Abstract

BackgroundOct4 is a major transcription factor related to stem cell self-renewal and differentiation. To fulfill its functions, it must be able to enter the nucleus and remain there to affect transcription. KPNA2, a member of the karyopherin family, plays a central role in nucleocytoplasmic transport. The objective of the current study was to examine the association between Oct4 and KPNA2 expression levels with regard to both the clinicopathological characteristics and prognoses of patients with non-small-cell lung cancer (NSCLC).MethodsImmunohistochemistry was used to detect the expression profile of Oct4 and KPNA2 in NSCLC tissues and adjacent noncancerous lung tissues. Real-time polymerase chain reaction and western blotting were used to detect the mRNA and protein expression profiles of Oct4 and KPNA2 in lung cancer cell lines. Small interfering RNAs were used to deplete Oct4 and KPNA2 expressions. Double immunofluorescence was used to detect Oct4 expression in KPNA2 knockdown cells. Co-immunoprecipitation was used to detect the interaction of Oct4 and KPNA2.ResultsOct4 was overexpressed in 29 of 102 (28.4%) human lung cancer samples and correlated with differentiation (P = 0.002) and TNM stage (P = 0.003). KPNA2 was overexpressed in 56 of 102 (54.9%) human lung cancer samples and correlated with histology (P = 0.001) and differentiation (P = 0.045). Importantly, Oct4 and KPNA2 expression levels correlated significantly (P < 0.01). Expression of Oct4 and KPNA2 was associated with short overall survival. In addition, depleting Oct4 and KPNA2 expression using small interfering RNAs inhibited proliferation in lung cancer cell lines. Real-time polymerase chain reaction and western blotting analysis indicated that reduction of KPNA2 expression significantly reduced mRNA and nucleoprotein levels of Oct4. Double immunofluorescence analysis revealed that nuclear Oct4 signals were reduced significantly in KPNA2 knockdown cells. Co-immunoprecipitation experiments revealed that KPNA2 interacts with Oct4 in lung cancer cell lines.ConclusionOct4 and KPNA2 play an important role in NSCLC progression. Oct4 nuclear localization may be mediated by its interaction with KPNA2.

Highlights

  • Oct4 is a major transcription factor related to stem cell self-renewal and differentiation

  • Expression levels of Oct4 and KPNA2 were analyzed by western blotting in a panel of lung cancer cell lines (A)

  • Overexpression of Oct4 and KPNA2 in non-small-cell lung cancer (NSCLC) tissues We investigated Oct4 and KPNA2 protein expression in 102 human NSCLC cancerous and precancerous tissue samples by IHC

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Summary

Introduction

Oct is a major transcription factor related to stem cell self-renewal and differentiation. The objective of the current study was to examine the association between Oct and KPNA2 expression levels with regard to both the clinicopathological characteristics and prognoses of patients with non-small-cell lung cancer (NSCLC). Known as POU5F1 (POU domain, class 5, transcription factor 1), is encoded by the POU5F1 gene in humans [1]. It is a homeodomain transcription factor of the POU family. Oct is normally found in totipotent or pluripotent stem cells of pregastrulation embryos and is essential to maintain their self-renewal [2]. The Oct transcription factor can be considered a master regulator of primarily reside in the cytoplasm. Only Oct4A has been proven to regulate pluripotency [9]

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