assess how combination therapy affected chemotactic motility in tumor cells, wound-healing migration and the Boyden chamber invasion assays were applied in vitro. Further, using western blots, the key signaling molecules and pathways in response to axitinib and AG490 combination treatment in anti tumor growth and anti EMT-mediated tumor metastasis were analyzed in Hela cells.Results: Therapy with axitinib and AG490 resulted in strong synergistic inhibition of proliferation, migration and cell cycle arrest without potently effect on apoptosis induction relative to AG490 monotherapy and control in vitro. Furthermore, phosphorylation of VEGFR2 (Tyr1175), JAK2 (Tyr1007/1008) and STAT3 (Tyr705) was completely blocked in parallel with significant reduction expressions of N-cadherin and obvious enhancement levels of E-cadherin through down-regulating Snail responding to combination treatment in cervical cancer cells.Conclusion:We first provided evidences that combination therapy of axitinib and AG490 significantly enhances anti-tumor effect via VEGFR2/JAK2/STAT3 signaling mediated growth arrest and EMT-mediated tumor metastasis inhibition, holds promise for an efficacious treatment of these advanced patients.</abstract>

Background: Epithelial to mesenchymal transition (EMT) not only confers tumor cells with a distinct advantage for metastatic dissemination, but also it provides tumor cells for proliferation and chemotherapy resistance. Thus, inhibiting this process using single or multiple agents, remains a field of intensive research. The development of EMT has been implicated in not only conferring cancer cells distant metastasis, but also providing tumor cells advantages for proliferation and chemotherapy resistance.Objective: We investigated whether axitinib synergistic interaction with AG490 could effectively block the growth and EMT-mediated tumor metastasis in cervical cancer in vitro.Methods: We addressed synergism effects on tumor growth, axitinib, AG490 alone and in any possible combinations on cell viability, apoptosis and cell cycle distribution were evaluated by XTT assay, Annexin V/propidium iodide staining and flow cytometric analysis. To assess how combination therapy affected chemotactic motility in tumor cells, wound-healing migration and the Boyden chamber invasion assays were applied in vitro. Further, using western blots, the key signaling molecules and pathways in response to axitinib and AG490 combination treatment in anti tumor growth and anti EMT-mediated tumor metastasis were analyzed in Hela cells.Results: Therapy with axitinib and AG490 resulted in strong synergistic inhibition of proliferation, migration and cell cycle arrest without potently effect on apoptosis induction relative to AG490 monotherapy and control in vitro. Furthermore, phosphorylation of VEGFR2 (Tyr1175), JAK2 (Tyr1007/1008) and STAT3 (Tyr705) was completely blocked in parallel with significant reduction expressions of N-cadherin and obvious enhancement levels of E-cadherin through down-regulating Snail responding to combination treatment in cervical cancer cells.Conclusion:We first provided evidences that combination therapy of axitinib and AG490 significantly enhances anti-tumor effect via VEGFR2/JAK2/STAT3 signaling mediated growth arrest and EMT-mediated tumor metastasis inhibition, holds promise for an efficacious treatment of these advanced patients.

Enhanced antitumor effect of axitinib synergistic interaction with AG490 via VEGFR2/JAK2/STAT3 signaling mediated epithelial-mesenchymal transition in cervical cancer in vitro

Department of Gynecology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200092, China

Department of Gynecology, Changhai Hospital, Second Military Medical University, Shanghai 200433,

Department of Gynecology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200092,

MD, Department of Gynecology, Changhai Hospital, Second Military Medical University, Shanghai 200433,

MD, Department of Gynecology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200092,

Asian Biomedicine

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Background: Epithelial to mesenchymal transition (EMT) not only confers tumor cells with a distinct advantage for metastatic dissemination, but also it...

Enhanced antitumor effect of axitinib synergistic interaction with AG490 via VEGFR2/JAK2/STAT3 signaling mediated epithelial-mesenchymal transition in cervical cancer in vitro

Article Category: Original article

Online veröffentlicht: 04. Feb. 2017

Seitenbereich: 39 - 49

DOI: https://doi.org/10.5372/1905-7415.0701.149

Schlüsselwörter
AG490, axitinib, EMT, Hela cells, JAK2, STAT3, VEGFR2

© 2017

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Enhanced antitumor effect of axitinib synergistic interaction with AG490 via VEGFR2/JAK2/STAT3 signaling mediated epithelial-mesenchymal transition in cervical cancer in vitro

Article Category: Original article

Online veröffentlicht: 04. Feb. 2017

Seitenbereich: 39 - 49

DOI: https://doi.org/10.5372/1905-7415.0701.149

SchlüsselwörterAG490, axitinib, EMT, Hela cells, JAK2, STAT3, VEGFR2

© 2017

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Schlüsselwörter
AG490, axitinib, EMT, Hela cells, JAK2, STAT3, VEGFR2