Role of the stem cell-associated intermediate filament nestin in malignant proliferation of non-small cell lung cancer

PLoS One. 2014 Feb 3;9(2):e85584. doi: 10.1371/journal.pone.0085584. eCollection 2014.

Abstract

Background: Nestin is associated with neoplastic transformation, but the mechanisms by which nestin contributes to invasion and malignancy of lung cancer remain unknown. Considering that proliferation is necessary for malignant behavior, we investigated the mechanism of nestin action in association with the proliferative properties of non-small cell lung cancer (NSCLC).

Methods: Nestin expression was examined in NSCLC specimens and cell lines. Associations with clinicopathological features, including prognosis and proliferative markers, were evaluated. Effects of nestin knockdown on proliferation and the signaling pathways involved were further investigated.

Results: Nestin was expressed in most cancer specimens and all the tumor cell lines analyzed. High nestin expression in malignant tissue was associated with high Ki-67 or PCNA levels and poor patient outcomes. Conversely, knockdown of nestin expression led to significant inhibition of tumor cell proliferation, decreased colony forming ability, and cell cycle G1 arrest. Furthermore, nestin knockdown resulted in inhibition of Akt and GSK3β activation.

Conclusions: Our data demonstrate that nestin expression in NSCLC cells is associated with poor prognosis of patients and tumor cell proliferation pathway. Downregulation of nestin efficiently inhibited lung cancer cell proliferation, which might be through affecting cell cycle arrest and Akt-GSK3β-Rb signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / metabolism*
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Cell Line, Tumor
  • Cell Proliferation*
  • Female
  • G1 Phase Cell Cycle Checkpoints / genetics
  • Gene Expression Regulation, Neoplastic
  • Glycogen Synthase Kinase 3 / metabolism
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Ki-67 Antigen / metabolism
  • Lung Neoplasms / genetics
  • Lung Neoplasms / metabolism*
  • Lung Neoplasms / pathology
  • Male
  • Microscopy, Fluorescence
  • Middle Aged
  • Neoplastic Stem Cells / metabolism*
  • Neoplastic Stem Cells / pathology
  • Nestin / genetics
  • Nestin / metabolism*
  • Prognosis
  • Proliferating Cell Nuclear Antigen / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • RNA Interference
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Ki-67 Antigen
  • Nestin
  • Proliferating Cell Nuclear Antigen
  • Proto-Oncogene Proteins c-akt
  • Glycogen Synthase Kinase 3

Grants and funding

This study was supported by grants from the National Basic Research Program of China (No. 2009CB522100 and 2010CB945400), the National Natural Science Foundation of China (No. 30971675, 30900729, and 31171398), and the Key Scientific and Technological Projects of Guangdong Province (No. 2007A032100003). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.