Literature DB >> 27352346

Adenovirus siMDM2 and NDRG2 Gene Therapy Inhibits Cell Proliferation and Induces Apoptosis of Squamous Cell Carcinoma.

Shouzhong Wang1,2, Nan Chen2, Na Dong1, Leihong Lu1, Liqian Liu1, Li Zhang3.   

Abstract

Squamous cell carcinoma (SCC) is one of the most common skin cancers. In the present study, we explored the effects of depletion of murine double minute gene 2 (MDM2) together with overexpression of N-myc downstream-regulated gene 2 (NDRG2) on cutaneous SCC. In order to achieve high efficiency of gene knockdown and overexpression in SCC-13 cells, recombinant adenovirus carrying siMDM2 and NDRG2 expression construct was produced. We found Ad-siMDM2, Ad-NDRG2, and Ad-siMDM2-NDRG2 infections inhibit the growth of SCC-13 cells in vitro, and Ad-siMDM2-NDRG2 infection has the highest inhibitory effect. Subcutaneous injections of Ad-siMDM2, Ad-NDRG2, and Ad-siMDM2-NDRG2 into SCC-13 xenograft nude mice resulted in the reduction of tumor volume. Moreover, we found that apoptosis protein caspase 3 was up-regulated in the Ad-siMDM2-, Ad-NDRG2-, and Ad-siMDM2-NDRG2-treated groups. Our data indicate that the adenovirus-mediated MDM2 silencing and NDRG2 overexpression can synergistically inhibit local cancer cell proliferation, induce apoptosis, and further prevent metastases of SCC. Our study provides a promising method that can be further developed as a new therapeutic approach against SCC.

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Keywords:  Gene silencing; Gene therapy; Murine double minute 2; N-myc downstream-regulated gene 2; Squamous cell carcinoma

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Year:  2015        PMID: 27352346     DOI: 10.1007/s12013-015-0691-8

Source DB:  PubMed          Journal:  Cell Biochem Biophys        ISSN: 1085-9195            Impact factor:   2.194


  2 in total

Review 1.  N-myc Downstream-Regulated Gene 2 (NDRG2) Function as a Positive Regulator of Apoptosis: A New Insight into NDRG2 as a Tumor Suppressor.

Authors:  Gayeon Kim; Seyeon Lim; Kwang Dong Kim
Journal:  Cells       Date:  2021-10-04       Impact factor: 6.600

2.  NDRG2 contributes to cisplatin sensitivity through modulation of BAK-to-Mcl-1 ratio.

Authors:  Soojong Park; Sang-Seok Oh; Ki Won Lee; Yeon-Kyeong Lee; Nae Yu Kim; Joo Heon Kim; Jiyun Yoo; Kwang Dong Kim
Journal:  Cell Death Dis       Date:  2018-01-18       Impact factor: 8.469

  2 in total

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