The American Journal of Surgery
Volume 199, Issue 4 , Pages 515-521, April 2010

Overexpression of LAPTM4B promotes growth of gallbladder carcinoma cells in vitro

  • Li Zhou, M.D.

      Affiliations

    • Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China
  • ,
  • Xiao-Dong He, M.D.

      Affiliations

    • Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China
  • ,
  • Jian-Chun Yu, M.D.

      Affiliations

    • Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China
    • Corresponding Author InformationCorresponding author: Tel.: 86-10-65296038; fax: 86-10-65296038
  • ,
  • Rou-Li Zhou, M.D.

      Affiliations

    • Department of Cell Biology, School of Basic Medical Sciences, Peking University, Beijing, China
  • ,
  • Hua Yang, Ph.D.

      Affiliations

    • Department of Cell Biology, School of Basic Medical Sciences, Peking University, Beijing, China
  • ,
  • Qiang Qu, M.D., Ph.D.

      Affiliations

    • Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China
  • ,
  • Jing-An Rui, M.D.

      Affiliations

    • Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China

Received 30 January 2009; received in revised form 16 March 2009 published online 03 December 2009.

Abstract 

Background

The overexpression of LAPTM4B-35 in gallbladder carcinoma (GBC) and its clinicopathologic and prognostic significance have been previously shown. Thus, this gene may play a role in the growth of GBC cells.

Methods

The pcDNA3-AE containing the complete open reading frame of LAPTM4B (lysosome-associated protein transmembrane-4β) and mock (pcDNA3) plasmids were transiently transfected into GBC-SD cells. Cell proliferation, cell cycle distribution, and protein expression were evaluated by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl-tetrazolium assay, flow cytometry, and Western blot, respectively.

Results

Cells transfected with pcDNA3-AE revealed accelerated proliferation, less serum dependence, and significant cell cycle progression compared with cells transfected with mock plasmid and parent cells. These phenotypes were accompanied by upregulated expression of C-myc, c-Fos, c-Jun, cyclin D1, and cyclin E and downregulated expression of P16 and P-27.

Conclusions

LAPTM4B overexpression promotes the growth of GBC cells in vitro by regulating the expression levels of some proliferation-associated proteins. Therefore, the LAPTM4B gene might be used as a novel therapeutic target of GBC.

Keywords: LAPTM4B, Transfection, Proliferation, Gallbladder carcinoma

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 This work was supported by a grant for the municipal key discipline of Beijing, China (HK100230446).

PII: S0002-9610(09)00509-1

doi:10.1016/j.amjsurg.2009.03.031

The American Journal of Surgery
Volume 199, Issue 4 , Pages 515-521, April 2010