West China Journal of Stomatology ›› 2017, Vol. 35 ›› Issue (4): 373-378.doi: 10.7518/hxkq.2017.04.006

• Orginal Article • Previous Articles     Next Articles

Effects of geranylgeranyltransferaseⅠsilencing on the proliferation of tongue squamous cancer cells

Ying Wang1(), Qimin Wang2, Jinghua Li3, Jinhong Han2,4, Lili Wang3, Chen Chao5, Jianhua Zhou2, Lei Tong2, Xufei Lu2,6, Yuan Zhou1, Yixiang Liao2, Zongxuan He2, Ning Li7, Lei Cao7, Wenjun Liu8, Zhenggang Chen2,9()   

  1. 1. College of Stomatology, Weifang Medical University, Weifang 261021, China
    2. Dept. of Oral and Maxillofacial Surgery, Qingdao Municipal Hospital, Qingdao 266071, China
    3. Central Lab, Qingdao Municipal Hospital, Qingdao 266071, China
    4. Dept. of Oral and Maxillofacial Surgery, YantaiStomatological Hospital, Yantai 264008, China
    5. Dept. of Surgery, Qingdao Clinical Hospital Affiliated to Nanjing Medical University, Qingdao 266071, China
    6. Dept. of Stomatology, Pudong Hospital of Jimo City, Qingdao 266234, China
    7. Postgraduate School, Dalian Medical University, Dalian 116044, China
    8. Dept. of Otorhinolaryngology, Qingdao Municipal Hospital, Qingdao 266071, China
    9. Dept. of Oral and Maxillofacial Surgery, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China
  • Received:2016-10-11 Revised:2017-04-09 Online:2017-08-01 Published:2017-08-01
  • Supported by:
    The National Natural Science Foundation of China (81372908);Project of Qingdao Municipal Health and Family Planning Commission (2014-WJZD009, 2013-WSZD011)

Abstract:

Objective This study aims to investigate the effect of geranylgeranyltransferaseⅠ (GGTase-Ⅰ) on the proliferation and growth of tongue squamous cancer cells. Methods Three small interfering RNAs (siRNAs) were designed on the basis of the GGTase-Ⅰ sequence in GeneBank. These siRNAs were then transfected into tongue squamous cancer cells Cal-27. The mRNA and protein expression of GGTase-Ⅰ and RhoA were examined by real-time quantitative polymerase chain reaction and Western blotting, respectively. The expression of Cyclin D1 and p21 were examined by Western blotting. The proliferation and growth ability were analyzed by cell counting kit-8 assay and flow cytometry. Results The mRNA and protein expression of GGTase-Ⅰ in Cal-27 was reduced significantly after the GGTase-Ⅰ siRNAs were transfected (P<0.05). No significant difference in RhoA mRNA and protein expression was detected (P>0.05). Cyclin D1 expression decreased, whereas p21 expression increased significantly. The cell cycle was altered, and the growth-proliferative activity was inhibited (P<0.05). Conclusion GGTase-Ⅰ siRNA can inhibit the expression of GGTase-Ⅰ and the proliferative activity of tongue squamous cancer cells. GGTase-Ⅰ may be a potential target for gene therapy in tongue squamous cell cancer.

Key words: geranylgeranyltransferaseⅠ, RhoA, tongue squamous cancer, proliferation, Cyclin D1, p21

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