4.1 Article

HIF-1α siRNA and Cisplatin in Combination SuppressTumor Growth in a Nude Mice Model of Esophageal Squamous Cell Carcinoma

Journal

ASIAN PACIFIC JOURNAL OF CANCER PREVENTION
Volume 13, Issue 2, Pages 473-477

Publisher

ASIAN PACIFIC ORGANIZATION CANCER PREVENTION
DOI: 10.7314/APJCP.2012.13.2.473

Keywords

RNA interference; HIF-1 alpha; cisplatin; esophageal squamous cell carcinoma

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Funding

  1. Natural Science Foundation for Doctoral Initiating Research of Guangdong Province [06300768]

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Introduction: The esophagus squamous cell carcinoma (ESCC) is one of the most deadly malignances, and a current challenge is the development of effective therapeutic agents. Our present work addressed the effect of HIF-1 alpha siRNA alone or in combination with cisplatin on the growth of ESCC in nude mice. Materials and Methods: Xenografts were established by inoculating ESCC TE-1 cells in nude mice, and transplanted tumors were treated with HIF-1 alpha siRNA, cisplatin alone or together. Growth was assessed by measuring tumor volume. HIF-1 alpha mRNA and protein expression were detected using RT-PCR and immunohistochemistry, respectively. Apoptosis of ESCC TE-1 cells was analyzed by flow cytometry. Results: In our nude mice model, HIF-1 alpha siRNA effectively inhibited the growth of transplanted ESCC, downregulating HIF-1 alpha mRNA and protein expression, and inducing ESCC TE-1 cell apoptosis. Notably when combinated with cisplatin, HIF-1 alpha siRNA showed synergistic interaction in suppressing tumor growth. Furthermore, the proportion of apoptotic cells in HIF-1 alpha siRNA plus cisplatin group was significantly higher than that in cisplatin or HIF-1 alpha siRNA-treated groups (P<0.05). Conclusions: Down-regulated HIF-1 alpha expression induced by siRNA could effectively suppress the growth of transplanted ESCC in vivo. HIF-1 alpha siRNA could enhance the cytotoxicity of cisplatin, which suggests that a combination of these two agents may have potential for therapy of advanced ESCC.

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