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Article Open Access

In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein

  • Authors:
    • Li Tian
    • Xiaoli Wang
    • Xingyun Li
    • Ben Liu
    • Wei Zhang
    • Jing Cao
    • Anhong Ning
    • Min Huang
    • Mintao Zhong
  • View Affiliations / Copyright

    Affiliations: Department of Medical Microbiology, Dalian Medical University, Dalian, Liaoning 116044, P.R. China
    Copyright: © Tian et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 3153-3160
    |
    Published online on: September 8, 2016
       https://doi.org/10.3892/ol.2016.5106
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Abstract

Cancer is one of the most significant health problems worldwide and thus the development of novel therapeutic agents with fewer side effects is required. The present study investigated the in vitro anticancer effects of a newly isolated fungal protein. In this study, Latcripin‑15 (LP‑15) regulator of chromosome condensation 1 (RCC1) domain protein, which is obtained from the Lentinula edodes C91‑3 fungal strain, was identified, cloned, expressed, purified and re‑folded to assess the in vitro antitumor activity of the protein. LP‑15 RCC1 full‑length cDNA was isolated from Lentinula edodes using 3' and 5'‑rapid amplification of cDNA ends and then cloned, expressed, purified and re‑folded in vitro. In addition, the effects of the isolated LP‑15 RCC1 protein's functional domain on the viability and apoptosis of human lung cancer A549 cells were assessed by 3‑(4,5‑dimethylthiazol‑2‑yl)‑2,5‑diphenyltetrazolium bromide assay, transmission electron microscopy, flow cytometry and Hoechst 33258 staining. The LP‑15 RCC1 functional domain protein was successfully expressed, purified and re‑folded in vitro. Treatment with the LP‑15 RCC1 functional domain protein significantly reduced tumor cell viability and induced apoptosis in A549 cells. The results of the present study indicate that the LP‑15 RCC1 functional domain requires further investigation as a novel therapeutic agent for cancer therapy.
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Copy and paste a formatted citation
Spandidos Publications style
Tian L, Wang X, Li X, Liu B, Zhang W, Cao J, Ning A, Huang M and Zhong M: In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein. Oncol Lett 12: 3153-3160, 2016.
APA
Tian, L., Wang, X., Li, X., Liu, B., Zhang, W., Cao, J. ... Zhong, M. (2016). In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein. Oncology Letters, 12, 3153-3160. https://doi.org/10.3892/ol.2016.5106
MLA
Tian, L., Wang, X., Li, X., Liu, B., Zhang, W., Cao, J., Ning, A., Huang, M., Zhong, M."In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein". Oncology Letters 12.5 (2016): 3153-3160.
Chicago
Tian, L., Wang, X., Li, X., Liu, B., Zhang, W., Cao, J., Ning, A., Huang, M., Zhong, M."In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein". Oncology Letters 12, no. 5 (2016): 3153-3160. https://doi.org/10.3892/ol.2016.5106
Copy and paste a formatted citation
x
Spandidos Publications style
Tian L, Wang X, Li X, Liu B, Zhang W, Cao J, Ning A, Huang M and Zhong M: In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein. Oncol Lett 12: 3153-3160, 2016.
APA
Tian, L., Wang, X., Li, X., Liu, B., Zhang, W., Cao, J. ... Zhong, M. (2016). In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein. Oncology Letters, 12, 3153-3160. https://doi.org/10.3892/ol.2016.5106
MLA
Tian, L., Wang, X., Li, X., Liu, B., Zhang, W., Cao, J., Ning, A., Huang, M., Zhong, M."In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein". Oncology Letters 12.5 (2016): 3153-3160.
Chicago
Tian, L., Wang, X., Li, X., Liu, B., Zhang, W., Cao, J., Ning, A., Huang, M., Zhong, M."In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein". Oncology Letters 12, no. 5 (2016): 3153-3160. https://doi.org/10.3892/ol.2016.5106
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