Background
Oct4, also 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. Oct4 is normally found in totipotent or pluripotent stem cells of pregastrulation embryos and is essential to maintain their self-renewal [
2]. Downregulation of Oct4 results in loss of stem cells [
3]. The Oct4 transcription factor can be considered a master regulator of maintenance and differentiation in pluripotent cells. Previous studies have indicated an involvement of Oct4 in tumorigenicity and malignancy of lung cancers [
4]. Oct4 might be a biomarker for assessing the prognosis of hepatocellular carcinoma and gastric cancer [
5,
6]. For patients with hypopharyngeal squamous cell carcinoma, Oct4 expression is an independent predictive factor [
7]. Oct4 expression has also been observed in human breast cancer stem-like cells, suggesting an involvement in self-renewal and tumorigenesis [
8]. Three isoforms of Oct4 have been identified – Oct4A, Oct4B, and Oct4B1. Oct4A is primarily localized in the nucleus, whereas Oct4B and Oct4B1 primarily reside in the cytoplasm. Currently, only Oct4A has been proven to regulate pluripotency [
9].
Transcription factors need to enter and remain in the nucleus to fulfill their functions. The Oct4 transcription factor homeodomain signature structure is important for both DNA binding and nucleocytoplasmic trafficking [
10,
11]. The importin transport system provides the machinery for nucleocytoplasmic transport. Nuclear protein transport is a complex process and aberrant expression of nuclear transport factors may result in profound deregulation of gene transcription [
12]. KPNA2 (importin α1), a member of the karyopherin (importin) family, plays a central role in nucleocytoplasmic transport [
13]. Together with importin-β, the KPNA2-bound cargo protein forms a ternary complex, which interacts with the nuclear pore complex and translocates into the nucleus, guided by a nuclear localization signal [
14]. A previous study showed that KPNA2 is mainly expressed in undifferentiated embryonic stem (ES) cells, and nuclear import of Oct4 is mediated by KPNA2 in mouse ES cells during differentiation into neurons [
15]. Oct4 and KPNA2 are reported to have a strong interaction in ES cells [
16]. In addition, KPNA2 was identified as a potential biomarker for non-small-cell lung cancer (NSCLC) by integration of the cancer cell secretome and tissue transcriptome [
17]. For lung cancer, however, very few reports have mentioned the two genes. This current study provides direct evidence for the interaction between Oct4 and KPNA2 and demonstrates that KPNA2 may contribute to Oct4 nuclear translocation in lung cancer.
Methods
Patient populations and clinical specimens
The Ethics Committee of the China Medical University approved this study. One hundred and two NSCLC samples and the corresponding normal lung tissues were obtained from the First Affiliated Hospital of China Medical University during 2004–2007. Tissues were formalin fixed and paraffin embedded. Before the operation, the patients had not received chemotherapy or radiotherapy. Histological types and differentiation degrees were categorized by the 2004 WHO standards, and TNM were classified according to the 2009 UICC TNM classification. Relevant clinical and pathological features (Table
1) were obtained from the patients’ files and/or by telephone interviews with the patient or their relatives.
Table 1
The expression of Oct4 and KPNA2 and their relationships with clinicopathological characteristics
Age (years) | | | | | | | |
<60 | 50 | 36(72.0) | 14(28.0) | 0.925 | 25(50.0) | 25(50.0) | 0.329 |
≥60 | 52 | 37(71.2) | 15(28.8) | | 21(40.4) | 31(59.6) | |
Gender | | | | | | | |
Male | 59 | 42(71.2) | 17(28.8) | 0.920 | 28(47.5) | 31(52.5) | 0.574 |
Female | 43 | 31(72.1) | 12(27.9) | | 18(41.9) | 25(58.1) | |
Smoke | | | | | | | |
Yes | 52 | 36(69.2) | 16(30.8) | 0.593 | 22(42.3) | 30(57.7) | 0.563 |
No | 50 | 37(74.0) | 13(26.0) | | 24(48.0) | 26(52.0) | |
Histology | | | | | | | |
Adenocarcinoma | 60 | 41(68.3) | 19(31.7) | 0.387 | 35(58.3) | 25(41.7) | 0.001* |
Squamous cell | 42 | 32(72.6) | 10(23.8) | | 11(26.2) | 31(73.8) | |
Carcinoma | | | | | | | |
Differentiation | | | | | | | |
Well | 38 | 34(89.5) | 4(10.5) | 0.002* | 22(57.9) | 16(42.1) | 0.045* |
Moderate-Poor | 64 | 39(60.9) | 25(39.1) | | 24(37.5) | 40(62.5) | |
TNM stage | | | | | | | |
I/II | 55 | 46(83.6) | 9(16.4) | 0.003* | 29(52.7) | 26(47.3) | 0.093 |
III/IV | 47 | 27(57.4) | 20(42.6) | | 17(36.2) | 30(63.8) | |
Angiolymphatic invasion | | | | | | | |
No | 57 | 44(77.2) | 13(22.8) | 0.156 | 25(43.9) | 32(56.1) | 0.777 |
Yes | 45 | 29(64.4) | 16(35.6) | | 21(46.7) | 24(53.3) | |
Immunohistochemistry (IHC) and scoring
The paraffin-embedded tissues were cut into 5-μm sections, placed on slides, and baked at 60°C for 120 min. The sections were de-paraffinized with xylenes and rehydrated. They were subjected to heat-induced antigen retrieval using citrate buffer (10 mM, pH 6.0) in a pressure cooker for 2 min and then cooled to room temperature for 20 min. The sections were treated with 3% hydrogen peroxide in methanol to quench the endogenous peroxidase activity, followed by incubation with normal serum to block nonspecific binding. The slides were then incubated with an anti-Oct4 antibody (1:100) (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA) and an anti-KPNA2 antibody (1:100) (Santa Cruz Biotechnology) overnight at 4°C, respectively. As a negative control for the staining procedure, the primary antibody was replaced with PBS. The second antibody was from an SP reagent kit (Zhongshan Biotechnology Company, Beijing, China). After washing, the tissue sections were treated with a biotinylated anti-mouse second antibody, followed by further incubation with streptavidin-horseradish peroxidase complex for 15 min. The sections were stained with diaminobenzidine and then counterstained with hematoxylin. The stained slides were reviewed and scored independently by two pathologists. The proportion (0: none; 1: < 25%; 2: 25–50%; 3: 51–75%; and 4: > 75%) and intensity (0, none; 1, weak; 2, intermediate; and 3, strong) scores were added to obtain a total score, which ranged from 0 to 7. Specimens were categorized into one of two groups according to their overall scores: (1) negative expression, < 4 points; (2) positive expression, 4–7 points.
Cell culture
Human lung cancer cell lines A549, LTE, 1299, and H460 were obtained from the American Type Culture Collection (Manassas, VA, USA). LK2 was obtained from the Japanese Cancer Research Resources Bank (Tokyo, Japan), SPC cells were obtained from the CCTCC (Chinese Center of Typical Culture Conserve, Wuhan, P.R. China). The cells were cultured in RPMI 1640 medium (Invitrogen, Carlsbad, CA, USA) containing 10% fetal calf serum (Invitrogen), 100 IU/ml penicillin (Sigma, St. Louis, MO, USA), and 100 μg/ml streptomycin (Sigma).
Western blot analysis
Total proteins from cell lines were extracted in lysis buffer (Thermo Fisher Scientific, Rockford, IL, USA) and quantified using the Bradford method. Each extracted protein sample (50 μg) was separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. After transferring to a polyvinylidene fluoride membrane, the membrane was incubated overnight at 4°C with the mouse monoclonal antibody against Oct4 (1:500, Santa Cruz Biotechnology), KPNA2 (1:500, Santa Cruz Biotechnology), β-actin (1:1000, Santa Cruz Biotechnology), or anti-lamin-B (1:500 Santa Cruz Biotechnology). After incubation with peroxidase-coupled anti-mouse IgG at 37°C for 2 h, the protein bands were visualized using ECL (Pierce, Rockford, IL, USA) and detected using the BioImaging Systems (UVP Inc., Upland, CA, USA). The relative amounts of protein were calculated with reference to the amount of β-actin protein.
Quantitative real-time polymerase chain reaction (PCR)
Total cellular RNA was extracted from cells using the RNeasy Mini kit from Qiagen (Hilden, Germany). Reverse transcription of 1 μg of RNA was performed using a high-capacity cDNA RT kit (Applied Biosystems, Foster City, CA, USA), following the manufacturer’s instructions. Quantitative real-time PCR was performed using a SYBR Green PCR master mix (Applied Biosystems) in a total volume of 20 μl on a 7900HT fast Real-Time PCR System (Applied Biosystems). A dissociation step was performed to generate a melting curve for confirmation of amplification specificity. β-actin was used as the reference gene. The relative levels of gene expression were represented as △Ct = Ct gene-Ct reference, and the fold change of gene expression was calculated by the 2-△△Ct method. Experiments were repeated in triplicate. The primer sequences were as follows: KPNA2 forward, 5′-CTGGGACATCAGAACAAACCAAG- 3′, KPNA2 reverse, 5′-ACACTGAGCCATCACCTGCAAT- 3′; Oct4 forward, 5′- CGCAAGCCCTCATTTCAC-3′; Oct4 reverse, 5′- CATCACCTCCACCACCTG-3′; β-actin forward, 5′-ATAGCACAGCCTGG ATAGCAACGTAC-3′, β-actin reverse, 5′-CACCTTCTACAATGAGCTGCGTGTG- 3′.
Immunofluorescence staining
Cells were placed into 96-well plain bottom plates, and fixed in 4% formaldehyde, permeabilized in 0.5% Triton X-100, and washed with PBS containing 1% of BSA (FACS buffer). After incubation with primary antibodies at 4°C overnight, the wells were washed with PBS three times. Appropriate secondary antibodies were added and incubated at 37°C for 30 min. The cells were then stained with 4′, 6-diamidino-2-phenylindole (DAPI) for 15 min. Specimens were examined using an epi-illumination fluorescence microscope BX50 (Olympus, Tokyo, Japan).
Knockdown of Oct4 and KPNA2 expression with small interfering RNA
Cells (1 × 104) were transfected with HiPerfect transfection reagent (Giagen, Germany), applying a combination of two sequence-validated, and knockdown-warranted siRNAs: KPNA2-siRNA (20 nM, each, 5′ -GCUCCUGCAUCAUGAUGAUTT-3′ and 5′-AUCAUCAUGAUGCAGGAGCTT-3′) and Oct4-siRNA (20 nM, each, 5′-CUGGGACACAGUAGAUAGATT-3′ and 5′-UCUAUCUACUGU GUCCCAGTT-3′), according to the manufacturer’s instructions (GenePharma Co., Ltd, Germany). After 96 h of treatment, the cells were split and re-transfected with siRNAs to guarantee efficient KPNA2 and Oct4 knockdown. A commercial GAPDH-siRNA served as a positive control (GenePharma). A green fluorescent protein-tagged, NCsiRNA (GenePharma) was used as an efficiency control and as a control for unspecific side effects. At 72 h after transfection, cell lysates were prepared for western blotting to determine the efficiency of gene expression ablation.
Cell proliferation assay
Cell proliferation was assayed using a Cell Counting Kit-8 solution (Dojindo, Gaithersburg, MD, USA), according to the manufacturer’s protocol. Briefly, cells were seeded at a concentration of 2 × 103 cells/100 μl/well in 96-well culture plates and treated with 10 μl/well of Cell Counting Kit-8H solution during the last 4 h of the culture. The optical density of the wells was measured at 450 nm using a microplate reader (Model450, Bio-Rad, Hercules, CA, USA).
Cells (1 × 103) were seeded into 6-cm dishes and maintained in growth medium. After 10 days, colonies were fixed with 80% methanol and stained with Giemsa (20 min.). Colonies were photographed and counted. The number of colonies with more than 50 cells was recorded.
Co-immunoprecipitation (CoIP)
Proteins were extracted with cellular lysis buffer. Equal amounts of protein were incubated with the KPNA2 specific antibody immobilized onto protein G-beads for 1 h at 4°C with gentle rotation. Beads were washed extensively with lysis buffer, boiled, and microcentrifuged. Proteins were detected with the anti-Oct4 antibody by western blotting.
Statistical analysis
SPSS version 13.0 for Windows was used for all analyses. The Chi-square test was used to compare positive staining rates between subgroups. Kaplan–Meier curves were plotted for survival analysis, and a log-rank test was performed based on the differences. The Student’s t-test was used to compare other data. A P-value of < 0.05 was considered statistically significant, and a P-value of < 0.01 was considered strongly statistically significant.
Discussion
In this study, we investigated the expression pattern and biological role of the transcription factor Oct4 and transport factor KPNA2 in 102 human NSCLC samples. Our results demonstrated that Oct4 and KPNA2 protein expression in lung cancer tissues is higher compared with corresponding normal lung tissue. We found a significant correlation between Oct4 upregulation and both differentiation and TNM stage. The expression of KPNA2 correlates with histology and differentiation. Although Oct4 and KPNA2 were expressed independently in some cases, they were more often co-localized to the same area. We also found that Oct4 and KPNA2 expressions were significantly correlated in human NSCLC tissues. This suggested that Oct4 and KPNA2 have an interaction in NSCLC. In addition, we demonstrated that Oct4 and KPNA2 upregulation correlated with a lower survival rate in NSCLC patients. This indicates that Oct4 and KPNA2 could represent novel biomarkers for distinguishing cancer from noncancerous lesions. At the same time, we found that Oct4 and KPNA2 expressions were co-positively correlated with shorter survival of NSCLC patients, compared with Oct4 and KPNA2 co-negative expression or Oct4 and KPNA2 single positive expression. Thus, combined analysis of Oct4 and KPNA2 expression in NSCLS was more informative than the analysis of either gene singly.
To validate the potential role of Oct4 and KPNA2 in lung cancer development, we employed siRNAs to knockdown Oct4 and KPNA2 expression in A549 and SPC cell lines. We found an impaired proliferation capacity and colony formation ability in both A549 and SPC cells after Oct4 or KPNA2 knockdown. These results suggest that Oct4 and KPNA2 expression were significantly correlated in lung cancer cells. High expression of these two proteins could promote the proliferation of lung cancer cells. Co-immunoprecipitation revealed that KPNA2 interacts with Oct4 in lung cancer cell lines. Moreover, knockdown of KPNA2 expression decreased the mRNA and nucleoprotein levels of Oct4. Double immunofluorescence analysis revealed that nuclear Oct4 signals were significantly reduced in the KPNA2 knockdown group.
The transcription factor Oct4 plays significant roles in maintaining pluripotency and self-renewal of embryonic stem cells and adult stem/progenitor cells anchored in a number of tissues [
18,
19]. Oct4 alone can induce pluripotency in mouse adult neural stem cells [
20]. Furthermore, Oct4 is an important determinant for the malignant potential of tumor cells and is accordingly not expressed in healthy and differentiated tissue [
21]. The Oct4 transcript can be detected in human embryonic carcinomas, testicular germ cell tumors, and seminomas [
22‐
24]. Knocking down Oct4 in tumor-initiating cells would lead to the loss of the self-renewal and proliferating capacities and result in CSC-like apoptosis of cancer cells [
25]. Our results contribute to the growing body of evidence that implicates Oct4 as a multifunctional factor involved in stem cell self-renewal and differentiation, as well as tumorigenesis and tumor progression. Recently, Oct4A was observed to contain a conserved nuclear localization signal (NLS), RKRKR, in its POU DNA binding domain [
26]. It is recognized by transport receptors that carry it from the cytoplasm to the nucleus. Tumorigenesis and tumor progression are associated with dysfunction of the nuclear transport machinery.
Karyopherin-α acts as a classical NLS receptor and mammalian cells have multiple Karyopherin-α genes that are classified into three subtypes that are differentially expressed in different tissues [
27‐
29]. A previous study indicated that KPNA2 is mainly expressed in undifferentiated ES cells [
15]. Overexpression of KPNA2 caused persistent expression of pluripotency marker genes, such as Oct4, in the absence of maintenance signals, and suppressed neural differentiation [
15]. Upregulation of KPNA2 expression has been implicated in several human cancers, including prostate cancer, esophageal squamous cell carcinoma, lung cancer, breast cancer, and infiltrative astrocytomas [
17,
30‐
34]. In breast tumor MCF7 cells, Oct4 expression was further increased by KPNA2 overexpression [
22]. In this study, we demonstrated that knocking down KPNA2 expression decreased the mRNA and nucleoprotein levels of Oct4. This indicated that KPNA2-associated Oct4 downstream signaling may contribute to the malignant phenotype of human lung cancer cells. Oct4 transcription could be influenced by gradually varying KPNA2 expression levels. KPNA2 silencing could therefore decrease the nuclear translocation of Oct4 and suppress the proliferative capacity of lung cancer cells. Thus, Oct4 may be one of the target proteins of nuclear transport receptor KPNA2 in lung cancer cells. However, reciprocal effects between KPNA2 expression and Oct4 should be addressed in future studies.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
XLL and XSJ designed the research and wrote the paper. MMS, XL, and HFL collected the cases. XLL, LLJ, MMS, and XL performed the research. XLL, HFL, and ZHL analyzed the data. ZHL and EHW edited the paper. All authors read and approved the final manuscript.